Diversity of Fishes
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
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. -
Order GASTEROSTEIFORMES PEGASIDAE Eurypegasus Draconis
click for previous page 2262 Bony Fishes Order GASTEROSTEIFORMES PEGASIDAE Seamoths (seadragons) by T.W. Pietsch and W.A. Palsson iagnostic characters: Small fishes (to 18 cm total length); body depressed, completely encased in Dfused dermal plates; tail encircled by 8 to 14 laterally articulating, or fused, bony rings. Nasal bones elongate, fused, forming a rostrum; mouth inferior. Gill opening restricted to a small hole on dorsolat- eral surface behind head. Spinous dorsal fin absent; soft dorsal and anal fins each with 5 rays, placed posteriorly on body. Caudal fin with 8 unbranched rays. Pectoral fins large, wing-like, inserted horizon- tally, composed of 9 to 19 unbranched, soft or spinous-soft rays; pectoral-fin rays interconnected by broad, transparent membranes. Pelvic fins thoracic, tentacle-like,withI spine and 2 or 3 unbranched soft rays. Colour: in life highly variable, apparently capable of rapid colour change to match substrata; head and body light to dark brown, olive-brown, reddish brown, or almost black, with dorsal and lateral surfaces usually darker than ventral surface; dorsal and lateral body surface often with fine, dark brown reticulations or mottled lines, sometimes with irregular white or yellow blotches; tail rings often encircled with dark brown bands; pectoral fins with broad white outer margin and small brown spots forming irregular, longitudinal bands; unpaired fins with small brown spots in irregular rows. dorsal view lateral view Habitat, biology, and fisheries: Benthic, found on sand, gravel, shell-rubble, or muddy bottoms. Collected incidentally by seine, trawl, dredge, or shrimp nets; postlarvae have been taken at surface lights at night. -
New Zealand Fishes a Field Guide to Common Species Caught by Bottom, Midwater, and Surface Fishing Cover Photos: Top – Kingfish (Seriola Lalandi), Malcolm Francis
New Zealand fishes A field guide to common species caught by bottom, midwater, and surface fishing Cover photos: Top – Kingfish (Seriola lalandi), Malcolm Francis. Top left – Snapper (Chrysophrys auratus), Malcolm Francis. Centre – Catch of hoki (Macruronus novaezelandiae), Neil Bagley (NIWA). Bottom left – Jack mackerel (Trachurus sp.), Malcolm Francis. Bottom – Orange roughy (Hoplostethus atlanticus), NIWA. New Zealand fishes A field guide to common species caught by bottom, midwater, and surface fishing New Zealand Aquatic Environment and Biodiversity Report No: 208 Prepared for Fisheries New Zealand by P. J. McMillan M. P. Francis G. D. James L. J. Paul P. Marriott E. J. Mackay B. A. Wood D. W. Stevens L. H. Griggs S. J. Baird C. D. Roberts‡ A. L. Stewart‡ C. D. Struthers‡ J. E. Robbins NIWA, Private Bag 14901, Wellington 6241 ‡ Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, 6011Wellington ISSN 1176-9440 (print) ISSN 1179-6480 (online) ISBN 978-1-98-859425-5 (print) ISBN 978-1-98-859426-2 (online) 2019 Disclaimer While every effort was made to ensure the information in this publication is accurate, Fisheries New Zealand does not accept any responsibility or liability for error of fact, omission, interpretation or opinion that may be present, nor for the consequences of any decisions based on this information. Requests for further copies should be directed to: Publications Logistics Officer Ministry for Primary Industries PO Box 2526 WELLINGTON 6140 Email: [email protected] Telephone: 0800 00 83 33 Facsimile: 04-894 0300 This publication is also available on the Ministry for Primary Industries website at http://www.mpi.govt.nz/news-and-resources/publications/ A higher resolution (larger) PDF of this guide is also available by application to: [email protected] Citation: McMillan, P.J.; Francis, M.P.; James, G.D.; Paul, L.J.; Marriott, P.; Mackay, E.; Wood, B.A.; Stevens, D.W.; Griggs, L.H.; Baird, S.J.; Roberts, C.D.; Stewart, A.L.; Struthers, C.D.; Robbins, J.E. -
HMS FMP Appendix F
