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Striped Bass
Can you tell the difference between a striped bass, a white bass and a striped bass hybrid? Anglers need to know the differences between these spe- cies because different sizes, seasons and creel limits apply to striped bass and striped bass hybrids, and to white bass. Knowing the differences between these species can also help you better understand Pennsylvania fishes and our wa- ters. These fish belong to the family Moronidae, temperate basses, also known as “true” basses. In Pennsylvania, this family also includes the white perch. Moronidae species are medium-sized to large-sized active predators and prized trophy and sport fishes. Some species live only in fresh water, while others are anadromous they spend much of their lives in salt water or brackish water but return to fresh water to spawn. Striped Bass Morone saxatilis Identification: The striped bass has a smoothly arched pro- file, slimmer and more streamlined than a striped bass hybrid, until it reaches a weight of five to 10 pounds, when its body becomes heavy-looking. The back is olive-green to steely blue- gray, sometimes almost black. The sides are silvery to pale rapidly and stay in brackish bays at the end of their downstream silvery-green, shading to white on the belly. There are seven float. Juveniles spend their first and second summers in the or eight distinct dark stripes that run laterally on the side of tidal Delaware River with most inhabitating that area from the the body. Striped bass have two dorsal fins, the front spiny- Schuylkill River downstream into the state of Delaware. -
Genetic Analysis of Whole Mitochondrial Genome of Lateolabrax Maculatus (Perciformes: Moronidae) Indicates the Presence of Two Populations Along the Chinese Coast
ZOOLOGIA 37: e49046 ISSN 1984-4689 (online) zoologia.pensoft.net RESEARCH ARTICLE Genetic analysis of whole mitochondrial genome of Lateolabrax maculatus (Perciformes: Moronidae) indicates the presence of two populations along the Chinese coast Jie Gong 1,2, Baohua Chen 1,2, Bijun Li 1, Zhixiong Zhou 1, Yue Shi 1, Qiaozhen Ke 1,3, Dianchang Zhang 4, Peng Xu 1,2,3 1Fujian Key Laboratory of Genetics and Breeding of Marine Organisms, Xiamen University. 361000 Xiamen, China. 2Shenzhen Research Institute, Xiamen University. 518000 Shenzhen, China. 3State Key Laboratory of Large Yellow Croaker Breeding, Ningde Fufa Fisheries Company Limited. 352130 Ningde, China. 4South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences. 510300 Guangzhou, China. Corresponding author: Peng Xu ([email protected]) http://zoobank.org/B5BBA46C-7FC5-44C3-B9CE-19F8E93FAA1C ABSTRACT. The whole mitochondrial genome of Lateolabrax maculatus (Cuvier, 1828) was used to investigate the reasons for the observed patterns of genetic differentiation among 12 populations in northern and southern China. The haplotype diversity and nucleotide diversity of L. maculatus were 0.998 and 0.00169, respectively. Pairwise FST values between popula- tions ranged from 0.001 to 0.429, correlating positively with geographic distance. Genetic structure analysis and haplotype network analysis indicated that these populations were split into two groups, in agreement with geographic segregation and environment. Tajima’s D values, Fu’s Fs tests and Bayesian skyline plot (BSP) indicated that a demographic expansion event may have occurred in the history of L. maculatus. Through selection pressure analysis, we found evidence of significant negative selection at the ATP6, ND3, Cytb, COX3, COX2 and COX1 genes. -
First Record of F2 Hybrid Striped Bass (Morone Chrysops ♀ × Morone Saxatilis ♂ × Morone Chrysops ♀ × Morone Saxatilis ♂) in Kemer Dam Lake
