What the Coelacanth Claim? a Significance of In-Situ Conservation
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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 -
Proceedings of the Fourth Forum of the Regional Network of Local Governments Implementing Integrated Coastal Management
PEMSEA/WP/2005/18 GEF/UNDP/IMO Regional Programme on Partnerships in Environmental Management for the Seas of East Asia Proceedings of the Fourth Forum of the Regional Network of Local Governments Implementing Integrated Coastal Management Building Better Coastal Governance through Stronger Local Alliance Bali, Indonesia 26-28 April 2005 PEMSEA/WP/2005/18 PROCEEDINGS OF THE FOURTH FORUM OF THE REGIONAL NETWORK OF LOCAL GOVERNMENTS IMPLEMENTING INTEGRATED COASTAL MANAGEMENT Building Better Coastal Governance through Stronger Local Alliance GEF/UNDP/IMO Regional Programme on Building Partnerships in Environmental Management for the Seas of East Asia (PEMSEA) RAS/98/G33/A/IG/19 Bali, Indonesia 26-28 April 2005 PROCEEDINGS OF THE FOURTH FORUM OF THE REGIONAL NETWORK OF LOCAL GOVERNMENTS IMPLEMENTING INTEGRATED COASTAL MANAGEMENT Building Better Coastal Governance through Stronger Local Alliance September 2005 This publication may be reproduced in whole or in part and in any form for educational or non-profit purposes or to provide wider dissemination for public response, provided prior written permission is obtained from the Regional Programme Director, acknowledgment of the source is made and no commercial usage or sale of the material occurs. PEMSEA would appreciate receiving a copy of any publication that uses this publication as a source. No use of this publication may be made for resale, any commercial purpose or any purpose other than those given above without a written agreement between PEMSEA and the requesting party. Published by the GEF/UNDP/IMO Regional Programme on Building Partnerships in Environmental Management for the Seas of East Asia Printed in Quezon City, Philippines PEMSEA. -
Coelacanth Discoveries in Madagascar, with AUTHORS: Andrew Cooke1 Recommendations on Research and Conservation Michael N
Coelacanth discoveries in Madagascar, with AUTHORS: Andrew Cooke1 recommendations on research and conservation Michael N. Bruton2 Minosoa Ravololoharinjara3 The presence of populations of the Western Indian Ocean coelacanth (Latimeria chalumnae) in AFFILIATIONS: 1Resolve sarl, Ivandry Business Madagascar is not surprising considering the vast range of habitats which the ancient island offers. Center, Antananarivo, Madagascar The discovery of a substantial population of coelacanths through handline fishing on the steep volcanic 2Honorary Research Associate, South African Institute for Aquatic slopes of Comoros archipelago initially provided an important source of museum specimens and was Biodiversity, Makhanda, South Africa the main focus of coelacanth research for almost 40 years. The advent of deep-set gillnets, or jarifa, for 3Resolve sarl, Ivandry Business catching sharks, driven by the demand for shark fins and oil from China in the mid- to late 1980s, resulted Center, Antananarivo, Madagascar in an explosion of coelacanth captures in Madagascar and other countries in the Western Indian Ocean. CORRESPONDENCE TO: We review coelacanth catches in Madagascar and present evidence for the existence of one or more Andrew Cooke populations of L. chalumnae distributed along about 1000 km of the southern and western coasts of the island. We also hypothesise that coelacanths are likely to occur around the whole continental margin EMAIL: [email protected] of Madagascar, making it the epicentre of coelacanth distribution in the Western Indian Ocean and the likely progenitor of the younger Comoros coelacanth population. Finally, we discuss the importance and DATES: vulnerability of the population of coelacanths inhabiting the submarine slopes of the Onilahy canyon in Received: 23 June 2020 Revised: 02 Oct. -
Identification of Important Marine Areas Using Ecologically Or Biologically Significant Areas
