1,940 results on '"White, William T."'
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2. Assessing Impacts and Local Perceptions Following the Incidental Introduction of tilapia (Cichlidae: Cichliformes) in a Remote Inland Fishery in Papua New Guinea
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Roeger, Darcy L., Amepou, Yolarnie, Chin, Andrew, Eisemberg, Carla C., Ibana, Dotty, White, William T., and Grant, Michael I.
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- 2024
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3. Beach showers as sources of contamination for sunscreen pollution in marine protected areas and areas of intensive beach tourism in Hawaii, USA
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Downs, C.A., Diaz-Cruz, M. Silvia, White, William T., Rice, Marc, Jim, Laura, Punihaole, Cindi, Dant, Mendy, Gautam, Krishna, Woodley, Cheryl M., Walsh, Kahelelani O., Perry, Jenna, Downs, Evelyn M., Bishop, Lisa, Garg, Achal, King, Kelly, Paltin, Tamara, McKinley, Ellen B., Beers, Axel I., Anbumani, Sadasivam, and Bagshaw, Jeff
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- 2022
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4. Taxonomy and Diversity of Extant Elasmobranchs
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White, William T., primary, O’Neill, Helen L., additional, and Naylor, Gavin J.P., additional
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- 2022
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5. Measuring Scientific Impact of Fisheries and Aquaculture Research-for-Development Projects in South East Asia and the Pacific
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Hiruy, Kiros, Murphy, Ray, Lewis, Tom, White, William T., and Purcell, Steven W.
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Research-for-development (R4D), as a mode of foreign aid, is a practical way to support developing countries. However, few studies have assessed the scientific impacts of R4D projects. Here, we applied an integrated assessment approach to evaluate the scientific impact of research projects commissioned by the Australian Centre for International Agricultural Research's Fisheries Program in the Asia-Pacific region between 2000 and 2012. We use publication metrics and expert panel reviews to examine trends in scientific outputs among 73 fisheries and aquaculture research projects. Among projects, there was considerable variation in publication types and outputs (including academic papers, magazine articles, policy reports, books, and book chapters), and projects produced, on average, 10 publications at a funded-dollar cost of AU$41,000 per publication. Bilateral and multilateral projects tended to produce more refereed journal articles and citations per funded dollar than single-country projects, and publication outputs were poor for certain countries. With the exception of fisheries projects, larger (more highly funded) projects did not produce more journal articles per funded dollar than smaller projects. Project duration had no significant effect on the number of refereed publications, citation rates, or total citations per funded dollar across projects. Aquaculture projects had greater publication impact, per funded dollar than fisheries projects. Beyond the bibliometric measures, qualitative findings indicated that scientific impact was strongly influenced by motivations of project leaders and their institutions. We identified disparate impact performance among industries and countries. These findings could inform future overseas aid investments, policies and strategies. This study offers useful benchmarks for gauging scientific impacts of R4D programs and shows the value of using approaches that go beyond bibliometric measures.
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- 2019
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6. Dichichthyidae, a New Family of Deepwater Sharks (Carcharhiniformes) from the Indo–West Pacific, with Description of a New Species
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White, William T., primary, Stewart, Andrew L., additional, O’Neill, Helen L., additional, and Naylor, Gavin J. P., additional
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- 2024
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7. Range extension of the Whitefin Swellshark Cephaloscyllium albipinnum (Scyliorhinidae) and possible implications for its conservation status
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White, William T., primary and Moore, Glenn I., additional
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- 2024
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8. First observation of a skate egg case nursery in the Ross Sea.
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Finucci, Brittany, Chin, Caroline, O'Neill, Helen L., White, William T., and Pinkerton, Matthew H.
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MARINE parks & reserves ,FISHERIES ,EGGS ,PLANT nurseries ,LARVAL dispersal - Abstract
Areas of importance to Southern Ocean skates are poorly defined. Here, we identify a deepwater skate egg case nursery in a discrete location at ~460 m depth off Cape Adare in the Southern Ocean. This is the first confirmed observation of a skate nursery area in the Ross Sea and only the second observation for the Southern Ocean. The morphology and size of the egg cases were consistent with the genus Bathyraja and most likely belong to the Bathyraja sp. (cf. eatonii). The nursery occurs within the "no take" General Protection Zone of the Ross Sea region marine protected area, where commercial fishing is prohibited. [ABSTRACT FROM AUTHOR]
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- 2024
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9. Phylogenomics reveals the deep ocean as an accelerator for evolutionary diversification in anglerfishes
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Miller, Elizabeth Christina, primary, Faucher, Rose, additional, Hart, Pamela B., additional, Rincon-Sandoval, Melissa, additional, Santaquiteria, Aintzane, additional, White, William T., additional, Baldwin, Carole C., additional, Miya, Masaki, additional, Betancur-R, Ricardo, additional, Tornabene, Luke, additional, Evans, Kory, additional, and Arcila, Dahiana, additional
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- 2023
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10. Extinction risk and conservation of the world's sharks and rays
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Dulvy, Nicholas K., Fowler, Sarah L., Musick, John A., Cavanagh, Rachel D., Kyne, Peter M., Harrison, Lucy R., Carlson, John K., Davidson, Lindsay N. K., Fordham, Sonja V., Francis, Malcolm P., Pollock, Caroline M., Simpfendorfer, Colin A., Burgess, George H., Carpenter, Kent E., Compagno, Leonard J. V., Ebert, David A., Gibson, Claudine, Heupel, Michelle R., Livingstone, Suzanne R., Sanciangco, Jonnell C., Stevens, John D., Valenti, Sarah, and White, William T.
