Memorandum of Understanding on the Conservation of Migratory Sharks Great White Shark Fact Sheet
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Luís M.D. Barcelos1, 2*, José M.N. Azevedo1, 3, Jürgen Pollerspöck4, and João P
ACTA ICHTHYOLOGICA ET PISCATORIA (2018) 48 (2): 189–194 DOI: 10.3750/AIEP/02436 REVIEW OF THE RECORDS OF THE SMALLTOOTH SAND TIGER SHARK, ODONTASPIS FEROX (ELASMOBRANCHII: LAMNIFORMES: ODONTASPIDIDAE), IN THE AZORES Luís M.D. Barcelos1, 2*, José M.N. Azevedo1, 3, Jürgen Pollerspöck4, and João P. Barreiros1, 2 1Centre for Ecology, Evolution, and Environmental Changes, Azorean Biodiversity Group, Angra do Heroísmo, Portugal 2Faculty of Agricultural and Environmental Sciences, University of the Azores, Angra do Heroísmo, Portugal 3Faculty of Sciences and Technology, University of the Azores, Ponta Delgada, Portugal 4Bavarian State Collection of Zoology, Munich, Germany Barcelos L.M.D., Azevedo J.M.N., Pollerspöck J., Barreiros J.P. 2018. Review of the records of the smalltooth sand tiger shark, Odontaspis ferox (Elasmobranchii: Lamniformes: Odontaspididae), in the Azores. Acta Ichthyol. Piscat. 48 (2): 189–194. Abstract. In recent years Azorean fishermen reported the presence of the smalltooth sand tiger shark,Odontaspis ferox (Risso, 1810), a very rare demersal shark species, associated with insular shelves and slopes, with occasional incursions into shallow waters and of poorly known biology and ecology. There are fourteen new records of this species, between 1996 and 2014, captured by spearfishing, harpoons, hand lines, or entangled in fishing gear in the Azores. These records were analysed and complemented with fishermen interviews, providing new locations and new biological data for this species. Also, specimens photographs were studied and post-mortem analysis were carefully carried out in one individual. This species is rare and captured only as bycatch in shallow waters. More detailed information on this species is critically needed in order to assess its conservation status and implement management guidelines. -
The Great White Shark Quick Questions
The Great White Shark Quick Questions 11 Great white sharks are the top of the ocean’s food chain. 1. Why do you think that the great white shark is at 22 They are the biggest fish on our planet which eat other the top of the ocean’s food chain? 32 fish and animals. They are known to live between thirty 45 and one hundred years old and can be found in all of the 55 world’s oceans, but they are mostly found in cool water 59 close to the coast. 2. Where are most great white sharks found? 69 Even though they are mostly grey, they get their name 78 from their white underbelly. The great white shark has 89 been known to grow up to six metres long and have 99 up to three hundred sharp teeth, in seven rows. Their 3. Find and copy the adjective that the author uses 109 amazing sense of smell allows them to hunt for prey, to describe the shark’s sense of smell. 119 such as seals, rays and small whales from miles away. 4. Number these facts from 1 to 3 to show the order they appear in the text. They live between thirty and one hundred years. They can grow up to six metres long. They have up to three hundred teeth. The Great White Shark Answers 11 Great white sharks are the top of the ocean’s food chain. 1. Why do you think that the great white shark is at 22 They are the biggest fish on our planet which eat other the top of the ocean’s food chain? 32 fish and animals. -
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. -
Great White Shark) on Appendix I of the Convention of International Trade in Endangered Species of Wild Fauna and Flora (CITES)
Prop. 11.48 Proposal to include Carcharodon carcharias (Great White Shark) on Appendix I of the Convention of International Trade in Endangered Species of Wild Fauna and Flora (CITES) A. PROPOSAL ..............................................................................................3 B. PROPONENT............................................................................................3 C. SUPPORTING STATEMENT....................................................................3 1. Taxonomy.........................................................................................................................3 1.1 Class.................................................................................................................................... 1.2 Order................................................................................................................................... 1.3 Family ................................................................................................................................. 1.4 Species ................................................................................................................................ 1.5 Scientific Synonyms............................................................................................................. 1.6 Common Names .................................................................................................................. 2. Biological Parameters......................................................................................................3 -
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. -
8Th MEETING of the SCIENTIFIC COMMITTEE New Zealand, 3 to 8 October 2020
