Annotated checklist of the living sharks,batoids and chimaeras (Chondrichthyes) of the world,with a focus on biogeographical diversity

An annotated checklist of the chondrichthyan fishes (sharks, batoids and chimaeras) of the world is presented. As of 7 November 2015, the number of species totals 1188, comprising 16 orders, 61 families and 199 genera. The checklist includes nine orders, 34 families, 105 genera and 509 species of sharks; six orders, 24 families, 88 genera and 630 species of batoids (skates and rays); one order, three families, six genera and 49 species of holocephalans (chimaeras). The most speciose shark orders are the Carcharhiniformes with 284 species, followed by the Squaliformes with 119. The most species‐rich batoid orders are the Rajiformes with 285 species and the Myliobatiformes with 210. This checklist represents the first global checklist of chondrichthyans to include information on maximum size, geographic and depth distributions, as well as comments on taxonomically problematic species and recent and regularly overlooked synonymizations. Furthermore, a detailed analysis of the biogeographical diversity of the species across 10 major areas of occurrence is given, including updated figures for previously published hotspots of chondrichthyan biodiversity, providing the detailed numbers of chondrichthyan species per major area, and revealing centres of distribution for several taxa     

Updated taxonomic list and conservation status of chondrichthyans from the exclusive economic zone of Venezuela,with first generic and specific records

Using the last taxonomic review of chondrichthyans of the world, we selected the species distributed in the north-western Atlantic Ocean (NWA) and compared it with the available published literature related to the class Chondrichthyes in the Venezuelan exclusive economic zone. We also revised information from worldwide databases such as: FAO (NWA-31 area), GBIF, iSpecies, IUCN and OBIS, as well as available museum collection databases. The taxonomic validity was checked using the Catalogue of Fishes of the California Academy of Sciences and recent references. The past published Venezuelan lists of chondrichthyans combined included nine orders, 30 families and 108 species. The updated list with 12 orders, 36 families and 122 species increased by three new orders, six families, three shark genera, nine shark species (one replacing another species), one chimaera genus, two chimaera species, three batoid genera and six batoid species (two replacing other species). Four holotype specimens (two sharks and two rays) are deposited in Venezuelan Museums. Most of the species have an IUCN conservation status, including four species catalogued as Critically Endangered, six as Endangered and 18 species as Vulnerable. Deep-sea fisheries, scientific exploration and taxonomic/genetic revisions might add future increments to the Venezuelan chondrichthyan list.     

Occipital spine of Orthacanthus (Xenacanthidae,Elasmobranchii): Structure and growth

The morphology of 16 occipital spines of the xenacanthid Orthacanthus from Upper Carboniferous deposits of Robinson (Kansas, USA), Nýřan (Czech Republic) and Puertollano (Spain) is described. The nonreplaced spines reveal the growth pattern of the shark. Moreover, the relationship between growth and paleoenvironmental conditions can be used to determine paleoecological conditions. Both external and internal morphology indicate that the spine was superficially inserted in the skin. During growth, the spine moved from a deep position in the dermis, in which trabecular dentine is formed, to a more superficial location in which centrifugally growing lamellar dentine was formed. Centripetally growing lamellar dentine was deposited more slowly than the centrifugally growing dentine; it obliterated the pulp cavity. The denticles are independent dermal elements formed by a dermal papilla and secondarily attached by dentine to the spine proper. The number of denticles per annual cycle and the density of denticulation vary with the growth rate. Moreover, the ratio of length of denticulated region to total length of the spine changes throughout ontogeny. In consequence, those features cannot be used for systematic purposes without a careful analysis of the variability. Centrifugally growing lamellar dentine in spines from Robinson shows a regular alternation of layers, suggesting tidal conditions in the environment in which the sharks lived. Monthly and seasonal cycles also occur. Tidal (lunar) cyclicity is also observed in the denticles: size and distance between denticles increase and decrease gradually, forming waves that are considered seasonal and yearly cycles. The observed regularity could be related to the variation in calcium phosphate deposition following the cyclical changes in water temperature produced in the tidal zone. Monthly and seasonal cycles are the result of the interaction of the solar and tidal (lunar) cycles. The cyclical pattern of growth is used to determine the age and growth rates. Orthacanthus was a fast‐growing shark like the Recent sharks Isurus, Mustelus, and Negaprion. J. Morphol. 242:1–45, 1999. © 1999 Wiley‐Liss, Inc.     

Bycatch and discarding patterns of dogfish and sharks taken in English and Welsh commercial fisheries

At-sea observer programmes can provide spatio-temporal data on the sizes and quantities of fish being either discarded or retained, including for species and size categories that may not be sampled effectively during scientific surveys. Such data were analysed for English and Welsh fisheries operating on the continental shelf of the North Sea ecoregion (ICES Divisions 4a–c and 7d) and Celtic Seas ecoregion (ICES Divisions 6a, 7a–c, e–k) for the period (2002–2016). These data were collated for four main gear types: beamtrawl, nephrops and otter trawls, and nets (including gillnets, tangle nets and trammel nets). Beamtrawlers caught proportionally more smaller individuals than otter trawlers, whilst nets were the most size-selective gear for larger sharks. Size-related discarding was observed, with smaller spurdog Squalus acanthias and starry smooth-hound Mustelus asterias (< 60 cm total length, L_T) usually being discarded. Such size-based selection was not evident for lesser-spotted dogfish Scyliorhinus canicula, which was generally landed as bait. Temporal changes in the discard–retention patterns were evident for S. acanthias and porbeagle Lamna nasus, with increased regulatory discarding as management measures became restrictive. A corresponding increase in the proportion of the non-quota M. asterias retained was also observed over the study period. Knowledge of the size-based discard–retention patterns by métier can also help inform on where future studies on discard survival could usefully be undertaken.     

