Osteoglossomorpha (Bonytongues)

Total Page:16

File Type:pdf, Size:1020Kb

Osteoglossomorpha (Bonytongues) Actinopterygian Relationships II Biology of Fishes 10.2.2012 Overview Group Projects Exam I (10.9.2012) Review (Actinopterygian Relationships I) Actinopterygian Relationships II Actinopterygian Relationships Sarcopterygii (lobe fins) Actinopterygii (ray fins) - Cladistia (bichirs, reedfish) - Chondrostei (sturgeons, paddlefishes) -Holostei (gars, bowfins) Neopterygii -Teleostei (teleosts, “modern fishes”) Actinopterygian Relationships II Chondrichthyes CRANIATES Sarcopterygii Vertebrates Osteichthyes Actinopterygii Actinopterygian Relationships II Teleostei (“modern fishes”) Caudal fin symmetrical – homocercal Uroneural bones in tail support upper lobe – both lobes Scales reduced – more flexible body Mobile premaxilla – suction feeding capabilities Advanced modes of locomotion and feeding, and therefore success (~24,000 species) Actinopterygian Relationships II Actinopterygian Relationships Sarcopterygii (lobe fins) Actinopterygii (ray fins) - Cladistia (bichirs, reedfish) - Chondrostei (sturgeons, paddlefishes) -Holostei (gars, bowfins) Neopterygii -Teleostei (teleosts, “modern fishes”) Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) (herrings, shad, relatives) -Clupeomorpha -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) Teleostei -Protacanthopterygii Neoteleostei Acanthomorpha Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) -Clupeomorpha (herrings, shad, relatives) -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) -Protacanthopterygii Neoteleostei Acanthomorpha Actinopterygian Relationships Elopomorpha (eels, tarpons, relatives) Most “primitive” teleosts (sister group to all other teleosts) Leptocephalus larvae Primarily marine Includes Tarpon, bonefish, ladyfish, morays, freshwater eels, gulper eels, swallower eels Elopomorpha Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) -Clupeomorpha (herrings, shad, relatives) -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) -Protacanthopterygii Neoteleostei Acanthomorpha Actinopterygian Relationships Osteoglossomorpha (bonytongues) Formerly most “primitive” teleosts Asia, Australia, North & South America, Africa Freshwater lakes and rivers; primarily tropical (2 N.American species) Bony tongues – well-developed teeth on tongue, bite against teeth on roof Arowana, arapaima, African butterflyfish, mooneyes, knifefishes, elephant fishes, gymnarchids Osteoglossomorpha Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) -Clupeomorpha (herrings, shad, relatives) -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) -Protacanthopterygii Neoteleostei Acanthomorpha Actinopterygian Relationships Clupeomorpha (herrings, shads, sardines, relatives) Mostly open water (pelagic), schooling, filter feeders 80% marine, large distribution Important commercial group Populations exhibit large fluctuations in abundance Otophysic – special connection between gas bladder and inner ear (increases hearing sensitivity) Herring, sardines, anchovies, shad, alewife, menhaden, pilchards, sprats Clupeomorpha Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) -Clupeomorpha (herrings, shad, relatives) -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) -Protacanthopterygii Neoteleostei Acanthomorpha Actinopterygian Relationships II Actinopterygian Relationships Ostariophysi 64% of all freshwater fishes Swim bladder divided into two parts – anterior for sound, posterior for buoyancy Produce and respond to alarm substance Includes Gonorynchiformes and Otophysi Actinopterygian Relationships Otophysi Weberian apparatus – series of bones transmits vibrations from swim bladder to inner ear; amplifies sound Cypriniformes (minnows, carps, relatives) Characiformes (characins, relatives) Siluriformes (catfishes) Gymnotiformes (“New World” knife fishes) Otophysi Cypriniformes Otophysi Characiformes Otophysi Siluriformes Otophysi Gymnotiformes Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) -Clupeomorpha (herrings, shad, relatives) -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) -Protacanthopterygii Neoteleostei Euteleostei Acanthomorpha Actinopterygian Relationships II Actinopterygian Relationships Euteleostei (“true teleosts”) 95% of all teleosts Stegural bones – uroneural with ossified outgrowth Protacanthopterygii Salmoniformes (salmon, trout, coregonids) Osmeriformes (smelt, galaxiids, salamanderfish) Esociformes (pikes, pickerels, mudminnows) Neoteleosts Protacanthopterygii Salmoniformes & Osmeriformes Protacanthopterygii Esociformes Actinopterygian Relationships Euteleostei (“true teleosts”) Protacanthopterygii Neoteleosts Rostral cartilage – lies between skull and upper jaws Retractor dorsalis – connects vertebral column to pharyngeal jaws Trend of pelvics moving forward and pectorals upward Stenopterygii, Aulopiformes, Scopelomorpha Primarily deep-sea marine fishes Actinopterygian Relationships II Holostei (gars, bowfins) Teleostei (teleosts “modern fishes”) - Elopomorpha (eels, tarpons, relatives) - Osteoglossomorpha (bonytongues) -Clupeomorpha (herrings, shad, relatives) -Ostariophysi (minnows, catfishes, characins, relatives) Euteleostei (“true teleosts”) -Protacanthopterygii Neoteleostei Acanthomorpha Actinopterygian Relationships Acanthomorpha Spiny-rayed teleosts Spines in dorsal and anal fins Lampridioformes Opahs and oarfish (up to 55 feet) marine Paracanthopterygii Actinopterygian Relationships Acanthomorpha Spiny-rayed teleosts Spines in dorsal and anal fins Lampridioformes Opahs and oarfish (up to 55 feet) marine Paracanthopterygii Actinopterygian Relationships II Actinopterygian Relationships Paracanthopterygii Mostly benthic marine fishes 20 freshwater species Cods, cavefishes, anglerfishes Actinopterygian Relationships II Neoteleostei Acanthomorpha (teleosts “modern fishes”) - Paracanthopterygii (cods, anglers, cavefishes) Acanthomorpha - Acanthopterygii Actinopterygian Relationships II Actinopterygian Relationships Acanthopterygii .
Recommended publications
  • The Phylogeny of Oncorhynchus (Euteleostei: Salmonidae) Based on Behavioral and Life History Characters
    Copeia, 2007(3), pp. 520–533 The Phylogeny of Oncorhynchus (Euteleostei: Salmonidae) Based on Behavioral and Life History Characters MANU ESTEVE AND DEBORAH A. MCLENNAN There is no consensus between morphological and molecular data concerning the relationships within the Pacific basin salmon and trout clade Oncorhynchus. In this paper we add another source of characters to the discussion. Phylogenetic analysis of 39 behavioral and life history traits produced one tree structured (O. clarki (O. mykiss (O. masou (O. kisutch (O. tshawytscha (O. nerka (O. keta, O. gorbuscha))))))). This topology is congruent with the phylogeny based upon Bayesian analysis of all available nuclear and mitochondrial gene sequences, with the exception of two nodes: behavior supports the morphological data in breaking the sister-group relationship between O. mykiss and O. clarki, and between O. kisutch and O. tshawytscha. The behavioral traits agreed with molecular rather than morphological data in placing O. keta as the sister-group of O. gorbuscha. The behavioral traits also resolve the molecular-based ambiguity concerning the placement of O. masou, placing it as sister to the rest of the Pacific basin salmon. Behavioral plus morphological data placed Salmo, not Salvelinus, as more closely related to Oncorhynchus, but that placement was only weakly supported and awaits collection of missing data from enigmatic species such as the lake trout, Salvelinus namaycush. Overall, the phenotypic characters helped resolve ambiguities that may have been created by molecular introgression, while the molecular traits helped resolve ambiguities introduced by phenotypic homoplasy. It seems reasonable therefore, that systematists can best respond to the escalating biodiversity crisis by forming research groups to gather behavioral and ecological information while specimens are being collected for morphological and molecular analysis.
