SPECIAL SCIENTIFIC REPORT-FISHERIES Na 631

Total Page:16

File Type:pdf, Size:1020Kb

SPECIAL SCIENTIFIC REPORT-FISHERIES Na 631 A UNITED STATES DEPARTMENT OF COMMERCE PUBLICATION U.S. DEPARTMENT OF COMMERCE NATIONAL OCEANIC AND ATMOSPHERIC ADMINISTRATION NATIONAL MARINE FISHERIES SERVICE Occurrence of Thiaminase in Some Common Aquatic Animals of the United States and Canada 1971 SPECIAL SCIENTIFIC REPORT-FISHERIES Na 631 UNITED STATES DEPARTMENT OF COMMERCE Maurice H. Stans, Secretary NATIONAL OCEANIC AND ATMOSPHERIC ADMINISTRATION Dr. Robert M. White, Administrator NATIONAL MARINE FISHERIES SERVICE Philip M. Roedel, Director Occurrence of Thiaminase in Some Common Aquatic Animals of the United States and Canada By R. A. GREIG and R. H. GNAEDINGER Special Scientific Report—Fisheries No. 631 Seattle, Washington July 1971 CONTENTS Page Introduction 1 Explanation of the tables 2 Discussion 2 Literature cited 3 TABLES 1. Thiaminase presence in freshwater animals 4 2. Thiaminase presence in marine animals 6 in Occurrence of Thiaminase in Some Common Aquatic Animals of the United States and Canada By R. A. GREIG National Marine Fisheries Service Technological Laboratory, Ann Arbor, Michigan 48107 and R. H. GNAEDINGER Pet Food Nutritional Research, Ralston-Purina Company, Checkerboard Square, St. Louis, Missouri 63199 ABSTRACT Two tables are presented that survey the presence or absence of thiaminase in freshwater and marine fish and shellfish. INTRODUCTION vitally important to animal feeders, particu- larly mink ranchers, for safety and economic The presence of thiaminase in fish that are reasons. routinely used raw in rations for animals can Also, scientific researchers at times need to cause a dietary deficiency. The disease in mink consider whether or not an aquatic animal is commonly called Chastek paralysis (Green, involved in their research contains thiaminase. Evans, and Carlson, 1937). Knowledge about For example, in biological research where the presence or absence of thiaminase in aquatic fishes are held in aquaria for feeding studies animals is therefore important to mink ranch- or other research, the presence of thiaminase ers and other animal feeders, scientific re- in the animals being fed to the fish could pos- searchers, commercial fish vendors, and others. sibly cause a vitamin deficiency or other prob- Thiaminase is an enzyme that destroys lems that could impede the research (Wolf, thiamine (vitamin Bi) and, like many enzymes, 1942). its activity is greatly reduced or destroyed up- Many species of aquatic organisms have been on heating to moderate temperatures (50°- assayed for thiaminase activity in various lab- 100° C). Thus, mink ranchers, for example, oratories throughout the world. Most of these assays, can cook the fish before feeding it to the animals however, were made in conjunction to avoid a Chastek paralysis problem (Lee, with specific research programs that were de- 1948; Gnaedinger and Krzeczkowski, 1966). signed to study a particular species native to However, mink ranchers generally prefer to the area of the research laboratory. As a re- avoid cooking the fish because mink show a sult, the data on the occurrence of thiaminase preference for raw fish and cooking adds to in aquatic specimens is scattered throughout the operational costs. Knowledge whether fish various research papers published over the do or do not contain thiaminase is therefore years. Deutsch and Hasler (1943) and Neilands by Stout, Oldfield, and Adair (1963), the ob- (1947) determined the thiaminase activity of servation was made that fish (yellow perch, a great number of freshwater and aquatic an- white perch, and hake in these experiments) imals. A number of important fishes and shell- generally considered to be thiaminase-free fish, however, were not examined by these could be found to contain thiaminase activity researchers but were investigated