Redalyc.Check List of Stomiiform, Aulopiform and Myctophiform Fishes
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BONY FISHES 602 Bony Fishes
click for previous page BONY FISHES 602 Bony Fishes GENERAL REMARKS by K.E. Carpenter, Old Dominion University, Virginia, USA ony fishes constitute the bulk, by far, of both the diversity and total landings of marine organisms encoun- Btered in fisheries of the Western Central Atlantic.They are found in all macrofaunal marine and estuarine habitats and exhibit a lavish array of adaptations to these environments. This extreme diversity of form and taxa presents an exceptional challenge for identification. There are 30 orders and 269 families of bony fishes presented in this guide, representing all families known from the area. Each order and family presents a unique suite of taxonomic problems and relevant characters. The purpose of this preliminary section on technical terms and guide to orders and families is to serve as an introduction and initial identification guide to this taxonomic diversity. It should also serve as a general reference for those features most commonly used in identification of bony fishes throughout the remaining volumes. However, I cannot begin to introduce the many facets of fish biology relevant to understanding the diversity of fishes in a few pages. For this, the reader is directed to one of the several general texts on fish biology such as the ones by Bond (1996), Moyle and Cech (1996), and Helfman et al.(1997) listed below. A general introduction to the fisheries of bony fishes in this region is given in the introduction to these volumes. Taxonomic details relevant to a specific family are explained under each of the appropriate family sections. The classification of bony fishes continues to transform as our knowledge of their evolutionary relationships improves. -
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. -
CHECKLIST and BIOGEOGRAPHY of FISHES from GUADALUPE ISLAND, WESTERN MEXICO Héctor Reyes-Bonilla, Arturo Ayala-Bocos, Luis E
ReyeS-BONIllA eT Al: CheCklIST AND BIOgeOgRAphy Of fISheS fROm gUADAlUpe ISlAND CalCOfI Rep., Vol. 51, 2010 CHECKLIST AND BIOGEOGRAPHY OF FISHES FROM GUADALUPE ISLAND, WESTERN MEXICO Héctor REyES-BONILLA, Arturo AyALA-BOCOS, LUIS E. Calderon-AGUILERA SAúL GONzáLEz-Romero, ISRAEL SáNCHEz-ALCántara Centro de Investigación Científica y de Educación Superior de Ensenada AND MARIANA Walther MENDOzA Carretera Tijuana - Ensenada # 3918, zona Playitas, C.P. 22860 Universidad Autónoma de Baja California Sur Ensenada, B.C., México Departamento de Biología Marina Tel: +52 646 1750500, ext. 25257; Fax: +52 646 Apartado postal 19-B, CP 23080 [email protected] La Paz, B.C.S., México. Tel: (612) 123-8800, ext. 4160; Fax: (612) 123-8819 NADIA C. Olivares-BAñUELOS [email protected] Reserva de la Biosfera Isla Guadalupe Comisión Nacional de áreas Naturales Protegidas yULIANA R. BEDOLLA-GUzMáN AND Avenida del Puerto 375, local 30 Arturo RAMíREz-VALDEz Fraccionamiento Playas de Ensenada, C.P. 22880 Universidad Autónoma de Baja California Ensenada, B.C., México Facultad de Ciencias Marinas, Instituto de Investigaciones Oceanológicas Universidad Autónoma de Baja California, Carr. Tijuana-Ensenada km. 107, Apartado postal 453, C.P. 22890 Ensenada, B.C., México ABSTRACT recognized the biological and ecological significance of Guadalupe Island, off Baja California, México, is Guadalupe Island, and declared it a Biosphere Reserve an important fishing area which also harbors high (SEMARNAT 2005). marine biodiversity. Based on field data, literature Guadalupe Island is isolated, far away from the main- reviews, and scientific collection records, we pres- land and has limited logistic facilities to conduct scien- ent a comprehensive checklist of the local fish fauna, tific studies. -
1 Exon Probe Sets and Bioinformatics Pipelines for All Levels of Fish Phylogenomics
