(Corydoras Paleatus) 1 Native Range and Status in the United States
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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, -
Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi
Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 (http://www.accessscience.com/) Article by: Boschung, Herbert Department of Biological Sciences, University of Alabama, Tuscaloosa, Alabama. Gardiner, Brian Linnean Society of London, Burlington House, Piccadilly, London, United Kingdom. Publication year: 2014 DOI: http://dx.doi.org/10.1036/1097-8542.680400 (http://dx.doi.org/10.1036/1097-8542.680400) Content Morphology Euteleostei Bibliography Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi The most recent group of actinopterygians (rayfin fishes), first appearing in the Upper Triassic (Fig. 1). About 26,840 species are contained within the Teleostei, accounting for more than half of all living vertebrates and over 96% of all living fishes. Teleosts comprise 517 families, of which 69 are extinct, leaving 448 extant families; of these, about 43% have no fossil record. See also: Actinopterygii (/content/actinopterygii/009100); Osteichthyes (/content/osteichthyes/478500) Fig. 1 Cladogram showing the relationships of the extant teleosts with the other extant actinopterygians. (J. S. Nelson, Fishes of the World, 4th ed., Wiley, New York, 2006) 1 of 9 10/7/2015 1:07 PM Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 Morphology Much of the evidence for teleost monophyly (evolving from a common ancestral form) and relationships comes from the caudal skeleton and concomitant acquisition of a homocercal tail (upper and lower lobes of the caudal fin are symmetrical). This type of tail primitively results from an ontogenetic fusion of centra (bodies of vertebrae) and the possession of paired bracing bones located bilaterally along the dorsal region of the caudal skeleton, derived ontogenetically from the neural arches (uroneurals) of the ural (tail) centra. -
Edna Assay Development
Environmental DNA assays available for species detection via qPCR analysis at the U.S.D.A Forest Service National Genomics Center for Wildlife and Fish Conservation (NGC). Asterisks indicate the assay was designed at the NGC. This list was last updated in June 2021 and is subject to change. Please contact [email protected] with questions. Family Species Common name Ready for use? Mustelidae Martes americana, Martes caurina American and Pacific marten* Y Castoridae Castor canadensis American beaver Y Ranidae Lithobates catesbeianus American bullfrog Y Cinclidae Cinclus mexicanus American dipper* N Anguillidae Anguilla rostrata American eel Y Soricidae Sorex palustris American water shrew* N Salmonidae Oncorhynchus clarkii ssp Any cutthroat trout* N Petromyzontidae Lampetra spp. Any Lampetra* Y Salmonidae Salmonidae Any salmonid* Y Cottidae Cottidae Any sculpin* Y Salmonidae Thymallus arcticus Arctic grayling* Y Cyrenidae Corbicula fluminea Asian clam* N Salmonidae Salmo salar Atlantic Salmon Y Lymnaeidae Radix auricularia Big-eared radix* N Cyprinidae Mylopharyngodon piceus Black carp N Ictaluridae Ameiurus melas Black Bullhead* N Catostomidae Cycleptus elongatus Blue Sucker* N Cichlidae Oreochromis aureus Blue tilapia* N Catostomidae Catostomus discobolus Bluehead sucker* N Catostomidae Catostomus virescens Bluehead sucker* Y Felidae Lynx rufus Bobcat* Y Hylidae Pseudocris maculata Boreal chorus frog N Hydrocharitaceae Egeria densa Brazilian elodea N Salmonidae Salvelinus fontinalis Brook trout* Y Colubridae Boiga irregularis Brown tree snake* -
Freshwater Ornamental Fish Commonly Cultured in Florida 1 Jeffrey E
Circular 54 Freshwater Ornamental Fish Commonly Cultured in Florida 1 Jeffrey E. Hill and Roy P.E. Yanong2 Introduction Unlike many traditional agriculture industries in Florida which may raise one or only a few different species, tropical Freshwater tropical ornamental fish culture is the largest fish farmers collectively culture hundreds of different component of aquaculture in the State of Florida and ac- species and varieties of fishes from numerous families and counts for approximately 95% of all ornamentals produced several geographic regions. There is much variation within in the US. There are about 200 Florida producers who and among fish groups with regard to acceptable water collectively raise over 800 varieties of freshwater