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Shark Cartilage, Cancer and the Growing Threat of Pseudoscience
[CANCER RESEARCH 64, 8485–8491, December 1, 2004] Review Shark Cartilage, Cancer and the Growing Threat of Pseudoscience Gary K. Ostrander,1 Keith C. Cheng,2 Jeffrey C. Wolf,3 and Marilyn J. Wolfe3 1Department of Biology and Department of Comparative Medicine, Johns Hopkins University, Baltimore, Maryland; 2Jake Gittlen Cancer Research Institute, Penn State College of Medicine, Hershey, Pennsylvania; and 3Registry of Tumors in Lower Animals, Experimental Pathology Laboratories, Inc., Sterling, Virginia Abstract primary justification for using crude shark cartilage extracts to treat cancer is based on the misconception that sharks do not, or infre- The promotion of crude shark cartilage extracts as a cure for cancer quently, develop cancer. Other justifications represent overextensions has contributed to at least two significant negative outcomes: a dramatic of experimental observations: concentrated extracts of cartilage can decline in shark populations and a diversion of patients from effective cancer treatments. An alleged lack of cancer in sharks constitutes a key inhibit tumor vessel formation and tumor invasions (e.g., refs. 2–5). justification for its use. Herein, both malignant and benign neoplasms of No available data or arguments support the medicinal use of crude sharks and their relatives are described, including previously unreported shark extracts to treat cancer (6). cases from the Registry of Tumors in Lower Animals, and two sharks with The claims that sharks do not, or rarely, get cancer was originally two cancers each. Additional justifications for using shark cartilage are argued by I. William Lane in a book entitled “Sharks Don’t Get illogical extensions of the finding of antiangiogenic and anti-invasive Cancer” in 1992 (7), publicized in “60 Minutes” television segments substances in cartilage. -
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. -
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. -
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. -
Evolutionary Relations of Hexanchiformes Deep-Sea Sharks Elucidated by Whole Mitochondrial Genome Sequences
Hindawi Publishing Corporation BioMed Research International Volume 2013, Article ID 147064, 11 pages http://dx.doi.org/10.1155/2013/147064 Research Article Evolutionary Relations of Hexanchiformes Deep-Sea Sharks Elucidated by Whole Mitochondrial Genome Sequences Keiko Tanaka,1 Takashi Shiina,1 Taketeru Tomita,2 Shingo Suzuki,1 Kazuyoshi Hosomichi,3 Kazumi Sano,4 Hiroyuki Doi,5 Azumi Kono,1 Tomoyoshi Komiyama,6 Hidetoshi Inoko,1 Jerzy K. Kulski,1,7 and Sho Tanaka8 1 Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1143, Japan 2 Fisheries Science Center, The Hokkaido University Museum, 3-1-1 Minato-cho, Hakodate, Hokkaido 041-8611, Japan 3 Division of Human Genetics, Department of Integrated Genetics, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka 411-8540, Japan 4 Division of Science Interpreter Training, Komaba Organization for Education Excellence College of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan 5 Shimonoseki Marine Science Museum, 6-1 Arcaport, Shimonoseki, Yamaguchi 750-0036, Japan 6 Department of Clinical Pharmacology, Division of Basic Clinical Science and Public Health, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1143, Japan 7 Centre for Forensic Science, The University of Western Australia, Nedlands, WA 6008, Australia 8 Department of Marine Biology, School of Marine Science and Technology, Tokai University, 3-20-1 Orido, Shimizu, Shizuoka 424-8610, Japan Correspondence should be addressed to Takashi Shiina; [email protected] Received 1 March 2013; Accepted 26 July 2013 Academic Editor: Dietmar Quandt Copyright © 2013 Keiko Tanaka et al. -
General Biology of Chondrichthyan Fishes
