BREAK-OUT SESSIONS at a GLANCE THURSDAY, 24 JULY, Afternoon Sessions
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§4-71-6.5 LIST of CONDITIONALLY APPROVED ANIMALS November
§4-71-6.5 LIST OF CONDITIONALLY APPROVED ANIMALS November 28, 2006 SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Plesiopora FAMILY Tubificidae Tubifex (all species in genus) worm, tubifex PHYLUM Arthropoda CLASS Crustacea ORDER Anostraca FAMILY Artemiidae Artemia (all species in genus) shrimp, brine ORDER Cladocera FAMILY Daphnidae Daphnia (all species in genus) flea, water ORDER Decapoda FAMILY Atelecyclidae Erimacrus isenbeckii crab, horsehair FAMILY Cancridae Cancer antennarius crab, California rock Cancer anthonyi crab, yellowstone Cancer borealis crab, Jonah Cancer magister crab, dungeness Cancer productus crab, rock (red) FAMILY Geryonidae Geryon affinis crab, golden FAMILY Lithodidae Paralithodes camtschatica crab, Alaskan king FAMILY Majidae Chionocetes bairdi crab, snow Chionocetes opilio crab, snow 1 CONDITIONAL ANIMAL LIST §4-71-6.5 SCIENTIFIC NAME COMMON NAME Chionocetes tanneri crab, snow FAMILY Nephropidae Homarus (all species in genus) lobster, true FAMILY Palaemonidae Macrobrachium lar shrimp, freshwater Macrobrachium rosenbergi prawn, giant long-legged FAMILY Palinuridae Jasus (all species in genus) crayfish, saltwater; lobster Panulirus argus lobster, Atlantic spiny Panulirus longipes femoristriga crayfish, saltwater Panulirus pencillatus lobster, spiny FAMILY Portunidae Callinectes sapidus crab, blue Scylla serrata crab, Samoan; serrate, swimming FAMILY Raninidae Ranina ranina crab, spanner; red frog, Hawaiian CLASS Insecta ORDER Coleoptera FAMILY Tenebrionidae Tenebrio molitor mealworm, -
Behaviour: an Important Diagnostic Tool for Lake Malawi Cichlids PDF
FISH and FISHERIES, 2002, 3, 213^224 Behaviour: an important diagnostic tool for Lake Malawi cichlids Jay R Stau¡er Jr1, Kenneth R McKaye2 & Ad F Konings3 1School of Forest Resources, Pennsylvania State University,University Park, Pennsylvania, PA16802, USA; 2Appalachian Laboratory,UMCES,301Braddock Road, Frostburg, Maryland, MD 21532, USA; 3Cichlid Press, PO Box13608, El Paso,Texas, T X 79913, USA Abstract Correspondence: Historically,the cichlid ¢shes of Lake Malawi, which probably represent one of the best Jay R. Stau¡er Jr, examples of rapid radiation of vertebrates, have been diagnosed with morphological School of Forest Resources, and genetic data. Many of the populations once thought to be conspeci¢c have been Pennsylvania State hypothesized to be separate species based on behavioural data. The use of behavioural University, data, as expressed in mate choice based on colour patterns or bower shapes, has been University Park, successfully used to diagnose both rock-dwelling and sand-dwelling cichlid species. Pennsylvania, PA Additionally,a combination of bower shapes and courtship patterns have been used as 16802, USA Tel.: þ1 814 863 0645 synapomorphies to diagnose genera within the Lake Malawi cichlid £ock. It is con- Fax: þ18148653725 cluded that taxonomists need to include behavioural data with morphological and E-mail:[email protected] genetic databases to diagnose species and to determine the phylogenetic relationships withinthis diverse assemblage of ¢shes. Received 5 Dec 2001 Accepted10Jun 2002 Keywords allopatry,behaviour, Cichlidae, -
Evidence of Hidden Diversity and Taxonomic Conflicts in Five Stream Fishes from the Eastern Zimbabwe Highlands Freshwater Ecoregion
A peer-reviewed open-access journal ZooKeys 768: 69–95Evidence (2018) of hidden diversity and taxonomic conflicts in five stream fishes... 69 doi: 10.3897/zookeys.768.21944 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Evidence of hidden diversity and taxonomic conflicts in five stream fishes from the Eastern Zimbabwe Highlands freshwater ecoregion Albert Chakona1,2, Wilbert T. Kadye2, Taurai Bere3, Daniel N. Mazungula1,2, Emmanuel Vreven4,5 1 South African Institute for Aquatic Biodiversity, Private Bag 1015, Grahamstown, South Africa, 6140 2 Department of Ichthyology and Fisheries Science, Rhodes University, P.O. Box 94, Grahamstown, South Africa, 6140 3 School of Wildlife, Ecology and Conservation, Chinhoyi University of Technology, P. Bag 7724, Chinhoyi, Zimbabwe 4 Royal Museum for Central Africa, Section of Vertebrates, Ichthyology, Leuvensesteenweg 