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by JAMSTEC Repository Identification of important marine areas using ecologically or biologically significant areas (EBSAs) criteria in the East to Southeast Asia region and comparison with existing registered areas for the purpose of conservation Takehisa Yamakitaa,*,‡, Kenji Sudob,* , Yoshie Jintsu-Uchifunea,, Hiroyuki Yamamotoa, Yoshihisa Shirayamaa aJapan Agency for Marine-Earth Science and Technology (JAMSTEC), 2-15 Natsushima-cho, Yokosuka, Kanagawa 237-0061, Japan bAkkeshi Marine Station, Field Science Center for Northern Biosphere, Hokkaido University, Aikappu 1, Akkeshi, Hokkaido 088-1113, Japan *These authors contributed equally to this manuscript; order was decided by the correspondence timeline ‡Corresponding author: Takehisa Yamakita Tel.: +81 46 867 9767 E-mail address:[email protected] 22 23 Abstract 24 The biodiversity of East to Southeast (E–SE) Asian waters is rapidly declining because 25 of anthropogenic effects ranging from local environmental pressures to global warming. 26 To improve marine biodiversity, the Aichi Biodiversity Targets were adopted in 2010. 27 The recommendation of the Subsidiary Body on Scientific, Technical and 28 Technological Advice (SBSTTA), encourages application of the ecologically or 29 biologically significant area (EBSA) process to identify areas for conservation. 30 However, there are few examples of the use of EBSA criteria to evaluate entire oceans. 31 In this article, seven criteria are numerically -
2 Existing Certification Systems for Fishery Products
Fisheries Partnership Agreement FPA 2006/20 FPA 15/IUU/08 ANNEX 2: INFORMATION NOTE ON IMPACT ASSESSMENT MISSION Council Regulation establishing a Community system to prevent, deter and eliminate illegal, unreported and unregulated fishing Oceanic Développement/Megapesca Lda 1. Introduction DG MARE of the European Commission has recruited consultants Oceanic Développement/Megapesca to undertake a study of the impacts of the new IUU fishing regulation in developing countries. A number of countries which represent different stages of development and fisheries conditions have been selected as candidates for detailed study. As part of this study the consultants will undertake field mission to each of the following countries: Ecuador, Indonesia, Mauritania, Mauritius, Morocco, Namibia, Senegal and Thailand. The duration of each field mission will be approximately one week. 2. Objectives of the Field Mission The field mission aims to meet with key governmental, industry and NGO stakeholders in the third country with a view to gathering data to: • Describe what are the national arrangements in place i) to regulate and monitor the fishing fleet flying its own flag, and ii) to ensure traceability of nationally landed and imported fisheries products • Define possible support measures which the Community could undertake, to increase the potential for successful implementation of the regulation in the third country, and to ameliorate any potential negative impacts. • Support the analysis and quantification of the positive and negative impacts of the newly adopted IUU fishing regulation, with particular reference to the certification scheme defined in Chapter III of the Regulation and its further provisions to provide cooperation and exchange of information with third countries in Chapters II, IV, VI and XI 3. -
The African Coelacanth Genome Provides Insights Into Tetrapod Evolution
OPEN ARTICLE doi:10.1038/nature12027 The African coelacanth genome provides insights into tetrapod evolution Chris T. Amemiya1,2*, Jessica Alfo¨ldi3*, Alison P. Lee4, Shaohua Fan5, Herve´ Philippe6, Iain MacCallum3, Ingo Braasch7, Tereza Manousaki5,8, Igor Schneider9, Nicolas Rohner10, Chris Organ11, Domitille Chalopin12, Jeramiah J. Smith13, Mark Robinson1, Rosemary A. Dorrington14, Marco Gerdol15, Bronwen Aken16, Maria Assunta Biscotti17, Marco Barucca17, Denis Baurain18, Aaron M. Berlin3, Gregory L. Blatch14,19, Francesco Buonocore20, Thorsten Burmester21, Michael S. Campbell22, Adriana Canapa17, John P. Cannon23, Alan Christoffels24, Gianluca De Moro15, Adrienne