by several if the fish was captured at a time when the other researchers. The purpose of this report, animal it fed on was not completely digested therefore, is to combine the listings of thiami- and this animal itself contained thiaminase. nase activity in aquatic animals that have ap- These findings are significant for several peared in the literature and also some recent reasons: (1) It is possible that some of the unpublished work at this laboratory into a animals listed in Tables 1 and 2 were found to comprehensive list of aquatic animals that have contain thiaminase because they were caught been assayed for thiaminase activity. at a time when their stomachs contained un- digested, thiaminase-containing feed. Also, the opposite could be true; that is, those species Explanation of the Tables listed as not containing thiaminase could at The list is presented in two tables: Table 1 times be found to contain thiaminase activity presents the information for freshwater ani- if captured with the undigested thiaminase- information for mals, and Table 2 presents the containing food in their stomachs. (2) The marine animals. The animals are listed alpha- findings could help to explain apparent dis- betically by common name. The scientific name crepancies that sometimes occur in regard to is also shown for each animal; the names were the reported thiaminase activity of a certain sci- taken from the publication (s) cited. The species. For example, burbot is listed in Table entific names relating to the unpublished data 1 as containing thiaminase when the animal of this laboratory are from the list published came from the Great Lakes; whereas, burbot by the American Fisheries Society (1960). did not contain thiaminase when captured from The part of the animal that was analyzed Rainy Lake, Minn. It is possible that the bur- for thiaminase is also shown in the tables. bot feeds on thiaminase-containing animals in Whether the whole animal or, for example, just the Great Lakes; whereas, the animals avail- the viscera was analyzed is important; this able for food in Rainy Lake are thiaminase- point will be further discussed later. Where free. Another possibility is that the burbot the source of the animal was given in the ori- from the Great Lakes was captured with un- ginal reference, this information is also given digested (thiaminase-containing) food in its in the tables. viscera, and the burbot from Rainy Lake was captured with completely digested food in its DISCUSSION viscera. Additional precautions that have to be con- most cases, the whole animal was analyzed In sidered in using the data presented in the tables in Tables 1 and 2. How- for the data presented are: The data do not indicate which animals the viscera ever, for some of the animals, only have the greatest concentration of thiaminase Thiaminase apparently or flesh was analyzed. and which have lesser concentrations of the the viscera more than in any concentrates in enzyme. In many respects this factor may not other part of the animal (Lee, 1948). Some be too important, at least with present lack researchers have found thiaminase to be pi-esent of knowledge about threshold concentrations in the viscera of some aquatic animals but not in regard to the ability of thiaminase to impair in the flesh of that same animal. For example, physiological activity of thiamine. In other Neilands (1947) found that viscera of lobster words, even a small amount of thiaminase in contained thiaminase, but the muscle did not. depending In over 30 marine and freshwater animals the animal could cause concern on studied by Neilands, however, the lobster the intended use of the animal. Thus, a mink proved the only example of such a relationship. rancher is not likely to feed raw, thiaminase- In other experiments by Neilands (1947) and containing fish to mink even though it was shown that the fish contained a relatively