    [Show full text]
  • Chapter 11 the Biology and Ecology of the Oceanic Whitetip Shark, Carcharhinus Longimanus
    Chapter 11 The Biology and Ecology of the Oceanic Whitetip Shark, Carcharhinus longimanus Ramón Bonfi l, Shelley Clarke and Hideki Nakano Abstract The oceanic whitetip shark (Carcharhinus longimanus) is a common circumtropical preda- tor and is taken as bycatch in many oceanic fi sheries. This summary of its life history, dis- tribution and abundance, and fi shery-related information is supplemented with unpublished data taken during Japanese tuna research operations in the Pacifi c Ocean. Oceanic whitetips are moderately slow-growing sharks that do not appear to have differential growth rates by sex, and individuals in the Atlantic and Pacifi c Oceans seem to grow at similar rates. They reach sexual maturity at approximately 170–200 cm total length (TL), or 4–7 years of age, and have a 9- to 12-month embryonic development period. Pupping and nursery areas are thought to exist in the central Pacifi c, between 0ºN and 15ºN. According to two demographic metrics, the resilience of C. longimanus to fi shery exploitation is similar to that of blue and shortfi n mako sharks. Nevertheless, reported oceanic whitetip shark catches in several major longline fi sheries represent only a small fraction of total shark catches, and studies in the Northwest Atlantic and Gulf of Mexico suggest that this species has suffered signifi cant declines in abundance. Stock assessment has been severely hampered by the lack of species-specifi c catch data in most fi sheries, but recent implementation of species-based reporting by the International Commission for the Conservation of Atlantic Tunas (ICCAT) and some of its member countries will provide better data for quantitative assessment.
    [Show full text]
  • 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.
    [Show full text]
  • Sea Monsters in Antiquity: a Classical and Zoological Investigation
    Sea Monsters in Antiquity: A Classical and Zoological Investigation Alexander L. Jaffe Harvard University Dept. of Organismic and Evolutionary Biology Class of 2015 Abstract: Sea monsters inspired both fascination and fear in the minds of the ancients. In this paper, I aim to examine several traditional monsters of antiquity with a multi-faceted approach that couples classical background with modern day zoological knowledge. Looking at the examples of the ketos and the sea serpent in Roman and Greek societies, I evaluate the scientific bases for representations of these monsters across of variety of media, from poetry to ceramics. Through the juxtaposition of the classical material and modern science, I seek to gain a greater understanding of the ancient conception of sea monsters and explain the way in which they were rationalized and depicted by ancient cultures. A closer look at extant literature, historical accounts, and artwork also helps to reveal a human sentiment towards the ocean and its denizens penetrating through time even into the modern day. “The Sea-monsters, mighty of limb and huge, the wonders of the sea, heavy with strength invincible, a terror for the eyes to behold and ever armed with deadly rage—many of these there be that roam the spacious seas...”1 Oppian, Halieutica 1 As the Greek poet Oppian so eloquently reveals, sea monsters inspired both fascination and fear in the minds of the ancients. From the Old Testament to Ovid, sources from throughout the ancient world show authors exercising both imagination and observation in the description of these creatures. Mythology as well played a large role in the creation of these beliefs, with such classic examples as Perseus and Andromeda or Herakles and Hesione.