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Quantitative Biology - Populations and Evolution - Abstract
The rapid expansion of human activities threatens ocean-wide biodiversity loss. Numerous marine animal populations have declined, yet it remains unclear whether these trends are symptomatic of a chronic accumulation of global marine extinction risk. We present the first systematic analysis of threat for a globally-distributed lineage of 1,041 chondrichthyan fishes - sharks, rays, and chimaeras. We estimate that one-quarter are threatened according to IUCN Red List criteria due to overfishing (targeted and incidental). Large-bodied, shallow-water species are at greatest risk and five out of the seven most threatened families are rays. Overall chondrichthyan extinction risk is substantially higher than for most other vertebrates, and only one-third of species are considered safe. Population depletion has occurred throughout the world's ice-free waters, but is particularly prevalent in the Indo-Pacific Biodiversity Triangle and Mediterranean Sea. Improved management of fisheries and trade is urgently needed to avoid extinctions and promote population recovery., Comment: Accepted for publication in eLIFE on 5th December 2013. 83 pages, 9 tables, 10 figures
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- 2013
11. A DNA sequence-based approach to the identification of shark and ray species and its implications for global elasmobranch diversity and parasitology
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Naylor, Gavin J. P., Caira, Janine N., 1957, Jensen, K. (Kirsten), 1971, Rosana, K. A. M., White, William T. (William Toby), 1977, Last, P. R., American Museum of Natural History Library, Naylor, Gavin J. P., Caira, Janine N., 1957, Jensen, K. (Kirsten), 1971, Rosana, K. A. M., White, William T. (William Toby), 1977, and Last, P. R.
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Chondrichthyes ,Classification ,coevolution ,Fishes ,Genetics ,Geographical distribution ,Host-parasite relationships ,Identification ,marine biodiversity ,mitochondrial DNA ,Molecular aspects ,NAD (Coenzyme) ,Nucleotide sequence ,Parasites ,Phylogeny ,Rays (Fishes) ,Sharks ,Variation - Published
- 2012
12. Revision of the genus Mustelus (Carcharhiniformes: Triakidae) in the northern Indian Ocean, with description of a new species and a discussion on the validity of M. walkeri and M. ravidus
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White, William T., Arunrugstichai, Sirachai, and Naylor, Gavin J.P.
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- 2021
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13. Sharks checking in to the sponge hotel: First internal use of sponges of the genus Agelas and family Irciniidae by banded sand catsharks Atelomycterus fasciatus.
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O'Neill, Helen L., White, William T., Pogonoski, John J., Alvarez, Belinda, Gomez, Oliver, and Keesing, John K.
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SAND , *DEMOSPONGIAE , *ECOLOGICAL niche , *HOTELS , *PREDATORY animals , *SHARKS - Abstract
Trawl surveys within and surrounding two northwestern Australian marine parks revealed banded sand catsharks Atelomycterus fasciatus (family Atelomycteridae) taking refuge within large sponges of the family Irciniidae (Demospongiae: Dictyoceratida) and the genus Agelas (Demospongiae: Agelasida: Agelasidae). Five sponges contained a total of 57 A. fasciatus, comprising both sexes and both immature and mature individuals ranging from 102 to 390 mm total length (TL). In the same surveys, only five A. fasciatus were captured unassociated with sponges, suggesting that sponges are an important microhabitat for A. fasciatus and may provide a daytime refuge from predators. A southerly range extension is also reported for this species. [ABSTRACT FROM AUTHOR]
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- 2024
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14. Sharks checking in to the sponge hotel: First internal use of sponges of the genus Agelas and family Irciniidae by banded sand catsharks Atelomycterus fasciatus
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O'Neill, Helen L., primary, White, William T., additional, Pogonoski, John J., additional, Alvarez, Belinda, additional, Gomez, Oliver, additional, and Keesing, John K., additional
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- 2023
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15. Elemental analysis of vertebrae discerns diadromous movements of threatened non‐marine elasmobranchs
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Grant, Michael I., primary, Kyne, Peter M., additional, James, Julie, additional, Hu, Yi, additional, Mukherji, Sushmita, additional, Amepou, Yolarnie, additional, Baje, Leontine, additional, Chin, Andrew, additional, Johnson, Grant, additional, Lee, Tegan, additional, Mahan, Brandon, additional, Wurster, Christopher, additional, White, William T., additional, and Simpfendorfer, Colin A., additional
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- 2023
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16. Refining mortality estimates in shark demographic analyses : a Bayesian inverse matrix approach
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Smart, Jonathan J., Punt, André E., Espinoza, Mario, White, William T., and Simpfendorfer, Colin A.
