Fish Diversity
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RESPIRATORY CONTROL in the LUNGFISH, NEOCERATODUS FORSTERI (KREFT) KJELL JOHANSEN, CLAUDE LENFANT and GORDON C
Comp. Biochem. Physiol., 1967, Vol. 20, pp. 835-854 RESPIRATORY CONTROL IN THE LUNGFISH, NEOCERATODUS FORSTERI (KREFT) KJELL JOHANSEN, CLAUDE LENFANT and GORDON C. GRIGG Abstract-1. Respiratory control has been studied in the lungfish, Neoceratodus forsteri by measuring ventilation (Ve), oxygen uptake (VO2), per cent O2 extraction from water, breathing rates of branchial and aerial respiration and changes in blood gas and pulmonary gas composition during exposure to hypoxia and hypercarbia. 2. Hypoxic water represents a strong stimulus for compensatory increase in both branchial and aerial respiration. Water ventilation increases by a factor of 3 or 4 primarily as a result of increased depth of breathing. 3. The ventilation perfusion ratio decreased during hypoxia because of a marked increase in cardiac output. Hypoxia also increased the fraction of total blood flow perfusing the lung. Injection of nitrogen into the lung evoked no compensatory changes. 4. It is concluded that the chemoreceptors eliciting the compensatory changes are located on the external side facing the ambient water or in the efferent branchial blood vessels. 5. Elevated pCO2 in the ambient water depressed the branchial respiration but stimulated aerial respiration. 6. It is suggested that the primary regulatory effect of the response to increased ambient pCO2 is to prevent CO2 from entering the animal, while the secondary stimulation of air breathing is caused by hypoxic stimulation of chemoreceptors located in the efferent branchial vessels. INTRODUCTION I t i s generally accepted that vertebrates acquired functional lungs before they possessed a locomotor apparatus for invasion of a terrestrial environment. Shortage of oxygen in the environment is thought to have been the primary driving force behind the development of auxiliary air breathing. -
The Ventricles
Guest Editorial Evolution of the Ventricles Solomon Victor, FRCS, FRCP We studied the evolution of ventricles by macroscopic examination of the hearts of Vijaya M. Nayak, MS marine cartilaginous and bony fish, and by angiocardiography and gross examination of Raveen Rajasingh, MPhil the hearts of air-breathing freshwater fish, frogs, turtles, snakes, and crocodiles. A right-sided, thin-walled ventricular lumen is seen in the fish, frog, turtle, and snake. In fish, there is external symmetry of the ventricle, internal asymmetry, and a thick- walled left ventricle with a small inlet chamber. In animals such as frogs, turtles, and snakes, the left ventricle exists as a small-cavitied contractile sponge. The high pressure generated by this spongy left ventricle, the direction of the jet, the ventriculoarterial ori- entation, and the bulbar spiral valve in the frog help to separate the systemic and pul- monary circulations. In the crocodile, the right aorta is connected to the left ventricle, and there is a complete interventricular septum and an improved left ventricular lumen when compared with turtles and snakes. The heart is housed in a rigid pericardial cavity in the shark, possibly to protect it from changing underwater pressure. The pericardial cavity in various species permits move- ments of the heart-which vary depending on the ventriculoarterial orientation and need for the ventricle to generate torque or spin on the ejected blood- that favor run-off into the appropriate arteries and their branches. In the lower species, it is not clear whether the spongy myocardium contributes to myocardial oxygenation. In human beings, spongy myocardium constitutes a rare form of congenital heart disease. -
ESS 345 Ichthyology
ESS 345 Ichthyology Evolutionary history of fishes 12 Feb 2019 (Who’s birthday?) Quote of the Day: We must, however, acknowledge, as it seems to me, that man with all his noble qualities... still bears in his bodily frame the indelible stamp of his lowly origin._______, (1809-1882) Evolution/radiation of fishes over time Era Cenozoic Fig 13.1 Fishes are the most primitive vertebrate and last common ancestor to all vertebrates They start the branch from all other living things with vertebrae and a cranium Chordata Notochord Dorsal hollow nerve cord Pharyngeal gill slits Postanal tail Urochordata Cephalochordata Craniates (mostly Vertebrata) Phylum Chordata sister is… Echinodermata Synapomorphy – They are deuterostomes Fish Evolutionary Tree – evolutionary innovations in vertebrate history Sarcopterygii Chondrichthyes Actinopterygii (fish) For extant fishes Osteichthyes Gnathostomata Handout Vertebrata Craniata Figure only from Berkeley.edu Hypothesis of fish (vert) origins Background 570 MYA – first large radiation of multicellular life – Fossils of the Burgess Shale – Called the Cambrian explosion Garstang Hypothesis 1928 Neoteny of sessile invertebrates Mistake that was “good” Mudpuppy First Vertebrates Vertebrates appear shortly after Cambrian explosion, 530 MYA – Conodonts Notochord replaced by segmented or partially segmented vertebrate and brain is enclosed in cranium Phylogenetic tree Echinoderms, et al. Other “inverts” Vertebrate phyla X Protostomes Deuterostomes Nephrozoa – bilateral animals First fishes were jawless appearing -