13, 3080, Tervuren, Belgium 5 KU Leuven, Department of Biology, Laboratory of Biodiversity and Evolutio- nary Genomics, Deberiotstraat 32, 3000 Leuven, Belgium Corresponding author: Albert Chakona ([email protected]) Academic editor: N. Bogutskaya | Received 30 October 2018 | Accepted 25 April 2018 | Published 19 June 2018 http://zoobank.org/9621930C-8C43-40D0-8554-684035E99FAA Citation: Chakona A, Kadye WT, Bere T, Mazungula DN, Vreven E (2018) Evidence of hidden diversity and taxonomic conflicts in five stream fishes from the Eastern Zimbabwe Highlands freshwater ecoregion. ZooKeys 768: 69–95. https://doi.org/10.3897/zookeys.768.21944 Abstract -
A Systematic Revision of the South American Freshwater Stingrays (Chondrichthyes: Potamotrygonidae) (Batoidei, Myliobatiformes, Phylogeny, Biogeography)
W&M ScholarWorks Dissertations, Theses, and Masters Projects Theses, Dissertations, & Master Projects 1985 A systematic revision of the South American freshwater stingrays (chondrichthyes: potamotrygonidae) (batoidei, myliobatiformes, phylogeny, biogeography) Ricardo de Souza Rosa College of William and Mary - Virginia Institute of Marine Science Follow this and additional works at: https://scholarworks.wm.edu/etd Part of the Fresh Water Studies Commons, Oceanography Commons, and the Zoology Commons Recommended Citation Rosa, Ricardo de Souza, "A systematic revision of the South American freshwater stingrays (chondrichthyes: potamotrygonidae) (batoidei, myliobatiformes, phylogeny, biogeography)" (1985). Dissertations, Theses, and Masters Projects. Paper 1539616831. https://dx.doi.org/doi:10.25773/v5-6ts0-6v68 This Dissertation is brought to you for free and open access by the Theses, Dissertations, & Master Projects at W&M ScholarWorks. It has been accepted for inclusion in Dissertations, Theses, and Masters Projects by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. INFORMATION TO USERS This reproduction was made from a copy of a document sent to us for microfilming. While the most advanced technology has been used to photograph and reproduce this document, the quality of the reproduction is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help clarify markings or notations which may appear on this reproduction. 1.The sign or “target” for pages apparently lacking from the document photographed is “Missing Pagefs)”. If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting through an image and duplicating adjacent pages to assure complete continuity. -
AC29 Doc. 35 A4
Extract from Eschmeyer, W. N., R. Fricke, and R. van der Laan (eds). CATALOG OF FISHES: GENERA, SPECIES, REFERENCES. Electronic version accessed 12 May 2017. AC29 Doc. 35 Annex / Annexe / Anexo 1 (English only / Seulement en anglais / Únicamente en inglés) Taxonomic Checklist of Fish taxa included in the Appendices at the 17th meeting of the Conference of the Parties (Johannesburg, 2016) Species information extracted from Eschmeyer, W.N., R. Fricke, and R. van der Laan (eds.) CATALOG OF FISHES: GENERA, SPECIES, REFERENCES. (http://researcharchive.calacademy.org/research/ichthyology/catal og/fishcatmain.asp). Online version of 28 April 2017 [This version was edited by Bill Eschmeyer.] accessed 12 May 2017 Copyright © W.N. Eschmeyer and California Academy of Sciences. All Rights reserved. Additional comments included by the Nomenclature Specialist of the CITES Animals Committee Reproduction for commercial purposes prohibited. Contents of this extract, prepared for AC29 by the Nomenclature Specialist for Fauna: Class Elasmobranchii Order Carcharhiniformes Family Carcharhinidae Genus Carcharias Species Carcharias falciformis (Bibron 1839) Page 3 Order Lamniformes Family Alopiidae Genus Alopias Rafinesque 1810 Page 6 Alopias pelagicus Nakamura 1935 Alopias superciliosus Lowe 1841 Alopias vulpinus (Bonnaterre 1788) Order Myliobatiformes Family Myliobatidae Genus Mobula Rafinesque 1810 Page 11 Mobula eregoodootenkee (Bleeker 1859) Mobula hypostoma (Bancroft 1831) AC29 Doc. 35; Annex / Annexe / Anexo 4 – p. 1 Extract from Eschmeyer, W. N., R. Fricke, and R. van der Laan (eds). CATALOG OF FISHES: GENERA, SPECIES, REFERENCES. Electronic version accessed 12 May 2017. Mobula japanica (Müller & Henle 1841) Mobula kuhlii (Valenciennes, in Müller & Henle 1841) Mobula mobular (Bonnaterre 1788) Mobula munkiana Notarbartolo-di-Sciara 1987 Mobula rochebrunei (Vaillant 1879) Mobula tarapacana (Philippi 1892) Mobula thurstoni (Lloyd 1908) Family Potamotrygonidae Page 21 Genus Paratrygon Duméril 1865 Paratrygon aiereba (Müller & Henle 1841). -