Turkish Journal of Zoology Turk J Zool (2014) 38: 637-641 http://journals.tubitak.gov.tr/zoology/ © TÜBİTAK Research Article doi:10.3906/zoo-1304-42 First record of F2 hybrid striped bass (Morone chrysops ♀ × Morone saxatilis ♂ × Morone chrysops ♀ × Morone saxatilis ♂) in Kemer Dam Lake 1, 2 Volkan KIZAK *, Yusuf GÜNER 1 Fisheries Faculty, Tunceli University, Tunceli, Turkey 2 Fisheries Faculty, Ege University, İzmir, Turkey Received: 26.04.2013 Accepted: 19.03.2014 Published Online: 14.07.2014 Printed: 13.08.2014 Abstract: The morphometric and meristic characters of 2 F2 hybrid striped bass (M. chrysops ♀ × M. saxatilis ♂ × M. chrysops ♀ × M. saxatilis ♂) from the family Moronidae are described. Two specimens were caught from Kemer Dam Lake. The body of the F2 hybrid striped bass was elongated, moderately compressed, and scaly. Dorsal surface and sides were silver and black to olive-gray, and the abdomen was white in color. Four or 5 longitudinal broken stripes ran above the lateral line to the caudal fin. The stripes were less visible behind the pectoral fins and below the lateral line. The bodies of the2 F specimens were deeper than 1/4 the fork length. The 2 dorsal fins were separated entirely. The first dorsal fin had 8–9 spines, and the second dorsal fin had a spine and 13–14 soft rays. The caudal fin was slightly forked. The anal fin had 3 spines with 12–14 soft rays. One tooth patch was present on the anterior of the tongue. According to our results, the fish were 2F hybrid striped bass offspring of 1F hybrid striped bass, which can reproduce naturally in Turkey. -
Highly Diversified Late Cretaceous Fish Assemblage Revealed by Otoliths (Ripley Formation and Owl Creek Formation, Northeast Mississippi, Usa)
Rivista Italiana di Paleontologia e Stratigrafia (Research in Paleontology and Stratigraphy) vol. 126(1): 111-155. March 2020 HIGHLY DIVERSIFIED LATE CRETACEOUS FISH ASSEMBLAGE REVEALED BY OTOLITHS (RIPLEY FORMATION AND OWL CREEK FORMATION, NORTHEAST MISSISSIPPI, USA) GARY L. STRINGER1, WERNER SCHWARZHANS*2 , GEORGE PHILLIPS3 & ROGER LAMBERT4 1Museum of Natural History, University of Louisiana at Monroe, Monroe, Louisiana 71209, USA. E-mail: [email protected] 2Natural History Museum of Denmark, Zoological Museum, Universitetsparken 15, DK-2100, Copenhagen, Denmark. E-mail: [email protected] 3Mississippi Museum of Natural Science, 2148 Riverside Drive, Jackson, Mississippi 39202, USA. E-mail: [email protected] 4North Mississippi Gem and Mineral Society, 1817 CR 700, Corinth, Mississippi, 38834, USA. E-mail: [email protected] *Corresponding author To cite this article: Stringer G.L., Schwarzhans W., Phillips G. & Lambert R. (2020) - Highly diversified Late Cretaceous fish assemblage revealed by otoliths (Ripley Formation and Owl Creek Formation, Northeast Mississippi, USA). Riv. It. Paleontol. Strat., 126(1): 111-155. Keywords: Beryciformes; Holocentriformes; Aulopiformes; otolith; evolutionary implications; paleoecology. Abstract. Bulk sampling and extensive, systematic surface collecting of the Coon Creek Member of the Ripley Formation (early Maastrichtian) at the Blue Springs locality and primarily bulk sampling of the Owl Creek Formation (late Maastrichtian) at the Owl Creek type locality, both in northeast Mississippi, USA, have produced the largest and most highly diversified actinopterygian otolith (ear stone) assemblage described from the Mesozoic of North America. The 3,802 otoliths represent 30 taxa of bony fishes representing at least 22 families. In addition, there were two different morphological types of lapilli, which were not identifiable to species level. -
APPENDIX 3: DELETION TABLES 3.1 Aluminum
APPENDIX 3: DELETION TABLES APPENDIX 3: DELETION TABLES 3.1 Aluminum TABLE 3.1.1: Deletion process for the Santa Ana River aluminum site-specific database. Phylum Class Order Family Genus/Species Common Name Code Platyhelminthes Turbellaria Tricladida Planarlidae Girardiaia tigrina Flatworm G Annelida Oligochaeta Haplotaxida Tubificidae Tubifex tubifex Worm F Mollusca Gastropoda Limnophila Physidae Physa sp. Snail G Arthropoda Branchiopoda Diplostraca Daphnidae Ceriodaphnia dubia Cladoceran O* Arthropoda Branchiopoda Diplostraca Daphnidae Daphnia magna Cladoceran O* Arthropoda Malacostraca Isopoda Asellidae Caecidotea aquaticus Isopod F Arthropoda Malacostraca Amphipoda Gammaridae Crangonyx pseudogracilis Amphipod F Arthropoda Malacostraca Amphipoda Gammaridae Gammarus pseudolimnaeus Amphipod G Arthropoda Insecta Plecoptera Perlidae Acroneuria sp. Stonefly O Arthropoda Insecta Diptera Chironomidae Tanytarsus dissimilis Midge G Chordata Actinopterygii Salmoniformes Salmonidae Oncorhynchus mykiss Rainbow trout D Chordata Actinopterygii Salmoniformes Salmonidae Oncorhynchus tschawytscha Chinook Salmon D Chordata Actinopterygii Salmoniformes Salmonidae Salmo salar Atlantic salmon D Chordata Actinopterygii Cypriniformes Cyprinidae Hybognathus amarus Rio Grande silvery minnow F Chordata Actinopterygii Cypriniformes Cyprinidae Pimephales promelas Fathead minnow S Chordata Actinopterygii Perifomes Centrarchidae Lepomis cyanellus Green sunfish S Chordata Actinopterygii Perifomes Centrarchidae Micropterus dolomieui Smallmouth bass G Chordata Actinopterygii -
Alteration of Growth and Temperature Tolerance of European Sea Bass
Turk. J. Fish.& Aquat. Sci. 20(5), 331-340 http://doi.org/10.4194/1303-2712-v20_5_01 R E S E A R C H P A P E R Alteration of Growth and Temperature Tolerance of European Sea Bass (Dicentrarchus labrax Linnaeus 1758) in Different Temperature and Salinity Combinations Hatice Asuman Yilmaz1,* , Serhat Turkmen2, Metin Kumlu1, Orhan Tufan 1 3 Eroldogan , Nafiye Perker 1Cukurova University, Department of Aquaculture, Faculty of Fisheries, 01330 Balcali Adana, Turkey. 2 Universidad de Las Palmas de Gran Canaria, Grupo de Investigación en Acuicultura (GIA), Transmontaña s/n, 35413 Arucas, Las Palmas, Canary Islands, Spain. 3Mediterranean Fisheries Research Production and Training Institute, Kepez Unit, 07001 Antalya, Turkey. Article History Abstract Received 23 January 2019 Accepted 10 July 2019 This study was performed to assess the combined effects of three salinities (0, 20 and First Online 26 July 2019 38 ppt) and three acclimation temperatures (15, 20 and 25°C) on growth performance, proximate composition and thermal tolerance of European Sea Bass (32 g) inhabiting Corresponding Author southern parts of the Mediterranean Sea. Highest fish final weight (83.8 g) was achieved at 25°C in freshwater (FW). Specific growth rate (SGR) at 25°C was about Tel.: +903223386060 twice higher than that at 15°C, while 20°C promoted an intermediate growth. The fish E-mail: [email protected] cultured in FW at 25°C displayed consistently lower FCR and better SGR than those in full strength seawater (SW). Salinity had strong influence on fillet protein and lipid Keywords compositions. Highest lipid content (14.9%) was found in fish held in brackish water CTMin (20 ppt), and the fish held in SW had the lowest lipid content. -
Biogeography of the Freshwater Fish of the Iberian Peninsula
BIOGEOGRAPHY OF THE FRESHWATER FISH OF THE IBERIAN PENINSULA J. A. Hernando and M. C.-Soriguer Faculty of Marine Science, University of Cádiz. Biology. Ap. de Correos no. 40. 11510 Puerto Real. Cádiz, Spain. Keywords: Iberian fish, Distribution, Biogeography, Allochthonous species, Sectorisation, Iberian peninsula, . ABSTRACT This paper reviews and presents new data on the composition and distribution of fish species in the continental waters of the Iberian Peninsula, and proposes a division of the Peninsula into three subregions: the Ebro-Cantabrian, the Atlantic and the Betico-Mediterranean, based on the distribution of the 45 species (native and endemic) in the 22 river basins with surface aseas of 990 square kilometres os more. INTRODUCTION sea and freshwater. The ecosystems of variable salinity lead us to consider marine species as forming part of the Iberian The lberian Peninsula is enormously interesting from an continental fauna. ichthyological point of view. Located at the Southwestern tip of Europe, it is a point of contact between North Atlantic and tropical coastal fish fauna. Much of its coastline is on the THE ICTHYOFAUNA OF THE IBERIAN Mediterranean, the Straits of Gibraltar, which separate the PENINSULA Mediterranean from the Atlantic, have always been more of a bridge than a barrier for North African and Iberian fauna. MYERS (1960) classified freshwater fish into three cate- The epicontinental fish fauna has also been affected by gories: primary, secondary and peripheral (vicariant, diadro- the geological history of the Peninsula. Possibilities for mous, sporadic and complementary). Under this classifica- dispersion have been, and still are, limited, due to the isola- tion, the continental fauna of the Iberian Peninsula consists tion caused by the Pyrenees and the Straits of Gibraltar. -
The Mystery of Morone: Solved at Last? Chris Scharpf
