A2 2-Sided NESP Sharks Rays of Nthn
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A New Stingray from South Africa
Nature Vol. 289 22 January 1981 221 A new stingray from South Africa from Alwyne Wheeler ICHTHYOLOGISTS are accustomed to the regular description of previously un recognized species of fishes, which if not a daily event at least happens so frequently as not to cause great comment. Previously undescribed genera are like wise not infrequently published, but higher categories are increasingly less common. The discovery of a new stingray, which is so different from all known rays as to require both a new family and a new suborder to accommodate its distinctive characters, is therefore a remarkable event. A recent paper by P.e. Heemstra and M.M. Smith (Ichthyological Bulletin oj the J. L.B. Smith Institute of Ichthyology 43, I; 1980) describes this most striking ray as Hexatrygon bickelli and discusses its differences from other batoid fishes. Surprisingly, this remarkable fish was not the result of some organized deep-sea fishing programme, but was found lying on the beach at Port Elizabeth. It was fresh but had suffered some loss of skin by sand abrasion on the beach, and the margins of its fins appeared desiccated in places. The way it was discovered leaves a tantalising question as to its normal habitat, but Heemstra and Smith suggest that it may live in moderately deep water of 400-1,000m. This suggestion is Ventral view of Hexatrygon bickelli supported by its general appearance (small eyes, thin black dorsal skin, f1acid an acellular jelly, while the underside is chimaeroids Rhinochimaera and snout) and the chemistry of its liver-oil. richly supplied with well developed Harriota, and there can be little doubt The classification of Hexatrygon ampullae of Lorenzini. -
Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011
August 2012 Indo-Pacific Division Indonesia Report No 6/12 Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011 Report Compiled By: Purwanto, Muhajir, Joanne Wilson, Rizya Ardiwijaya, and Sangeeta Mangubhai August 2012 Indo-Pacific Division Indonesia Report No 6/12 Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011 Report Compiled By: Purwanto, Muhajir, Joanne Wilson, Rizya Ardiwijaya, and Sangeeta Mangubhai Published by: TheNatureConservancy,Indo-PacificDivision Purwanto:TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia.Email: [email protected] Muhajir: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia.Email: [email protected] JoanneWilson: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia. RizyaArdiwijaya:TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur, Bali,Indonesia.Email: [email protected] SangeetaMangubhai: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2, Sanur,Bali,Indonesia.Email: [email protected] Suggested Citation: Purwanto,Muhajir,Wilson,J.,Ardiwijaya,R.,Mangubhai,S.2012.CoralReefMonitoringinKofiau andBooIslandsMarineProtectedArea,RajaAmpat,WestPapua.2009-2011.TheNature Conservancy,Indo-PacificDivision,Indonesia.ReportN,6/12.50pp. © 2012012012201 222 The Nature Conservancy AllRightsReserved.Reproductionforanypurposeisprohibitedwithoutpriorpermission. AllmapsdesignedandcreatedbyMuhajir. CoverPhoto: -
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 -
Chondrichthyes: Dasyatidae)
1 Ichthyological Exploration of Freshwaters/IEF-1089/pp. 1-6 Published 16 February 2019 LSID: http://zoobank.org/urn:lsid:zoobank.org:pub:DFACCD8F-33A9-414C-A2EC-A6DA8FDE6BEF DOI: http://doi.org/10.23788/IEF-1089 Contemporary distribution records of the giant freshwater stingray Urogymnus polylepis in Borneo (Chondrichthyes: Dasyatidae) Yuanita Windusari*, Muhammad Iqbal**, Laila Hanum*, Hilda Zulkifli* and Indra Yustian* Stingrays (Dasyatidae) are found in marine (con- species entering, or occurring in freshwater. For tinental, insular shelves and uppermost slopes, example, Fluvitrygon oxyrhynchus and F. signifer one oceanic species), brackish and freshwater, and were only known from five or fewer major riverine are distributed across tropical to warm temperate systems (Compagno, 2016a-b; Last et al., 2016a), waters of the Atlantic, Indian and Pacific oceans though recent surveys yielded a single record of (Nelson et al., 2016). Only a small proportion of F. oxyrhynchus and ten records of F. signifier in the dasyatid rays occur in freshwater, and include Musi drainage, South Sumatra, indicating that obligate freshwater species (those found only in both species are more widely distributed than freshwater) and euryhaline species (those that previously expected (Iqbal et al., 2017, 2018). move between freshwater and saltwater) (Last et Particularly, the dasyatid fauna of Borneo al., 2016a). Recently, a total of 89 species of Dasy- includes the giant freshwater stingray Urogymnus atidae has been confirmed worldwide (Last et al., polylepis. The occurrence of U. polylepis in Borneo 2016a), including 14 species which are known to has been reported from Sabah and Sarawak in enter or live permanently in freshwater habitats of Malaysia and the Mahakam basin in Kaliman- Southeast Asia [Brevitrygon imbricata, Fluvitrygon tan of Indonesia (Monkolprasit & Roberts, 1990; kittipongi, F. -
Stingray Injuries
Stingray Injuries FINDLAY E. RUSSELL, M.D. inflicted by stingrays are com¬ the integumentary sheath surrounding the INJURIESmon in several areas of the coastal waters spine is ruptured and the venom escapes into of North America (1-4). Approximately 750 the victim's tissues. In withdrawing the spine, people a year along our coasts are stung by the integumentary sheath may be torn free and these elasmobranchs. The largest number of remain in the wound. stings are reported from southern California, Unlike the injuries inflicted by many venom¬ the Gulf of California, the Gulf of Mexico, and ous animals, wounds produced by the stingray the south Atlantic coast (5). may be large and severely lacerated, requiring Of 1,097 stingray injuries reported over a 5- extensive debridement and surgical closure. A year period in the United States (5, tf), 232 sting no wider than 5 mm. may produce a were seen by a physician at some time during wound 3.5 cm. long (#), and larger stings may the course of the recovery of the victim. Sixty- produce wounds 7 inches long (7). Occasion¬ two patients were hospitalized; the majority of ally, the sting itself may be broken off in the these required surgical closure of their wounds wound. or treatment for secondary infection, or both. The sting, or caudal spine, is a bilaterally ser¬ At least 10 of the 62 victims were hospitalized rated dentinal structure located on the dorsal for treatment for overexuberant first aid care. surface of the animal's tail. The sharp serra¬ Only eight patients were hospitalized for the tions are curved cephalically and as such are treatment of the systemic effects produced by responsible for the lacerating effects as the sting the venom. -
Biology, Husbandry, and Reproduction of Freshwater Stingrays
Biology, husbandry, and reproduction of freshwater stingrays. Ronald G. Oldfield University of Michigan, Department of Ecology and Evolutionary Biology Museum of Zoology, 1109 Geddes Ave., Ann Arbor, MI 48109 U.S.A. E-mail: [email protected] A version of this article was published previously in two parts: Oldfield, R.G. 2005. Biology, husbandry, and reproduction of freshwater stingrays I. Tropical Fish Hobbyist. 53(12): 114-116. Oldfield, R.G. 2005. Biology, husbandry, and reproduction of freshwater stingrays II. Tropical Fish Hobbyist. 54(1): 110-112. Introduction In the freshwater aquarium, stingrays are among the most desired of unusual pets. Although a couple species have been commercially available for some time, they remain relatively uncommon in home aquariums. They are often avoided by aquarists due to their reputation for being fragile and difficult to maintain. As with many fishes that share this reputation, it is partly undeserved. A healthy ray is a robust animal, and problems are often due to lack of a proper understanding of care requirements. In the last few years many more species have been exported from South America on a regular basis. As a result, many are just recently being captive bred for the first time. These advances will be making additional species of freshwater stingray increasingly available in the near future. This article answers this newly expanded supply of wild-caught rays and an anticipated increased The underside is one of the most entertaining aspects of a availability of captive-bred specimens by discussing their stingray. In an aquarium it is possible to see the gill slits and general biology, husbandry, and reproduction in order watch it eat, as can be seen in this Potamotrygon motoro. -
AC30 Doc. 20 A1
AC30 Doc. 20 Annex 1 (in the original language / dans la langue d’origine / en el idioma original) Responses to Notification to the Parties No 2018/041 Table of Contents Australia 2 China 14 Colombia 16 European Union 18 Indonesia 22 Mexico 52 New Zealand 56 Peru 59 Philippines 65 United States of America 67 Uruguay 116 Florida International University 121 The Pew Charitable Trusts 123 Wildlife Conservation Society 125 Notification 2018/041 Request for new information on shark and ray conservation and management activities, including legislation Australia is pleased to provide the following response to Notification 2018/041 ‘Request for new information on shark and ray conservation and management activities, including legislation’. This document is an update of the information submitted in 2017 in response to Notification 2017/031. The Australian Government is committed to the sustainable use of fisheries resources and the conservation of marine ecosystems and biodiversity. In particular, we are committed to the conservation of shark species in Australian waters and on the high seas. The Australian Government manages some fisheries directly, others are managed by state and territory governments. The Australian Government also regulates the export of commercially harvested marine species. Australia cooperates internationally to protect sharks by implementing our Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) obligations, and by working with regional fisheries management organisations on the management of internationally straddling and highly migratory stocks. For more information on Australia’s fisheries management and international cooperation see the Australian Government Department of the Environment and Energy’s fisheries webpages at http://www.environment.gov.au/marine/fisheries. -
Sawfish and River Sharks Multispecies Recovery Plan
Sawfish and River Sharks Multispecies Recovery Plan 2015 The issues paper linked to this plan is obtainable from: http://www.environment.gov.au/resource/recovery-plan-sawfish-and-river-sharks © Copyright Commonwealth of Australia 2015 Sawfish and River Sharks Multispecies Recovery Plan is licensed by the Commonwealth of Australia for use under a Creative Commons Attribution 4.0 licence with the exception of the Coat of Arms of the Commonwealth of Australia, the logo of the agency responsible for publishing the report, content supplied by third parties, and any images depicting people. For licence conditions see: https://creativecommons.org/licenses/by/4.0/. This report should be attributed as ‘Sawfish and River Sharks Multispecies Recovery Plan, Commonwealth of Australia 2015’. The Commonwealth of Australia has made all reasonable efforts to identify content supplied by third parties using the following format ‘© Copyright, [name of third party] ’. Disclaimer The views and opinions expressed in this publication are those of the authors and do not necessarily reflect those of the Australian Government or the Minister for the Environment. While reasonable efforts have been made to ensure that the contents of this publication are factually correct, the Commonwealth does not accept responsibility for the accuracy or completeness of the contents, and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of, or reliance on, the contents of this publication. Image Credits Front Cover: Largetooth sawfish (Pristis pristis) in the Daly River (© Copyright, Richard Pillans). Back Cover: Green sawfish (Pristis zijsron) juvenile from Pilbara (© Copyright, Richard Pillans). -
Class Wars: Chondrichthyes and Osteichthyes Dominance in Chesapeake Bay, 2002-2012
Class Wars: Chondrichthyes and Osteichthyes dominance in Chesapeake Bay, 2002-2012. 01 July 2013 Introduction The objective of this analysis was to demonstrate a possible changing relationship between two Classes of fishes, Osteichthyes (the bony fishes) and Chondrichthyes (the cartilaginous fishes) in Chesapeake Bay based on 11 years of monitoring. If any changes between the two Classes appeared to be significant, either statistically or anecdotally, the data were explored further in an attempt to explain the variation. The Class Osteichthyes is characterized by having a skeleton made of bone and is comprised of the majority of fish species worldwide, while the Chondrichthyes skeleton is made of cartilage and is represented by the sharks, skates, and rays (the elasmobranch fishes) and chimaeras1. Many shark species are generally categorized as apex predators, while skates and rays and some smaller sharks can be placed into the mesopredator functional group (Myers et al., 2007). By definition, mesopredators prey upon a significant array of lower trophic groups, but also serve as the prey base for apex predators. Global demand for shark and consequential shark fishing mortality, estimated at 97 million sharks in 2010 (Worm et al., 2013), is hypothesized to have contributed to the decline of these apex predators in recent years (Baum et al., 2003 and Fowler et al., 2005), which in turn is suggested to have had a cascading effect on lower trophic levels—an increase in mesopredators and subsequent decrease in the prey base (Myers et al., 2007). According to 10 years of trawl survey monitoring of Chesapeake Bay, fish species composition of catches has shown a marked change over the years (Buchheister et al., 2013). -
A Practical Key for the Identification of Large Fish Rostra 145-160 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; Download
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Spixiana, Zeitschrift für Zoologie Jahr/Year: 2015 Band/Volume: 038 Autor(en)/Author(s): Lange Tabea, Brehm Julian, Moritz Timo Artikel/Article: A practical key for the identification of large fish rostra 145-160 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de SPIXIANA 38 1 145-160 München, August 2015 ISSN 0341-8391 A practical key for the identification of large fish rostra (Pisces) Tabea Lange, Julian Brehm & Timo Moritz Lange, T., Brehm, J. & Moritz, T. 2015. A practical key for the identification of large fish rostra (Pisces). Spixiana 38 (1): 145-160. Large fish rostra without data of origin or determination are present in many museum collections or may appear in customs inspections. In recent years the inclu- sion of fish species on national and international lists for the protection of wildlife resulted in increased trading regulations. Therefore, useful identification tools are of growing importance. Here, we present a practical key for large fish rostra for the families Pristidae, Pristiophoridae, Xiphiidae and Istiophoridae. This key allows determination on species level for three of four families. Descriptions of the rostrum characteristics of the respective taxa are given. Tabea Lange, Lindenallee 38, 18437 Stralsund Julian Brehm, Königsallee 5, 95448 Bayreuth Timo Moritz, Deutsches Meeresmuseum, Katharinenberg 14-20, 18439 Stralsund; e-mail: [email protected] Introduction Polyodon spathula is equipped with a spoon-like rostrum which is used as an electrosensory organ Rostra are found in many fish species and can for locating plankton in water columns (Wilkens & be used for hunting (Wueringer et al. -
Northern River Shark, Glyphis Garricki
Published Date: 1 March 2019 Northern River Shark, Glyphis garricki Report Card Depleted assessment IUCN Red List IUCN Red List Australian Refer to Global Assessment Global Critically Endangered Assessment Assessment Assessors Pogonoski, J. & Pollard, D. Report Card Remarks Rare species with possibly very few mature individuals remaining Summary The Northern River Shark is a rare species found in northern Australia and Papua New Guinea. It is suggested that fewer than 250 mature individuals exist. It is threatened by fishing pressure and is presumably taken as bycatch in commercial and recreational fisheries. Habitat Source: White et al. 2015. License: CC By degradation is another likely Attribution. threat due to its coastal and estuarine distribution. It is listed as Endangered on the Environment Protection Biodiversity Conservation Act 1999 list of threatened species and hence protected under Commonwealth law. A recovery plan has been developed. Until abundance can be proven to be greater than suspected levels, it is assessed as Critically Endangered (IUCN) and in Australia, Overfished (SAFS). Distribution The distribution of the Northern River Shark is uncertain. It occurs in marine, freshwater and estuarine habitats and is known to occur in several areas in Western Australia (Ord and King Rivers, King Sound and Joseph Bonaparte Gulf) and Northern Territory (South and East Alligator Rivers and Wessel islands) (Last and Stevens 2009). It has been confirmed as occurring in Papua New Guinea with the finding of two individuals in the coastal marine waters of the Daru region (White et al. 2015). This was the first confirmed record of this species in Papua New Guinea since the 1970s (White et al. -
Complete Mitochondrial DNA Genome of Bonnethead Shark, Sphyrna Tiburo, and Phylogenetic Relationships Among Main Superorders of Modern Elasmobranchs
Meta Gene 7 (2016) 48–55 Contents lists available at ScienceDirect Meta Gene journal homepage: www.elsevier.com/locate/mgene Complete mitochondrial DNA genome of bonnethead shark, Sphyrna tiburo, and phylogenetic relationships among main superorders of modern elasmobranchs Píndaro Díaz-Jaimes a,⁎, Natalia J. Bayona-Vásquez a, Douglas H. Adams b, Manuel Uribe-Alcocer a a Laboratorio de Genética de Organismos Acuáticos, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Apdo. Postal 70-305, México D.F. 04510, Mexico b Florida Fish and Wildlife Conservation Commission, Fish and Wildlife Research Institute, 1220 Prospect Avenue, Suite 285, Melbourne, FL 32901, USA article info abstract Article history: Elasmobranchs are one of the most diverse groups in the marine realm represented by 18 orders, 55 families and Received 2 September 2015 about 1200 species reported, but also one of the most vulnerable to exploitation and to climate change. Phyloge- Revised 18 November 2015 netic relationships among main orders have been controversial since the emergence of the Hypnosqualean Accepted 19 November 2015 hypothesis by Shirai (1992) that considered batoids as a sister group of sharks. The use of the complete Available online 24 November 2015 mitochondrial DNA (mtDNA) may shed light to further validate this hypothesis by increasing the number of Keywords: informative characters. We report the mtDNA genome of the bonnethead shark Sphyrna tiburo, and compare it Bonnethead with mitogenomes of other 48 species to assess phylogenetic relationships. The mtDNA genome of S. tiburo,is Mitogenome quite similar in size to that of congeneric species but also similar to the reported mtDNA genome of other Phylogeny Carcharhinidae species.