th 8 MEETING OF THE SCIENTIFIC COMMITTEE New Zealand, 3 to 8 October 2020 SC8-DW14 Interactions with marine mammals, seabirds, reptiles, other species of concern New Zealand PO Box 3797, Wellington 6140, New Zealand P: +64 4 499 9889 – F: +64 4 473 9579 – E: [email protected] www.sprfmo.int SC8-DW14 South Pacific Regional Fisheries Management Organisation 8th Meeting of the Scientific Committee Online meeting hosted by New Zealand, 3–8 October 2020 Interactions with marine mammals, seabirds, reptiles (turtles), and other species of concern in bottom fisheries to 2019 Martin Cryer1, Igor Debski2, Shane W. Geange2, Tiffany D. Bock3, Marco Milardi3 3 September 2020 1. Fisheries New Zealand, Ministry for Primary Industries, Nelson, New Zealand 2. Department of Conservation, Wellington, New Zealand 3. Fisheries New Zealand, Ministry for Primary Industries, Wellington, New Zealand 1 SC8-DW14 Contents 1. Purpose of paper ............................................................................................................. 3 2. Requirements of CMM-03-2020 and CMM-02-2020 ....................................................... 3 3. Reported interactions ..................................................................................................... 3 4. Discussion of seabird interactions ................................................................................... 5 5. Processes for verifying records and updating databases ................................................. 6 6. Acknowledgments .......................................................................................................... -
Body Length Estimation of Neogene Macrophagous Lamniform Sharks (Carcharodon and Otodus) Derived from Associated Fossil Dentitions
Palaeontologia Electronica palaeo-electronica.org Body length estimation of Neogene macrophagous lamniform sharks (Carcharodon and Otodus) derived from associated fossil dentitions Victor J. Perez, Ronny M. Leder, and Teddy Badaut ABSTRACT The megatooth shark, Otodus megalodon, is widely accepted as the largest mac- rophagous shark that ever lived; and yet, despite over a century of research, its size is still debated. The great white shark, Carcharodon carcharias, is regarded as the best living ecological analog to the extinct megatooth shark and has been the basis for all body length estimates to date. The most widely accepted and applied method for esti- mating body size of O. megalodon was based upon a linear relationship between tooth crown height and total body length in C. carcharias. However, when applying this method to an associated dentition of O. megalodon (UF-VP-311000), the estimates for this single individual ranged from 11.4 to 41.1 m. These widely variable estimates showed a distinct pattern, in which anterior teeth resulted in lower estimates than pos- terior teeth. Consequently, previous paleoecological analyses based on body size esti- mates of O. megalodon may be subject to misinterpretation. Herein, we describe a novel method based on the summed crown width of associated fossil dentitions, which mitigates the variability associated with different tooth positions. The method assumes direct proportionality between the ratio of summed crown width to body length in eco- logically and taxonomically related fossil and modern species. Total body lengths were estimated from 11 individuals, representing five lamniform species: Otodus megal- odon, Otodus chubutensis, Carcharodon carcharias, Carcharodon hubbelli, and Carcharodon hastalis. -
Acoustic Tracking of Bigeye Thresher Shark Alopias Superciliosus in the Eastern Pacific Ocean
MARINE ECOLOGY PROGRESS SERIES Vol. 265: 255–261, 2003 Published December 31 Mar Ecol Prog Ser Acoustic tracking of bigeye thresher shark Alopias superciliosus in the eastern Pacific Ocean Hideki Nakano*, Hiroaki Matsunaga, Hiroaki Okamoto, Makoto Okazaki National Research Institute of Far Seas Fisheries, 5-7-1 Shimizu-Orido, Shizuoka 424-8633, Japan ABSTRACT: Acoustic telemetry was used to identify the short-term horizontal and vertical movement patterns of the bigeye thresher shark Alopias superciliosus in the eastern tropical Pacific Ocean dur- ing the summer of 1996. Two immature female sharks, 175 and 124 cm PCL (precaudal length), were tracked for 96 and 70 h, respectively, demonstrating very distinct crepuscular vertical migrations sim- ilar to those reported for the megamouth shark. The bigeye threshers stayed at 200 to 500 m depth during the day and at 80 to 130 m at night. The deepest dive extends the known depth distribution of the species to 723 m. No ‘fly-glide’ behavior (rapid ascents followed by slower acute-angled descents) was observed for the 2 sharks. However, the opposite behavioral pattern of slow ascents and rela- tively rapid descents during the night was observed. Since bigeye threshers have large eyes extend- ing upwards onto the dorsal surface of the cranium, it may be more efficient for them to hunt prey which are highlighted against the sea surface from below. Estimated mean swimming speed over the ground ranged from 1.32 to 2.02 km h–1, similar to swordfish and megamouth sharks, and slower than that reported for tunas, billfishes, and other pelagic sharks. -
How Solitary Are White Sharks: Social Interactions Or Just Spatial Proximity?