L. Edkins14, Lin Fan3, Anna Maria Fausto20, Nathalie Feiner5,25, Mariko Forconi17, Junaid Gamieldien24, Sante Gnerre3, Andreas Gnirke3, Jared V. Goldstone26, Wilfried Haerty27, Mark E. Hahn26, Uljana Hesse24, Steve Hoffmann28, Jeremy Johnson3, Sibel I. Karchner26, Shigehiro Kuraku5{, Marcia Lara3, Joshua Z. Levin3, Gary W. Litman23, Evan Mauceli3{, Tsutomu Miyake29, M. Gail Mueller30, David R. Nelson31, Anne Nitsche32, Ettore Olmo17, Tatsuya Ota33, Alberto Pallavicini15, Sumir Panji24{, Barbara Picone24, Chris P. Ponting27, Sonja J. Prohaska34, Dariusz Przybylski3, Nil Ratan Saha1, Vydianathan Ravi4, Filipe J. Ribeiro3{, Tatjana Sauka-Spengler35, Giuseppe Scapigliati20, Stephen M. J. Searle16, Ted Sharpe3, Oleg Simakov5,36, Peter F. Stadler32, John J. Stegeman26, Kenta Sumiyama37, Diana Tabbaa3, Hakim Tafer32, Jason Turner-Maier3, Peter van Heusden24, Simon White16, Louise Williams3, Mark Yandell22, Henner Brinkmann6, Jean-Nicolas Volff12, Clifford J. Tabin10, Neil Shubin38, Manfred Schartl39, David B. Jaffe3, John H. Postlethwait7, Byrappa Venkatesh4, Federica Di Palma3, Eric S. Lander3, Axel Meyer5,8,25 & Kerstin Lindblad-Toh3,40 The discovery of a living coelacanth specimen in 1938 was remarkable, as this lineage of lobe-finned fish was thought to have become extinct 70 million years ago. -
Making a Big Splash with Louisiana Fishes
Making a Big Splash with Louisiana Fishes Written and Designed by Prosanta Chakrabarty, Ph.D., Sophie Warny, Ph.D., and Valerie Derouen LSU Museum of Natural Science To those young people still discovering their love of nature... Note to parents, teachers, instructors, activity coordinators and to all the fishermen in us: This book is a companion piece to Making a Big Splash with Louisiana Fishes, an exhibit at Louisiana State Universi- ty’s Museum of Natural Science (MNS). Located in Foster Hall on the main campus of LSU, this exhibit created in 2012 contains many of the elements discussed in this book. The MNS exhibit hall is open weekdays, from 8 am to 4 pm, when the LSU campus is open. The MNS visits are free of charge, but call our main office at 225-578-2855 to schedule a visit if your group includes 10 or more students. Of course the book can also be enjoyed on its own and we hope that you will enjoy it on your own or with your children or students. The book and exhibit was funded by the Louisiana Board Of Regents, Traditional Enhancement Grant - Education: Mak- ing a Big Splash with Louisiana Fishes: A Three-tiered Education Program and Museum Exhibit. Funding was obtained by LSUMNS Curators’ Sophie Warny and Prosanta Chakrabarty who designed the exhibit with Southwest Museum Services who built it in 2012. The oarfish in the exhibit was created by Carolyn Thome of the Smithsonian, and images exhibited here are from Curator Chakrabarty unless noted elsewhere (see Appendix II). -
Giant Fossil Coelacanths from the Late Cretaceous of the Eastern
^rfij^i^v^^™, - » v ' - - 4 j/ N ^P"" ,- V ^™ V- -*^ >•;:-* ' ^ * -r;' David R. Schwimmer, Geologist, Columbus State University Introduction In Autumn, 1987, a sizeable mass of fossil bone was discovered by amateur collectors in the bed of a small creek in eastern Alabama. The bone-bearing rock, some 300 kg in weight, was collected by a party led by G. Dent Williams and transferred to the paleontology laboratory at Columbus State University. Williams prepared most of the material using air percussion tools, and I further cleared some bones with acetic acid. A mandible (lower jaw bone) of 502 mm length was the first bone prepared from the material. It strangely lacked evidence of both teeth and tooth sockets, and it was covered medially with coarse denticulation resembling #40 grit sandpaper. The jawbone conformed with no recognizable North American Late Cretaceous fish or four-legged animal, and, given the large size of the mandible, my initial search for an identification ranged from ankylosaurid dinosaurs, to mosasaurs, to the larger contemporary fish, such as Xiphactinus. Nothing known in the Late Cretaceous of North America matched the mandible nor any other bone which was subsequently prepared from this matrix. J.D. Stewart of the L.A. County Museum was prior fossil record of a North American coelacanth is concurrently studying fossils of small marine Diplurus newarki, from freshwater deposits of earliest coelacanths from the Late Cretaceous of western Kansas, Jurassic age (ca. 205 Myr.: Schaeffer, 1941, 1952). USA (which were also a new discovery at the time: see Forey (1981) and Maisey (1991) recognized two sub- Stewart et al., 1991). -
Class SARCOPTERYGII Order COELACANTHIFORMES
click for previous page Coelacanthiformes: Latimeriidae 3969 Class SARCOPTERYGII Order COELACANTHIFORMES LATIMERIIDAE (= Coelacanthidae) Coelacanths by S.L. Jewett A single species occurring in the area. Latimeria menadoensis Pouyaud, Wirjoatmodjo, Rachmatika, Tjakrawidjaja, Hadiaty, and Hadie, 1999 Frequent synonyms / misidentifications: None / Nearly identical in appearance to Latimeria chalumnae Smith, 1939 from the western Indian Ocean. FAO names: En - Sulawesi coelacanth. Diagnostic characters: A large robust fish. Caudal-peduncle depth nearly equal to body depth. Head robust, with large eye, terminal mouth, and large soft gill flap extending posteriorly from opercular bone. Dorsal surface of snout with pits and reticulations comprising part of sensory system. Three large, widely spaced pores on each side of snout, 1 near tip of snout and 2 just anterior to eye, connecting internally to rostral organ. Anterior nostrils form small papillae located at dorsolateral margin of mouth, at anterior end of pseudomaxillary fold (thick, muscularized skin which replaces the maxilla in coelacanths). Ventral side of head with prominent paired gular plates, longitudinally oriented along midline; skull dorsally with pronounced paired bony plates, just above and behind eyes, the posterior margins of which mark exterior manifestation of intracranial joint (or hinge) that divides braincase into anterior and posterior portions (found only in coelacanths). First dorsal fin typical, with 8 stout bony rays. Second dorsal (28 rays), anal (30), paired pectoral (each 30 to 33), and paired pelvic (each 33) fins lobed, i.e. each with a fleshy base, internally supported by an endoskeleton with which terminal fin rays articulate. Caudal fin atypical, consisting of 3 parts: upper and lower portions with numerous rays more or less symmetrically arranged along dorsal and ventral midlines, and a separate smaller terminal portion (sometimes called epicaudal fin) with symmetrically arranged rays. -
Giant Mesozoic Coelacanths (Osteichthyes, Actinistia) Reveal High Body Size Disparity Decoupled from Taxic Diversity
Giant Mesozoic Coelacanths (Osteichthyes, Actinistia) Reveal High Body Size Disparity Decoupled From Taxic Diversity Lionel Cavin ( [email protected] ) Natural History Museum of Geneva André Piuz Natural History Museum of Geneva Christophe Ferrante Natural History Museum of Geneva Guillaume Guinot Institut des Sciences de l'Evolution de Montpellier Research Article Keywords: morphological evolution, taxic diversication, Genomic and physiological characteristics Posted Date: March 2nd, 2021 DOI: https://doi.org/10.21203/rs.3.rs-245480/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License 1 2 Giant Mesozoic coelacanths (Osteichthyes, Actinistia) reveal high 3 body size disparity decoupled from taxic diversity 4 5 Lionel Cavin1*, André Piuz1, Christophe Ferrante1,2 & Guillaume Guinot3 6 7 8 1 Department of Geology and Palaeontology, Natural History Museum of Geneva, Geneva, 9 Switzerland 10 2 Department of Earth Sciences, University of Geneva, Rue des Maraîchais 13, 1205 Genève, 11 Switzerland 12 3 Institut des Sciences de l’Evolution de Montpellier (Université de Montpellier, CNRS, IRD, 13 EPHE), Montpellier, France 14 15 * Corresponding author 16 Email: [email protected] 17 1 18 Abstract 19 20 The positive correlation between speciation rates and morphological evolution expressed by 21 body size is a macroevolutionary trait of vertebrates. Although taxic diversification and 22 morphological evolution are slow in coelacanths, their fossil record indicates that large and 23 small species coexisted, which calls into question the link between morphological and body 24 size disparities. Here, we describe and reassess fossils of giant coelacanths. Two genera 25 reached up to 5 meters long, placing them among the ten largest bony fish that ever lived. -