bioRxiv preprint doi: https://doi.org/10.1101/2020.02.18.949735; this version posted February 19, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Exon probe sets and bioinformatics pipelines for all levels of fish phylogenomics 2 3 Lily C. Hughes1,2,3,*, Guillermo Ortí1,3, Hadeel Saad1, Chenhong Li4, William T. White5, Carole 4 C. Baldwin3, Keith A. Crandall1,2, Dahiana Arcila3,6,7, and Ricardo Betancur-R.7 5 6 1 Department of Biological Sciences, George Washington University, Washington, D.C., U.S.A. 7 2 Computational Biology Institute, Milken Institute of Public Health, George Washington 8 University, Washington, D.C., U.S.A. 9 3 Department of Vertebrate Zoology, National Museum of Natural History, Smithsonian 10 Institution, Washington, D.C., U.S.A. 11 4 College of Fisheries and Life Sciences, Shanghai Ocean University, Shanghai, China 12 5 CSIRO Australian National Fish Collection, National Research Collections of Australia, 13 Hobart, TAS, Australia 14 6 Sam Noble Oklahoma Museum of Natural History, Norman, O.K., U.S.A. 15 7 Department of Biology, University of Oklahoma, Norman, O.K., U.S.A. 16 17 *Corresponding author: Lily C. Hughes, [email protected]. 18 Current address: Department of Organismal Biology and Anatomy, University of Chicago, 19 Chicago, IL. 20 21 Keywords: Actinopterygii, Protein coding, Systematics, Phylogenetics, Evolution, Target 22 capture 23 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.02.18.949735; this version posted February 19, 2020. -
Acanthopterygii, Bone, Eurypterygii, Osteology, Percomprpha
Research in Zoology 2014, 4(2): 29-42 DOI: 10.5923/j.zoology.20140402.01 Comparative Osteology of the Jaws in Representatives of the Eurypterygian Fishes Yazdan Keivany Department of Natural Resources (Fisheries Division), Isfahan University of Technology, Isfahan, 84156-83111, Iran Abstract The osteology of the jaws in representatives of 49 genera in 40 families of eurypterygian fishes, including: Aulopiformes, Myctophiformes, Lampridiformes, Polymixiiformes, Percopsiformes, Mugiliformes, Atheriniformes, Beloniformes, Cyprinodontiformes, Stephanoberyciformes, Beryciformes, Zeiformes, Gasterosteiformes, Synbranchiformes, Scorpaeniformes (including Dactylopteridae), and Perciformes (including Elassomatidae) were studied. Generally, in this group, the upper jaw consists of the premaxilla, maxilla, and supramaxilla. The lower jaw consists of the dentary, anguloarticular, retroarticular, and sesamoid articular. In higher taxa, the premaxilla bears ascending, articular, and postmaxillary processes. The maxilla usually bears a ventral and a dorsal articular process. The supramaxilla is present only in some taxa. The dentary is usually toothed and bears coronoid and posteroventral processes. The retroarticular is small and located at the posteroventral corner of the anguloarticular. Keywords Acanthopterygii, Bone, Eurypterygii, Osteology, Percomprpha following method for clearing and staining bone and 1. Introduction cartilage provided in reference [18]. A camera lucida attached to a Wild M5 dissecting stereomicroscope was used Despite the introduction of modern techniques such as to prepare the drawings. The bones in the first figure of each DNA sequencing and barcoding, osteology, due to its anatomical section are arbitrarily shaded and labeled and in reliability, still plays an important role in the systematic the others are shaded in a consistent manner (dark, medium, study of fishes and comprises a major percent of today’s and clear) to facilitate comparison among the taxa. -
Fao/Government Cooperative Programme Scientific Basis