The Mystery of Morone: Solved at last? Chris Scharpf Winter 2019 American Currents 36 THE MYSTERY OF MORONE: SOLVED AT LAST? Christopher Scharpf Baltimore, Maryland Morone, the Temperate Basses, is a small but commercially, recre- Now, over two centuries years later, I have found a clue that ationally, and culturally important genus of fishes native to fresh may explain this mysterious name. According to the Etymologi- waters of central and eastern North America, and brackish and cal and Pronouncing Dictionary of the English Language (5th ed., marine waters along the Western Atlantic and Gulf coasts. Mo- 1879), “morone” is a noun for a “deep crimson colour like the un- rone is also the type genus of the family Moronidae, which con- ripe mulberry.” In other words, it’s another word for—or an ar- tains one other genus, Dicentrarchus, the European Seabasses of chaic variation of—maroon. the Eastern Atlantic and Mediterranean. Despite the 200-year Sure enough, Mitchill indicated red, ruddy, or rusty (i.e., ma- pedigree of its name, and the fact that its species are among the roon-like) colors in all four of the species he included in his genus most studied fishes in the world, ichthyologists have long puzzled Morone. over what “Morone” means. With the help of a 19th-century ety- • M. pallida, “White Perch of New York” — “anal and mological dictionary, I offer an explanation. pectoral fins and chin ruddy” [a junior synonym of the Morone was proposed by Samuel Latham Mitchill (1764–1831), White Perch, Morone americana (Gmelin 1789)] a physician from New York State in the days when surgeon and • M. -
Comprehensive Phylogeny of Ray-Finned Fishes (Actinopterygii) Based on Transcriptomic and Genomic Data
Comprehensive phylogeny of ray-finned fishes (Actinopterygii) based on transcriptomic and genomic data Lily C. Hughesa,b,1,2, Guillermo Ortía,b,1,2, Yu Huangc,d,1, Ying Sunc,e,1, Carole C. Baldwinb, Andrew W. Thompsona,b, Dahiana Arcilaa,b, Ricardo Betancur-R.b,f, Chenhong Lig, Leandro Beckerh, Nicolás Bellorah, Xiaomeng Zhaoc,d, Xiaofeng Lic,d, Min Wangc, Chao Fangd, Bing Xiec, Zhuocheng Zhoui, Hai Huangj, Songlin Chenk, Byrappa Venkateshl,2, and Qiong Shic,d,2 aDepartment of Biological Sciences, The George Washington University, Washington, DC 20052; bNational Museum of Natural History, Smithsonian Institution, Washington, DC 20560; cShenzhen Key Lab of Marine Genomics, Guangdong Provincial Key Lab of Molecular Breeding in Marine Economic Animals, Beijing Genomics Institute Academy of Marine Sciences, Beijing Genomics Institute Marine, Beijing Genomics Institute, 518083 Shenzhen, China; dBeijing Genomics Institute Education Center, University of Chinese Academy of Sciences, 518083 Shenzhen, China; eChina National GeneBank, Beijing Genomics Institute-Shenzhen, 518120 Shenzhen, China; fDepartment of Biology, University of Puerto Rico–Rio Piedras, San Juan 00931, Puerto Rico; gKey Laboratory of Exploration and Utilization of Aquatic Genetic Resources, Shanghai Ocean University, Ministry of Education, 201306 Shanghai, China; hLaboratorio de Ictiología y Acuicultura Experimental, Universidad Nacional del Comahue–CONICET, 8400 Bariloche, Argentina; iProfessional Committee of Native Aquatic Organisms and Water Ecosystem, China Fisheries Association, 100125 Beijing, China; jCollege of Life Science and Ecology, Hainan Tropical Ocean University, 572022 Sanya, China; kYellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 266071 Qingdao, China; and lComparative Genomics Laboratory, Institute of Molecular and Cell Biology, A*STAR, Biopolis, 138673 Singapore Edited by Scott V. -
Striped Bass
Maine 2015 Wildlife Action Plan Revision Report Date: January 13, 2016 Morone saxatilis (Striped Bass) Priority 2 Species of Greatest Conservation Need (SGCN) Class: Actinopterygii (Ray-finned Fishes) Order: Perciformes (Perch-like Fishes) Family: Moronidae (Temperate Basses) General comments: none No Species Conservation Range Maps Available for Striped Bass SGCN Priority Ranking - Designation Criteria: Risk of Extirpation: NA State Special Concern or NMFS Species of Concern: NA Recent Significant Declines: Striped Bass is currently undergoing steep population declines, which has already led to, or if unchecked is likely to lead to, local extinction and/or range contraction. Notes: ASMFC Stock Assessment Regional Endemic: NA High Regional Conservation Priority: Committee on the Status of Endangered Wildlife in Canada (COSEWIC): Status: E, Last Examination: 11/1/2012, Change: In a higher risk category, Canada Occurence: NB, NS, Atlantic Ocean Atlantic States Marine Fisheries Commission Stock Assessments: Status: Unstable/Increasing, Status Comment: In 2012, the Atlantic striped bass stock was not overfished or experiencing overfishing based on the points estimates of fully-recruited fishing mortality and female spawning stock biomass relative to the reference points defined in this assessment. Reference: Atlantic States Marine Fisheries Commission. 