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- 2018
17. Categorising use patterns of non-marine environments by elasmobranchs and a review of their extinction risk
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Grant, Michael I., Kyne, Peter M., Simpfendorfer, Colin A., White, William T., and Chin, Andrew
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- 2019
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18. Shape-preserving erosion controlled by the graded microarchitecture of shark tooth enameloid
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Amini, Shahrouz, Razi, Hajar, Seidel, Ronald, Werner, Daniel, White, William T., Weaver, James C., Dean, Mason N., and Fratzl, Peter
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- 2020
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19. A median fin derived from the lateral plate mesoderm and the origin of paired fins
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Tzung, Keh-Weei, primary, Lalonde, Robert L., additional, Prummel, Karin D., additional, Mahabaleshwar, Harsha, additional, Moran, Hannah R., additional, Stundl, Jan, additional, Cass, Amanda N., additional, Le, Yao, additional, Lea, Robert, additional, Dorey, Karel, additional, Tomecka, Monika J., additional, Zhang, Changqing, additional, Brombacher, Eline C., additional, White, William T., additional, Roehl, Henry H., additional, Tulenko, Frank J., additional, Winkler, Christoph, additional, Currie, Peter D., additional, Amaya, Enrique, additional, Davis, Marcus C., additional, Bronner, Marianne E., additional, Mosimann, Christian, additional, and Carney, Tom J., additional
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- 2023
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20. What came first, the shark or the egg? Discovery of a new species of deepwater shark by investigation of egg case morphology
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White, William T., primary, O'Neill, Helen L., additional, Devloo‐Delva, Floriaan, additional, Nakaya, Kazuhiro, additional, and Iglésias, Samuel P., additional
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- 2023
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21. Discovery of a new mode of oviparous reproduction in sharks and its evolutionary implications
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Nakaya, Kazuhiro, White, William T., and Ho, Hsuan-Ching
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- 2020
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22. DNA capture reveals transoceanic gene flow in endangered river sharks
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Li, Chenhong, Corrigan, Shannon, Yang, Lei, Straube, Nicolas, Harris, Mark, Hofreiter, Michael, White, William T., and Naylor, Gavin J. P.
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- 2015
23. Species in Disguise: A New Species of Hornshark from Northern Australia (Heterodontiformes: Heterodontidae).
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White, William T., Mollen, Frederik H., O'Neill, Helen L., Yang, Lei, and Naylor, Gavin J. P.
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PECTORAL fins , *SPECIES , *ZEBRAS - Abstract
A new species of hornshark is described from northwestern Australia based on six whole specimens and a single egg case. Heterodontus marshallae n. sp. was previously considered to be conspecific with H. zebra from the Western Pacific. The new species differs from H. zebra in the sequence of its NADH2 gene, several morphological characters, egg case morphology and key coloration features. Despite the coloration being similar between H. marshallae n. sp. and H. zebra, i.e., pale background with 22 dark brown bands and saddles, they differ consistently in two key aspects. Firstly, the snout of H. marshallae n. sp. has a dark semicircular bar, usually bifurcated for most of its length vs. a pointed, triangular shaped dark marking in H. zebra. Secondly, H. zebra has a dark bar originating below the posterior gill slits and extending onto anterior pectoral fin, which is absent in H. marshallae n. sp. The Heterodontus marshallae n. sp. is endemic to northwestern Australia and occurs in deeper waters (125–229 m) than H. zebra (0–143 m). [ABSTRACT FROM AUTHOR]
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- 2023
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24. Concordance and Discordance in the Phylogenomics of the Wrasses and Parrotfishes (Teleostei: Labridae)
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Hughes, Lily C, primary, Nash, Chloe M, additional, White, William T, additional, and Westneat, Mark W, additional
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- 2022
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25. Life history of the silvertip shark Carcharhinus albimarginatus from Papua New Guinea
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Smart, Jonathan J., Chin, Andrew, Baje, Leontine, Tobin, Andrew J., Simpfendorfer, Colin A., and White, William T.