General biology of Chondrichthyan fi shes By Terence I. Walker Gummy shark (Mustelus antarcticus) (© Ken Hoppen, [email protected]) Chondrichthyan teeth vary in size and shape between the GENERAL BIOLOGY OF various groups of these animals. The upper and lower jaws of CHONDRICHTHYAN FISHES sharks and rays bear teeth that are embedded in the gums rather than attached to the jaws, and are continuously replaced. The By Terence I. Walker teeth of chimaeras are non-replaceable and attached to grinding tooth plates in a beak-like arrangement. Many demersal Marine and Freshwater Systems, Primary Industries Research sharks, such as the bullhead sharks, have small, sharp teeth for Victoria, PO Box 114, Queenscliff, Victoria, 3225 Australia grasping their prey, and fl attened back teeth for crushing hard shell. Other demersal sharks, such as the hound sharks and the rays, have all fl attened teeth. Pelagic species have larger Background sharp teeth more suited to cutting their prey. The whale shark (Rhincodon typus), basking shark (Cetorhinus maximus), and Sharks and rays belong to the group Elasmobranchii. manta ray (Manta birostris) lack teeth and have evolved gill Chimaeras, the nearest relatives, belong to the group rakers for straining out plankton from large volumes of water Holocephali. The Elasmobranchii and Holocephali together taken in through the gaping mouth and passed out over the gills comprise the Chondrichthyes. as the animal breathes. Chondrichthyans form only a small proportion of all living The vertebral column comprises a series of vertebrae held in fi shes. They share many features with the other fi sh, known as place by connective tissue, and provides the animal with a the bony fi shes, but they also have several features that separate fl exible body. -
Chondrichthyes: Carcharhiniformes: Scyliorhinidae) from the Gulf of Aden
Zootaxa 3881 (1): 001–016 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3881.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:809A2B3B-2C2C-4D26-A50F-6D5185D3BD6A Apristurus breviventralis, a new species of deep-water catshark (Chondrichthyes: Carcharhiniformes: Scyliorhinidae) from the Gulf of Aden JUNRO KAWAUCHI1,4, SIMON WEIGMANN2 & KAZUHIRO NAKAYA3 1Chair of Marine Biology and Biodiversity (Systematic Ichthyology), Graduate School of Fisheries Sciences, Hokkaido University, 3- 3-1 Minato-cho, Hakodate Hokkaido 041-8611, Japan. E-mail: junro@ frontier.hokudai.ac.jp 2Biocenter Grindel and Zoological Museum, University of Hamburg, Section Ichthyology, Martin-Luther-King-Platz 3, D-20146 Hamburg, Germany. E-mail: [email protected] 3Hokkaido University, 3-1-1 Minato-cho, Hakodate, Hokkaido 041-8611, Japan. E-mail: [email protected] 4Corresponding author Abstract A new deep-water catshark of the genus Apristurus Garman, 1913 is described based on nine specimens from the Gulf of Aden in the northwestern Indian Ocean. Apristurus breviventralis sp. nov. belongs to the ‘brunneus group’ of the genus and is characterized by having pectoral-fin tips reaching beyond the midpoint between the paired fin bases, a much shorter pectoral-pelvic space than the anal-fin base, a low and long-based anal fin, and a first dorsal fin located behind pelvic-fin insertion. The new species most closely resembles the western Atlantic species Apristurus canutus, but is distinguishable in having greater nostril length than internarial width and longer claspers in adult males. -
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. -
Ore Bin / Oregon Geology Magazine / Journal
State of Oregon The ORE BIN· Department of Geology Volume 34,no. 10 and Mineral Industries 1069 State Office BI dg. October 1972 Portland Oregon 97201 FOSSil SHARKS IN OREGON Bruce J. Welton* Approximately 21 species of sharks, skates, and rays are either indigenous to or occasionally visit the Oregon coast. The Blue Shark Prionace glauca, Soup-fin Shark Galeorhinus zyopterus, and the Dog-fish Shark Squalus acanthias commonly inhabit our coastal waters. These 21 species are represented by 16 genera, of which 10 genera are known from the fossi I record in Oregon. The most common genus encountered is the Dog-fish Shark Squalus. The sharks, skates, and rays, (all members of the Elasmobranchii) have a fossil record extending back into the Devonian period, but many major groups became extinct before or during the Mesozoic. A rapid expansion in the number of new forms before the close of the Mesozoic gave rise to practically all the Holocene families living today. Paleozoic shark remains are not known from Oregon, but teeth of the Cretaceous genus Scapanorhyn chus have been collected from the Hudspeth Formation near Mitchell, Oregon. Recent work has shown that elasmobranch teeth occur in abundance west of the Cascades in marine Tertiary strata ranging in age from late Eocene to middle Miocene (Figures 1 and 2). All members of the EIasmobranchii possess a cartilaginous endoskeleton which deteriorates rapidly upon death and is only rarely preserved in the fossil record. Only under exceptional conditions of preservation, usually in a highly reducing environment, will cranial or postcranial elements be fossilized. -
Report on the Status of Mediterranean Chondrichthyan Species
United Nations Environment Programme Mediterranean Action Plan Regional Activity Centre For Specially Protected Areas REPORT ON THE STATUS OF MEDITERRANEAN CHONDRICHTHYAN SPECIES D. CEBRIAN © L. MASTRAGOSTINO © R. DUPUY DE LA GRANDRIVE © Note : The designations employed and the presentation of the material in this document do not imply the expression of any opinion whatsoever on the part of UNEP concerning the legal status of any State, Territory, city or area, or of its authorities, or concerning the delimitation of their frontiers or boundaries. © 2007 United Nations Environment Programme Mediterranean Action Plan Regional Activity Centre for Specially Protected Areas (RAC/SPA) Boulevard du leader Yasser Arafat B.P.337 –1080 Tunis CEDEX E-mail : [email protected] Citation: UNEP-MAP RAC/SPA, 2007. Report on the status of Mediterranean chondrichthyan species. By Melendez, M.J. & D. Macias, IEO. Ed. RAC/SPA, Tunis. 241pp The original version (English) of this document has been prepared for the Regional Activity Centre for Specially Protected Areas (RAC/SPA) by : Mª José Melendez (Degree in Marine Sciences) & A. David Macías (PhD. in Biological Sciences). IEO. (Instituto Español de Oceanografía). Sede Central Spanish Ministry of Education and Science Avda. de Brasil, 31 Madrid Spain [email protected] 2 INDEX 1. INTRODUCTION 3 2. CONSERVATION AND PROTECTION 3 3. HUMAN IMPACTS ON SHARKS 8 3.1 Over-fishing 8 3.2 Shark Finning 8 3.3 By-catch 8 3.4 Pollution 8 3.5 Habitat Loss and Degradation 9 4. CONSERVATION PRIORITIES FOR MEDITERRANEAN SHARKS 9 REFERENCES 10 ANNEX I. LIST OF CHONDRICHTHYAN OF THE MEDITERRANEAN SEA 11 1 1. -
Biodiversity Series Background Document for Basking Shark
Background Document for Basking shark Cetorhinus maximus Biodiversity Series 2009 OSPAR Convention Convention OSPAR The Convention for the Protection of the La Convention pour la protection du milieu Marine Environment of the North-East Atlantic marin de l'Atlantique du Nord-Est, dite (the “OSPAR Convention”) was opened for Convention OSPAR, a été ouverte à la signature at the Ministerial Meeting of the signature à la réunion ministérielle des former Oslo and Paris Commissions in Paris anciennes Commissions d'Oslo et de Paris, on 22 September 1992. The Convention à Paris le 22 septembre 1992. La Convention entered into force on 25 March 1998. It has est entrée en vigueur le 25 mars 1998. been ratified by Belgium, Denmark, Finland, La Convention a été ratifiée par l'Allemagne, France, Germany, Iceland, Ireland, la Belgique, le Danemark, la Finlande, Luxembourg, Netherlands, Norway, Portugal, la France, l’Irlande, l’Islande, le Luxembourg, Sweden, Switzerland and the United Kingdom la Norvège, les Pays-Bas, le Portugal, and approved by the European Community le Royaume-Uni de Grande Bretagne and Spain. et d’Irlande du Nord, la Suède et la Suisse et approuvée par la Communauté européenne et l’Espagne. Acknowledgement This report has been prepared by the Association pour l'Etude et la Conservation des Sélaciens (APECS) and Ms Amelia Curd (France). Thanks are also due for contributions provided by Colin Speedie, Sarah Fowler, David Sims, Jean-Luc Solandt Photo acknowledgement: Cover page: Basking shark, wikipedia Contents Background Document -
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.