FI:GCP/RLA/140/JPN TECHNICAL DOCUMENT No. 4 FAO/GOVERNMENT COOPERATIVE PROGRAMME SCIENTIFIC BASIS FOR ECOSYSTEM-BASED MANAGEMENT IN THE LESSER ANTILLES INCLUDING INTERACTIONS WITH MARINE MAMMALS AND OTHER TOP PREDATORS CRUISE REPORT FOR THE LAPE ECOSYSTEM SURVEY ON RV CELTIC EXPLORER (CE0607) FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS Barbados, 2006 FI:GCP/RLA/140/JPN TECHNICAL DOCUMENT No. 4 FAO/GOVERNMENT COOPERATIVE PROGRAMME SCIENTIFIC BASIS FOR ECOSYSTEM-BASED MANAGEMENT IN THE LESSER ANTILLES INCLUDING INTERACTIONS WITH MARINE MAMMALS AND OTHER TOP PREDATORS CRUISE REPORT FOR THE LAPE ECOSYSTEM SURVEY ON RV CELTIC EXPLORER (CE0607) Lesser Antilles Pelagic Ecosystem Project (GCP/RLA/140/JPN) Bridgetown, Barbados FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS Barbados, 2006 This technical report is one of a series of reports prepared during the course of the project identified on the title page. The conclusions and recommendations given in the report are those considered appropriate at the time of its preparation. They may be modified in the light of further knowledge gained at subsequent stages of the project. The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries All rights reserved. Reproduction and dissemination of material in this information product for educational or other non-commercial purposes are authorized without any prior written permission from the copyright holders provided the source is fully acknowledged. -
Updated Checklist of Marine Fishes (Chordata: Craniata) from Portugal and the Proposed Extension of the Portuguese Continental Shelf
European Journal of Taxonomy 73: 1-73 ISSN 2118-9773 http://dx.doi.org/10.5852/ejt.2014.73 www.europeanjournaloftaxonomy.eu 2014 · Carneiro M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:9A5F217D-8E7B-448A-9CAB-2CCC9CC6F857 Updated checklist of marine fishes (Chordata: Craniata) from Portugal and the proposed extension of the Portuguese continental shelf Miguel CARNEIRO1,5, Rogélia MARTINS2,6, Monica LANDI*,3,7 & Filipe O. COSTA4,8 1,2 DIV-RP (Modelling and Management Fishery Resources Division), Instituto Português do Mar e da Atmosfera, Av. Brasilia 1449-006 Lisboa, Portugal. E-mail: [email protected], [email protected] 3,4 CBMA (Centre of Molecular and Environmental Biology), Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. E-mail: [email protected], [email protected] * corresponding author: [email protected] 5 urn:lsid:zoobank.org:author:90A98A50-327E-4648-9DCE-75709C7A2472 6 urn:lsid:zoobank.org:author:1EB6DE00-9E91-407C-B7C4-34F31F29FD88 7 urn:lsid:zoobank.org:author:6D3AC760-77F2-4CFA-B5C7-665CB07F4CEB 8 urn:lsid:zoobank.org:author:48E53CF3-71C8-403C-BECD-10B20B3C15B4 Abstract. The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. -
Morphology and Mathematics. by D'arcy Wentworth Thompson. The
( 857 ) XXVII.—Morphology and Mathematics. By D'Arcy Wentworth Thompson. (Read December 7, 1914. MS. received February 1, 1915. Issued separately June 22, 1915.) The study of Organic Form, which we call by GOETHE'S name of Morphology, is but a portion of that wider Science of Form which deals with the forms assumed by matter under all aspects and conditions, and, in a still wider sense, with Forms which are theoretically imaginable. The study of Form may be descriptive merely, or it may become analytical. We begin by describing the shape of an object in the simple words of common speech : we end by denning it in the precise language of mathematics ; and the one method tends to follow the other in strict scientific order and historical continuity. Thus, fer instance, the form of the earth, of a raindrop or a rainbow, the shape of the hanging chain, or the path of a stone thrown up into the air, may all be described, however inadequately, in common words ; but when we have learned to comprehend and to define the sphere, the catenary, or the parabola, we have made a wonderful and perhaps a manifold advance. The mathematical definition of a "form" has a quality of precision which was quite lacking in our earlier stage of mere description ; it is expressed in few words, or