low Fish. Wildl. Serv., Fish. Ind. Res. level of thiaminase activity. In this case, the 2(4): 55-59. mink rancher would cook the fish to be on the 5. GNAEDINGER, R. H., and R. A. safe side. According to the results of research KRZECZKOWSKI. by Gnaedinger and Krzeczkowski ( 1966) , it ap- 1966. Heat inactivation of thiaminase pears that fish with various concentrations of in whole fish. Commer. Fish. Rev. thiaminase activity all have to be heated to 28(8): 11-14. about the same temperature time relationship 6. GREEN, R. G., C. A. EVANS, and to give complete destruction of thiaminase ac- W. E. CARLSON. tivity. Therefore, a mink rancher probably 1937. A summary of Chastek paral- should not give fish with "low" levels of thi- ysis studies. Minn. Wildl. Dis. In- aminase a milder heat treatment than fish with vest. 3: 173-177. "high" levels of thiaminase. 7. JONES, W. G. Different analytic methods were used by the 1960. Fishery resources for animal various researchers to obtain the data pre- food. U.S. Fish Wildl. Serv., Fish. sented in the tables. That is, the presence or Lean. 501, 22 p. absence of thiaminase was observed through 8. LEE, C. F. various chemical methodologies or biological 1948. Thiaminase in fishery products: feeding studies; it is possible that one method A review. Commer. Fish. Rev. of detection could show the presence of thi- 10(4): 7-17. aminase, whereas another method would show 9. LEE, C. F., and W. CLEGG. that the thiaminase was absent in the animal. 1955. Technical Note No. 31 — Generally, the chemical methods for thiaminase Weight range, proximate composi- activity are believed capable of detecting low- tion and thiaminase content of fish er levels of thiaminase than the biological taken in shallow water trawling in methods. northern Gulf of Mexico. Commer. Fish. Rev. 17(3): 21-23. 10. MELNICK, D., M. HOCHBERG, and LITERATURE CITED B. L. OSER. 1945. Physiological availability of the 1. AMERICAN FISHERIES SOCIETY. vitamins. II. The effect of dietary 1960. A list of common and scien- thiaminase in fish products. J. Nutr. tific names of fishes from the Unit- 30(2): 81-88. ed States and Canada. 2nd ed. 11. NEILANDS, J. B.
Recommended publications
  • Fish and Mammals in the Economy of an Ancient Peruvian Kingdom
    Proc. Natl. Acad. Sci. USA Vol. 96, pp. 6564–6570, May 1999 Anthropology This contribution is part of the special series of Inaugural Articles by members of the National Academy of Sciences elected on April 29, 1997. Fish and mammals in the economy of an ancient Peruvian kingdom JOYCE MARCUS*, JEFFREY D. SOMMER, AND CHRISTOPHER P. GLEW Museum of Anthropology, 1109 Geddes Avenue, University of Michigan, Ann Arbor, MI 48109-1079 Contributed by Joyce Marcus, April 8, 1999 ABSTRACT Fish and mammal bones from the coastal Yunga and Chaupi Yunga site of Cerro Azul, Peru shed light on economic specialization just before the Inca conquest of A.D. 1470. The site devoted In Quechua, the language of the Inca, the Peruvian coast was itself to procuring anchovies and sardines in quantity for divided into yunga and chaupi yunga. The yunga, or coast shipment to agricultural communities. These small fish were proper, is an arid strip along the ocean, rarely extending inland dried, stored, and eventually transported inland via caravans more than 50 km. Beyond that point, it merges with the chaupi of pack llamas. Cerro Azul itself did not raise llamas but yunga, a piedmont zone at the base of the Andes. The chaupi obtained charqui (or dried meat) as well as occasional whole yunga is cut by stream canyons supporting trees, shrubs, and adult animals from the caravans. Guinea pigs were locally grasses that are rare to absent in the yunga. raised. Some 20 species of larger fish were caught by using In ancient times, one could hunt deer and guanaco in these nets; the more prestigious varieties of these show up mainly in piedmont canyons.