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. -
Last Meal Reflects Spiral-Shaped Intestine 6 January 2016
Last meal reflects spiral-shaped intestine 6 January 2016 performed statistical analyses that revealed unknown patterns of distribution of the intestinal structure", explains Marcelo Sánchez. All of this led to the finding that Saurichthys had a straight stomach and a spiral valve. Energetic lifestyle The findings by the Zurich-based paleontologists unveil previously unexpected convergences with the gastrointestinal anatomy of present-day sharks and rays. "The anatomy of the gastrointestinal tract of Saurichthys, in particular the many windings in Extinct predatory fish Saurichthys. Credit: UZH the spiral valve, show the most original digestion organs of earlier fishes", says Thodoris Argyriou, a PhD student at the Paleontological Institute and Museum of the University of Zurich. The spiral A last meal provides new insights: The fossilized valve of Saurichthys indicates an energy-laden food remains of the extinct predatory fish lifestyle that was adjusted to the predatory and Saurichthys reflect its spiral-shaped intestine. The reproductive behavior of the genus. "The large spiral valve in fossils from Southern Switzerland is number of windings increased the surface area for similar to that of sharks and rays. Paleontologists digestion, which is sure to have provided the fish from the University of Zurich have thus closed a with more energy", says Thodoris Argyriou. gap in the knowledge concerning the evolution of the gastrointestinal tract in vertebrates. More information: Thodoris Argyriou et al. Exceptional preservation reveals gastrointestinal A last supper has provided some interesting anatomy and evolution in early actinopterygian findings. The digested and undigested remains of fishes, Scientific Reports (2016). DOI: the last meal eaten by a Saurichthys, a Triassic 10.1038/srep18758 bony fish, were discovered in a extraordinary case of preservation that paleontologists at the University of Zurich were quick to take advantage of. -
Fishes Scales & Tails Scale Types 1
Phylum Chordata SUBPHYLUM VERTEBRATA Metameric chordates Linear series of cartilaginous or boney support (vertebrae) surrounding or replacing the notochord Expanded anterior portion of nervous system THE FISHES SCALES & TAILS SCALE TYPES 1. COSMOID (most primitive) First found on ostracaderm agnathans, thick & boney - composed of: Ganoine (enamel outer layer) Cosmine (thick under layer) Spongy bone Lamellar bone Perhaps selected for protection against eurypterids, but decreased flexibility 2. GANOID (primitive, still found on some living fish like gar) 3. PLACOID (old scale type found on the chondrichthyes) Dentine, tooth-like 4. CYCLOID (more recent scale type, found in modern osteichthyes) 5. CTENOID (most modern scale type, found in modern osteichthyes) TAILS HETEROCERCAL (primitive, still found on chondrichthyes) ABBREVIATED HETEROCERCAL (found on some primitive living fish like gar) DIPHYCERCAL (primitive, found on sarcopterygii) HOMOCERCAL (most modern, found on most modern osteichthyes) Agnatha (class) [connect the taxa] Cyclostomata (order) Placodermi Acanthodii (class) (class) Chondrichthyes (class) Osteichthyes (class) Actinopterygii (subclass) Sarcopterygii (subclass) Dipnoi (order) Crossopterygii (order) Ripidistia (suborder) Coelacanthiformes (suborder) Chondrostei (infra class) Holostei (infra class) Teleostei (infra class) CLASS AGNATHA ("without jaws") Most primitive - first fossils in Ordovician Bottom feeders, dorsal/ventral flattened Cosmoid scales (Ostracoderms) Pair of eyes + pineal eye - present in a few living fish and reptiles - regulates circadian rhythms Nine - seven gill pouches No paired appendages, medial nosril ORDER CYCLOSTOMATA (60 spp) Last living representatives - lampreys & hagfish Notochord not replaced by vertebrae Cartilaginous cranium, scaleless body Sea lamprey predaceous - horny teeth in buccal cavity & on tongue - secretes anti-coaggulant Lateral Line System No stomach or spleen 5 - 7 year life span - adults move into freshwater streams, spawn, & die. -
Sight for Sore Eyes: Ancient Fish See Colour 19 September 2005