in still briefer symbols, and these words or symbols are so pregnant with meaning that thought itself is economised ; we are brought by means of it in touch with GALILEO'S aphorism, that " the Book of Nature is written in characters of Geometry." Next, we soon reach through mathematical analysis to mathematical synthesis ; we discover homologies or identities which were not obvious before, and which our descriptions obscured rather than revealed : as, for instance, when we learn that, however we hold our chain, or however we fire our bullet, the contour of the one or the path of the other is always mathematically homologous. -
Sardinella
A CHECK.LIST OF THE FISHES OF INDIA, BURMA AND CEYLON. PART II. CLUPEIFORMES, BATHYCLUPEIFORMES, GALAXIIFORMES, SCOPELIFORMES AND ATELEOPIl~"ORMES. By K. S. l\iISRA, D.Se., F.Z.S., ,,1ssistant Superintendent, Zoological Survey of India, Kaiser Castle, Banaras Gantt. CONTENTS. PAGE. INTRODUOTION •• 382 SYSTEMATIC ACCOUNT 382 Class TELEOSTOMI 382 Subclass ACTINOPTERYGII 382 Order CLUPEIFOR)IES (ISOSPONDYLI, MALACOPTERYGII S. STR., 382 THRISSO)IORPHI). Suborder CLUPEOIDEI .. 382 Superfamily ELOPOIDAE 382 Family ELOPIDAE 382 Elopa 8aurU8 L. 382 Family MEGALOPIDA.E 383 M egalopa cyprinoides (Brouss.) 383 Su perfamily ALBULOIDAE 383 Family ALBULIDAE 383 Albula vulpe8 (L.) 384 Superfamily CLUPEOIDAE ... 384 Family CL UPEIDAE .' 384 SU bfamily DU88umieriini 384- Dussumieria acuta (C.V.) ". 384 Dus8umieria hasselti Blkr. 384 Ehirava jluviatiz.i8 Deraniyagala 385 Stolephorus malabaricu.9 Day 385 Subfamily Clupeini 385 IJarengula, punctata (RUpp.) 385 , Ilarcngula 'l:itteta (C. V .) .. 386 Sardinella albella.<C.V.) 386 Sardinella clupeoides (Blkr.) 387 Sardinella dayi Reg. 387 Saidinella jimbriata (C.V.) .. 387 Sa-rdinella gibbosa (Blkr.) 387 Sarain,ella longiceps C. V. 388 Sardinella melon1#tra (C.) 388 Sard·inella 8inden~i8 (Day) 389 Sardinella sirm (RliPll.) 389 Hilsu U·isha (Ham.) 389 HUsa !'anglt'rta (Blkr.) 390 390 lli/sa tol~ (C.v.) ., . [ 377 ] Q 378 Records of tll.e Indian Museum. [VOL. XLV .P~OE. (}ac1lUsia chapra (Ham.) 391 GadU8ia vari8!Jata (Day) 391 l(owala coval (C.) · . 392 Oarica Bohoma Ham. 392 Ilisha brachllsom:a (Blkr.) .. 3\J2 llisha elongata (Benn.) .. 393 llish.Q jiligera (C. V.) Ii • 393 llislla indica (Swns.) .. 393 ilisha kampeni (Web. & de Bfrt.) 394 llisha leach.enaulti (C.V.) , . -
Marine Fishes of the Azores: an Annotated Checklist and Bibliography
MARINE FISHES OF THE AZORES: AN ANNOTATED CHECKLIST AND BIBLIOGRAPHY. RICARDO SERRÃO SANTOS, FILIPE MORA PORTEIRO & JOÃO PEDRO BARREIROS SANTOS, RICARDO SERRÃO, FILIPE MORA PORTEIRO & JOÃO PEDRO BARREIROS 1997. Marine fishes of the Azores: An annotated checklist and bibliography. Arquipélago. Life and Marine Sciences Supplement 1: xxiii + 242pp. Ponta Delgada. ISSN 0873-4704. ISBN 972-9340-92-7. A list of the marine fishes of the Azores is presented. The list is based on a review of the literature combined with an examination of selected specimens available from collections of Azorean fishes deposited in museums, including the collection of fish at the Department of Oceanography and Fisheries of the University of the Azores (Horta). Personal information collected over several years is also incorporated. The geographic area considered is the Economic Exclusive Zone of the Azores. The list is organised in Classes, Orders and Families according to Nelson (1994). The scientific names are, for the most part, those used in Fishes of the North-eastern Atlantic and the Mediterranean (FNAM) (Whitehead et al. 1989), and they are organised in alphabetical order within the families. Clofnam numbers (see Hureau & Monod 1979) are included for reference. Information is given if the species is not cited for the Azores in FNAM. Whenever available, vernacular names are presented, both in Portuguese (Azorean names) and in English. Synonyms, misspellings and misidentifications found in the literature in reference to the occurrence of species in the Azores are also quoted. The 460 species listed, belong to 142 families; 12 species are cited for the first time for the Azores. -