    [Show full text]
  • (Galeichthys Peruvianus) Otoliths
    THE UNIVERSITY OF ALABAMA University Libraries Oxygen Isotope Record of the 1997–1998 El Niño in Peruvian Sea Catfish (Galeichthys peruvianus) Otoliths C. Fred T. Andrus – University of Georgia Douglas E. Crowe – University of Georgia Christopher S. Romanek – University of Georgia Deposited 01/16/2018 Citation of published version: Andrus, C., Crowe, D., Romanek, C. (2002): Oxygen Isotope Record of the 1997–1998 El Niño in Peruvian Sea Catfish (Galeichthys peruvianus) Otoliths. Paleoceanography, 17(4). DOI: https://doi.org/10.1029/2001PA000652 © 2002. American Geophysical Union. All Rights Reserved. PALEOCEANOGRAPHY, VOL. 17, NO. 4, 1053, doi:10.1029/2001PA000652, 2002 Oxygen isotope record of the 1997–1998 El Nin˜o in Peruvian sea catfish (Galeichthys peruvianus) otoliths C. Fred T. Andrus, Douglas E. Crowe, and Christopher S. Romanek1 Department of Geology, University of Georgia, Athens, Georgia, USA Received 2 May 2001; revised 9 January 2002; accepted 23 January 2002; published 11 October 2002. [1] Sagittal otoliths of the Peruvian sea catfish Galeichthys peruvianus were collected from the north coast of Peru during and after the 1997–1998 El Nin˜o. The otoliths were analyzed via laser microprobe and micromilling techniques for oxygen isotope composition through ontogeny to document their use as an El Nin˜o-Southern Oscillation (ENSO) proxy. Results were compared to theoretical calculations for the d18O of otolith aragonite using measured sea surface temperatures (SST) and d18O values for local seawater assuming equilibrium oxygen isotope fractionation was achieved. All otoliths recorded the 1997–1998 El Nin˜o event as well as seasonal temperature variations. These ENSO events were recorded in otolith aragonite as significant negative excursions in d18O that reflected the increased temperature of local marine waters.
    [Show full text]
  • A Checklist of Texas Fresh-Water Fishes By
    A Checklist of I Texas Fresh-Water Fishes By CLARK HUBBS Department of Zoology The University of Texas DIVISION OF INLAND FISHERIES TEXAS GAME AND FISH COMMISSION Austin, Texas Marion Toole, Director IF Series - No. 3 Revised Dec. 1958 FOREWORD A checklist of Texas fresh-water fishes by CLARK HUBBS This checklist is modified from that of Hubbs (1957a). A number of changes have been made in nomenclature. Notropis roseus and N. deliciosus have been changed to N. texanus and N. strarnineus, re­ spectively, following Suttkus (1958). Etheostorna whipplei and E. m·tesiae have been changed to E. radiosum following a re-examina­ tion of available material. Two species have been added, Garnbusia senilis, following Hubbs (1958), and Eucinoslornus argenteus, a marine species collected in a .coastal stream near Brownsville. Two species which had not been described in the previous checklist are given their names, Gambusia geiseri, following Hubbs and Springer (1957), and G. helerochir, following Hubbs (1957b). The primary difference between the checklists is the addition of information on the distribution of fishes within the state to this list. The general concepts follow those given in a previous report (Hubbs, 1957c), but emphasize the ranges of the individual species rather than the distributional patterns. The range designations follow the common names of all species. The numbers refer to the modified game areas shovvn on the map. If the fish inhabits only a part of the area, it is so designated by preceding the number with letters (N. for north, etc.) indicating· the pai·t of the area inhabited by the species.
    [Show full text]
  • Molecular Clocks Provide New Insights Into the Evolutionary History of Galeichthyine Sea Catfishes
    ORIGINAL ARTICLE doi:10.1111/j.1558-5646.2009.00640.x MOLECULAR CLOCKS PROVIDE NEW INSIGHTS INTO THE EVOLUTIONARY HISTORY OF GALEICHTHYINE SEA CATFISHES Ricardo Betancur-R.1,2 and Jonathan W. Armbruster1 1Department of Biological Sciences, Auburn University, 331 Funchess Hall, Auburn, Alabama 36849 2E-mail: [email protected] Received August 28, 2008 Accepted January 7, 2009 Intercontinental distributions in the southern hemisphere can either be the result of Gondwanan vicariance or more recent transoceanic dispersal. Transoceanic dispersal has come into vogue for explaining many intercontinental distributions; however, it has been used mainly for organisms that can float or raft between the continents. Despite their name, the Sea Catfishes (Ariidae) have limited dispersal ability, and there are no examples of nearshore ariid genera with a transoceanic distribution except for Galeichthys where three species occur in southern Africa and one in the Peruvian coast. A previous study suggested that the group originated in Gondwana, and that the species arrived at their current range after the breakup of the supercontinent in the Early Cretaceous. To test this hypothesis, we infer molecular phylogenies (mitochondrial cytochrome b, ATP synthase 8/6, 12S, and 16S; nuclear rag2; total ∼4 kb) and estimate intercontinental divergence via molecular clocks (penalized-likelihood, Bayesian relaxed clock, and universal clock rates in fishes). Age ranges for cladogenesis of African and South American lineages are 15.4–2.5 my, far more recent than would be suggested by Gondwanan vicariance; thus, the distribution of galeichthyines must be explained by dispersal or more recent vicariant events. The nested position of the Peruvian species (Galeichthys peruvianus) within the African taxa is robust, suggesting that the direction of the dispersal was from Africa to South America.