Cop17 Doc. 87
Original language: English CoP17 Doc. 87 CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ____________________ Seventeenth meeting of the Conference of the Parties Johannesburg (South Africa), 24 September - 5 October 2016 Species specific matters Maintenance of the Appendices FRESHWATER STINGRAYS (POTAMOTRYGONIDAE SPP.) 1. This document has been submitted by the Animals Committee.* Background 2. At its 16th meeting (CoP16, Bangkok, 2013), the Conference of the Parties adopted the following interrelated decisions on freshwater stingrays: Directed to the Secretariat 16.130 The Secretariat shall issue a Notification requesting the range States of freshwater stingrays (Family Potamotrygonidae) to report on the conservation status and management of, and domestic and international trade in the species. Directed to the Animals Committee 16.131 The Animals Committee shall establish a working group comprising the range States of freshwater stingrays in order to evaluate and duly prioritize the species for inclusion in CITES Appendix II. 16.132 The Animals Committee shall consider all information submitted on freshwater stingrays in response to the request made under Decision 16.131 above, and shall: a) identify species of priority concern, including those species that meet the criteria for inclusion in Appendix II of the Convention; b) provide specific recommendations to the range States of freshwater stingrays; and c) submit a report at the 17th meeting of the Conference of the Parties on the progress made by the working group, and its recommendations and conclusions. * The geographical designations employed in this document do not imply the expression of any opinion whatsoever on the part of the CITES Secretariat (or the United Nations Environment Programme) concerning the legal status of any country, territory, or area, or concerning the delimitation of its frontiers or boundaries. -
Fish, Various Invertebrates
Zambezi Basin Wetlands Volume II : Chapters 7 - 11 - Contents i Back to links page CONTENTS VOLUME II Technical Reviews Page CHAPTER 7 : FRESHWATER FISHES .............................. 393 7.1 Introduction .................................................................... 393 7.2 The origin and zoogeography of Zambezian fishes ....... 393 7.3 Ichthyological regions of the Zambezi .......................... 404 7.4 Threats to biodiversity ................................................... 416 7.5 Wetlands of special interest .......................................... 432 7.6 Conservation and future directions ............................... 440 7.7 References ..................................................................... 443 TABLE 7.2: The fishes of the Zambezi River system .............. 449 APPENDIX 7.1 : Zambezi Delta Survey .................................. 461 CHAPTER 8 : FRESHWATER MOLLUSCS ................... 487 8.1 Introduction ................................................................. 487 8.2 Literature review ......................................................... 488 8.3 The Zambezi River basin ............................................ 489 8.4 The Molluscan fauna .................................................. 491 8.5 Biogeography ............................................................... 508 8.6 Biomphalaria, Bulinis and Schistosomiasis ................ 515 8.7 Conservation ................................................................ 516 8.8 Further investigations ................................................. -
The African Butterfly Peacock Aulonocara Jacobfreibergi “Eureka Red” by John Moyles