Zootaxa, First Report of Aulopus (Teleostei: Aulopidae) From
Zootaxa 2628: 27–42 (2010) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2010 · Magnolia Press ISSN 1175-5334 (online edition) First report of Aulopus (Teleostei: Aulopidae) from Southwestern Atlantic, with a review of records and a key to Western Atlantic Aulopoidei species ALFREDO CARVALHO-FILHO1,4, GUY MARCOVALDI2, CLÁUDIO L. S. SAMPAIO3, M. ISABEL G. PAIVA2 & LUIZ A. G. DUARTE2 1Fish-Bizz Ltda. Rua Maria Garcez, 39, São Paulo, SP, 05424-070, Brasil 2Projeto Tamar-ICMBio. Avenida do Farol Garcia D´Ávila, s/n, Praia do Forte, Mata de São João, BA, 48280-000, Brasil 3Universidade Federal de Alagoas, Unidade de Ensino Penedo. Av. Beira Rio s/n°, Centro Histórico, Penedo, AL. 57.200-000 4Corresponding author. E-mail: [email protected] Abstract In this second paper dedicated to report on deep-sea fishes from Brazilian waters, mainly from Bahia, the presence of one family and three species of Aulopoidei is reported for the first time from Brazilian waters: the aulopid Aulopus filamentosus (royal flagfin), the synodontids Saurida normani and Synodus poeyi (shortjaw lizardfish and offshore lizardfish, respectively). The presence of Synodus saurus and Saurida suspicio in Brazilian waters is discussed, and a key to the Western Atlantic Aulopoidei is provided. Key words: Lizardfishes, flagfin, Aulopus, Saurida, Synodus, Aulopidae, Synodontidae, deep-sea fishes Introduction According to Davis (2010), the world-wide marine and usually deep-sea, benthic or pelagic Aulopiformes order, contains 16 families, split in 3 suborders of extant taxa: Alepisauroidei (Alepisauridae, Bathysauridae, Bathysauroididae, Bathysauropsidae, Chlorophthalmidae, Evermannellidae, Giganturidae, Ipnopidae, Notosudidae, Paralepididae, Scopelarchidae and Sudidae), Paraulopoidei (Paraulopidae), and Aulopoidei (Aulopidae, Pseudotrichonotidae, and Synodontidae). -
Olfactory Organs in the Deep Sea Hatchetfish <I>Sternoptyx
NOTES BULLETIN OF MARINE SCIENCE, 53(3): 1163-1167, 1993 OLFACTORY ORGANS IN THE DEEP SEA HATCHETFISH STERNOPTYX DIAPHANA (STOMIIFORMES, STERNOPTYCHIDAE) Ronald C. Baird and George Y. Jumper It has been estimated that more than 80% of the deep sea fish fauna living at depths greater than 1,000 m exhibit sexual dimorphism in the olfactory system (Marshall, 1967). The most common form of dimorphism involves development oflarge, complex olfactory receptors in males while in females the olfactory system is regressed or microsmatic. Marshall also notes that in contrast, mesopelagic fishes living at depths less than 1,000 m generally have well-developed olfactory systems in both sexes and sexual dimorphism is uncommon. Recently, sexual dimorphism was reported in the olfactory organs of two me- sopelagic sternoptychids Argyropelecus hemigymnus and Valenciennellus tri- punctulatus by Baird et aI., 1990. Unlike many of the deeper living fishesdescribed by Marshall (op. cit.) the olfactory systems in females of these species are relatively well developed. The potential advantages of chemical communication to mate location in deep- sea fishes have been explored by Jumper and Baird (1991) and the use of odor cues appears to greatly enhance mate location in A. hemigymnus. The nasal rosettes of the hatchetfish Sternoptyx diaphana do not exhibit di- morphism. More importantly, the nasal rosettes of both sexes in S. diaphana are much smaller in size, and considerably less complex in structure than in A. hemi- gymnus. In this article, we describe the external morphology of the olfactory organs in sexually mature individuals of S. diaphana, compare them to that found in A.