    [Show full text]
  • Evaluación De La Extracción De Galeichthys Peruvianus “Bagre Con Fajas” En El Litoral Del Departamento De Lambayeque 2007-2012
    UNIVERSIDAD NACIONAL PEDRO RUIZ GALLO FACULTAD DE CIENCIAS BIOLÓGICAS PROGRAMA DE TITULACIÓN – I EN CIENCIAS BIOLÓGICAS Evaluación de la extracción de Galeichthys peruvianus “Bagre con fajas” en el litoral del departamento de Lambayeque 2007-2012 INFORME DE INVESTIGACIÓN Para optar el título profesional de licenciado en: BIOLOGÍA - PESQUERÍA - ZOOLOGÍA PRESENTADA POR Br. Jabo Abad Carito Paola Lambayeque-Perú 2016 i UNIVERSIDAD NACIONAL PEDRO RUIZ GALLO FACULTAD DE CIENCIAS BIOLÓGICAS PROGRAMA DE TITULACIÓN – I EN CIENCIAS BIOLÓGICAS Evaluación de la extracción de Galeichthys peruvianus “Bagre con fajas” en el litoral del departamento de Lambayeque 2007-2012 - INFORME DE INVESTIGACIÓN Para optar el título profesional de licenciado en: BIOLOGÍA - PESQUERÍA - ZOOLOGÍA PRESENTADA POR Br. Jabo Abad Carito Paola APROBADO POR: _______________________ _______________________ MSc. Jhon Wiston García López MSc. Marco Antonio Guzman Tello PRESIDENTE SECRETARIO _______________________ _______________________ Dra. Marlene E. Cardozo Quinteros MSc. Clara Aurora Cueva Castillo VOCAL PATROCINADORA ABRIL, 2016 ii DEDICATORIA A mis padres ANTERO JABO OGOÑA MARIA CELINDA ABAD TORRES Por sus enseñanzas e incondicional apoyo y sacrificio. Tener su esencia lo es todo para mí. A mis hermanos ROXANA, JAVIER, OMAR, WILSON, JANET, PAMELA Y LORENA Por su esencia de cada uno en mí. Ustedes son mis siete maravillas de mi vida. A mis pocos pero bonísimos amigos ZOILA, JEANNETTE, OMAR. Por su amistad a prueba de fuego. Ustedes representan aquellos hermanos de la vida. ii AGRADECIMIENTO Mi infinito y eterno agradecimiento al señor de todos: DIOS, Porque gracias a su AMOR INFINITO, tengo todo para ser feliz. Él me fortalece…… Mis más sinceros agradecimientos, a los profesores de la Facultad de Ciencias Biológicas, por sus enseñanzas en mi formación personal y profesional….