Molecular characterization of marine and coastal fishes of Bangladesh through DNA barcodes

This study describes the molecular characterization of marine and coastal fishes of Bangladesh based on the mitochondrial cytochrome c oxidase subunit I (COI) gene as a marker. A total of 376 mitochondrial COI barcode sequences were obtained from 185 species belonging to 146 genera, 74 families, 21 orders, and two classes of fishes. The mean length of the sequences was 652 base pairs. In Elasmobranchii (Sharks and rays), the average Kimura two parameter (K2P) distances within species, genera, families, and orders were 1.20%, 6.07%, 11.08%, and 14.68%, respectively, and for Actinopterygii, the average K2P distances within species, genera, families, and orders were 0.40%, 6.36%, 14.10%, and 24.07%, respectively. The mean interspecies distance was 16‐fold higher than the mean intraspecies distance. The K2P neighbor‐joining (NJ) trees based on the sequences generally clustered species in accordance with their taxonomic position. A total of 21 species were newly recorded in Bangladesh. High efficiency and fidelity in species identification and discrimination were demonstrated in the present study by DNA barcoding, and we conclude that COI sequencing can be used as an authentic identification marker for Bangladesh marine fish species.     

Performance of shark teeth during puncture and draw: implications for the mechanics of cutting

The performance of an organism's feeding apparatus has obvious implications for its fitness and survival. However, the majority of studies that focus on chondrichthyan feeding have largely ignored the role of teeth. Studying the functional morphology of shark teeth not only elucidates the biological role that teeth play in feeding, but also provides insight specifically into the evolution of shark feeding because teeth are often the only structures available in the fossil record. In the present study, we investigate the puncture and draw performance of three general categories of extant teeth, tearing‐type, cutting‐type, and cutting–clutching type, as well as three fossil morphologies, utilizing a universal testing system. Differences in puncturing performance occurred among different prey items, indicating that not all ‘soft’ prey items are alike. The majority of teeth were able to puncture different prey items, and differences in puncture performance also occurred among tooth types; however, few patterns emerged. In some cases, broader triangular teeth were less effective at puncturing than narrow‐cusped teeth. There were no differences between the maximum draw forces and maximum puncture forces. Many of the shark teeth in the present study were not only able to perform draw and puncture equally well, but also many tooth morphologies were functionally equivalent to each other. The findings obtained in the present study lend little support to the belief that shark tooth morphology is a good predictor of biological role. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100 , 271–286.     

Development and microstructure of tooth histotypes in the blue shark,Prionace glauca (Carcharhiniformes: Carcharhinidae) and the great white shark,Carcharodon carcharias (Lamniformes: Lamnidae)

Elasmobranchs exhibit two distinct arrangements of mineralized tissues in the teeth that are known as orthodont and osteodont histotypes. Traditionally, it has been said that orthodont teeth maintain a pulp cavity throughout tooth development whereas osteodont teeth are filled with osteodentine and lack a pulp cavity when fully developed. We used light microscopy, scanning electron microscopy, and high‐resolution micro‐computed tomography to compare the structure and development of elasmobranch teeth representing the two histotypes. As an example of the orthodont histotype, we studied teeth of the blue shark, Prionace glauca (Carcharhiniformes: Carcharhinidae). For the osteodont histotype, we studied teeth of the great white shark, Carcharodon carcharias (Lamniformes: Lamnidae). We document similarities and differences in tooth development and the microstructure of tissues in these two species and review the history of definitions and interpretations of elasmobranch tooth histotypes. We discuss a possible correlation between tooth histotype and tooth replacement and review the history of histotype differentiation in sharks. We find that contrary to a long held misconception, there is no orthodentine in the osteodont teeth of C. carcharias. J. Morphol. 276:797–817, 2015. © 2015 Wiley Periodicals, Inc.     

Biology meets engineering: The structural mechanics of fossil and extant shark teeth

The majority of studies on the evolution and function of feeding in sharks have focused primarily on the movement of cranial components and muscle function, with little integration of tooth properties or function. As teeth are subjected to sometimes extreme loads during feeding, they undergo stress, strain, and potential failure. As attributes related to structural strength such as material properties and overall shape may be subjected to natural selection, both prey processing ability and structural parameters must be considered to understand the evolution of shark teeth. In this study, finite element analysis was used to visualize stress distributions of fossil and extant shark teeth during puncture, unidirectional draw (cutting), and holding. Under the loading and boundary conditions here, which are consistent with bite forces of large sharks, shark teeth are structurally strong. Teeth loaded in puncture have localized stress concentrations at the cusp apex that diminish rapidly away from the apex. When loaded in draw and holding, the majority of the teeth show stress concentrations consistent with well designed cantilever beams. Notches result in stress concentration during draw and may serve as a weak point; however they are functionally important for cutting prey during lateral head shaking behavior. As shark teeth are replaced regularly, it is proposed that the frequency of tooth replacement in sharks is driven by tooth wear, not tooth failure. As the tooth tip and cutting edges are worn, the surface areas of these features increase, decreasing the amount of stress produced by the tooth. While this wear will not affect the general structural strength of the tooth, tooth replacement may also serve to keep ahead of damage caused by fatigue that may lead to eventual tooth failure. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.