2013. ASMFC Striped Bass Technical Committee. 2013 Update of the Striped Bass Stock Assessment using Final 2012 Data. Available from: http://www.asmfc.org/fisheries-science/stock- assessments#StockAssessments -
The Striped Bass Fishery of the Gulf of Mexico, United States
The Stri1Jecl Ba~s Fishery of the Gulf of Mexico, U 11ited States: A Regional Ma11agement Plan 2006 Revisio11 Gttlf States ~'larine Fisheries Commissio11 I\.Im·ch 2006 fliumber l Ji Gulf States Marine Fisheries Commission Commissioners and Proxies ALABAMA Senator Butch Gautreaux Barnett Lawley, Commissioner 1015 Clothilde Avenue Alabama Department of Conservation Morgan City, LA 70380 and Natural Resources 64 North Union Street Mr. Wilson Gaidry Montgomery, AL 36130-1901 8911 Park Avenue Proxy: Houma, LA 70363 Vernon Minton, Director Alabama Marine Resources Division MISSISSIPPI P.O. Drawer 458 William Walker, Executive Director Gulf Shores, AL 36547 Mississippi Department of Marine Resources 1141 Bayview Avenue, Suite 101 Senator Gary G. Tanner Biloxi, MS 39530 5750 McDonald Road Proxy: Theodore, AL 36582 William S. “Corky” Perret Mississippi Department of Marine Resources Chris Nelson 1141 Bayview Avenue, Suite 101 Bon Secour Fisheries, Inc. Biloxi, MS 39530 P.O. Box 60 Bon Secour, AL 36511 Senator Tommy Gollott 235 Bay View Avenue FLORIDA Biloxi, MS 39530 Ken Haddad, Executive Director Florida Fish and Wildlife Conservation Commission Mr. Joe Gill Jr. 620 South Meridian Street Joe Gill Consulting, LLC Tallahassee, FL 32399-1600 P.O. Box 535 Proxy: Ocean Springs, MS 39566-0535 Virginia Vail FWC Division of Marine Fisheries TEXAS 620 South Meridian Street Robert L. Cook, Executive Director Tallahassee, FL 32399-1600 Texas Parks and Wildlife Department 4200 Smith School Road Senator Nancy Argenziano Austin, TX 78744 1120 North Suncoast Boulevard Proxy Crystal River, FL 34429 Mike Ray Coastal Fisheries Division Hayden R. Dempsey Texas Parks and Wildlife Department Greenberg Traurig, P.A. -
Family-Group Names of Fossil Fishes
© European Journal of Taxonomy; download unter http://www.europeanjournaloftaxonomy.eu; www.zobodat.at European Journal of Taxonomy 466: 1–167 ISSN 2118-9773 https://doi.org/10.5852/ejt.2018.466 www.europeanjournaloftaxonomy.eu 2018 · Van der Laan R. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:1F74D019-D13C-426F-835A-24A9A1126C55 Family-group names of fossil fi shes Richard VAN DER LAAN Grasmeent 80, 1357JJ Almere, The Netherlands. Email: [email protected] urn:lsid:zoobank.org:author:55EA63EE-63FD-49E6-A216-A6D2BEB91B82 Abstract. The family-group names of animals (superfamily, family, subfamily, supertribe, tribe and subtribe) are regulated by the International Code of Zoological Nomenclature. Particularly, the family names are very important, because they are among the most widely used of all technical animal names. A uniform name and spelling are essential for the location of information. To facilitate this, a list of family- group names for fossil fi shes has been compiled. I use the concept ‘Fishes’ in the usual sense, i.e., starting with the Agnatha up to the †Osteolepidiformes. All the family-group names proposed for fossil fi shes found to date are listed, together with their author(s) and year of publication. The main goal of the list is to contribute to the usage of the correct family-group names for fossil fi shes with a uniform spelling and to list the author(s) and date of those names. No valid family-group name description could be located for the following family-group names currently in usage: †Brindabellaspidae, †Diabolepididae, †Dorsetichthyidae, †Erichalcidae, †Holodipteridae, †Kentuckiidae, †Lepidaspididae, †Loganelliidae and †Pituriaspididae.