APPENDIX F U.S. WEST COAST HIGHLY MIGRATORY SPECIES: LIFE HISTORY ACCOUNTS AND ESSENTIAL FISH HABITAT DESCRIPTIONS (Originally Appendix A to the FMP) U.S. West Coast Highly Migratory Species Plan Development Team Pacific Fishery Management Council Originally Available January 16, 2003 HMS FMP - Appendix F i June 2007 TABLE OF CONTENTS REVIEW OF METHODS AND DEFINITIONS.............................................F-1 1.0SHARKS ....................................................................F-1 1.1Common Thresher ...........................................................F-1 1.1.8 Essential Fish Habitat for Common Thresher ................................F-4 1.2Pelagic Thresher.............................................................F-5 1.2.8 Essential Fish Habitat for Pelagic Thresher..................................F-6 1.3Bigeye Thresher .............................................................F-7 1.3.8 Essential Fish Habitat for Bigeye Thresher ..................................F-9 1.4Shortfin Mako ...............................................................F-9 1.4.8 Essential Fish Habitat for Shortfin Mako ...................................F-12 1.5Blue Shark.................................................................F-12 1.5.8 Essential Fish Habitat for Blue Shark......................................F-16 2.0TUNAS.......................................................................F-16 2.1Albacore ..................................................................F-16 2.1.8 Essential Fish Habitat for Albacore .......................................F-20 -
Download/18.8620Dc61698d96b1904a2/1554132043883/SRC Report%20Nordic%20Food%20Systems.Pdf (Accessed on 1 October 2019)
foods Article Mesopelagic Species and Their Potential Contribution to Food and Feed Security—A Case Study from Norway Anita R. Alvheim, Marian Kjellevold , Espen Strand, Monica Sanden and Martin Wiech * Institute of Marine Research, P.O. Box 1870, Nordnes, NO-5817 Bergen, Norway; [email protected] (A.R.A.); [email protected] (M.K.); [email protected] (E.S.); [email protected] (M.S.) * Correspondence: [email protected]; Tel.: +47-451-59-792 Received: 7 February 2020; Accepted: 11 March 2020; Published: 16 March 2020 Abstract: The projected increase in global population will demand a major increase in global food production. There is a need for more biomass from the ocean as future food and feed, preferentially from lower trophic levels. In this study, we estimated the mesopelagic biomass in three Norwegian fjords. We analyzed the nutrient composition in six of the most abundant mesopelagic species and evaluated their potential contribution to food and feed security. The six species make up a large part of the mesopelagic biomass in deep Norwegian fjords. Several of the analyzed mesopelagic species, especially the fish species Benthosema glaciale and Maurolicus muelleri, were nutrient dense, containing a high level of vitamin A1, calcium, selenium, iodine, eicopentaenoic acid (EPA), docosahexaenoic acid (DHA) and cetoleic acid. We were able to show that mesopelagic species, whose genus or family are found to be widespread and numerous around the globe, are nutrient dense sources of micronutrients and marine-based ingredients and may contribute significantly to global food and feed security. Keywords: mesopelagic; nutrients; Benthosema glaciale; Maurolicus muelleri; trace elements; minerals; fatty acids; vitamin A; vitamin D 1. -
Fishes-Of-The-Salish-Sea-Pp18.Pdf
NOAA Professional Paper NMFS 18 Fishes of the Salish Sea: a compilation and distributional analysis Theodore W. Pietsch James W. Orr September 2015 U.S. Department of Commerce NOAA Professional Penny Pritzker Secretary of Commerce Papers NMFS National Oceanic and Atmospheric Administration Kathryn D. Sullivan Scientifi c Editor Administrator Richard Langton National Marine Fisheries Service National Marine Northeast Fisheries Science Center Fisheries Service Maine Field Station Eileen Sobeck 17 Godfrey Drive, Suite 1 Assistant Administrator Orono, Maine 04473 for Fisheries Associate Editor Kathryn Dennis National Marine Fisheries Service Offi ce of Science and Technology Fisheries Research and Monitoring Division 1845 Wasp Blvd., Bldg. 178 Honolulu, Hawaii 96818 Managing Editor Shelley Arenas National Marine Fisheries Service Scientifi c Publications Offi ce 7600 Sand Point Way NE Seattle, Washington 98115 Editorial Committee Ann C. Matarese National Marine Fisheries Service James W. Orr National Marine Fisheries Service - The NOAA Professional Paper NMFS (ISSN 1931-4590) series is published by the Scientifi c Publications Offi ce, National Marine Fisheries Service, The NOAA Professional Paper NMFS series carries peer-reviewed, lengthy original NOAA, 7600 Sand Point Way NE, research reports, taxonomic keys, species synopses, fl ora and fauna studies, and data- Seattle, WA 98115. intensive reports on investigations in fi shery science, engineering, and economics. The Secretary of Commerce has Copies of the NOAA Professional Paper NMFS series are available free in limited determined that the publication of numbers to government agencies, both federal and state. They are also available in this series is necessary in the transac- exchange for other scientifi c and technical publications in the marine sciences. -