    [Show full text]
  • Huchen (Hucho Hucho) ERSS
    Huchen (Hucho hucho) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, April 2011 Revised, January 2019, February 2019 Web Version, 4/30/2019 Photo: Liquid Art. Licensed under CC-SA 4.0 International. Available: https://commons.wikimedia.org/wiki/File:Danube_Salmon_-_Huchen_(Hucho_hucho).jpg. (January 2019). 1 Native Range and Status in the United States Native Range From Froese and Pauly (2019): “Europe: Danube drainage [Austria, Bosnia and Herzegovina, Bulgaria, Croatia, Germany, Hungary, Italy, Romania, Serbia, Slovakia, Slovenia, Switzerland, and Ukraine].” “Population has declined [in Slovenia] due to pollution and river regulation. Conservation measures include artificial propagation and stocking [Povz 1996]. Status of threat: Regionally extinct [Bianco and Ketmaier 2016].” 1 “Considered locally extinct (extirpated) in 1990 [in Switzerland] [Vilcinskas 1993].” “Extinct in the wild in 2000 [in Czech Republic] [Lusk and Hanel 2000]. This species is a native species in the basin of the Black Sea (the rivers Morava and Dyje). At present, its local and time- limited occurrence depends on the stocking material from artificial culture. Conditions that will facilitate the formation of a permanent population under natural conditions are not available [Lusk et al. 2004]. […] Status of threat: extinct in the wild [Lusk et al. 2011].” From Freyhof and Kottelat (2008): “The species is severely fragmented within the Danube drainage, where most populations exclusively depend on stocking and natural reproduction is very limited due to habitat alterations and flow regime changes.” From Grabowska et al. (2010): “The exceptional case is huchen (or Danubian salmon), Hucho hucho. The huchen’s native range in Poland was restricted to two small rivers (Czarna Orawa and Czadeczka) of the Danube River basin, […]” Status in the United States Froese and Pauly (2019) report an introduction to the United States between 1870 and 1874 that did not result in an established population.
    [Show full text]
  • Crestfish Lophotus Lacepede (Giorna, 1809) and Scalloped Ribbonfish Zu Cristatus (Bonelli, 1819) in the Northern Coast of Sicily, Italy
    ISSN: 0001-5113 ACTA ADRIAT., ORIGINAL SCIENTIFIC PAPER AADRAY 58(1): 137 - 146, 2017 Occurrence of two rare species from order Lampriformes: Crestfish Lophotus lacepede (Giorna, 1809) and scalloped ribbonfish Zu cristatus (Bonelli, 1819) in the northern coast of Sicily, Italy Fabio FALSONE1, Michele Luca GERACI1, Danilo SCANNELLA1, Charles Odilichukwu R. OKPALA1, Giovan Battista GIUSTO1, Mar BOSCH-BELMAR2, Salvatore GANCITANO1 and Gioacchino BONO1 1Institute for the Coastal Marine Environment, IAMC‑CNR, 91026 Mazara del Vallo, Sicily, Italy 2Consorzio Nazionale Interuniversitario per le Scienze del Mare (CoNISMa), Rome, Italy Corresponding author, e‑mail: [email protected] The bony fish Lophotus lacepede (Giorna, 1809) and Zu cristatus (Bonelli, 1819) are the two species rarely recorded within the Mediterranean basin, usually reported as accidentally captured in depth (mesopelagic) fishing operations. In the current work, we present the first record of L. lacepede and Z. cristatus in fishing catches from southwestern Tyrrhenian Sea. Moreover, in order to improve existent biological/ecological knowledge, some bio-related aspects such as feeding aspect, sexual maturity and age estimate have been discussed. Key words: crestfish, scalloped ribbonfish, meristic features, vertebrae, growth ring INTRODUCTION species of Lophotidae family, the L. lacepede inhabits the epipelagic zone, although it could The target species of this study (Lophotus also be recorded in most oceans from the surface lacepede and Zu cristatus) belong to Lophotidae up to 1000 m depth (HEEMSTRA, 1986; PALMER, (Bonaparte, 1845) and Trachipteridae (Swain- 1986; OLNEY, 1999). First record of this spe- son, 1839) families respectively, including the cies in the Mediterranean Basin was from the Lampriformes order (consisted of 7 families).