The African Butterfly Peacock Aulonocara jacobfreibergi “Eureka Red” By John Moyles Aulonocara jacobfreibergi (Johnson, 1974) is also called the African butterfly peacock and the fairy peacock. They are endemic to Malawi and are found throughout the lake of the same name. There are several geographical variants of the Aulonocara species in the hobby, including Eureka, Mamela, Otter Point, Hongi Island, Cape Kaiser, Lemon Jake, among others. These should never be housed together as they will readily cross-breed. Only one geographical race should be kept in the same aquarium. Description Males of this species differ from most other Peacocks in their broad, wide white dorsal and caudal fin margins. Females are easily confused with other peacock females, because they are grayish-brown in color with vertical banding on the body and have rounded anal and dorsal fins. Butterfly peacocks are further distinguished from other Peacocks by their large size. They can grow to lengths of up to 8 or 9 inches, but often can breed at half that size. Another distinguishing characteristic of the Butterfly Peacock is its moderate to deeply forked tail fin, which gives it the appearance of a swallow's tail. The “Eureka” variant is an aquarium strain that was developed by line breeding specimens from Otter Point, Malawi. The males have blue throughout head, body and fins. Lower half of the head is blue and the upper part of the dorsal region is orange/red. Anal fin may show red. Dorsal fin has the trademark white/light blue blaze. Diet Butterfly peacocks are specialized feeders. In the wild they mostly consume zooplankton (insect larvae and crustaceans) in the wild. -
ECOLOGY of NORTH AMERICAN FRESHWATER FISHES
ECOLOGY of NORTH AMERICAN FRESHWATER FISHES Tables STEPHEN T. ROSS University of California Press Berkeley Los Angeles London © 2013 by The Regents of the University of California ISBN 978-0-520-24945-5 uucp-ross-book-color.indbcp-ross-book-color.indb 1 44/5/13/5/13 88:34:34 AAMM uucp-ross-book-color.indbcp-ross-book-color.indb 2 44/5/13/5/13 88:34:34 AAMM TABLE 1.1 Families Composing 95% of North American Freshwater Fish Species Ranked by the Number of Native Species Number Cumulative Family of species percent Cyprinidae 297 28 Percidae 186 45 Catostomidae 71 51 Poeciliidae 69 58 Ictaluridae 46 62 Goodeidae 45 66 Atherinopsidae 39 70 Salmonidae 38 74 Cyprinodontidae 35 77 Fundulidae 34 80 Centrarchidae 31 83 Cottidae 30 86 Petromyzontidae 21 88 Cichlidae 16 89 Clupeidae 10 90 Eleotridae 10 91 Acipenseridae 8 92 Osmeridae 6 92 Elassomatidae 6 93 Gobiidae 6 93 Amblyopsidae 6 94 Pimelodidae 6 94 Gasterosteidae 5 95 source: Compiled primarily from Mayden (1992), Nelson et al. (2004), and Miller and Norris (2005). uucp-ross-book-color.indbcp-ross-book-color.indb 3 44/5/13/5/13 88:34:34 AAMM TABLE 3.1 Biogeographic Relationships of Species from a Sample of Fishes from the Ouachita River, Arkansas, at the Confl uence with the Little Missouri River (Ross, pers. observ.) Origin/ Pre- Pleistocene Taxa distribution Source Highland Stoneroller, Campostoma spadiceum 2 Mayden 1987a; Blum et al. 2008; Cashner et al. 2010 Blacktail Shiner, Cyprinella venusta 3 Mayden 1987a Steelcolor Shiner, Cyprinella whipplei 1 Mayden 1987a Redfi n Shiner, Lythrurus umbratilis 4 Mayden 1987a Bigeye Shiner, Notropis boops 1 Wiley and Mayden 1985; Mayden 1987a Bullhead Minnow, Pimephales vigilax 4 Mayden 1987a Mountain Madtom, Noturus eleutherus 2a Mayden 1985, 1987a Creole Darter, Etheostoma collettei 2a Mayden 1985 Orangebelly Darter, Etheostoma radiosum 2a Page 1983; Mayden 1985, 1987a Speckled Darter, Etheostoma stigmaeum 3 Page 1983; Simon 1997 Redspot Darter, Etheostoma artesiae 3 Mayden 1985; Piller et al. -
Induced Spawning and Reproductive Variables of the Catfish Lophiosilurus Alexandri Steindachner, 1876 (Siluriformes: Pseudopimelodidae)
Neotropical Ichthyology, 11(3):607-614, 2013 Copyright © 2013 Sociedade Brasileira de Ictiologia Induced spawning and reproductive variables of the catfish Lophiosilurus alexandri Steindachner, 1876 (Siluriformes: Pseudopimelodidae) Hélio Batista dos Santos1, Edson Vieira Sampaio2, Fábio Pereira Arantes3 and Yoshimi Sato2 Lophiosilurus alexandri is an endemic fish from the São Francisco River basin, Brazil. The aim of this study was to induce L. alexandri to spawn and to obtain data on several reproductive variables for this species. For induced spawning, adults were submitted to Cyprinus carpio pituitary homogenate (CPH). Nine of the 12 females (75%) responded positively to the treatment. The stripping of oocytes was performed 8.4 h after the second dose of CPH with the water temperature maintained at 26ºC. The number of stripped oocytes per gram of ova was 74 ± 5 oocytes g-1, and the mean oocyte diameter was 3.1 ± 0.2 and 3.6 ± 0.2 mm, before and