    [Show full text]
  • LNG to Power Project ADDITIONAL MARINE BIODIVERSITY STUDY
    LNG to Power Project ADDITIONAL MARINE BIODIVERSITY STUDY February 2018 – 16-3489 LNG TO POWER PROJECT MARINE BIOTA REPORT Table of Contents 1 ADDITIONAL MARINE BIODIVERSITY STUDY ............................................................................................... 1-1 1.1 INTRODUCTION ......................................................................................................................................... 1-1 1.1.1 Objectives .............................................................................................................................................. 1-1 1.1.2 Methodology ......................................................................................................................................... 1-2 1.1.3 Overview................................................................................................................................................ 1-2 1.1.4 Sampling Stations for Fish ..................................................................................................................... 1-3 1.2 FISH (PHYLLUM CHORDATA) ...................................................................................................................... 1-4 1.2.1 Survey for Fish ....................................................................................................................................... 1-4 1.3 DOLPHINS AND WHALES ............................................................................................................................ 1-7 1.4 MARINES TURTLES
    [Show full text]
  • Essential Fish Habitat
    12/12/16 Final Report 5-Year Review of Essential Fish Habitat Requirements Including Review of Habitat Areas of Particular Concern and Adverse Effects of Fishing and Non-Fishing in the Fishery Management Plans of the Gulf of Mexico December 2016 This is a publication of the Gulf of Mexico Fishery Management Council Pursuant to National Oceanic and Atmospheric Administration Award No. NA15NMF4410011. This page intentionally blank 5-Year Review of EFH i COVER SHEET Name of Action Essential Fish Habitat 5-Year Review Responsible Agencies and Contact Persons Gulf of Mexico Fishery Management Council 813-348-1630 2203 North Lois Avenue, Suite 1100 813-348-1711 (fax) Tampa, Florida 33607 [email protected] Claire Roberts ([email protected]) http://www.gulfcouncil.org National Marine Fisheries Service 727-824-5305 Southeast Regional Office 727-824-5308 (fax) 263 13th Avenue South http://sero.nmfs.noaa.gov St. Petersburg, Florida 33701 David Dale ([email protected]) Type of Action ( ) Administrative ( ) Legislative () Draft (X) Final 5-Year Review of EFH ii ABBREVIATIONS USED IN THIS DOCUMENT AP Advisory Panel CL Carapace length CMP Coastal Migratory Pelagic Resources in the Gulf of Mexico and Atlantic Region Council Gulf of Mexico Fishery Management Council DO Dissolved oxygen EA Environmental Assessment EEZ Exclusive Economic Zone EFH Essential Fish Habitat FEIS Final Environmental Impact Statement ER Eco-region F Instantaneous fishing mortality rate FL Fork length FMC Fishery management council FMP Fishery Management
    [Show full text]
  • Annual Reproductive Cycle of Gafftopsail Catfish,Bagre Marinus
    Mendoza-Carranza *3 11/11/05 1:35 PM Page 275 Hidrobiológica 2005, 15 (3): 275-282 Annual reproductive cycle of gafftopsail catfish, Bagre marinus (Ariidae) in a tropical coastal environment in the Gulf of Mexico Ciclo reproductivo anual del bagre bandera Bagre marinus (Ariidae) en un ambiente tropical costero del Golfo de México Manuel Mendoza-Carranza1 and Arlette Hernández-Franyutti2 1Departmento de Pesquerías Artesanales El Colegio de la Frontera Sur – ECOSUR-Unidad Villahermosa A.P. 1042 Admon. de Correos No.2 Col Atasta,Villahermosa, Tabasco C.P. 86100 México. email: [email protected] 2 Histology Laboratory. Universidad Juárez Autónoma de Tabasco. Carretera Vhsa-Cardenas Km 0.5. 86000, Villahermosa, Tabasco, México. Mendoza-Carranza M. and A. Hernández-Franyutti. 2005. Annual reproductive cycle of gafftopsail catfish, Bagre marinus (Ariidae) in a tropical coastal environment in the Gulf of Mexico. Hidrobiológica 15 (3): 275-282. ABSTRACT Reproductive cycle of gafftopsail catfish (Bagre marinus) and its relation to environmental variables were analyzed, based on specimens collected randomly from commercial landings of long line artisan fleet of the Chiltepec Barrier, Tabasco State. Gonadosomatic index showed that this species had one reproductive period per year (May - August). Reproduction occurs in shallow coastal waters at high temperatures (27.0 - 29.0°C) under heavy precipitation conditions (170- 333 mm). Female condition factor had a similar behavior than the gonadosomatic index, reaching high values (0.61 to 0.63) during May through July, although a high value of 0.64 was observed during March. A decrease on the condition factor in males from July (0.55) to October (0.50) was related to the energetic cost of oral incubation.