    [Show full text]
  • Characterization of the G Protein-Coupled Receptor Family
    www.nature.com/scientificreports OPEN Characterization of the G protein‑coupled receptor family SREB across fsh evolution Timothy S. Breton1*, William G. B. Sampson1, Benjamin Cliford2, Anyssa M. Phaneuf1, Ilze Smidt3, Tamera True1, Andrew R. Wilcox1, Taylor Lipscomb4,5, Casey Murray4 & Matthew A. DiMaggio4 The SREB (Super‑conserved Receptors Expressed in Brain) family of G protein‑coupled receptors is highly conserved across vertebrates and consists of three members: SREB1 (orphan receptor GPR27), SREB2 (GPR85), and SREB3 (GPR173). Ligands for these receptors are largely unknown or only recently identifed, and functions for all three are still beginning to be understood, including roles in glucose homeostasis, neurogenesis, and hypothalamic control of reproduction. In addition to the brain, all three are expressed in gonads, but relatively few studies have focused on this, especially in non‑mammalian models or in an integrated approach across the entire receptor family. The purpose of this study was to more fully characterize sreb genes in fsh, using comparative genomics and gonadal expression analyses in fve diverse ray‑fnned (Actinopterygii) species across evolution. Several unique characteristics were identifed in fsh, including: (1) a novel, fourth euteleost‑specifc gene (sreb3b or gpr173b) that likely emerged from a copy of sreb3 in a separate event after the teleost whole genome duplication, (2) sreb3a gene loss in Order Cyprinodontiformes, and (3) expression diferences between a gar species and teleosts. Overall, gonadal patterns suggested an important role for all sreb genes in teleost testicular development, while gar were characterized by greater ovarian expression that may refect similar roles to mammals. The novel sreb3b gene was also characterized by several unique features, including divergent but highly conserved amino acid positions, and elevated brain expression in pufer (Dichotomyctere nigroviridis) that more closely matched sreb2, not sreb3a.
    [Show full text]
  • Development of the Muscles Associated with the Mandibular and Hyoid Arches in the Siberian Sturgeon, Acipenser Baerii (Acipenseriformes: Acipenseridae)
    Received: 31 May 2017 | Revised: 24 September 2017 | Accepted: 29 September 2017 DOI: 10.1002/jmor.20761 RESEARCH ARTICLE Development of the muscles associated with the mandibular and hyoid arches in the Siberian sturgeon, Acipenser baerii (Acipenseriformes: Acipenseridae) Peter Warth1 | Eric J. Hilton2 | Benjamin Naumann1 | Lennart Olsson1 | Peter Konstantinidis3 1Institut fur€ Spezielle Zoologie und Evolutionsbiologie mit Phyletischem Abstract Museum, Friedrich-Schiller-Universität Jena, The skeleton of the jaws and neurocranium of sturgeons (Acipenseridae) are connected only Germany through the hyoid arch. This arrangement allows considerable protrusion and retraction of the 2 Department of Fisheries Science, Virginia jaws and is highly specialized among ray-finned fishes (Actinopterygii). To better understand the Institute of Marine Science, College of unique morphology and the evolution of the jaw apparatus in Acipenseridae, we investigated the William & Mary, Gloucester Point, Virginia development of the muscles of the mandibular and hyoid arches of the Siberian sturgeon, Aci- 3Department of Fisheries and Wildlife, Oregon State University, Corvallis, Oregon penser baerii. We used a combination of antibody staining and formalin-induced fluorescence of tissues imaged with confocal microscopy and subsequent three-dimensional reconstruction. These Correspondence data were analyzed to address the identity of previously controversial and newly discovered mus- Peter Warth, Institut fur€ Spezielle Zoologie cle portions. Our results indicate that the anlagen of the muscles in A. baerii develop similarly to und Evolutionsbiologie mit Phyletischem Museum, Friedrich-Schiller-Universität Jena, those of other actinopterygians, although they differ by not differentiating into distinct muscles. Erbertstr. 1, 07743 Jena, Germany. This is exemplified by the subpartitioning of the m. adductor mandibulae as well as the massive m.