Sight for sore eyes: ancient fish see colour 19 September 2005 The Australian lungfish - one of the world’s oldest pigments, are bigger in lungfish than for any other fishes and related to our ancient ancestors - may animal with a backbone. This probably makes them have been viewing rivers in technicolour long more sensitive to light. before dinosaurs roamed the Earth. “We keep discovering ways in which these animals Recent work by postgraduate student Helena are quite different from other fish,” Helena says. Bailes at the University of Queensland Australia, “Their eyes seem designed to optimise both has found these unusual fish have genes for five sensitivity and colour vision with large cells different forms of visual pigment in their eyes. containing different visual pigments.” Humans only have three. She now is hoping that behavioural research can Helena is one of 13 early-career researchers who find out how these fish are using their eyes for have presented their work to the public and the colour vision in the wild. media for the first time as part of the national program Fresh Science. “We may then learn what Queensland rivers look like to some of their oldest inhabitants, before those Night and day (colour) vision are controlled by inhabitants are wiped out,” Bailes says. different light sensing cells known respectively as rods and cones. Humans have a single type of rod and three types of cone, each containing a different pigment gene tuned to red, green and blue wavelengths. Lungfish possess two additional pigments that were lost in mammals, Bailes says. -
Supporting Information
Supporting Information Clarke et al. 10.1073/pnas.1607237113 Major Axes of Shape Variation and Their Anatomical a comparison: the crown teleost vs. stem teleost comparison on Correlates molecular timescales. Here, the larger SL dataset delivers a All relative warp axes that individually account for >5% of the majority of trees where crown teleosts possess significantly variation across the species sampled are displayed in Table S3. higher rates than stem teleosts, whereas the CS and pruned SL Morphospaces derived from the first three axes, containing all datasets find this result in a large minority (Fig. S3). 398 Mesozoic neopterygian species in our shape dataset, are Overall, these results suggest that choice of size metric is presented in Fig. S1. Images of sampled fossil specimens are also relatively unimportant for our dataset, and that the overall size included in Fig. S1 to illustrate the anatomical correlates of and taxonomic samplings of the dataset are more likely to in- shape axes. The positions of major neopterygian clades in mor- fluence subsequent results, despite those factors having a rela- phospace are indicated by different colors in Fig. S2. Major tively small influence here. Nevertheless, choice of metric may be teleost clades are presented in Fig. S2A and major holostean important for other datasets (e.g., different groups of organisms clades in Fig. S2B. or datasets of other biological/nonbiological structures), because RW1 captures 42.53% of the variance, reflecting changes from it is possible to envisage scenarios where the choice of size metric slender-bodied taxa to deep-bodied taxa (Fig. S1 and Table S3). -
The Histology of the Digestive Tract of the Chimaroid Fish, Hydrolagus
'PRE HISTOLOGY OF THE DIGEST IVE TRACT OF THE CHIMAEROID FISH, HYDROLA.GUS COLLIE! (LAY AND BENN:&rT) by GALEN EDWARD CLOTHIER A THESIS submitted to OREGON STATE COLLEGE in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE June 1957 IIFBOTST Redacted for Privacy Frofeasor o,f BooI"oilr 0baLrrsn of $epartuant of Zoology & 0harst of XaJor Redacted for Privacy Cha,Lruaa Sob,oo1 0mduatr Oonntttec Redacted for Privacy Dcen ef Sraduato Sohool Date thccls te Brosoated tJrpcd by largaret $loth!.tr ACKNOWLEDGMENTS I would like to express my appreciation and gratitude to my major professor, Dr . Ernst J. Dornfeld , for the training, advice , assistance and encouragement given me during this investigation. Dr . Alfred Owczarzak of Oregon State College deserves special thanks for assistance and advice concerning t he photographs which accompany this thesis . I would like also to express my gratitude to Dr . Paul Ilg and his staff at the Friday Harbor Laboratories for collecting the fish used in this study. '!'ABLE OF CONTENTS Page INTRODUCTION • • • • • • • • • • • • . .. • • • .l MATERIALS AND METHODS • • • • • • • • • • • • 6 OBSERVATIONS • • • • • • • • • • • • • • • • • • 8 Gross anatomical features • • • • • • • • • 8 Microscopic anatomy • • • • • • • • • • • • ll DISCUSSION • • • • • • • • • . .. • • • • • • • 23 SUMMARY AND COUCLUSIONS • • • • • • • • • • • • 29 BJELIOGRAPHY • • • • • • • • • • • • • • • • • • 31 APPENDIX EXPLANATION OP PLATES • • • •• • • • • • • • • • 35 Plate I • • • • • • • • • • • • • • • . . -
History of Fishes - Structural Patterns and Trends in Diversification