Deep Sea Squid Communicate by Glowing Like E-Readers
Deep Sea Squid Communicate by Glowing Like E-Readers April 17, 20205:00 AM ET LAUREN SOMMER A Humboldt squid shows its colors in the lights of a remotely operated vehicle off the coast of California. Deep in the Pacific Ocean, six-foot-long Humboldt squid are known for being aggressive, cannibalistic and, according to new research, good communicators. Known as "red devils," the squid can rapidly change the color of their skin, making different patterns to communicate, something other squid species are known to do. But Humboldt squid live in almost total darkness more than 1,000 feet below the surface, so their patterns aren't very visible. Instead, according to a new study, they create backlighting for the patterns by making their bodies glow, like the screen of an e-reader. "Right now, what blows my mind is there's probably squid talking to each other in the deep ocean and they're probably sharing all sorts of cool information," said Ben Burford, a graduate student at Stanford University. Humboldt squid crowd together in large, fast-moving groups to feed on small fish and other prey. "When you watch them it looks like frenzy," Burford said. "But if you pay close attention, they're not touching each other. They're not bumping into each other." Scientists used deep water footage of Humboldt squid to study the changing patterns on their skin. Burford and his colleagues studied deep-water footage taken by the Monterey Bay Aquarium Research Institute's remotely operated vehicles off the California coast. They found the squid make around 30 different patterns of lines, stripes and patches. -
Sea Resources
TEACHER BACKGROUND Unit 6 - The Deep Sea Pacific Viperfish The Pacific viperfish feeds on lanternfish and squid. It has a very large mouth and fang-like teeth. Once the viperfish catches something, it won't get away. Its size ranges from 22-30 cm. Notice the two rows of photophores. Look at the long, thin ray on the back (dorsal) fin. How might the ray help attract a tasty meal? Deep Sea Squid This squid can grow to 30 cm in length. Its photophores adjust to match the ocean twilight. It can move very quickly forward or backward. The two longest tentacles grab and hold its prey. The smaller tentacles move the prey to its mouth. The eyes are of different sizes. Scientists don't know why. Do you have any ideas? Lanternfish The lanternfish is very common in the deep water. It lives where there is some light. It has very large eyes. The lanternfish swims up and down every day. It stays in the deep water during the day. It moves closer to the surface at night. Scientists think lanternfish may move like this to feed. They are not sure. Its photophores may help it find and communicate with other lanternfish. It grows to about 13cm in length. Anglerfish The anglerfish can grow to 10 cm in length. It has an appendage that looks like a fishing pole and lure. The "lure" is a large photophore. It may help attract prey. It is hard to find and keep mates in the deep sea. The anglerfish has a solution. -
Fish Species Recorded During Deepwater Trawl Surveys on the Continental Shelf and the Porcupine Bank, 2006-2008
Fish species recorded during deepwater trawl surveys on the continental shelf and the Porcupine Bank, 2006-2008 GRAHAM JOHNSTON, BRENDAN O’HEA AND LEONIE DRANSFELD Marine Institute, Rinville, Oranmore, Galway The Marine Institute and the National University of Ireland, Galway conducted a deepwater survey each September from 2006-2008 from the RV Celtic Explorer using BT184 deepwater nets with type-D ground gear (ICES 2006). Fish, benthic and hydrographic data were collected. Two-hour fishing trawls (time on bottom) took place in three locations on the continental slope to the north and west of Ireland, and on the Porcupine Bank. The survey objectives were to collect biological data on the main deepwater