This Is a Peer Reviewed Version Of
This is a peer reviewed version of the following article: Tulloch, A., Auerbach, N., Avery- Gomm, S., Bayraktarov, E., Butt, N., Dickman, C.R., Ehmke, G., Fisher, D.O., Grantham, H., Holden, M.H., Lavery, T.H., Leseberg, N.P., Nicholls, M., O’Connor, J., Roberson, L., Smyth, A.K., Stone, Z., Tulloch, V., Turak, E., Wardle, G.M., Watson, J.E.M. (2018) A decision tree for assessing the risks and benefits of publishing biodiversity data, Nature Ecology & Evolution, Vol. 2, pp. 1209-1217; which has been published in final form at: https://doi.org/10.1038/s41559-018-0608-1 1 2 A decision tree for assessing the risks and benefits of publishing 3 biodiversity data 4 Ayesha I.T. Tulloch1,2,3*, Nancy Auerbach4, Stephanie Avery-Gomm4, Elisa Bayraktarov4, Nathalie Butt4, Chris R. 5 Dickman3, Glenn Ehmke5, Diana O. Fisher4, Hedley Grantham2, Matthew H. Holden4, Tyrone H. Lavery6, 6 Nicholas P. Leseberg1, Miles Nicholls7, James O’Connor5, Leslie Roberson4, Anita K. Smyth8, Zoe Stone1, 7 Vivitskaia Tulloch4, Eren Turak9,10, Glenda M. Wardle3, James E.M. Watson1,2 8 1. School of Earth and Environmental Sciences, The University of Queensland, St. Lucia Queensland 4072, 9 Australia 10 2. Wildlife Conservation Society, Global Conservation Program, 2300 Southern Boulevard, Bronx NY 11 10460-1068, USA 12 3. Desert Ecology Research Group, School of Life and Environmental Sciences, University of Sydney, 13 Sydney NSW 2006, Australia 14 4. School of Biological Sciences, The University of Queensland, St. Lucia, Brisbane Queensland 4072, 15 Australia 16 5. BirdLife Australia, Melbourne VIC 3053, Australia 17 6. -
New Coelacanth Material from the Middle Triassic of Eastern Switzerland, and Comments on the Taxic Diversity of Actinistans
Swiss J Geosci (2013) 106:161–177 DOI 10.1007/s00015-013-0143-7 New coelacanth material from the Middle Triassic of eastern Switzerland, and comments on the taxic diversity of actinistans Lionel Cavin • Heinz Furrer • Christian Obrist Received: 1 February 2013 / Accepted: 9 August 2013 / Published online: 16 November 2013 Ó Swiss Geological Society 2013 Abstract New coelacanth material from the Middle Tri- preserved on the holotype and allows the addition of new assic Prosanto Formation of the Ducan and Landwasser characters to a previously published data matrix of acti- area near Davos in eastern Switzerland, Canton Graubu¨n- nistians. A phylogenetic analysis is performed, which den, is described. A sub-complete individual is visible in supports that Ticinepomis is nested among the Latimeri- ventral view, and shows details of its branchial apparatus. idae. The diversity of post-Palaeozoic coelacanths is In particular, it possesses relatively large teeth on the assessed. The taxic diversity of observed occurrences ceratobranchials, and possible ossified hypobranchials. shows a peak in the Early Triassic and a peak in the Late Few diagnostic characters are observable, and most of them Jurassic, as detected in previous studies. When ghost lin- are visible on the mandibles preserved in lateral view. This eages are included in the computation, the Late Jurassic specimen shares characters with Ticinepomis peyeri,a peak is smoothened. By comparing the taxic diversity smaller form from the Middle Triassic of Monte San curves with the curve of average ghost lineage duration, we Giorgio, whose holotype is re-described in part here. A conclude that the Early Triassic peak of diversity was second specimen, a fragmentary caudal skeleton shows the probably caused by a biological radiation, whereas the Late typical supplementary lobe of coelacanths, and meristic Jurassic peak of observed diversity is probably the result of characters indicating probable close affinities with T.