    [Show full text]
  • Fishes of the Charlotte Harbor Estuarine System, Florida Gregg R
    Gulf of Mexico Science Volume 22 Article 1 Number 2 Number 2 2004 Fishes of the Charlotte Harbor Estuarine System, Florida Gregg R. Poulakis Florida Fish and Wildlife Conservation Commission Richard E. Matheson Jr. Florida Fish and Wildlife Conservation Commission Michael E. Mitchell Florida Fish and Wildlife Conservation Commission David A. Blewett Florida Fish and Wildlife Conservation Commission Charles F. Idelberger Florida Fish and Wildlife Conservation Commission DOI: 10.18785/goms.2202.01 Follow this and additional works at: https://aquila.usm.edu/goms Recommended Citation Poulakis, G. R., R. E. Matheson Jr., M. E. Mitchell, D. A. Blewett nda C. F. Idelberger. 2004. Fishes of the Charlotte Harbor Estuarine System, Florida. Gulf of Mexico Science 22 (2). Retrieved from https://aquila.usm.edu/goms/vol22/iss2/1 This Article is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Gulf of Mexico Science by an authorized editor of The Aquila Digital Community. For more information, please contact [email protected]. Poulakis et al.: Fishes of the Charlotte Harbor Estuarine System, Florida Gulf of Mexico Science, 2004(2), pp. 117-150 Fishes of the Charlotte Harbor Estuarine System, Florida GREGG R. POULAIUS, RICHARD E. MATHESON JR., MICHAEL E. MITCHELL, DAVID A. BLEWETT, AND CHARLES F. lDELBERGER To date, 255 fish species in 95 families have been reliably reported from the Charlotte Harbor estuarine system in southwest Florida. The species list was com­ piled from recent fishery-independent collections, a review of reports and peer­ reviewed literature, and examination of cataloged specimens at the Florida Mu­ seum of Natural History.
    [Show full text]
  • Monophyly, Affinities, and Subfamilial Clades of Sea Catfishes (Siluriformes: Ariidae)
    133 Ichthyol. Explor. Freshwaters, Vol. 18, No. 2, pp. 133-143, 9 figs., 1 tab., June 2007 © 2007 by Verlag Dr. Friedrich Pfeil, München, Germany – ISSN 0936-9902 Monophyly, affinities, and subfamilial clades of sea catfishes (Siluriformes: Ariidae) , , Arturo Acero P.* *** and Ricardo Betancur-R.** *** Abstract The sea catfish family Ariidae is a natural group defined by four anatomical synapomorphies: lapillus otolith extraordinarily developed, bones of the otic capsules (prootic, pterotic, exoccipital, and epioccipital) profoundly inflated, presence of a well-developed ventral process of basioccipital, and male mouthbrooding of eggs and embryos. Recent studies, based on molecular and morphological evidence, agree that the sister group to ariids is the freshwater family Anchariidae from Madagascar; however, there is no consensus about the phylogenetic relationships of the Ariidae + Anchariidae clade among other siluroid families. The family Ariidae can be di- vided into two monophyletic lineages. Galeichthyinae, new subfamily, including one genus and four species, is defined by one derived morphological state: postcleithral process fused to the posterior dorsal process of cleithrum, forming a fan-shaped lamina. The subfamily Ariinae, including the remaining ariids, is characterized by four anatomical synapomorphies: posterior process of epioccipital produced and connected to the sustentaculum of Weberian apparatus, ventral process of basioccipital and ventral ossification of complex vertebra forming an aortic tunnel, presence of anterodorsal bony block of the orbitosphenoids, and absence of anterior nuchal plate. Additionally, mitochondrial and nuclear evidence strongly support the monophyly of the Ariidae (three amino acid synapomorphies) and its subfamilies (Galeichthyinae, six amino acid autapomorphies of Galeichthys peruvia- nus; Ariinae, four amino acid synapomorphies).
