“King of Shark Fins” with Their Reputed Quality and Texture (Yeung 儘管群翅廣為人知,但以鰩魚鰭為研究目標 Et Al., 2005; Lam, 2010)
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The Fishing and Illegal Trade of the Angelshark DNA Barcoding
Fisheries Research 206 (2018) 193–197 Contents lists available at ScienceDirect Fisheries Research journal homepage: www.elsevier.com/locate/fishres The fishing and illegal trade of the angelshark: DNA barcoding against T misleading identifications ⁎ Ingrid Vasconcellos Bunholia, Bruno Lopes da Silva Ferrettea,b, , Juliana Beltramin De Biasia,b, Carolina de Oliveira Magalhãesa,b, Matheus Marcos Rotundoc, Claudio Oliveirab, Fausto Forestib, Fernando Fernandes Mendonçaa a Laboratório de Genética Pesqueira e Conservação (GenPesC), Instituto do Mar (IMar), Universidade Federal de São Paulo (UNIFESP), Santos, SP, 11070-102, Brazil b Laboratório de Biologia e Genética de Peixes (LBGP), Instituto de Biociências de Botucatu (IBB), Universidade Estadual Paulista (UNESP), Botucatu, SP, 18618-689, Brazil c Acervo Zoológico da Universidade Santa Cecília (AZUSC), Universidade Santa Cecília (Unisanta), Santos, SP, 11045-907, Brazil ARTICLE INFO ABSTRACT Handled by J Viñas Morphological identification in the field can be extremely difficult considering fragmentation of species for trade Keywords: or high similarity between congeneric species. In this context, the shark group belonging to the genus Squatina is Conservation composed of three species distributed in the southern part of the western Atlantic. These three species are Endangered species classified in the IUCN Red List as endangered, and they are currently protected under Brazilian law, which Fishing monitoring prohibits fishing and trade. Molecular genetic tools are now used for practical taxonomic identification, parti- Forensic genetics cularly in cases where morphological observation is prevented, e.g., during fish processing. Consequently, DNA fi Mislabeling identi cation barcoding was used in the present study to track potential crimes against the landing and trade of endangered species along the São Paulo coastline, in particular Squatina guggenheim (n = 75) and S. -
WHERE DO SAWFISH LIVE? Educator Information for Student Activity 4
WHERE DO SAWFISH LIVE? Educator Information For Student Activity 4 Lesson Summary: This lesson examines the diversity of locations and habitats where sawfish are found throughout the world. Vocabulary: Distribution, habitats Background Information: There are six recognized species of sawfish throughout the world. In this activity the distribution range of each species will be discussed and mapped. Information on each species can be found in the “Sawfish In Peril” teaching binder within each of the species profiles. Materials: Copies of activity map sheets and species profile laminated cards w/maps Pencils: colored pencils recommended Procedure: This activity begins by getting students to look at the different maps of sawfish species distribution. Have each student color in a map template of the distribution of a favorite sawfish species or have students form groups to color the maps for each species. Discussion Questions: Where do sawfish live? What habitats do sawfish reside in? Where would you go if you wanted to see a sawfish? Extension Activities: For more advanced students, the following questions can be discussed: What determines where sawfish species live? Do sawfish prefer certain water temperatures and habitat types? In the past, did sawfish have larger distribution then they do currently? If so, why do you think that is? www.flmnh.ufl.edu/fish 6-14 © 2010 Florida Museum of Natural History WHERE DO SAWFISH LIVE? Educator Information For Student Activity 4 Maps of sawfish species geographical distribution (from the species profiles): Smalltooth Sawfish (P. pectinata) Freshwater Sawfish (P. microdon) Largetooth Sawfish (P. perotteti) Dwarf Sawfish (P. clavata) Green Sawfish (P. -
Bibliography Database of Living/Fossil Sharks, Rays and Chimaeras (Chondrichthyes: Elasmobranchii, Holocephali) Papers of the Year 2016
www.shark-references.com Version 13.01.2017 Bibliography database of living/fossil sharks, rays and chimaeras (Chondrichthyes: Elasmobranchii, Holocephali) Papers of the year 2016 published by Jürgen Pollerspöck, Benediktinerring 34, 94569 Stephansposching, Germany and Nicolas Straube, Munich, Germany ISSN: 2195-6499 copyright by the authors 1 please inform us about missing papers: [email protected] www.shark-references.com Version 13.01.2017 Abstract: This paper contains a collection of 803 citations (no conference abstracts) on topics related to extant and extinct Chondrichthyes (sharks, rays, and chimaeras) as well as a list of Chondrichthyan species and hosted parasites newly described in 2016. The list is the result of regular queries in numerous journals, books and online publications. It provides a complete list of publication citations as well as a database report containing rearranged subsets of the list sorted by the keyword statistics, extant and extinct genera and species descriptions from the years 2000 to 2016, list of descriptions of extinct and extant species from 2016, parasitology, reproduction, distribution, diet, conservation, and taxonomy. The paper is intended to be consulted for information. In addition, we provide information on the geographic and depth distribution of newly described species, i.e. the type specimens from the year 1990- 2016 in a hot spot analysis. Please note that the content of this paper has been compiled to the best of our abilities based on current knowledge and practice, however, -
Sharks in Crisis: a Call to Action for the Mediterranean
REPORT 2019 SHARKS IN CRISIS: A CALL TO ACTION FOR THE MEDITERRANEAN WWF Sharks in the Mediterranean 2019 | 1 fp SECTION 1 ACKNOWLEDGEMENTS Written and edited by WWF Mediterranean Marine Initiative / Evan Jeffries (www.swim2birds.co.uk), based on data contained in: Bartolí, A., Polti, S., Niedermüller, S.K. & García, R. 2018. Sharks in the Mediterranean: A review of the literature on the current state of scientific knowledge, conservation measures and management policies and instruments. Design by Catherine Perry (www.swim2birds.co.uk) Front cover photo: Blue shark (Prionace glauca) © Joost van Uffelen / WWF References and sources are available online at www.wwfmmi.org Published in July 2019 by WWF – World Wide Fund For Nature Any reproduction in full or in part must mention the title and credit the WWF Mediterranean Marine Initiative as the copyright owner. © Text 2019 WWF. All rights reserved. Our thanks go to the following people for their invaluable comments and contributions to this report: Fabrizio Serena, Monica Barone, Adi Barash (M.E.C.O.), Ioannis Giovos (iSea), Pamela Mason (SharkLab Malta), Ali Hood (Sharktrust), Matthieu Lapinksi (AILERONS association), Sandrine Polti, Alex Bartoli, Raul Garcia, Alessandro Buzzi, Giulia Prato, Jose Luis Garcia Varas, Ayse Oruc, Danijel Kanski, Antigoni Foutsi, Théa Jacob, Sofiane Mahjoub, Sarah Fagnani, Heike Zidowitz, Philipp Kanstinger, Andy Cornish and Marco Costantini. Special acknowledgements go to WWF-Spain for funding this report. KEY CONTACTS Giuseppe Di Carlo Director WWF Mediterranean Marine Initiative Email: [email protected] Simone Niedermueller Mediterranean Shark expert Email: [email protected] Stefania Campogianni Communications manager WWF Mediterranean Marine Initiative Email: [email protected] WWF is one of the world’s largest and most respected independent conservation organizations, with more than 5 million supporters and a global network active in over 100 countries. -
Extinction Risk and Conservation of the World's Sharks and Rays
RESEARCH ARTICLE elife.elifesciences.org Extinction risk and conservation of the world’s sharks and rays Nicholas K Dulvy1,2*, Sarah L Fowler3, John A Musick4, Rachel D Cavanagh5, Peter M Kyne6, Lucy R Harrison1,2, John K Carlson7, Lindsay NK Davidson1,2, Sonja V Fordham8, Malcolm P Francis9, Caroline M Pollock10, Colin A Simpfendorfer11,12, George H Burgess13, Kent E Carpenter14,15, Leonard JV Compagno16, David A Ebert17, Claudine Gibson3, Michelle R Heupel18, Suzanne R Livingstone19, Jonnell C Sanciangco14,15, John D Stevens20, Sarah Valenti3, William T White20 1IUCN Species Survival Commission Shark Specialist Group, Department of Biological Sciences, Simon Fraser University, Burnaby, Canada; 2Earth to Ocean Research Group, Department of Biological Sciences, Simon Fraser University, Burnaby, Canada; 3IUCN Species Survival Commission Shark Specialist Group, NatureBureau International, Newbury, United Kingdom; 4Virginia Institute of Marine Science, College of William and Mary, Gloucester Point, United States; 5British Antarctic Survey, Natural Environment Research Council, Cambridge, United Kingdom; 6Research Institute for the Environment and Livelihoods, Charles Darwin University, Darwin, Australia; 7Southeast Fisheries Science Center, NOAA/National Marine Fisheries Service, Panama City, United States; 8Shark Advocates International, The Ocean Foundation, Washington, DC, United States; 9National Institute of Water and Atmospheric Research, Wellington, New Zealand; 10Global Species Programme, International Union for the Conservation -
