Fish Dissection Guide
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Bony Fish Guide
This guide will help you to complete the Bony Fish Observation Worksheet. Bony Fish Guide Fish (n.) An ectothermic (cold-blooded) vertebrate (with a backbone) aquatic (lives in water) animal that moves with the help of fins (limbs with no fingers or toes) and breathes with gills. This definition might seem very broad, and that is because fish are one of the most diverse groups of animals on the planet—there are a lot of fish in the sea (not to mention rivers, lakes and ponds). In fact, scientists count at least 32,000 species of fish—more than any other type of vertebrate. Fish are split into three broad classes: Jawless Fish Cartilaginous Fish Bony Fish (hagfish, lampreys, etc.) (sharks, rays, skates, etc.) (all other fish) This guide will focus on the Bony Fish. There are at least 28,000 species of bony fish, and they are found in almost every naturally occurring body of water on the planet. Bony fish range in size: • Largest: ocean sunfish (Mola mola), 11 feet, over 5,000 pounds • Smallest: dwarf pygmy goby (Pandaka pygmaea), ½ inch, a fraction of an ounce (This image is life size.) The following guide will help you learn more about the bony fish you can find throughout the New England Aquarium. Much of the guide is keyed to the Giant Ocean Tank, but can be applied to many kinds of fish. Even if you know nothing about fish, you can quickly learn a few things: The shape of a fish’s body, the position of its mouth and the shape of its tail can give you many clues as to its behavior and adaptations. -
Respiratory Disorders of Fish
This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Disorders of the Respiratory System in Pet and Ornamental Fish a, b Helen E. Roberts, DVM *, Stephen A. Smith, DVM, PhD KEYWORDS Pet fish Ornamental fish Branchitis Gill Wet mount cytology Hypoxia Respiratory disorders Pathology Living in an aquatic environment where oxygen is in less supply and harder to extract than in a terrestrial one, fish have developed a respiratory system that is much more efficient than terrestrial vertebrates. The gills of fish are a unique organ system and serve several functions including respiration, osmoregulation, excretion of nitroge- nous wastes, and acid-base regulation.1 The gills are the primary site of oxygen exchange in fish and are in intimate contact with the aquatic environment. In most cases, the separation between the water and the tissues of the fish is only a few cell layers thick. Gills are a common target for assault by infectious and noninfectious disease processes.2 Nonlethal diagnostic biopsy of the gills can identify pathologic changes, provide samples for bacterial culture/identification/sensitivity testing, aid in fungal element identification, provide samples for viral testing, and provide parasitic organisms for identification.3–6 This diagnostic test is so important that it should be included as part of every diagnostic workup performed on a fish. -
Alcolapia Grahami ERSS
Lake Magadi Tilapia (Alcolapia grahami) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, March 2015 Revised, August 2017, October 2017 Web Version, 8/21/2018 1 Native Range and Status in the United States Native Range From Bayona and Akinyi (2006): “The natural range of this species is restricted to a single location: Lake Magadi [Kenya].” Status in the United States No records of Alcolapia grahami in the wild or in trade in the United States were found. The Florida Fish and Wildlife Conservation Commission has listed the tilapia Alcolapia grahami as a prohibited species. Prohibited nonnative species (FFWCC 2018), “are considered to be dangerous to the ecology and/or the health and welfare of the people of Florida. These species are not allowed to be personally possessed or used for commercial activities.” Means of Introductions in the United States No records of Alcolapia grahami in the United States were found. 1 Remarks From Bayona and Akinyi (2006): “Vulnerable D2 ver 3.1” Various sources use Alcolapia grahami (Eschmeyer et al. 2017) or Oreochromis grahami (ITIS 2017) as the accepted name for this species. Information searches were conducted under both names to ensure completeness of the data gathered. 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing According to Eschmeyer et al. (2017), Alcolapia grahami (Boulenger 1912) is the current valid name for this species. It was originally described as Tilapia grahami; it has also been known as Oreoghromis grahami, and as a synonym, but valid subspecies, of -
Lecture 8 – Head and Jaw Osteology
Lecture 8 – Head and Jaw osteology More derived fishes (Ray finned fishes) The variability of the jaw structure of bony fishes provides an explanation for the extensive adaptive radiation in the group and why they are so diverse and occupy almost every aquatic niche available. Skull diversity (A) carp, Cyprinus carpio, (B) vampire characin, Hydrolycus scomberoides, (C) catfish Arius felis. (D) cod Gadus morhua. (E) large-mouth bass, Micropterus salmoides (F) The parrotfish Scarus guacamaia. Scale bar = 10 mm WESTNEAT 2004 From an evolutionary standpoint, fishes were the first animals to develop bony jaws. Versatile jaws and multiple feeding strategies allowed fishes to fill, or radiate into, a diverse range of niches. They have evolved to feed in all possible ways – sucking, biting, scraping, nipping, crushing etc. The head of a teleost has 5 main regions: Cranium, jaws, cheeks, hydroid arch, opercula. The head of a fish has five main regions • 1) The CRANIUM is composed of the bones providing direct support and protection to the brain and the visual, Anterior Posterior olfactory, and auditory organs. Below the cranium is the parashenoid bone. • Parasphenoid plays a role in the jaws as Features of the neurocranium sensu lato (from Caranx it acts as a hard melampygus, lateral aspect, left, and posterior aspect, right). A = prevomer, B = ethmoid, C = frontal, D = palate supraoccipital, E = pterotic, F = exoccipital, G = basioccipital, H = foramen magnum, I = parasphenoid, J = orbit. The five main regions Bowfin 2) The JAWS • Lower Jaw – has an Angular articular and dentary bone • Angular articular- The paired bones form the posterior part of either side of the lower jaw and articulate with the suspensorium. -
Invasive Species of the Pacific Northwest
Invasive Species of the Pacific Northwest: Green Sunfish Lepomis cyanellus Derek Arterburn FISH 423: Olden 12.5.14 Figure 1: Adult Green sunfish Lepomis cyanellus . Photo from http://www.freshwater-fishing- news.com/fish-species-north -america/green-sunfish/ Classification Lepomis cyanellus may have a few teeth, Order: Perciformes which can be found on the tongue. Family: Centrarchidae Additional distinguishing marks are the 7-12 Genus: Lepomis parallel diffused dark bars running ventral to Species: cyanellus dorsal along the side of L. cyanellus, and the bluish-green pattern. The bluish-green Identification coloration takes place on the mainly black/dark brown/olive body, composed of Adult Green Sunfish, Lepomis ctenoid scales, which fades to a lighter cyanellus, commonly reach a total length of ventral color. The dark sides of L. cyanellus 31cm, with juveniles ranging from 12-15cm. are contrast with a yellow/cream ventral Adult Green Sunfish have been known to coloration (Cockerell 1913). The thick reach a maximum weight of one kilogram caudal peduncle is without an adipose fin, (2.2lbs). L. cyanellus is a deep bodied, and the peduncle runs to a rounded, slightly laterally compressed species, with a lateral forked, homocercal caudal fin. The paired line running from the operculum to the fins on Lepomis cyanellus are derived in caudal peduncle. The posterior of the orientation. The Green Sunfish has lateral operculum has a characteristic dark spot placement of the pectoral fins with vertical relatively the same size as the eye, and the insertion, anterior pelvic fins, and spines same size spot may also be found at the base found on the anal and dorsal fins. -
Percomorph Phylogeny: a Survey of Acanthomorphs and a New Proposal