    [Show full text]
  • Siluriformes: Ariidae) As Inferred from Mitochondrial, Nuclear, and Morphological Evidence
    Available online at www.sciencedirect.com MOLECULAR PHYLOGENETICS W ScienceDirect AND EVOLUTION ELSEVIER Molecular Phylogenetics and Evolution 45 (2007) 339-357 www.elsevier.com/locate/ympev Systematics and biogeography of New World sea catfishes (Siluriformes: Ariidae) as inferred from mitochondrial, nuclear, and morphological evidence Ricardo Betancur-R. ^''''*, Arturo Acero P. '^, Eldredge Bermingham ^, Richard Cooke ^ ^ Department of Biological Sciences, Auburn University, 331 Funchess Hall, Auburn, AL 36849, USA Smithsonian Tropical Research Institute, Apartado 2072, Balboa, Panama Universidad Nacional de Colombia (Instituto de Ciencias Naturales), Cerro Punta Betín, Apartado 1016 (INVEMAR), Santa Marta, Colombia Received 23 December 2006; accepted 15 February 2007 Available online 28 February 2007 Abstract Ariid or sea catfishes include around 150 species that inhabit marine, brackish, and freshwater environments along world's tropical and subtropical continental shelves. Phylogenetic relationships for 46 New World and three Old World species of ariids were hypothesized using maximum parsimony and Bayesian inference reconstruction criteria on 2842 mitochondrial (cytochrome b, ATP synthase 8 and 6, ribosomal 12S and 16S) and 978 nuclear (rag2) nucleotide sites. The molecular topologies were compared to a previously compiled morphological data- set that was expanded herein to a total of 25 ariid species and 55 characters. Mitochondrial data yielded clades highly resolved at subfamilial, generic, and intrageneric levels. Nuclear rag2 reconstructions showed poor resolution at supra- and intrageneric levels, but provided support for the monophyly of most genera (except Ariopsis and Cathorops) as well as for the subfamihal clades. The hypothesized phylogeny derived from the morphological data was congruent with the molecular topologies at infrafamilial and generic levels.
    [Show full text]
  • Reproductive Biology and Trophic Niche of Hardhead Catfish in the Northern Gulf of Mexico
    Louisiana State University LSU Digital Commons LSU Master's Theses Graduate School January 2020 Reproductive Biology and Trophic Niche of Hardhead Catfish in the Northern Gulf of Mexico Lucas G. Pensinger Louisiana State University and Agricultural and Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_theses Part of the Marine Biology Commons, and the Oceanography Commons Recommended Citation Pensinger, Lucas G., "Reproductive Biology and Trophic Niche of Hardhead Catfish in the Northern Gulf of Mexico" (2020). LSU Master's Theses. 5046. https://digitalcommons.lsu.edu/gradschool_theses/5046 This Thesis is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Master's Theses by an authorized graduate school editor of LSU Digital Commons. For more information, please contact [email protected]. REPRODUCTIVE BIOLOGY AND TROPHIC NICHE OF HARDHEAD CATFISH IN THE NORTHERN GULF OF MEXICO A Thesis Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Master of Science in The Department of Oceanography and Coastal Science by Lucas G. Pensinger B.S., University of Delaware, 2017 May 2020 Acknowledgements I cannot start anywhere else but thanking my advisor, Dr. Steve Midway, whose advice and guidance throughout my time as LSU have been invaluable in my growth as a researcher, a scientist, and a writer. Similarly, I would like to thank my committee members, Dr. Chris Green and Dr. Mike Polito, for their constant willingness to answer questions and provide guidance for my thesis.
    [Show full text]