An Introduction to the Classification of Elasmobranchs
An introduction to the classification of elasmobranchs 17 Rekha J. Nair and P.U Zacharia Central Marine Fisheries Research Institute, Kochi-682 018 Introduction eyed, stomachless, deep-sea creatures that possess an upper jaw which is fused to its cranium (unlike in sharks). The term Elasmobranchs or chondrichthyans refers to the The great majority of the commercially important species of group of marine organisms with a skeleton made of cartilage. chondrichthyans are elasmobranchs. The latter are named They include sharks, skates, rays and chimaeras. These for their plated gills which communicate to the exterior by organisms are characterised by and differ from their sister 5–7 openings. In total, there are about 869+ extant species group of bony fishes in the characteristics like cartilaginous of elasmobranchs, with about 400+ of those being sharks skeleton, absence of swim bladders and presence of five and the rest skates and rays. Taxonomy is also perhaps to seven pairs of naked gill slits that are not covered by an infamously known for its constant, yet essential, revisions operculum. The chondrichthyans which are placed in Class of the relationships and identity of different organisms. Elasmobranchii are grouped into two main subdivisions Classification of elasmobranchs certainly does not evade this Holocephalii (Chimaeras or ratfishes and elephant fishes) process, and species are sometimes lumped in with other with three families and approximately 37 species inhabiting species, or renamed, or assigned to different families and deep cool waters; and the Elasmobranchii, which is a large, other taxonomic groupings. It is certain, however, that such diverse group (sharks, skates and rays) with representatives revisions will clarify our view of the taxonomy and phylogeny in all types of environments, from fresh waters to the bottom (evolutionary relationships) of elasmobranchs, leading to a of marine trenches and from polar regions to warm tropical better understanding of how these creatures evolved. -
Updated Checklist of Marine Fishes (Chordata: Craniata) from Portugal and the Proposed Extension of the Portuguese Continental Shelf
European Journal of Taxonomy 73: 1-73 ISSN 2118-9773 http://dx.doi.org/10.5852/ejt.2014.73 www.europeanjournaloftaxonomy.eu 2014 · Carneiro M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:9A5F217D-8E7B-448A-9CAB-2CCC9CC6F857 Updated checklist of marine fishes (Chordata: Craniata) from Portugal and the proposed extension of the Portuguese continental shelf Miguel CARNEIRO1,5, Rogélia MARTINS2,6, Monica LANDI*,3,7 & Filipe O. COSTA4,8 1,2 DIV-RP (Modelling and Management Fishery Resources Division), Instituto Português do Mar e da Atmosfera, Av. Brasilia 1449-006 Lisboa, Portugal. E-mail: [email protected], [email protected] 3,4 CBMA (Centre of Molecular and Environmental Biology), Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. E-mail: [email protected], [email protected] * corresponding author: [email protected] 5 urn:lsid:zoobank.org:author:90A98A50-327E-4648-9DCE-75709C7A2472 6 urn:lsid:zoobank.org:author:1EB6DE00-9E91-407C-B7C4-34F31F29FD88 7 urn:lsid:zoobank.org:author:6D3AC760-77F2-4CFA-B5C7-665CB07F4CEB 8 urn:lsid:zoobank.org:author:48E53CF3-71C8-403C-BECD-10B20B3C15B4 Abstract. The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. -
UNEP/CMS/COP13/Doc.28.2.9 MIGRATORY 24 September 2019