BULLETIN OF MARINE SCIENCE, 52(1): 554-626, 1993 PERCOMORPH PHYLOGENY: A SURVEY OF ACANTHOMORPHS AND A NEW PROPOSAL G. David Johnson and Colin Patterson ABSTRACT The interrelationships of acanthomorph fishes are reviewed. We recognize seven mono- phyletic terminal taxa among acanthomorphs: Lampridiformes, Polymixiiformes, Paracan- thopterygii, Stephanoberyciformes, Beryciformes, Zeiformes, and a new taxon named Smeg- mamorpha. The Percomorpha, as currently constituted, are polyphyletic, and the Perciformes are probably paraphyletic. The smegmamorphs comprise five subgroups: Synbranchiformes (Synbranchoidei and Mastacembeloidei), Mugilomorpha (Mugiloidei), Elassomatidae (Elas- soma), Gasterosteiformes, and Atherinomorpha. Monophyly of Lampridiformes is justified elsewhere; we have found no new characters to substantiate the monophyly of Polymixi- iformes (which is not in doubt) or Paracanthopterygii. Stephanoberyciformes uniquely share a modification of the extrascapular, and Beryciformes a modification of the anterior part of the supraorbital and infraorbital sensory canals, here named Jakubowski's organ. Our Zei- formes excludes the Caproidae, and characters are proposed to justify the monophyly of the group in that restricted sense. The Smegmamorpha are thought to be monophyletic principally because of the configuration of the first vertebra and its intermuscular bone. Within the Smegmamorpha, the Atherinomorpha and Mugilomorpha are shown to be monophyletic elsewhere. Our Gasterosteiformes includes the syngnathoids and the Pegasiformes -
Anatomy and Go Fish! Background
Anatomy and Go Fish! Background Introduction It is important to properly identify fi sh for many reasons: to follow the rules and regulations, for protection against sharp teeth or protruding spines, for the safety of the fi sh, and for consumption or eating purposes. When identifying fi sh, scientists and anglers use specifi c vocabulary to describe external or outside body parts. These body parts are common to most fi sh. The difference in the body parts is what helps distinguish one fi sh from another, while their similarities are used to classify them into groups. There are approximately 29,000 fi sh species in the world. In order to identify each type of fi sh, scientists have grouped them according to their outside body parts, specifi cally the number and location of fi ns, and body shape. Classifi cation Using a system of classifi cation, scientists arrange all organisms into groups based on their similarities. The fi rst system of classifi cation was proposed in 1753 by Carolus Linnaeus. Linnaeus believed that each organism should have a binomial name, genus and species, with species being the smallest organization unit of life. Using Linnaeus’ system as a guide, scientists created a hierarchical system known as taxonomic classifi cation, in which organisms are classifi ed into groups based on their similarities. This hierarchical system moves from largest and most general to smallest and most specifi c: kingdom, phylum, class, order, family, genus, and species. {See Figure 1. Taxonomic Classifi cation Pyramid}. For example, fi sh belong to the kingdom Animalia, the phylum Chordata, and from there are grouped more specifi cally into several classes, orders, families, and thousands of genus and species. -
Humboldt Bay Fishes
Humboldt Bay Fishes ><((((º>`·._ .·´¯`·. _ .·´¯`·. ><((((º> ·´¯`·._.·´¯`·.. ><((((º>`·._ .·´¯`·. _ .·´¯`·. ><((((º> Acknowledgements The Humboldt Bay Harbor District would like to offer our sincere thanks and appreciation to the authors and photographers who have allowed us to use their work in this report. Photography and Illustrations We would like to thank the photographers and illustrators who have so graciously donated the use of their images for this publication. Andrey Dolgor Dan Gotshall Polar Research Institute of Marine Sea Challengers, Inc. Fisheries And Oceanography [email protected] [email protected] Michael Lanboeuf Milton Love [email protected] Marine Science Institute [email protected] Stephen Metherell Jacques Moreau [email protected] [email protected] Bernd Ueberschaer Clinton Bauder [email protected] [email protected] Fish descriptions contained in this report are from: Froese, R. and Pauly, D. Editors. 2003 FishBase. Worldwide Web electronic publication. http://www.fishbase.org/ 13 August 2003 Photographer Fish Photographer Bauder, Clinton wolf-eel Gotshall, Daniel W scalyhead sculpin Bauder, Clinton blackeye goby Gotshall, Daniel W speckled sanddab Bauder, Clinton spotted cusk-eel Gotshall, Daniel W. bocaccio Bauder, Clinton tube-snout Gotshall, Daniel W. brown rockfish Gotshall, Daniel W. yellowtail rockfish Flescher, Don american shad Gotshall, Daniel W. dover sole Flescher, Don stripped bass Gotshall, Daniel W. pacific sanddab Gotshall, Daniel W. kelp greenling Garcia-Franco, Mauricio louvar -
The Opercular Mouth-Opening Mechanism of Largemouth Bass Functions As a 3D Four-Bar Linkage with Three Degrees of Freedom Aaron M
© 2017. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2017) 220, 4612-4623 doi:10.1242/jeb.159079 RESEARCH ARTICLE The opercular mouth-opening mechanism of largemouth bass functions as a 3D four-bar linkage with three degrees of freedom Aaron M. Olsen1,*,‡,§, Ariel L. Camp2,‡ and Elizabeth L. Brainerd2 ABSTRACT (Greene, 1983), the thorax and wings of flying insects (Wootton, The planar, one degree of freedom (1-DoF) four-bar linkage is an 2009), and multiple skeletal elements in the skulls of fishes important model for understanding the function, performance and (Ballintijn, 1969; Westneat, 1990). In addition, four-bar models evolution of numerous biomechanical systems. One such system is have been used to evaluate functional hypotheses by comparing in vivo the opercular mechanism in fishes, which is thought to function like a simulated and kinematics (Westneat, 1991; Van four-bar linkage to depress the lower jaw. While anatomical and Wassenbergh et al., 2005; Roos et al., 2009), to measure how behavioral observations suggest some form of mechanical coupling, force and motion are transmitted through musculoskeletal systems previous attempts to model the opercular mechanism as a planar (Aerts and Verraes, 1984; Adriaens et al., 2001; Van Wassenbergh four-bar have consistently produced poor model fits relative to et al., 2013), and to examine the distribution and evolution of observed kinematics. Using newly developed, open source functional diversity (Westneat, 1995; Alfaro et al., 2004, 2005; mechanism fitting software, we fitted multiple three-dimensional Wainwright et al., 2004; Hulsey and García de León, 2005). (3D) four-bar models with varying DoF to in vivo kinematics in In biomechanical studies, four-bar models have been applied largemouth bass to test whether the opercular mechanism functions most extensively to the skulls of fishes. -
Biodiversity of Arctic Marine Fishes: Taxonomy and Zoogeography
Mar Biodiv DOI 10.1007/s12526-010-0070-z ARCTIC OCEAN DIVERSITY SYNTHESIS Biodiversity of arctic marine fishes: taxonomy and zoogeography Catherine W. Mecklenburg & Peter Rask Møller & Dirk Steinke Received: 3 June 2010 /Revised: 23 September 2010 /Accepted: 1 November 2010 # Senckenberg, Gesellschaft für Naturforschung and Springer 2010 Abstract Taxonomic and distributional information on each Six families in Cottoidei with 72 species and five in fish species found in arctic marine waters is reviewed, and a Zoarcoidei with 55 species account for more than half list of families and species with commentary on distributional (52.5%) the species. This study produced CO1 sequences for records is presented. The list incorporates results from 106 of the 242 species. Sequence variability in the barcode examination of museum collections of arctic marine fishes region permits discrimination of all species. The average dating back to the 1830s. It also incorporates results from sequence variation within species was 0.3% (range 0–3.5%), DNA barcoding, used to complement morphological charac- while the average genetic distance between congeners was ters in evaluating problematic taxa and to assist in identifica- 4.7% (range 3.7–13.3%). The CO1 sequences support tion of specimens collected in recent expeditions. Barcoding taxonomic separation of some species, such as Osmerus results are depicted in a neighbor-joining tree of 880 CO1 dentex and O. mordax and Liparis bathyarcticus and L. (cytochrome c oxidase 1 gene) sequences distributed among gibbus; and synonymy of others, like Myoxocephalus 165 species from the arctic region and adjacent waters, and verrucosus in M. scorpius and Gymnelus knipowitschi in discussed in the family reviews. -