fishes. In quality parameters, feeding and nutrition, and mode of 2003 alone, farm-gate value of Florida-raised tropical fish reproduction. Some farms specialize in one or a few fish was about US$47.2 million. Given the additional economic groups, while other farms produce a wide spectrum of effects of tropical fish trade such as support industries, aquatic livestock. wholesalers, retail pet stores, and aquarium product manufacturing, the importance to Florida is tremendous. Fish can be grouped in a number of different ways. One major division in the industry which has practical signifi- Florida’s tropical ornamental aquaculture industry is cance is that between egg-laying species and live-bearing concentrated in Hillsborough, Polk, and Miami-Dade species. The culture practices for each division are different, counties with additional farms throughout the southern requiring specialized knowledge and equipment to succeed. half of the state. Historic factors, warm climate, the proxim- ity to airports and other infrastructural considerations This publication briefly reviews the more common groups (ready access to aquaculture equipment, supplies, feed, etc.) of freshwater tropical ornamental fishes cultured in Florida are the major reasons for this distribution. -
Zootaxa, Pisces, Actinopterygii, Cyprinodontiformes, Rivulidae
Zootaxa 928: 1–20 (2005) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 928 Copyright © 2005 Magnolia Press ISSN 1175-5334 (online edition) Kryptolebias sepia n. sp. (Actinopterygii: Cyprinodontiformes: Riv- ulidae), a new killifish from the Tapanahony River drainage in southeast Surinam FRANS B. M. VERMEULEN1 & TOMAS HRBEK2* 1 Tanki Leendert 194 c, Noord, Aruba; [email protected] 2 Department of Biology, University of Puerto Rico Rio Piedras, San Juan, PR 00931, Puerto Rico; [email protected] * Correspondence to: TOMAS HRBEK Abstract Kryptolebias sepia n. sp. is described from small forest tributaries of the Tapanahony and Palumeu Rivers which form part of the Upper Marowijne River system in southeast of Surinam. This species is distinguished from all other Kryptolebias spp. and Rivulus spp. by strong melanism on the body, its ability to change color pattern rapidly, the lack of strong sexual dimorphism, and the presence of pronounced adult/juvenile dichromatism. Key words: Rivulus, Kryptolebias, Guyana Shield, mtDNA, speciation, molecular phylogeny, biodiversity Introduction The fauna and flora of the Guyana shield is particularly rich. While extensive floristic sur- veys have been undertaken, relatively little work has been conducted on the fish fauna of this region. Most surveys have been done in Venezuela, and Brazilian surveys have con- centrated primarily on the middle Rio Negro drainage. The first and last major survey of Guyana was conducted by Eigenmann in 1909 (Eigenmann 1912), and more recently his route has been retraced by researchers focusing on loricariid catfishes (Hardman et al. 2002). A survey of freshwater fishes of French Guiana has also been published (Keith et al. -
Siluriformes: Callichthyidae) in the Subterranean Domain of Northern and Northeastern Brazil
13 4 297 Tencatt et al NOTES ON GEOGRAPHIC DISTRIBUTION Check List 13 (4): 297–303 https://doi.org/10.15560/13.4.297 First report of armored catfishes Callichthyinae Bonaparte, 1838 (Siluriformes: Callichthyidae) in the subterranean domain of northern and northeastern Brazil Luiz Fernando Caserta Tencatt,1 Bruno Ferreira dos Santos,2 Maria Elina Bichuette3 1 Universidade Estadual de Maringá, Coleção Ictiológica do Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura e Programa de Pós- Graduação em Ecologia de Ambientes Aquáticos Continentais, Av. Colombo, 5790, 87020-900 Maringá, Paraná, Brazil. 2 Universidade Federal de Mato Grosso do Sul, Programa de Pós-Graduação em Biologia Animal, Av. Costa e Silva, 79070-900 Campo Grande, Mato Grosso do Sul, Brazil. 3 Universidade Federal de São Carlos, Departamento de Ecologia e Biologia Evolutiva, Laboratório de Estudos Subterrâneos, Rodovia Washington Luis, km 235, 13565-905 São Carlos, São Paulo, Brazil. Corresponding author: Luiz Fernando Caserta Tencatt, [email protected] Abstract The first occurrence of the armored catfishes of the subfamily Callichthynae is reported in subterranean water bodies of northern and northeastern Brazil. The records include 3 species, each occurring in 1 of the 3 caves in the central and northeastern regions of Brazil: Callichthys callichthys from Casa do Caboclo cave, Sergipe state; Hoplosternum lit- torale from the Gruna da Lagoa do Meio, Bahia state; and Megalechis thoracata, from Casa de Pedra cave, Tocantins state. Keywords Camboatá, cave, hypogean habitat, karstic areas, Neotropical region. Academic editor: Bárbara Calegari | Received 2 March 2017 | Accepted 10 June 2017 | Published 14 August 2017 Citation: Tencatt LFC, Ferreira dos Santos B, Bichuette ME (2017) First report of armored catfishes Callichthyinae( Bonaparte, 1838) (Siluriformes: Callichthyidae) in the subterranean domain. -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
John Todaro Angelfish
T H E O N - L I N E J O U R N A L O F T H E B R O O K L Y N A Q U A R I U M S O C I E T Y QVOL. 32 UATI MAY - JUNE 2019 No. 5 CA AngelfishA - Pteropyllum scalare Photo: John Todaro 1 108 Y EARSOF E DUCATING A QUARISTS AQUATICA VOL. 32 MAY • JUNE 2 0 1 9 N O . 5 C ONTENTS PAGE 2 THE AQUATICA STAFF PAGE 29 THE SCARLET BADIS. A report on Dario dario a beautiful PAGE 3 CALENDAR OF EVENTS. small fish and how to breed them. BAS Events for the year 2019. MIKE HELLWEG - MAS PAGE 4 MAKING YOUR OWN FISH PAGE 32 WHY SOUTHEAST ASIA FOOD. How to make your own AND AUSTRALIA’S CORAL homemade fish foods. REEFS BECOME SO RICH IN STAFF WRITER - www.pethelpful.com SPECIES. Dive into the coral reefs of Southeast Asia or Australia and you’ll likely PAGE 6 AN OLD FAVORITE REVISITED: spot a wrasse. But which of the hundreds of THE PARADISE FISH. The Paradise fish kinds of wrasses will you see? is the granddaddy of all tropical fish. STEPH YIN - New York Times 10/17/2018 JOHN TODARO - BAS PAGE 34 WHERE DID FISH FIRST EVOLVE? THE PAGE 7 ORGANIC DISEASE TREATMENTS. ANSWER MAY BE SHALLOW. Some had armor Supplemental measures to help your fish fight off and spikes. Many lacked jaws. They evolved in the diseases and recover from them. shallow coasts around super continents and they ANTHONY P. -
Resolving Cypriniformes Relationships Using an Anchored Enrichment Approach Carla C
Stout et al. BMC Evolutionary Biology (2016) 16:244 DOI 10.1186/s12862-016-0819-5 RESEARCH ARTICLE Open Access Resolving Cypriniformes relationships using an anchored enrichment approach Carla C. Stout1*†, Milton Tan1†, Alan R. Lemmon2, Emily Moriarty Lemmon3 and Jonathan W. Armbruster1 Abstract Background: Cypriniformes (minnows, carps, loaches, and suckers) is the largest group of freshwater fishes in the world (~4300 described species). Despite much attention, previous attempts to elucidate relationships using molecular and morphological characters have been incongruent. In this study we present the first phylogenomic analysis using anchored hybrid enrichment for 172 taxa to represent the order (plus three out-group taxa), which is the largest dataset for the order to date (219 loci, 315,288 bp, average locus length of 1011 bp). Results: Concatenation analysis establishes a robust tree with 97 % of nodes at 100 % bootstrap support. Species tree analysis was highly congruent with the concatenation analysis with only two major differences: monophyly of Cobitoidei and placement of Danionidae. Conclusions: Most major clades obtained in prior molecular studies were validated as monophyletic, and we provide robust resolution for the relationships among these clades for the first time. These relationships can be used as a framework for addressing a variety of evolutionary questions (e.g. phylogeography, polyploidization, diversification, trait evolution, comparative genomics) for which Cypriniformes is ideally suited. Keywords: Fish, High-throughput -
Corydoras Tukano, a New Species of Corydoradine Catfish from the Rio Tiquié, Upper Rio Negro Basin, Brazil (Ostariophysi: Siluriformes: Callichthyidae)
Neotropical Ichthyology, 1(2):83-91, 2003 Copyright © 2003 Sociedade Brasileira de Ictiologia Corydoras tukano, a new species of corydoradine catfish from the rio Tiquié, upper rio Negro basin, Brazil (Ostariophysi: Siluriformes: Callichthyidae) Marcelo R. Britto* and Flávio C.T. Lima** A new Corydoras species from the rio Tiquié, upper rio Negro system, Amazonas, Brazil, is described. This taxon was previously referred to as “Corydoras species ‘Asher’”, “Corydoras cf. reynoldsi”, and “Corydoras aff. reynoldsi” in the aquarist literature. The new taxon can be distinguished from all its congeners, except Corydoras reynoldsi and C. weitzmani, by its color pattern, consisting of three large, dark blotches, the first one (“mask”) on the head, across the eye; the second one on the trunk at the level of dorsal fin; and the third one on the trunk at the level of the adipose fin. It can be distinguished from Corydoras reynoldsi mainly by the development of trunk blotches; and from C. weitzmani by the presence of a dusky saddle between the dorsal and adipose fins, the second trunk blotch extending vertically from the adipose-fin base to the anal-fin base, and the presence of four dark stripes in the caudal fin. Uma nova espécie de Corydoras do rio Tiquié, bacia do alto rio Negro, estado do Amazonas, Brasil, é descrita. Este táxon foi anteriormente citado na literatura aquarista como “Corydoras species ‘Asher’”, “Corydoras cf. reynoldsi” e “Corydoras aff. reynoldsi”. O novo táxon pode ser distinguido de todos seus congêneres, exceto Corydoras reynoldsi e C. weitzmani, por seu padrão de colorido, que consiste em três grandes manchas pretas, a primeira (“máscara”) na cabeça, através do olho; a segunda no tronco, no nível da nadadeira dorsal; e a terceira no tronco, no nível da nadadeira adiposa. -
Investigations in Fish Control
INVESTIGATIONS IN FISH CONTROL 82. Investigations in Fish Control: Index to Numbers 1-72,1964-76 UNITED STATES DEPARTMENT OF THE INTERIOR FISH AND WILDLIFE SERVICE Investigations in Fish Control, published by the Fish and Wildlife Service, include reports on the results of work at the Service's Fish Control Laboratories at La Crosse, Wis., and Warm Springs, Ga., and reports of other studies related to that work. Though each report is regarded as a separate publication, several may be issued under a single cover, for economy. [See Investigations in Fish Control 47-50 (in one cover) for list of issues published prior to 1970.] (Reports 41 through 43 are in one cover.) 41. Identification of MS-222 Residues in Selected Fish Tissues by Thin Layer Chromatog- raphy, by John L. Alien, Charles W. Luhning, and Paul D. Harman. 1970. 7 pp. 42. Dynamics of MS-222 in the Blood and Brain of Freshwater Fishes During Anesthesia, by Joseph B. Hunn. 1970.8 pp. 43. Effect of MS-222 on Electrolyte and Water Content in the Brain of Rainbow Trout, by Wayne A. Willford. 1970. 7 pp. 44. A Review of Literature on TFM (3-trifluormethyl-4-nitrophenol) as a Lamprey Larvi- cide, by Rosalie A. Schnick. 1972.31 pp. (Reports 45 and 46 are in one cover.) 45. Residues of MS-222 in Northern Pike, Muskellunge, and Walleye, by John L. Alien, Charles W. Luhning, and Paul D. Harman. 1972. 8 pp. 46. Methods of Estimating the Half-Life of Biological Activity of Toxic Chemicals in Water, by Leif L. -
Global Catfish Biodiversity 17
American Fisheries Society Symposium 77:15–37, 2011 © 2011 by the American Fisheries Society Global Catfi sh Biodiversity JONATHAN W. ARMBRUSTER* Department of Biological Sciences, Auburn University 331 Funchess, Auburn University, Alabama 36849, USA Abstract.—Catfi shes are a broadly distributed order of freshwater fi shes with 3,407 cur- rently valid species. In this paper, I review the different clades of catfi shes, all catfi sh fami- lies, and provide information on some of the more interesting aspects of catfi sh biology that express the great diversity that is present in the order. I also discuss the results of the widely successful All Catfi sh Species Inventory Project. Introduction proximately 10.8% of all fi shes and 5.5% of all ver- tebrates are catfi shes. Renowned herpetologist and ecologist Archie Carr’s But would every one be able to identify the 1941 parody of dichotomous keys, A Subjective Key loricariid catfi sh Pseudancistrus pectegenitor as a to the Fishes of Alachua County, Florida, begins catfi sh (Figure 2A)? It does not have scales, but it with “Any damn fool knows a catfi sh.” Carr is right does have bony plates. It is very fl at, and its mouth but only in part. Catfi shes (the Siluriformes) occur has long jaws but could not be called large. There is on every continent (even fossils are known from a barbel, but you might not recognize it as one as it Antarctica; Figure 1); and the order is extremely is just a small extension of the lip. There are spines well supported by numerous complex synapomor- at the front of the dorsal and pectoral fi ns, but they phies (shared, derived characteristics; Fink and are not sharp like in the typical catfi sh.