fish species and invertebrates. Fishing hauls were carried out at five depths, 500 m, 750 m, 1000 m, 1500 m, and 1800 m, in each of three areas (Fig. 1) chosen to repeat observations made during exploratory deepwater surveys by Ireland and Scotland in the 1990s (Connolly and Kelly 1994). The number of hauls at each depth varied from year to year, as a result of technical limitations in 2006 and variations in bottom type. The numbers of fish recorded should not be used to interpret changes in abundance between years. The number of successful hauls in each area is provided in Table 1. In Table 2 we present a record of each of the fish species identified during these surveys, and the total number of these caught each year. Specimens were identified using UNESCO guides (Whitehead et al. 1984-1986), to species level where possible. Where individuals were damaged, they were identified only to genus or family. -
Sharksof Oregon
Sharksof Oregon Illustrations by Michael Cole oceanscape.aquarium.org Basking Shark Cetorhinus maximus These are one of the largest fish in the world, second only to their aptly-named cousin, the Whale Shark. Basking Sharks are very unusual-looking, with large heads that are almost completely encircled by gills. As their name implies, they are often found “basking” near the water’s surface, filtering krill and other zooplankton through their gaping mouths. The gills of the shark are lined with cartilaginous structures called “rakers” which help snag and hold food as they sweep through the water. Aside from their great size and large mouths, Basking Sharks can also be identified by a a hook-shaped snout and a large dorsal fin that can flop from one side to the other when out of the water. Due to their size and shape, they are often mistaken for Great White Sharks although they are more docile in temperament and do not pose any threat to human beings. Range and Habitat: The Basking Shark can be found in both the northern and southern hemispheres, from the subarctic and subantarctic waters to temperate waters along the continental shelves. Because the sharks follow the ocean’s current, they often migrate over vast distances. Although they spend most of their time in the open ocean, they will venture closer to shore, sometimes even entering bays, as food sources change. Status of Conservation: Changes in ocean currents and weather may be encouraging unusual numbers of Basking Sharks to more Southern latitudes, rather than the Canadian waters where they are usually spotted. -
Mifish, a Set of Universal PCR Primers for Metabarcoding
Downloaded from http://rsos.royalsocietypublishing.org/ on July 31, 2015 MiFish, a set of universal PCR primers for rsos.royalsocietypublishing.org metabarcoding Research environmental DNA from Cite this article: Miya M et al.2015MiFish,a fishes: detection of more set of universal PCR primers for metabarcoding environmental DNA from fishes: detection of more than 230 subtropical than 230 subtropical marine species. R. Soc. open sci. 2: 150088. http://dx.doi.org/10.1098/rsos.150088 marine species M. Miya1,2,Y.Sato2,3,T.Fukunaga4,T.Sado1,2, Received: 26 February 2015 J. Y. Poulsen1,2,5,K.Sato6, T. Minamoto2,7, Accepted:25June2015 S. Yamamoto2,7, H. Yamanaka2,8,H.Araki2,9, M. Kondoh2,8 and W. Iwasaki2,4,10 Subject Category: 1Department of Zoology, Natural History Museum and Institute, Chiba 260-8682, Japan Biology (whole organism) 2CREST, Japan Science and Technology Agency, Saitama 332-0012, Japan 3Tohoku Medical Megabank Organization, Tohoku University, Miyagi 980-8573, Japan Subject Areas: 4Department of Computational Biology, The University of Tokyo, Chiba 277-8568, Japan ecology/environmental science/ 5Fish Section, Australian Museum, Sydney, New South Wales 2010, Australia taxonomy and systematics 6Okinawa Churashima Research Center, Okinawa 905-0206, Japan 7Graduate School of Human Development and Environment, Kobe University, Keywords: Hyogo 657-8501, Japan metabarcoding, MiSeq, environmental DNA, 8Faculty of Science and Technology, Ryukoku University, Shiga 520-2194, Japan 9 mitogenome, resource management, Research Faculty of Agriculture, Hokkaido University, Hokkaido 060-8589, Japan 10 community ecology Department of Biological Sciences, The University of Tokyo, Tokyo 133-0032, Japan We developed a set of universal PCR primers (MiFish-U/E) Author for correspondence: for metabarcoding environmental DNA (eDNA) from M.