after hydration, respectively. The oocytes were opaque, yellowish, demersal, highly adhesive, and covered by a gelatinous coat. The total fecundity was 4,534 ± 671 oocytes, and the fertilization rate was 59%. The initial and final fertilities were 2,631 ± 740 and 1,542 ± 416 embryos, respectively. Larval hatching occurred up to 56 h after fertilization, and the larvae had a total length of 8.4 ± 0.1 mm. This work provides important biological information for L. alexandri that can be used for management and conservation of this species. Lophiosilurus alexandri é um peixe endêmico da bacia do rio São Francisco, Brasil. O objetivo do trabalho foi induzir L. -
Otolith Description and Age-And-Growth of Kurtus Gulliveri from Northern Australia
Journal of Fish Biology (2004) 65, 354–362 doi:10.1111/j.1095-8649.2004.00454.x,availableonlineathttp://www.blackwell-synergy.com Otolith description and age-and-growth of Kurtus gulliveri from northern Australia T. M. BERRA* AND D. D. ADAY Department of Evolution, Ecology and Organismal Biology, The Ohio State University, Mansfield, OH 44906, U.S.A. (Received 15 July 2003, Accepted 22 April 2004) The sagitta of Kurtus gulliveri was ovate, moderately thick with the following attributes: lateral surface convex, mesial surface flat; dorsal margin sinuate, posterior margin rounded ventrally, ventral margin rounded and irregular; sulcus divided into ostium and cauda by constriction of dorsal and ventral margins, heterosulcoid, colliculum heteromorph; dorsal depression large and distinct, ventral groove close to margin in larger otoliths; rostrum broad and antirostrum small, separated by wide, shallow excisural notch. Otolith size was moderate, average 4Á6% standard length (LS), typical for a perciform. Annuli on 78 whole sagittae were read, and 15% of these were transversely sectioned for verification of the annuli. Males ranged from 94 to 235 mm LS and females from 95 to 284 mm LS. There was little difference in size distribution of the sample between the sexes, perhaps due to a 6 month spawning season over which young were continually added to the population. Some sexual dimorphism was noted, however, as age 2 year females were significantly larger than males of the same age. The largest fish aged was a 284 mm LS, 3 year-old female, and the oldest age reached was 4 years by two males. It appears likely that most spawning females are 2 years old, but some larger 1 year old fish may attain sexual maturity. -
Multilocus Molecular Phylogeny of the Suckermouth Armored Catfishes
Molecular Phylogenetics and Evolution xxx (2014) xxx–xxx Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Multilocus molecular phylogeny of the suckermouth armored catfishes (Siluriformes: Loricariidae) with a focus on subfamily Hypostominae ⇑ Nathan K. Lujan a,b, , Jonathan W. Armbruster c, Nathan R. Lovejoy d, Hernán López-Fernández a,b a Department of Natural History, Royal Ontario Museum, 100 Queen’s Park, Toronto, Ontario M5S 2C6, Canada b Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, Ontario M5S 3B2, Canada c Department of Biological Sciences, Auburn University, Auburn, AL 36849, USA d Department of Biological Sciences, University of Toronto Scarborough, Toronto, Ontario M1C 1A4, Canada article info abstract Article history: The Neotropical catfish family Loricariidae is the fifth most species-rich vertebrate family on Earth, with Received 4 July 2014 over 800 valid species. The Hypostominae is its most species-rich, geographically widespread, and eco- Revised 15 August 2014 morphologically diverse subfamily. Here, we provide a comprehensive molecular phylogenetic reap- Accepted 20 August 2014 praisal of genus-level relationships in the Hypostominae based on our sequencing and analysis of two Available online xxxx mitochondrial and three nuclear loci (4293 bp total). Our most striking large-scale systematic discovery was that the tribe Hypostomini, which has traditionally been recognized as sister to tribe Ancistrini based Keywords: on morphological data, was nested within Ancistrini. This required recognition of seven additional tribe- Neotropics level clades: the Chaetostoma Clade, the Pseudancistrus Clade, the Lithoxus Clade, the ‘Pseudancistrus’ Guiana Shield Andes Mountains Clade, the Acanthicus Clade, the Hemiancistrus Clade, and the Peckoltia Clade.