History of fishes - Structural Patterns and Trends in Diversification AGNATHANS = Jawless • Class – Pteraspidomorphi • Class – Myxini?? (living) • Class – Cephalaspidomorphi – Osteostraci – Anaspidiformes – Petromyzontiformes (living) Major Groups of Agnathans • 1. Osteostracida 2. Anaspida 3. Pteraspidomorphida • Hagfish and Lamprey = traditionally together in cyclostomata Jaws = GNATHOSTOMES • Gnathostomes: the jawed fishes -good evidence for gnathostome monophyly. • 4 major groups of jawed vertebrates: Extinct Acanthodii and Placodermi (know) Living Chondrichthyes and Osteichthyes • Living Chondrichthyans - usually divided into Selachii or Elasmobranchi (sharks and rays) and Holocephali (chimeroids). • • Living Osteichthyans commonly regarded as forming two major groups ‑ – Actinopterygii – Ray finned fish – Sarcopterygii (coelacanths, lungfish, Tetrapods). • SARCOPTERYGII = Coelacanths + (Dipnoi = Lung-fish) + Rhipidistian (Osteolepimorphi) = Tetrapod Ancestors (Eusthenopteron) Close to tetrapods Lungfish - Dipnoi • Three genera, Africa+Australian+South American ACTINOPTERYGII Bichirs – Cladistia = POLYPTERIFORMES Notable exception = Cladistia – Polypterus (bichirs) - Represented by 10 FW species - tropical Africa and one species - Erpetoichthys calabaricus – reedfish. Highly aberrant Cladistia - numerous uniquely derived features – long, independent evolution: – Strange dorsal finlets, Series spiracular ossicles, Peculiar urohyal bone and parasphenoid • But retain # primitive Actinopterygian features = heavy ganoid scales (external -
BMC Ecology Biomed Central
BMC Ecology BioMed Central Research article Open Access Visual ecology of the Australian lungfish (Neoceratodus forsteri) Nathan S Hart*1, Helena J Bailes1,2, Misha Vorobyev1,3, N Justin Marshall1 and Shaun P Collin1 Address: 1School of Biomedical Sciences, The University of Queensland, Brisbane, QLD 4072, Australia, 2Faculty of Life Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK and 3Department of Optometry and Vision Science, The University of Auckland, Private Bag 92019, Auckland, New Zealand Email: Nathan S Hart* - [email protected]; Helena J Bailes - [email protected]; Misha Vorobyev - [email protected]; N Justin Marshall - [email protected]; Shaun P Collin - [email protected] * Corresponding author Published: 18 December 2008 Received: 27 August 2008 Accepted: 18 December 2008 BMC Ecology 2008, 8:21 doi:10.1186/1472-6785-8-21 This article is available from: http://www.biomedcentral.com/1472-6785/8/21 © 2008 Hart et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: The transition from water to land was a key event in the evolution of vertebrates that occurred over a period of 15–20 million years towards the end of the Devonian. Tetrapods, including all land-living vertebrates, are thought to have evolved from lobe-finned (sarcopterygian) fish that developed adaptations for an amphibious existence. -
Tetrapod Limb and Sarcopterygian Fin Regeneration Share a Core Genetic
ARTICLE Received 28 Apr 2016 | Accepted 27 Sep 2016 | Published 2 Nov 2016 DOI: 10.1038/ncomms13364 OPEN Tetrapod limb and sarcopterygian fin regeneration share a core genetic programme Acacio F. Nogueira1,*, Carinne M. Costa1,*, Jamily Lorena1, Rodrigo N. Moreira1, Gabriela N. Frota-Lima1, Carolina Furtado2, Mark Robinson3, Chris T. Amemiya3,4, Sylvain Darnet1 & Igor Schneider1 Salamanders are the only living tetrapods capable of fully regenerating limbs. The discovery of salamander lineage-specific genes (LSGs) expressed during limb regeneration suggests that this capacity is a salamander novelty. Conversely, recent paleontological evidence supports a deeper evolutionary origin, before the occurrence of salamanders in the fossil record. Here we show that lungfishes, the sister group of tetrapods, regenerate their fins through morphological steps equivalent to those seen in salamanders. Lungfish de novo transcriptome assembly and differential gene expression analysis reveal notable parallels between lungfish and salamander appendage regeneration, including strong downregulation of muscle proteins and upregulation of oncogenes, developmental genes and lungfish LSGs. MARCKS-like protein (MLP), recently discovered as a regeneration-initiating molecule in salamander, is likewise upregulated during early stages of lungfish fin regeneration. Taken together, our results lend strong support for the hypothesis that tetrapods inherited a bona fide limb regeneration programme concomitant with the fin-to-limb transition. 1 Instituto de Cieˆncias Biolo´gicas, Universidade Federal do Para´, Rua Augusto Correa, 01, Bele´m66075-110,Brazil.2 Unidade Genoˆmica, Programa de Gene´tica, Instituto Nacional do Caˆncer, Rio de Janeiro 20230-240, Brazil. 3 Benaroya Research Institute at Virginia Mason, 1201 Ninth Avenue, Seattle, Washington 98101, USA. 4 Department of Biology, University of Washington 106 Kincaid, Seattle, Washington 98195, USA.