Behav Ecol Sociobiol DOI 10.1007/s00265-016-2179-y ORIGINAL ARTICLE How solitary are white sharks: social interactions or just spatial proximity? R. Findlay1 & E. Gennari2,3 & M. Cantor1 & D. P. Tittensor 1,4 Received: 23 October 2015 /Revised: 24 June 2016 /Accepted: 28 June 2016 # Springer-Verlag Berlin Heidelberg 2016 Abstract the evidence that large pelagic shark species are generally White sharks (Carcharodon carcharias) are circumglobally solitary and display limited social behaviour. distributed large apex predators. While ecologically impor- tant, there is very limited study of their social behaviour. Significance statement Although evident in other large, apex marine predators (e.g. Large pelagic shark species are important top predators, but toothed whales) and smaller elasmobranchs (e.g. blacktip reef we know little about their social behaviour. We tested the sharks), the ability of any large pelagic elasmobranch to dem- ability of white sharks (C. carcharias) to form groups and onstrate social preferences, tolerance or grouping behaviour is display social preferences for other individuals when they largely unknown. Here, we test whether white sharks in a congregate at scavenging events in a coastal environment, near-coastal environment form non-random associations with where social interactions may be more likely. We found that other conspecifics or simply share the same space at the same white sharks co-occur at random, displaying no preferred or time. We photo-identified 323 individuals—74 % juvenile avoided associations for other individuals. Nevertheless, there females (175–300 cm)—during chumming events at six dif- was a minor influence of biological traits, with individuals ferent sites in Mossel Bay, South Africa, over a 6-year period aggregating according to gender and, possibly, body size. -
Sand Tiger − Carcharias Taurus Overall Vulnerability Rank = High
Sand Tiger − Carcharias taurus Overall Vulnerability Rank = High Biological Sensitivity = High Climate Exposure = High Data Quality = 79% of scores ≥ 2 Expert Data Expert Scores Plots Scores Quality (Portion by Category) Carcharias taurus Low Moderate Stock Status 3.1 1.8 High Other Stressors 1.8 1.8 Very High Population Growth Rate 3.8 2.6 Spawning Cycle 1.8 2.4 Complexity in Reproduction 1.8 1.8 Early Life History Requirements 1.0 3.0 Sensitivity to Ocean Acidification 1.0 2.4 Prey Specialization 1.3 2.8 Habitat Specialization 1.3 3.0 Sensitivity attributes Sensitivity to Temperature 1.3 3.0 Adult Mobility 1.0 3.0 Dispersal & Early Life History 1.0 3.0 Sensitivity Score High Sea Surface Temperature 3.9 3.0 Variability in Sea Surface Temperature 1.0 3.0 Salinity 2.8 3.0 Variability Salinity 1.2 3.0 Air Temperature 1.0 3.0 Variability Air Temperature 1.0 3.0 Precipitation 1.0 3.0 Variability in Precipitation 1.0 3.0 Ocean Acidification 4.0 2.0 Exposure variables Variability in Ocean Acidification 1.0 2.2 Currents 2.1 1.0 Sea Level Rise 1.2 1.5 Exposure Score High Overall Vulnerability Rank High Sand Tiger (Carcharias taurus) Overall Climate Vulnerability Rank: High (76% certainty from bootstrap analysis). Climate Exposure: High. Two exposure factors contributed to this score: Ocean Surface Temperature (3.9) and Ocean Acidification (4.0). Sand Tiger Shark are pelagic but associate with benthic habitats. Biological Sensitivity: High. Two attributes scored above 3.0: Population Growth Rate (3.8) and Stock Status (3.1).