Module De Formation Poisson D'eau Douce
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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, -
Taxonomy and Biochemical Genetics of Some African Freshwater Fish Species
_________________________________________________________________________Swansea University E-Theses Taxonomy and biochemical genetics of some African freshwater fish species. Abban, Edward Kofi How to cite: _________________________________________________________________________ Abban, Edward Kofi (1988) Taxonomy and biochemical genetics of some African freshwater fish species.. thesis, Swansea University. http://cronfa.swan.ac.uk/Record/cronfa43062 Use policy: _________________________________________________________________________ This item is brought to you by Swansea University. Any person downloading material is agreeing to abide by the terms of the repository licence: copies of full text items may be used or reproduced in any format or medium, without prior permission for personal research or study, educational or non-commercial purposes only. The copyright for any work remains with the original author unless otherwise specified. The full-text must not be sold in any format or medium without the formal permission of the copyright holder. Permission for multiple reproductions should be obtained from the original author. Authors are personally responsible for adhering to copyright and publisher restrictions when uploading content to the repository. Please link to the metadata record in the Swansea University repository, Cronfa (link given in the citation reference above.) http://www.swansea.ac.uk/library/researchsupport/ris-support/ TAXONOMY AND BIOCHEMICAL GENETICS OF SOME AFRICAN FRESHWATER FISH SPECIES. BY EDWARD KOFI ABBAN A Thesis submitted for the degree of Ph.D. UNIVERSITY OF WALES. 1988 ProQuest Number: 10821454 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. -
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 -
Phylogenetic Relationships Within the Speciose Family Characidae
Oliveira et al. BMC Evolutionary Biology 2011, 11:275 http://www.biomedcentral.com/1471-2148/11/275 RESEARCH ARTICLE Open Access Phylogenetic relationships within the speciose family Characidae (Teleostei: Ostariophysi: Characiformes) based on multilocus analysis and extensive ingroup sampling Claudio Oliveira1*, Gleisy S Avelino1, Kelly T Abe1, Tatiane C Mariguela1, Ricardo C Benine1, Guillermo Ortí2, Richard P Vari3 and Ricardo M Corrêa e Castro4 Abstract Background: With nearly 1,100 species, the fish family Characidae represents more than half of the species of Characiformes, and is a key component of Neotropical freshwater ecosystems. The composition, phylogeny, and classification of Characidae is currently uncertain, despite significant efforts based on analysis of morphological and molecular data. No consensus about the monophyly of this group or its position within the order Characiformes has been reached, challenged by the fact that many key studies to date have non-overlapping taxonomic representation and focus only on subsets of this diversity. Results: In the present study we propose a new definition of the family Characidae and a hypothesis of relationships for the Characiformes based on phylogenetic analysis of DNA sequences of two mitochondrial and three nuclear genes (4,680 base pairs). The sequences were obtained from 211 samples representing 166 genera distributed among all 18 recognized families in the order Characiformes, all 14 recognized subfamilies in the Characidae, plus 56 of the genera so far considered incertae sedis in the Characidae. The phylogeny obtained is robust, with most lineages significantly supported by posterior probabilities in Bayesian analysis, and high bootstrap values from maximum likelihood and parsimony analyses. -
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 ................................................. -
BREAK-OUT SESSIONS at a GLANCE THURSDAY, 24 JULY, Afternoon Sessions