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- 2017
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26. Further description of the Kerguelen sandpaper skate Bathyraja irrasa (Rajiformes: Arhynchobatidae) based on additional specimens, including egg cases and embryos
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White, William T., primary, O'Neill, Helen L., additional, Cleeland, Jaimie, additional, and Lamb, Tim D., additional
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- 2022
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27. The impact of paleoclimatic changes on body size evolution in marine fishes
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Troyer, Emily M., primary, Betancur-R, Ricardo, additional, Hughes, Lily C., additional, Westneat, Mark, additional, Carnevale, Giorgio, additional, White, William T., additional, Pogonoski, John J., additional, Tyler, James C., additional, Baldwin, Carole C., additional, Ortí, Guillermo, additional, Brinkworth, Andrew, additional, Clavel, Julien, additional, and Arcila, Dahiana, additional
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- 2022
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28. Concordance and Discordance in the Phylogenomics of the Wrasses and Parrotfishes (Teleostei: Labridae).
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Hughes, Lily C, Nash, Chloe M, White, William T, and Westneat, Mark W
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CORAL reefs & islands ,CORAL reef fishes ,WRASSES ,OSTEICHTHYES ,TIME perception - Abstract
Phylogenomic analysis of large genome-wide sequence data sets can resolve phylogenetic tree topologies for large species groups, help test the accuracy of and improve resolution for earlier multi-locus studies and reveal the level of agreement or concordance within partitions of the genome for various tree topologies. Here we used a target-capture approach to sequence 1088 single-copy exons for more than 200 labrid fishes together with more than 100 outgroup taxa to generate a new data-rich phylogeny for the family Labridae. Our time-calibrated phylogenetic analysis of exon-capture data pushes the root node age of the family Labridae back into the Cretaceous to about 79 Ma years ago. The monotypic Centrogenys vaigiensis , and the order Uranoscopiformes (stargazers) are identified as the sister lineages of Labridae. The phylogenetic relationships among major labrid subfamilies and within these clades were largely congruent with prior analyses of select mitochondrial and nuclear datasets. However, the position of the tribe Cirrhilabrini (fairy and flame wrasses) showed discordance, resolving either as the sister to a crown julidine clade or alternatively sister to a group formed by the labrines, cheilines and scarines. Exploration of this pattern using multiple approaches leads to slightly higher support for this latter hypothesis, highlighting the importance of genome-level data sets for resolving short internodes at key phylogenetic positions in a large, economically important groups of coral reef fishes. More broadly, we demonstrate how accounting for sources of biological variability from incomplete lineage sorting and exploring systematic error at conflicting nodes can aid in evaluating alternative phylogenetic hypotheses. [coral reefs; divergence time estimation; exon-capture; fossil calibration; incomplete lineage sorting.] [ABSTRACT FROM AUTHOR]
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- 2023
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29. Centrophorus uyato
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White, William T., Guallart, Javier, Ebert, David A., Naylor, Gavin J. P., Mo, Ana Veríssi, Cotton, Charles F., Harris, Mark, Serena, Fabrizio, and Iglésias, Samuel P.
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Centrophorus ,Animalia ,Squaliformes ,Centrophorus uyato ,Biodiversity ,Centrophoridae ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Centrophorus uyato (Rafinesque, 1810) Little Gulper Shark Synonymy. Dalatias nocturnus Rafinesque, 1810: 11, pl. 14, fig. 3 (Type locality: Sicily, Italy)— Cuvier, 1818: 455; Cuvier, 1829: 392; Cuvier, 1837: 246; Swainson, 1838: 129, 160; Swainson, 1839: 313; Duméril, 1865: 436; Jordan & Evermann, 1917: 77; Bigelow & Schroeder, 1948: 500. Spinax uyatus — Bonaparte, 1834: 49, fig. 2 (Italy); Bonaparte, 1846: 16 (Mediterranean); Böhlke, 1984: 158. Acanthias uyatus — Müller & Henle, 1839: 85 (Mediterranean); Gray, 1851: vii, 71 (Mediterranean); Steindachner, 1864: 27; Duméril, 1865: 439 (Algerian coast, Mediterranean); Barbosa du Bocage & de Brito Capello, 1866: 7, 21; Günther, 1870: 419 (Mediterranean); Canestrini, 1872: 40; Steindachner, 1875: 466; Moreau, 1881: 346 (Mediterranean); Réguis, 1882: 72; Rochebrune, 1883: 47 (Senegal and Gambia); Hilgendorf, 1884: 518; Duncan, 1891: 35 (Mediterranean); Moreau, 1892: 39; