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Horizontal and Vertical Movements of Longfin Makos (Isurus Paucus)
101 Abstract—The longfin mako (Isurus paucus) is a poorly studied oceanic Horizontal and vertical movements of longfin shark taken in fisheries throughout makos (Isurus paucus) tracked with satellite- its worldwide range in temperate and tropical waters. Satellite-linked linked tags in the northwestern Atlantic Ocean tags were deployed to investigate the movements of 2 mature males, 1 one tagged in the northeastern Gulf Robert E. Hueter (contact author) of Mexico (GOM) and the other off John P. Tyminski1 northern Cuba. Horizontal tracks John J. Morris1 estimated by using likelihood meth- 2 ods were similar for these sharks; Alexei Ruiz Abierno comparable movements were docu- Jorge Angulo Valdes2,3 mented from the GOM, through the Straits of Florida and the Ba- Email address for contact author: [email protected] hamas, and into the open Atlantic Ocean where they converged on the 1 Center for Shark Research Mid-Atlantic Bight. Depth and tem- Mote Marine Laboratory perature ranges were 0–1767 m and 1600 Ken Thompson Parkway 4.0–28.8°C. A diel pattern of vertical Sarasota, Florida 34236 movement was evident for both in- 2 Centro de Investigaciones Marinas dividuals, along with regular forays Universidad de la Habana from cold daytime depths to warmer Calle 16, No. 114 e/ 1ra y 3ra near-surface waters, possibly as an Miramar, Playa, La Habana CP 11300, Cuba adaptation for thermoregulation. The vertical movements of longfin 3 School of Natural Resources and Environment makos allow them to exploit verti- University of Florida cally migrating prey but these move- P.O. Box 116455 ments increase their vulnerability to Gainesville, Florida 32611 pelagic longlining. -
Diurnal Patterns in Gulf of Mexico Epipelagic Predator Interactions with Pelagic Longline Gear: Implications for Target Species Catch Rates and Bycatch Mitigation
Bull Mar Sci. 93(2):573–589. 2017 research paper https://doi.org/10.5343/bms.2016.1008 Diurnal patterns in Gulf of Mexico epipelagic predator interactions with pelagic longline gear: implications for target species catch rates and bycatch mitigation 1 National Marine Fisheries Eric S Orbesen 1 * Service, Southeast Fisheries 1 Science Center, 75 Virginia Beach Derke Snodgrass 2 Drive, Miami, Florida 33149. Geoffrey S Shideler 1 2 University of Miami, Rosenstiel Craig A Brown School of Marine & Atmospheric John F Walter 1 Science, 4600 Rickenbacker Causeway, Miami, Florida 33149. * Corresponding author email: <[email protected]>. ABSTRACT.—Bycatch in pelagic longline fisheries is of substantial international concern, and the mitigation of bycatch in the Gulf of Mexico has been considered as an option to help restore lost biomass following the 2010 Deepwater Horizon oil spill. The most effective bycatch mitigation measures operate upon a differential response between target and bycatch species, ideally maintaining target catch while minimizing bycatch. We investigated whether bycatch vs target catch rates varied between day and night sets for the United States pelagic longline fishery in the Gulf of Mexico by comparing the influence of diel time period and moon illumination on catch rates of 18 commonly caught species/species groups. A generalized linear model approach was used to account for operational and environmental covariates, including: year, season, water temperature, hook type, bait, and maximum hook depth. Time of day or moon -
Can Threshold Foraging Responses of Basking Sharks Be Used to Estimate Their Metabolic Rate?
MARINE ECOLOGY PROGRESS SERIES Vol. 200: 289-296,2000 Published July 14 Mar Ecol Prog Ser ~ NOTE Can threshold foraging responses of basking sharks be used to estimate their metabolic rate? David W. Sims* Department of Zoology, University of Aberdeen. Tillydrone Avenue. Aberdeen AB24 2TZ. United Kingdom ABSTRACT: Empirical and theoretical determinations of There are 3 species of filter-feeding shark, the whale minimum threshold prey densities for filter-feeding basking shark ~hi~~~d~~typus of warm-temperate and tropical sharks Cetorhinus maximus were used to test the idea that threshold foraging behaviour could provide a means for esti- seas worldwide, the basking shark Cetorhinus max- mating oxygen consumption (a proxy for metabolic rate). The im~~that inhabits warm-temperate to boreal waters threshold feeding levelrepres&nts the prey density at which circumglobally, and the megamouth shark Mega- there will be no net energy gain (energy intake equals expen- chasms pelagjos occurs in the Pacific and At- diture). Basking sharks were observed to cease feeding at lantic, primarily in deep water (Compagno 1984, Yano their theoretical threshold; thus, the assumption underpin- ning the concept presented here was that over the narrow et They are the largest marine verte- range of zooplankton prey densities that induce 'switching' brates attaining body lengths of up to 14, 10 and 6 m re- between feeding and non-feeding in basking sharks, the spectively. Comparatively little is known about the bi- energetic value of the minimum threshold prey density is ology of planktivorous sharks despite the fact that they equivalent to the shark's instantaneous level of energy expen- diture. -
Early Stages of Fishes in the Western North Atlantic Ocean Volume
ISBN 0-9689167-4-x Early Stages of Fishes in the Western North Atlantic Ocean (Davis Strait, Southern Greenland and Flemish Cap to Cape Hatteras) Volume One Acipenseriformes through Syngnathiformes Michael P. Fahay ii Early Stages of Fishes in the Western North Atlantic Ocean iii Dedication This monograph is dedicated to those highly skilled larval fish illustrators whose talents and efforts have greatly facilitated the study of fish ontogeny. The works of many of those fine illustrators grace these pages. iv Early Stages of Fishes in the Western North Atlantic Ocean v Preface The contents of this monograph are a revision and update of an earlier atlas describing the eggs and larvae of western Atlantic marine fishes occurring between the Scotian Shelf and Cape Hatteras, North Carolina (Fahay, 1983). The three-fold increase in the total num- ber of species covered in the current compilation is the result of both a larger study area and a recent increase in published ontogenetic studies of fishes by many authors and students of the morphology of early stages of marine fishes. It is a tribute to the efforts of those authors that the ontogeny of greater than 70% of species known from the western North Atlantic Ocean is now well described. Michael Fahay 241 Sabino Road West Bath, Maine 04530 U.S.A. vi Acknowledgements I greatly appreciate the help provided by a number of very knowledgeable friends and colleagues dur- ing the preparation of this monograph. Jon Hare undertook a painstakingly critical review of the entire monograph, corrected omissions, inconsistencies, and errors of fact, and made suggestions which markedly improved its organization and presentation. -
Lamna Nasus) Inferred from a Data Mining in the Spanish Longline Fishery Targeting Swordfish (Xiphias Gladius) in the Atlantic for the 1987-2017 Period
SCRS/2020/073 Collect. Vol. Sci. Pap. ICCAT, 77(6): 89-117 (2020) SIZE AND AREA DISTRIBUTION OF PORBEAGLE (LAMNA NASUS) INFERRED FROM A DATA MINING IN THE SPANISH LONGLINE FISHERY TARGETING SWORDFISH (XIPHIAS GLADIUS) IN THE ATLANTIC FOR THE 1987-2017 PERIOD J. Mejuto1, A. Ramos-Cartelle1, B. García-Cortés1 and J. Fernández-Costa1 SUMMARY A total of 5,136 size observations of porbeagle were recovered for the period 1987-2017. The GLM results explained very moderately the variability of the sizes considering three main factors, suggesting minor but significant differences in some cases especially for the year factor and non-significant differences in other factors depending on the analysis. The greatest differences in the standardized mean length between some zones were caused by some large fish of unidentified sex. The standardized mean length data for the northern zones showed stability throughout the time series, very stable range of mean values and very few differences between sexes. The size distribution for northern areas indicated an FL-overall mean of 158 cm. The size showed a normal distribution confirming that a small fraction of individuals of this stock/s is available in the oceanic areas where the North Atlantic fleet is regularly fishing and the fishes are not fully recruited to those areas and / or this fishing gear up to 160 cm. The data suggests that some individuals could sporadically reach some intertropical areas of the eastern Atlantic. RÉSUMÉ Un total de 5.136 observations de taille de requins-taupes communs ont été récupérées pour la période 1987-2017. Les résultats du GLM expliquent très modérément la variabilité des tailles en tenant compte de trois facteurs principaux, ce qui suggère des différences mineures mais significatives dans certains cas, notamment pour le facteur année et des différences non significatives pour d'autres facteurs selon le type d’analyse. -
Electrosensory Pore Distribution and Feeding in the Basking Shark Cetorhinus Maximus (Lamniformes: Cetorhinidae)
Vol. 12: 33–36, 2011 AQUATIC BIOLOGY Published online March 3 doi: 10.3354/ab00328 Aquat Biol NOTE Electrosensory pore distribution and feeding in the basking shark Cetorhinus maximus (Lamniformes: Cetorhinidae) Ryan M. Kempster*, Shaun P. Collin The UWA Oceans Institute and the School of Animal Biology, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia ABSTRACT: The basking shark Cetorhinus maximus is the second largest fish in the world, attaining lengths of up to 10 m. Very little is known of its sensory biology, particularly in relation to its feeding behaviour. We describe the abundance and distribution of ampullary pores over the head and pro- pose that both the spacing and orientation of electrosensory pores enables C. maximus to use passive electroreception to track the diel vertical migrations of zooplankton that enable the shark to meet the energetic costs of ram filter feeding. KEY WORDS: Ampullae of Lorenzini · Electroreception · Filter feeding · Basking shark Resale or republication not permitted without written consent of the publisher INTRODUCTION shark Rhincodon typus and the megamouth shark Megachasma pelagios, which can attain lengths of up Electroreception is an ancient sensory modality that to 14 and 6 m, respectively (Compagno 1984). These 3 has evolved independently across the animal kingdom filter-feeding sharks are among the largest living in multiple groups (Scheich et al. 1986, Collin & White- marine vertebrates (Compagno 1984) and yet they are head 2004). Repeated independent evolution of elec- all able to meet their energetic costs through the con- troreception emphasises the importance of this sense sumption of tiny zooplankton. -
Order LAMNIFORMES ODONTASPIDIDAE Sand Tiger Sharks Iagnostic Characters: Large Sharks
click for previous page Lamniformes: Odontaspididae 419 Order LAMNIFORMES ODONTASPIDIDAE Sand tiger sharks iagnostic characters: Large sharks. Head with 5 medium-sized gill slits, all in front of pectoral-fin bases, Dtheir upper ends not extending onto dorsal surface of head; eyes small or moderately large, with- out nictitating eyelids; no nasal barbels or nasoral grooves; snout conical or moderately depressed, not blade-like;mouth very long and angular, extending well behind eyes when jaws are not protruded;lower labial furrows present at mouth corners; anterior teeth enlarged, with long, narrow, sharp-edged but unserrated cusps and small basal cusplets (absent in young of at least 1 species), the upper anteriors separated from the laterals by a gap and tiny intermediate teeth; gill arches without rakers; spiracles present but very small. Two moderately large high dorsal fins, the first dorsal fin originating well in advance of the pelvic fins, the second dorsal fin as large as or somewhat smaller than the first dorsal fin;anal fin as large as second dorsal fin or slightly smaller; caudal fin short, asymmetrical, with a strong subterminal notch and a short but well marked ventral lobe. Caudal peduncle not depressed, without keels; a deep upper precaudal pit present but no lower pit. Intestinal valve of ring type, with turns closely packed like a stack of washers. Colour: grey or grey-brown to blackish above, blackish to light grey or white, with round or oval dark spots and blotches vari- ably present on 2 species. high dorsal fins upper precaudal eyes without pit present nictitating eyelids intestinal valve of ring type Habitat, biology, and fisheries: Wide-ranging, tropical to cool-temperate sharks, found inshore and down to moderate depths on the edge of the continental shelves and around some oceanic islands, and in the open ocean. -
The Denticle Surface of Thresher Shark Tails: Three-Dimensional Structure and Comparison to Other Pelagic Species
Received: 3 April 2020 Revised: 14 May 2020 Accepted: 21 May 2020 DOI: 10.1002/jmor.21222 RESEARCH ARTICLE The denticle surface of thresher shark tails: Three-dimensional structure and comparison to other pelagic species Meagan Popp1 | Connor F. White1 | Diego Bernal2 | Dylan K. Wainwright1 | George V. Lauder1 1Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Abstract Massachusetts Shark skin denticles (scales) are diverse in morphology both among species and 2 Department of Biology, University of across the body of single individuals, although the function of this diversity is poorly Massachusetts Dartmouth, Dartmouth, Massachusetts understood. The extremely elongate and highly flexible tail of thresher sharks pro- vides an opportunity to characterize gradients in denticle surface characteristics Correspondence George V. Lauder, Museum of Comparative along the length of the tail and assess correlations between denticle morphology and Zoology, 26 Oxford Street, Cambridge, MA tail kinematics. We measured denticle morphology on the caudal fin of three mature 02138. Email: [email protected] and two embryo common thresher sharks (Alopias vulpinus), and we compared thresher tail denticles to those of eleven other shark species. Using surface Funding information National Oceanic and Atmospheric profilometry, we quantified 3D-denticle patterning and texture along the tail of Administration, Grant/Award Number: threshers (27 regions in adults, and 16 regions in embryos). We report that tails of NA16NMF4270231; National Science Foundation, Grant/Award Numbers: IOS- thresher embryos have a membrane that covers the denticles and reduces surface 1354593, GRF DGE-1144152; Office of Naval roughness. In mature thresher tails, surfaces have an average roughness of 5.6 μm Research, Grant/Award Numbers: N00014-09-1-0352, N000141410533 which is smoother than some other pelagic shark species, but similar in roughness to blacktip, porbeagle, and bonnethead shark tails. -
Population Structure and Biology of Shortfin Mako, Isurus Oxyrinchus, in the South-West Indian Ocean
CSIRO PUBLISHING Marine and Freshwater Research http://dx.doi.org/10.1071/MF13341 Population structure and biology of shortfin mako, Isurus oxyrinchus, in the south-west Indian Ocean J. C. GroeneveldA,E, G. Cliff B, S. F. J. DudleyC, A. J. FoulisA, J. SantosD and S. P. WintnerB AOceanographic Research Institute, PO Box 10712, Marine Parade 4056, Durban, South Africa. BKwaZulu-Natal Sharks Board, Private Bag 2, Umhlanga Rocks 4320, South Africa. CFisheries Management, Department of Agriculture, Forestry and Fisheries, Private Bag X2, Rogge Bay 8012, South Africa. DNorwegian College of Fishery Science, University of Tromsø, NO-9037, Tromsø, Norway. ECorresponding author. Email: [email protected] Abstract. The population structure, reproductive biology, age and growth, and diet of shortfin makos caught by pelagic longliners (2005–10) and bather protection nets (1978–2010) in the south-west Indian Ocean were investigated. The mean fork length (FL) of makos measured by observers on longliners targeting tuna, swordfish and sharks was similar, and decreased from east to west, with the smallest individuals occurring near the Agulhas Bank edge, June to November. Nearly all makos caught by longliners were immature, with equal sex ratio. Makos caught by bather protection nets were significantly larger, males were more frequent, and 93% of males and 55% of females were mature. Age was assessed from band counts of sectioned vertebrae, and a von Bertalanffy growth model fitted to sex-pooled length-at-age data predicted a À1 birth size (L0) of 90 cm, maximum FL (LN) of 285 cm and growth coefficient (k) of 0.113 y . -
Porbeagle Shark Lamna Nasus
Porbeagle Shark Lamna nasus Lateral View (♀) Ventral View (♀) COMMON NAMES APPEARANCE Porbeagle Shark, Atlantic Mackerel Shark, Blue Dog, Bottle-nosed • Heavily built but streamlined mackerel shark. Shark, Beaumaris Shark, Requin-Taupe Commun (Fr), Marrajo • Moderately long conical snout with a relatively large eyes. Sardinero (Es), Tiburón Sardinero (Es), Tintorera (Es). • Large first dorsal fin with a conspicuous white free rear tip. SYNONYMS • Second dorsal fin and anal fin equal-sized and set together. Squalus glaucus (Gunnerus, 1758), Squalus cornubicus (Gmelin, 1789), • Lunate caudal fin with strong keel and small secondary keel. Squalus pennanti (Walbaum, 1792), Lamna pennanti (Desvaux, 1851), Squalus monensis (Shaw, 1804), Squalus cornubiensis (Pennant, 1812), • Dorsally dark blue to grey with no patterning. Squalus selanonus (Walker, 1818), Selanonius walkeri (Fleming, 1828), • Ventrally white. Lamna punctata (Storer, 1839), Oxyrhina daekyi (Gill, 1862), Lamna • Maximum length of 365cm, though rarely to this size. NE MED ATL philippi (Perez Canto, 1886), Lamna whitleyi (Phillipps, 1935). DISTRIBUTION The Porbeagle Shark is a large, streamlined mackerel shark with a In the northern conical snout and powerful body. The first dorsal fin is large and hemisphere, the originates above or slightly behind the pectoral fins. It has a free rear Porbeagle Shark tip which is white. The second dorsal fin is tiny and is set above the occurs only in the anal fin, to which it is comparable in size. The caudal fin is strong and North Atlantic and lunate with a small terminal notch. The caudal keel is strong and, Mediterranean, uniquely for the northeast Atlantic, a smaller secondary caudal keel is whilst in the present. -
XIV. Appendices
Appendix 1, Page 1 XIV. Appendices Appendix 1. Vertebrate Species of Alaska1 * Threatened/Endangered Fishes Scientific Name Common Name Eptatretus deani black hagfish Lampetra tridentata Pacific lamprey Lampetra camtschatica Arctic lamprey Lampetra alaskense Alaskan brook lamprey Lampetra ayresii river lamprey Lampetra richardsoni western brook lamprey Hydrolagus colliei spotted ratfish Prionace glauca blue shark Apristurus brunneus brown cat shark Lamna ditropis salmon shark Carcharodon carcharias white shark Cetorhinus maximus basking shark Hexanchus griseus bluntnose sixgill shark Somniosus pacificus Pacific sleeper shark Squalus acanthias spiny dogfish Raja binoculata big skate Raja rhina longnose skate Bathyraja parmifera Alaska skate Bathyraja aleutica Aleutian skate Bathyraja interrupta sandpaper skate Bathyraja lindbergi Commander skate Bathyraja abyssicola deepsea skate Bathyraja maculata whiteblotched skate Bathyraja minispinosa whitebrow skate Bathyraja trachura roughtail skate Bathyraja taranetzi mud skate Bathyraja violacea Okhotsk skate Acipenser medirostris green sturgeon Acipenser transmontanus white sturgeon Polyacanthonotus challengeri longnose tapirfish Synaphobranchus affinis slope cutthroat eel Histiobranchus bathybius deepwater cutthroat eel Avocettina infans blackline snipe eel Nemichthys scolopaceus slender snipe eel Alosa sapidissima American shad Clupea pallasii Pacific herring 1 This appendix lists the vertebrate species of Alaska, but it does not include subspecies, even though some of those are featured in the CWCS. -
Can Sharks Be Saved? a Global Plan of Action for Shark Conservation in the Regime of the Convention on Migratory Species
Seattle Journal of Environmental Law Volume 5 Issue 1 Article 15 5-31-2015 Can Sharks be Saved? A Global Plan of Action for Shark Conservation in the Regime of the Convention on Migratory Species James Kraska Leo Chan Gaskins Follow this and additional works at: https://digitalcommons.law.seattleu.edu/sjel Part of the Education Commons, Environmental Law Commons, Intellectual Property Law Commons, Internet Law Commons, Land Use Law Commons, Natural Resources Law Commons, Science and Technology Law Commons, and the Water Law Commons Recommended Citation Kraska, James and Gaskins, Leo Chan (2015) "Can Sharks be Saved? A Global Plan of Action for Shark Conservation in the Regime of the Convention on Migratory Species," Seattle Journal of Environmental Law: Vol. 5 : Iss. 1 , Article 15. Available at: https://digitalcommons.law.seattleu.edu/sjel/vol5/iss1/15 This Article is brought to you for free and open access by the Student Publications and Programs at Seattle University School of Law Digital Commons. It has been accepted for inclusion in Seattle Journal of Environmental Law by an authorized editor of Seattle University School of Law Digital Commons. Can Sharks be Saved? A Global Plan of Action for Shark Conservation in the Regime of the Convention on Migratory Species James Kraska† and Leo Chan Gaskins‡ Shark populations throughout the world are at grave risk; some spe- cies have declined by 95 percent. The most recent IUCN (Interna- tional Union for the Conservation of Nature) assessment by the Shark Specialist Group (SSG) found that one-fourth of shark and ray spe- cies face the prospect of extinction.