2008 Joint Meeting (JMIH), Montreal, Canada BREAK-OUT SESSIONS AT A GLANCE THURSDAY, 24 JULY, Afternoon Sessions ROOM Salon Drummond West & Center Salons A&B Salons 6&7 SESSION/ Fish Ecology I Herp Behavior Fish Morphology & Histology I SYMPOSIUM MODERATOR J Knouft M Whiting M Dean 1:30 PM M Whiting M Dean Can She-male Flat Lizards (Platysaurus broadleyi) use Micro-mechanics and material properties of the Multiple Signals to Deceive Male Rivals? tessellated skeleton of cartilaginous fishes 1:45 PM J Webb M Paulissen K Conway - GDM The interopercular-preopercular articulation: a novel Is prey detection mediated by the widened lateral line Variation In Spatial Learning Within And Between Two feature suggesting a close relationship between canal system in the Lake Malawi cichlid, Aulonocara Species Of North American Skinks Psilorhynchus and labeonin cyprinids (Ostariophysi: hansbaenchi? Cypriniformes) 2:00 PM I Dolinsek M Venesky D Adriaens Homing And Straying Following Experimental Effects of Batrachochytrium dendrobatidis infections on Biting for Blood: A Novel Jaw Mechanism in Translocation Of PIT Tagged Fishes larval foraging performance Haematophagous Candirú Catfish (Vandellia sp.) 2:15 PM Z Benzaken K Summers J Bagley - GDM Taxonomy, population genetics, and body shape The tale of the two shoals: How individual experience A Key Ecological Trait Drives the Evolution of Monogamy variation of Alabama spotted bass Micropterus influences shoal behaviour in a Peruvian Poison Frog punctulatus henshalli 2:30 PM M Pyron K Parris L Chapman -
DNA Barcoding Discriminates Freshwater Fishes from Southeastern Nigeria and Provides River System-Level Phylogeographic Resoluti
Mitochondrial DNA, 2011; Early Online: 1–9 DNA barcoding discriminates freshwater fishes from southeastern Nigeria and provides river system-level phylogeographic resolution within some species CHRISTOPHER D. NWANIa, SVEN BECKERb, HEATHER E. BRAIDb, EMMANUEL F. UDEc, OKECHUKWU I. OKOGWUa, & ROBERT HANNERb aDepartment of Applied Biology, Ebonyi State University, Abakaliki, Nigeria, bDepartment of Integrative Biology, Biodiversity Institute of Ontario, University of Guelph, Guelph, Ontario, Canada, and cFisheries and Aquaculture, Ebonyi State University, Abakaliki, Nigeria (Received 17 August 2010; revised 28 October 2010; accepted 28 October 2010) Abstract Background and aims: Fishes are the main animal protein source for human beings and play a vital role in aquatic ecosystems and food webs. Fish identification can be challenging, especially in the tropics (due to high diversity), and this is particularly true for larval forms or fragmentary remains. DNA barcoding, which uses the 50 region of the mitochondrial cytochrome c oxidase subunit I (cox1) as a target gene, is an efficient method for standardized species-level identification for biodiversity assessment and conservation, pending the establishment of reference sequence libraries. Materials and methods: In this study, fishes were collected from three rivers in southeastern Nigeria, identified morphologically, and imaged digitally. DNA was extracted, PCR-amplified, and the standard barcode region was bidirectionally sequenced for 363 individuals belonging to 70 species in 38 genera. All specimen provenance data and associated sequence information were For personal use only. recorded in the barcode of life data systems (BOLD; www.barcodinglife.org). Analytical tools on BOLD were used to assess the performance of barcoding to identify species. Results: Using neighbor-joining distance comparison, the average genetic distance was 60-fold higher between species than within species, as pairwise genetic distance estimates averaged 10.29% among congeners and only 0.17% among conspecifics. -
Citharinus Citharus in Anambra River Flood System, Southeastern Nigeria
American Journal of Agricultural Science 2015; 2(2): 63-69 Published online April 10, 2015 (http://www.aascit.org/journal/ajas) Gut Helminth Parasites of Citharinus citharus in Anambra River Flood System, Southeastern Nigeria Uneke Bilikis Iyabo Fisheries and Hydrobiology, Dept of Applied Biology, Faculty of Biological Sciences, Ebonyi State University, Abakaliki, Ebonyi State, Nigeria Email address [email protected] Citation Keywords Uneke Bilikis Iyabo. Gut Helminth Parasites of Citharinus citharus in Anambra River Flood Citharinus citharus , System, Southeastern Nigeria. American Journal of Agricultural Science. Prevalence, Vol. 2, No. 2, 2015, pp. 63-69. Gut Helminth Parasites, Procamallanus Laeviconchus, Abstract Cithariniella citharini , A total of forty (40) Citharinus citharus (Geoffroy Saint-Hilaire, 1809), order Infection Rate, (Characiformes) and family (Citharinidae) were purchased randomly from local Nigeria fishermen who fished in Anambra River from May to October 2012 and examined for the gut helminth parasites. Macroscopic and microscopic examinations were used for parasite isolation and identification. Ten (25.0%) of the fish examined were infected with the two species of helminth parasites Procamallanus laeviconchus and Cithariniella Received: March 19, 2015 citharini . The parasites were isolated which were restricted to the intestine, except for P. Revised: March 30, 2015 laeviconchus , which was also found in the oesophagus and stomach. P. laeviconchus was Accepted: March 31, 2015 identified in the majority of the fish with a prevalence rate of 15.0% while C. citharini was identified in the minority with an infection rate of 10.0%. The highest prevalence (30.0%) of the helminth infection was recorded in fish with total lengths ranging from 35cm-39.9cm while those with lengths ranging from 20cm-24.9cm recorded the lowest prevalence (11.7%). -
A Review of the Systematic Biology of Fossil and Living Bony-Tongue Fishes, Osteoglossomorpha (Actinopterygii: Teleostei)
Neotropical Ichthyology, 16(3): e180031, 2018 Journal homepage: www.scielo.br/ni DOI: 10.1590/1982-0224-20180031 Published online: 11 October 2018 (ISSN 1982-0224) Copyright © 2018 Sociedade Brasileira de Ictiologia Printed: 30 September 2018 (ISSN 1679-6225) Review article A review of the systematic biology of fossil and living bony-tongue fishes, Osteoglossomorpha (Actinopterygii: Teleostei) Eric J. Hilton1 and Sébastien Lavoué2,3 The bony-tongue fishes, Osteoglossomorpha, have been the focus of a great deal of morphological, systematic, and evolutio- nary study, due in part to their basal position among extant teleostean fishes. This group includes the mooneyes (Hiodontidae), knifefishes (Notopteridae), the abu (Gymnarchidae), elephantfishes (Mormyridae), arawanas and pirarucu (Osteoglossidae), and the African butterfly fish (Pantodontidae). This morphologically heterogeneous group also has a long and diverse fossil record, including taxa from all continents and both freshwater and marine deposits. The phylogenetic relationships among most extant osteoglossomorph families are widely agreed upon. However, there is still much to discover about the systematic biology of these fishes, particularly with regard to the phylogenetic affinities of several fossil taxa, within Mormyridae, and the position of Pantodon. In this paper we review the state of knowledge for osteoglossomorph fishes. We first provide an overview of the diversity of Osteoglossomorpha, and then discuss studies of the phylogeny of Osteoglossomorpha from both morphological and molecular perspectives, as well as biogeographic analyses of the group. Finally, we offer our perspectives on future needs for research on the systematic biology of Osteoglossomorpha. Keywords: Biogeography, Osteoglossidae, Paleontology, Phylogeny, Taxonomy. Os peixes da Superordem Osteoglossomorpha têm sido foco de inúmeros estudos sobre a morfologia, sistemática e evo- lução, particularmente devido à sua posição basal dentre os peixes teleósteos. -
01 Astyanax Final Version.Indd
Vertebrate Zoology 59 (1) 2009 31 31 – 40 © Museum für Tierkunde Dresden, ISSN 1864-5755, 29.05.2009 Osteology of the African annual killifi sh genus Callopanchax (Teleostei: Cyprinodontiformes: Nothobranchiidae) and phylogenetic implications WILSON J. E. M. COSTA Laboratório de Ictiologia Geral e Aplicada, Departamento de Zoologia, Universidade Federal do Rio de Janeiro, Caixa Postal 68049, CEP 21944-970, Rio de Janeiro, Brazil E-mail: wcosta(at)acd.ufrj.br Received on May 5, 2008, accepted on October 6, 2008. Published online at www.vertebrate-zoology.de on May 15, 2009. > Abstract Osteological structures of Callopanchax are fi rst described and illustrated. Twenty-six characters derived from comparisons of osseous structures among some aplocheiloid fi shes provided evidence supporting hypotheses of relationships among three western African genera (Callopanchax, Scriptaphyosemion and Archiaphyosemion), as proposed in recent molecular analysis. The clade comprising Callopanchax, Scriptaphyosemion and Archiaphyosemion is supported by a laterally displaced antero-proximal process of the fourth ceratobranchial. The sister group relationship between Callopanchax and Scriptaphyosemion is supported by a constriction on the posterior portion of the parasphenoid, an anterior expansion of the hyomandibula, a rectangular basihyal cartilage, an anterior pointed process on the fi rst vertebra, and a long ventrally directed hemal prezygapophysis on the preural centrum 2. Monophyly of Callopanchax is supported by a convexity on the dorsal margin of the opercle, a long interarcual cartilage, and long neural prezygapophyses on the anterior caudal vertebrae. > Key words Killifi shes, Callopanchax, Africa, Osteology, Annual fi shes. Introduction COSTA, 1998a, 2004) and among genera and species of the Rivulidae (e. g., COSTA, 1998b, 2005, 2006a, b). -
Three New Endemic Aphyosemion Species (Cyprinodontiformes: Nothobranchiidae) from the Massif Du Chaillu in the Upper Louessé River System, Republic of the Congo
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/321875026 Three new endemic Aphyosemion species (Cyprinodontiformes: Nothobranchiidae) from the Massif du Chaillu in the upper Louessé River system, Republic of the Congo Article in Zootaxa · January 2018 DOI: 10.11646/zootaxa.4369.1.3 CITATIONS READS 0 587 6 authors, including: Jouke van der Zee Gina Walsh Hogeschool Arnhem and Nijmegen Flora Fauna & Man Ecological Services Ltd. 18 PUBLICATIONS 29 CITATIONS 9 PUBLICATIONS 48 CITATIONS SEE PROFILE SEE PROFILE Valdie Nina Boukaka Mikembi Michiel Nell Jonker Institut National Recherche en Sciences Exactes et Naturelle Biotech Innovation Research Development & Consulting 5 PUBLICATIONS 0 CITATIONS 6 PUBLICATIONS 0 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Effects of microplastics and pharmaceuticals on trophic interactions View project Functional Ecology of Afrotropical Streams in the Republic of Congo, west-central Africa View project All content following this page was uploaded by Gina Walsh on 17 September 2018. The user has requested enhancement of the downloaded file. Zootaxa 4369 (1): 063–092 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2018 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4369.1.3 http://zoobank.org/urn:lsid:zoobank.org:pub:946093ED-9309-4D85-A473-32566D631B19 Three new endemic Aphyosemion species (Cyprinodontiformes: Nothobranchiidae) from the Massif du Chaillu in the upper Louessé River system, Republic of the Congo JOUKE R. VAN DER ZEE1, GINA WALSH2,3,8, VALDIE N. -
Assessment of Fecundity of Brycinus Macrolepidotus in Akomoje Water Reservoir, Abeokuta, South West, Nigeria
Egyptian Journal of Aquatic Biology & Fisheries Zoology Department, Faculty of Science, Ain Shams University, Cairo, Egypt. ISSN 1110 – 6131 Vol. 23(1): 245 -252 (2019) www.ejabf.journals.ekb.eg Assessment of fecundity of Brycinus macrolepidotus in Akomoje water reservoir, Abeokuta, South West, Nigeria Ajiboye, Elijah Olusegun1; Adeosun, Festus Idowu1*; Oghenochuko, Mavis Titilayo Oghenebrorhie1, 2 1- Department of Aquaculture and Fisheries Management, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria 2- Animal Science Program, Department of Agriculture, Landmark University, Omu-Aran, Kwara State, Nigeria ARTICLE INFO ABSTRACT Article History: Overfishing and threat of extinction globally has been a topic of Received: Nov. 23, 2018 concern in the fisheries sub-sector over the years. This study assessed Accepted: Jan.30, 2019 some aspect of the biology of Brycinus macrolepidotus in Akomoje Online: Feb. 2019 reservoir, lower River Ogun, Nigeria. A total number of 838 fish _______________ specimens were collected bi-monthly for a nine month period from commercial catches using cast nets and long line. A total number of 51 Keywords: mature female were selected for fecundity analysis which was limited to Brycinus macrolepidotus only sexually gravid female fish. Length and weight of experimental fish Akomoje reservoir were measured. Data were subjected to analysis of variance (ANOVA), Fecundity descriptive and inferential statistics. Correlation statistics was carried out Abeokuta to ascertain relationship between absolute and relative fecundity with Nigeria length and weight of fish. Length and weight of experimental fish ranged between 14.5-39.4 cm and 938-1956 g. The relative fecundity ranged between 441 and 3,597 eggs with a mean of 1,702±0.16 eggs while absolute fecundity ranged from 5,838 to 39,208 eggs with a mean of 14,326±0.52 eggs.