    [Show full text]
  • Highly Diversified Late Cretaceous Fish Assemblage Revealed by Otoliths (Ripley Formation and Owl Creek Formation, Northeast Mississippi, Usa)
    Rivista Italiana di Paleontologia e Stratigrafia (Research in Paleontology and Stratigraphy) vol. 126(1): 111-155. March 2020 HIGHLY DIVERSIFIED LATE CRETACEOUS FISH ASSEMBLAGE REVEALED BY OTOLITHS (RIPLEY FORMATION AND OWL CREEK FORMATION, NORTHEAST MISSISSIPPI, USA) GARY L. STRINGER1, WERNER SCHWARZHANS*2 , GEORGE PHILLIPS3 & ROGER LAMBERT4 1Museum of Natural History, University of Louisiana at Monroe, Monroe, Louisiana 71209, USA. E-mail: [email protected] 2Natural History Museum of Denmark, Zoological Museum, Universitetsparken 15, DK-2100, Copenhagen, Denmark. E-mail: [email protected] 3Mississippi Museum of Natural Science, 2148 Riverside Drive, Jackson, Mississippi 39202, USA. E-mail: [email protected] 4North Mississippi Gem and Mineral Society, 1817 CR 700, Corinth, Mississippi, 38834, USA. E-mail: [email protected] *Corresponding author To cite this article: Stringer G.L., Schwarzhans W., Phillips G. & Lambert R. (2020) - Highly diversified Late Cretaceous fish assemblage revealed by otoliths (Ripley Formation and Owl Creek Formation, Northeast Mississippi, USA). Riv. It. Paleontol. Strat., 126(1): 111-155. Keywords: Beryciformes; Holocentriformes; Aulopiformes; otolith; evolutionary implications; paleoecology. Abstract. Bulk sampling and extensive, systematic surface collecting of the Coon Creek Member of the Ripley Formation (early Maastrichtian) at the Blue Springs locality and primarily bulk sampling of the Owl Creek Formation (late Maastrichtian) at the Owl Creek type locality, both in northeast Mississippi, USA, have produced the largest and most highly diversified actinopterygian otolith (ear stone) assemblage described from the Mesozoic of North America. The 3,802 otoliths represent 30 taxa of bony fishes representing at least 22 families. In addition, there were two different morphological types of lapilli, which were not identifiable to species level.
    [Show full text]
  • Lab 9 - an Introduction to Marine Fishes
    Name ___________________________________ Lab 9 - An introduction to marine fishes NOTE: these taxonomic groups have many more species than those shown today; each specimen is but a representative of its particular family or order. PLEASE HANDLE SPECIMENS CAREFULLY!!!! Superclass Agnatha (jawless fishes; ~80 spp.) Class Myxini Order Myxiniformes Family Myxinidae; Hagfish (Myxine glutinosa) Class Cephalaspidomorphi Order Petromyzontiformes Family Petromyzontidae; Sea lamprey (Petromyzon marinus) 1) What are some key differences between Myxinids and Petromyzontids? Superclass Gnathostomata (jawed fishes) Class Chondrichthyes (cartilaginous fishes) Subclass Elasmobranchii (shark-like fishes; 800 spp) Order Squatiniformes; Angel shark (Squatina dumerili) Order Squaliformes; Spiny dogfish (Squalus acanthias) Order Rajiformes; Clearnose skate (Raja eglanteria), Guitarfish (Rhinobatos sp.) Subclass Holocephali (chimaeras; 30 spp) Order Chimaeriformes; Spotted chimaera (Hydrolagus colliei) 2) What are two features that clearly distinguish the order Rajiformes (skates) from sharks? 3) Where in the water column would you expect to find a chimaera? Why? Class Teleostomi (bony fishes) Superorder Clupeomorpha Order Clupeiformes Family Clupeidae; Atlantic herring (Clupea harengus), Menhaden (Brevoortia tyrannus) Family Engraulidae; Anchovy (Anchoa nasuta) 4) What characteristics most clearly separate these two families? 5) These fishes tend to travel in schools. What purpose might the silvery stripe down their sides serve? (Hint: think about this from
    [Show full text]
  • Current Knowledge on the European Mudminnow, Umbra Krameri Walbaum, 1792 (Pisces: Umbridae)
    ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Annalen des Naturhistorischen Museums in Wien Jahr/Year: 1995 Band/Volume: 97B Autor(en)/Author(s): Wanzenböck Josef Artikel/Article: Current knowledge on the European mudminnow, Umbra krameri Walbaum, 1792 (Pisces: Umbridae). 439-449 ©Naturhistorisches Museum Wien, download unter www.biologiezentrum.at Ann. Naturhist. Mus. Wien 97 B 439 - 449 Wien, November 1995 Current knowledge on the European mudminnow, Umbra krameri WALBAUM, 1792 (Pisces: Umbridae) J. Wanzenböck* Abstract The present paper summarizes the current knowledge on the European mudminnow {Umbra krameri WALBAUM, 1792) with respect to systematics, taxonomy, and ecology. Key words: Umbridae, Umbra krameri, systematics, taxonomy, ecology. Zusammenfassung Die vorliegende Arbeit faßt den derzeitigen Wissensstand über den Europäischen Hundsfisch {Umbra kra- meri WALBAUM, 1792) unter Berücksichtigung systematischer, taxonomischer und ökologischer Aspekte zusammen. Names, taxonomy, and systematics Scientific name: Umbra krameri WALBAUM, 1792 Common names: Based on BLANC & al. (1971) and LINDBERG & HEARD (1972). Names suggested by the author are given at first, those marked with an asterix (*) are given in BLANC & al. (1971). German: Europäischer Hundsfisch, Hundsfisch*, Ungarischer Hundsfisch Hungarian: Lâpi póc* Czech: Tmavec hnëdy*, Blatnâk tmavy Slovak: Blatniak* Russian: Evdoshka, Umbra* Ukrainian: Boboshka (Dniestr), Evdoshka, Lezheboka
    [Show full text]
  • Convergent Evolution of Weakly Electric Fishes from Floodplain Habitats in Africa and South America
    Environmental Biology of Fishes 49: 175–186, 1997. 1997 Kluwer Academic Publishers. Printed in the Netherlands. Convergent evolution of weakly electric fishes from floodplain habitats in Africa and South America Kirk O. Winemiller & Alphonse Adite Department of Wildlife and Fisheries Sciences, Texas A&M University, College Station, TX 77843, U.S.A. Received 19.7.1995 Accepted 27.5.1996 Key words: diet, electrogenesis, electroreception, foraging, morphology, niche, Venezuela, Zambia Synopsis An assemblage of seven gymnotiform fishes in Venezuela was compared with an assemblage of six mormyri- form fishes in Zambia to test the assumption of convergent evolution in the two groups of very distantly related, weakly electric, noctournal fishes. Both assemblages occur in strongly seasonal floodplain habitats, but the upper Zambezi floodplain in Zambia covers a much larger area. The two assemblages had broad diet overlap but relatively narrow overlap of morphological attributes associated with feeding. The gymnotiform assemblage had greater morphological variation, but mormyriforms had more dietary variation. There was ample evidence of evolutionary convergence based on both morphology and diet, and this was despite the fact that species pairwise morphological similarity and dietary similarity were uncorrelated in this dataset. For the most part, the two groups have diversified in a convergent fashion within the confines of their broader niche as nocturnal invertebrate feeders. Both assemblages contain midwater planktivores, microphagous vegetation- dwellers, macrophagous benthic foragers, and long-snouted benthic probers. The gymnotiform assemblage has one piscivore, a niche not represented in the upper Zambezi mormyriform assemblage, but present in the form of Mormyrops deliciousus in the lower Zambezi and many other regions of Africa.
    [Show full text]