Observation on the Urinogenital Papilla and Sexual Dimorphism in Some Indian Gobiids (Gobiidae: Teleostei)
Observation on the urinogenital papilla and sexual dimorphism in some Indian gobiids (Gobiidae: Teleostei) Item Type article Authors Har, S.P. Download date 05/10/2021 03:51:48 Link to Item http://hdl.handle.net/1834/32378 Journal of the Indian Fisheries Association 7 27,2000, 7-17 OBSERVATION ON THE URINOGENITAL PAPILLA AND SEXUAL DIMORPHISM IN SOME INDIAN GOBIIDS (GOBIIDAE: TELEOSTEI) SAKTI HAR Department of Zoology, Ranwnanda College, Bishnupur, Bankura-722122. W. Bengal, India. ABSTRACT A thorough comparative study on the urinogenital papilla and sexual dimorphism has been made for the first time in both the sexes of twelve Indian gobiids- Glassogobius giuris (Han1ilton); Acentrogobius cyanomos (Bleeker); Eleotriodes muralis (Valenciennes); Parapocryptes serperaster (Richardson); Apocryptes bato (Hamilton); Scartclaos viridis (Hamilton); Boleophthalmus boddarti (Pallas), Periophthalmus schlosseri (Pallas); P. koelreuteri (Pallas); Taenioides anguillaris (Linnaeus); T. buchanani (Day); Odontamblyopus rubicundus (Hamilton). The urinogenital papilla, originating as a free muscular organ from the ventral surface of the body-wall and shortly behind anus, is present in both the sexes. It is an important organ of primary sex recognition in all species. In case of male the papilla is conical, broad at the base and in female it is either flattened, distally truncated or bluntly rounded. The presence of permanent colour mark over the specific region of the body surface is another secondary sexual character in a few species. Besides, colouration may also be a nuptial secondary sex character developed in some during peak breeding season. The enlargement and colouration of the organ is subject to seasonal variations parallel to the seasonal gonadal cycle. -
Sensory Biology of Aquatic Animals
Jelle Atema Richard R. Fay Arthur N. Popper William N. Tavolga Editors Sensory Biology of Aquatic Animals Springer-Verlag New York Berlin Heidelberg London Paris Tokyo JELLE ATEMA, Boston University Marine Program, Marine Biological Laboratory, Woods Hole, Massachusetts 02543, USA Richard R. Fay, Parmly Hearing Institute, Loyola University, Chicago, Illinois 60626, USA ARTHUR N. POPPER, Department of Zoology, University of Maryland, College Park, MD 20742, USA WILLIAM N. TAVOLGA, Mote Marine Laboratory, Sarasota, Florida 33577, USA The cover Illustration is a reproduction of Figure 13.3, p. 343 of this volume Library of Congress Cataloging-in-Publication Data Sensory biology of aquatic animals. Papers based on presentations given at an International Conference on the Sensory Biology of Aquatic Animals held, June 24-28, 1985, at the Mote Marine Laboratory in Sarasota, Fla. Bibliography: p. Includes indexes. 1. Aquatic animals—Physiology—Congresses. 2. Senses and Sensation—Congresses. I. Atema, Jelle. II. International Conference on the Sensory Biology - . of Aquatic Animals (1985 : Sarasota, Fla.) QL120.S46 1987 591.92 87-9632 © 1988 by Springer-Verlag New York Inc. x —• All rights reserved. This work may not be translated or copied in whole or in part without the written permission of the publisher (Springer-Verlag, 175 Fifth Avenue, New York 10010, U.S.A.), except for brief excerpts in connection with reviews or scholarly analysis. Use in connection with any form of Information storage and retrieval, electronic adaptation, Computer Software, or by similar or dissimilar methodology now known or hereafter developed is forbidden. The use of general descriptive names, trade names, trademarks, etc.