CONVENTION ON UNEP/CMS/COP13/Doc.28.2.9 MIGRATORY 24 September 2019 SPECIES Original: English 13th MEETING OF THE CONFERENCE OF THE PARTIES Gandhinagar, India, 17 - 22 February 2020 Agenda Item 28.2 PROPOSAL FOR A CONCERTED ACTION FOR THE COMMON GUITARFISH (Rhinobatos rhinobatos) AND BOTTLENOSE WEDGEFISH (Rhynchobatus australiae) ALREADY ON APPENDIX II OF THE CONVENTION, AND THE FAMILIES RHINOBATIDAE AND GLAUCOSTEGIDAE Summary: The IUCN Shark Specialist Group has submitted the attached proposal for a Concerted Action for the Common Guitarfish (Rhinobatos rhinobatos) and Bottlenose Wedgefish (Rhynchobatus australiae), in accordance with the process elaborated in Resolution 12.28. In addition to the aforementioned CMS-listed species, the families Rhinobatidae, Rhinidae and Glaucostegidae are proposed for Concerted Action because of their similar conservation needs. *The geographical designations employed in this document do not imply the expression of any opinion whatsoever on the part of the CMS Secretariat (or the United Nations Environment Programme) concerning the legal status of any country, territory, or area, or concerning the delimitation of its frontiers or boundaries. The responsibility for the contents of the document rests exclusively with its author UNEP/CMS/COP13/Doc.28.2.9 PROPOSAL FOR A CONCERTED ACTION FOR THE COMMON GUITARFISH (Rhinobatos rhinobatos) AND BOTTLENOSE WEDGEFISH (Rhynchobatus australiae) ALREADY ON APPENDIX II OF THE CONVENTION, AND THE FAMILIES RHINOBATIDAE AND GLAUCOSTEGIDAE (i). Proponent: International Union For Conservation of Nature - IUCN Species Survival Commission’s Shark Specialist Group (IUCN SSG) The IUCN SSG has long been a trusted source of science-based information and advice on sharks and their relatives (Class Chondrichthyes: sharks, rays, and chimaeras) and provides leadership for the conservation of threatened species and populations of all chondrichthyan fishes. -
Dwarf Sawfish Pristis Clavata
MARINE BIODIVERSITY hub 40° SPECIES INFORMATION SHEET No. 3 Dwarf SawfishPristis clavata 20° Distribution Although once more widespread in the Indo-West Pacific Ocean, the Dwarf Sawfish may now be restricted to northern Australia, where it occurs in tidal reaches of rivers, estuaries and coastal 0° waters of the Kimberley (WA), NT, Gulf of Carpentaria and Cape York (QLD). Conservation Status ? International (IUCN Red List of Threatened Species): Endangered 20° Australia: Vulnerable Northern Territory: Vulnerable • Dwarf Sawfish is a protected species throughout Australia. • It has declined across its global range and it now appears to be extinct outside of Australia. • Northern Australia therefore represents the last 40° population stronghold (although its status here is also of conservation concern). Dwarf Sawfish Identification Rostral teeth evenly-spaced and occur along the Front of the first dorsal fin is over, or slightly behind, whole rostrum: the origin of the pelvic fins: 100° 120° 140° 160° 180° Dwarf Sawfish Biology Habitat • Occurs in shallow-water coastal and estuarine waters, and in the tidal reaches of rivers (but does not occur in freshwater). • Size at birth is estimated at 60–81 cm long. • Despite its name, maximum size is small relative only to other sawfish species; Dwarf Sawfish grow to at least 3.2 m long. • Pregnant females give birth to live young, but it is unknown how many pups they have. • Tracking of a few Dwarf Sawfish showed that they rested in inundated mangrove forests at high tide and moved out onto subtidal mudflats at low tide. They moved up to 10 km each tidal cycle and often returned to the same area to rest at high tide. -
Life-History Characteristics of the Eastern Shovelnose Ray, Aptychotrema Rostrata (Shaw, 1794), from Southern Queensland, Australia
CSIRO PUBLISHING Marine and Freshwater Research, 2021, 72, 1280–1289 https://doi.org/10.1071/MF20347 Life-history characteristics of the eastern shovelnose ray, Aptychotrema rostrata (Shaw, 1794), from southern Queensland, Australia Matthew J. Campbell A,B,C, Mark F. McLennanA, Anthony J. CourtneyA and Colin A. SimpfendorferB AQueensland Department of Agriculture and Fisheries, Agri-Science Queensland, Ecosciences Precinct, GPO Box 267, Brisbane, Qld 4001, Australia. BCentre for Sustainable Tropical Fisheries and Aquaculture and College of Science and Engineering, James Cook University, 1 James Cook Drive, Townsville, Qld 4811, Australia. CCorresponding author. Email: [email protected] Abstract. The eastern shovelnose ray (Aptychotrema rostrata) is a medium-sized coastal batoid endemic to the eastern coast of Australia. It is the most common elasmobranch incidentally caught in the Queensland east coast otter trawl fishery, Australia’s largest penaeid-trawl fishery. Despite this, age and growth studies on this species are lacking. The present study estimated the growth parameters and age-at-maturity for A. rostrata on the basis of sampling conducted in southern Queensland, Australia. This study showed that A. rostrata exhibits slow growth and late maturity, which are common life- history strategies among elasmobranchs. Length-at-age data were analysed within a Bayesian framework and the von Bertalanffy growth function (VBGF) best described these data. The growth parameters were estimated as L0 ¼ 193 mm À1 TL, k ¼ 0.08 year and LN ¼ 924 mm TL. Age-at-maturity was found to be 13.3 years and 10.0 years for females and males respectively. The under-sampling of larger, older individuals was overcome by using informative priors, reducing bias in the growth and maturity estimates. -
(Etp) Species in West Africa
Issue Brief AN OVERVIEW OF THE ILLEGAL HARVEST OF AQUATIC ENDANGERED, THREATENED OR PROTECTED (ETP) SPECIES IN WEST AFRICA AQUATIC WILDMEAT: THE PLIGHT OF THREATENENED AQUATIC SPECIES Throughout West Africa, declining fisheries resources and rising human populations have accelerated the displacement WHAT IS AQUATIC BUSHMEAT? of many communities from their traditional food sources. This Aquatic wild meat, sometimes referred to in turn is driving new forms of aquatic meat consumption, as as aquatic bushmeat, is defined as the meat well as the rise of illegal local and international trade aimed at of aquatic species harvested and used by revenue generation. As a consequence, this aquatic harvest is humans as food resources, medicines and/ now seriously impacting large aquatic mammal, reptile and avian or cultural/ traditional items (e.g. religious biodiversity in the region. This aquatic harvest is ‘falling through items). Aquatic wildmeat includes marine the cracks’ between environment and fisheries Ministries, mammals such as manatees, cetaceans and agencies and international processes. hippopotamus, reptiles such as crocodiles and marine turtles, fish (sharks and rays), and In West Africa, as worldwide, aquatic species have been aquatic birds (herons, pelicans and storks harvested for decades by local populations. Some of the most amongst others). famous human uses are (1) the trade of the hawksbill marine turtle’ shell (bekko) through Japanese networks, (2) the consumption of manatee’s or marine turtle’s meat by coastal populations and (3) the harvest of sharks for their fins for the Asian market (Miliken & Tokunaga 1987; Groombridge & Luxmoore 1989; Diop & Dossa 2011). A WIDE VARIETY OF AQUATIC SPECIES ARE THREATENED Over time, aquatic bushmeat consumption, increasing human populations and poorly enforced measures punishing the use or trade of these aquatic species, could threaten the survival of many aquatic species. -
Age, Growth and Reproductive Biology of Two Endemic Demersal
ZOOLOGIA 37: e49318 ISSN 1984-4689 (online) zoologia.pensoft.net RESEARCH ARTICLE Age, growth and reproductive biology of two endemic demersal bycatch elasmobranchs: Trygonorrhina fasciata and Dentiraja australis (Chondrichthyes: Rhinopristiformes, Rajiformes) from Eastern Australia Marcelo Reis1 , Will F. Figueira1 1University of Sydney, School of Life and Environmental Sciences. Edgeworth David Building (A11), Room 111, Sydney, NSW 2006, Australia. [email protected] Corresponding author: Marcelo Reis ([email protected]) http://zoobank.org/51FFF676-C96D-4B1A-A713-15921D9844BF ABSTRACT. Bottom-dwelling elasmobranchs, such as guitarfishes, skates and stingrays are highly susceptible species to bycatch due to the overlap between their distribution and area of fishing operations. Catch data for this group is also often merged in generic categories preventing species-specific assessments. Along the east coast of Australia, the Eastern Fiddler Ray, Trygonorrhina fasciata (Muller & Henle, 1841), and the Sydney Skate, Dentiraja australis (Macleay, 1884), are common components of bycatch yet there is little information about their age, growth and reproductive timing, making impact assessment difficult. In this study the age and growth (from vertebral bands) as well as reproductive parameters of these two species are estimated and reported based on 171 specimens of Eastern Fiddler Rays (100 females and 71 males) and 81 Sydney Skates (47 females and 34 males). Based on von Bertalanffy growth curve fits, Eastern Fiddler Rays grew to larger sizes than Sydney Skate but did so more slowly (ray: L∞ = 109.61, t0 = 0.26 and K = 0.20; skate: L∞ = 51.95, t0 = -0.99 and K = 0.34 [both sexes combined]). Both species had higher liver weight ratios (HSI) during austral summer.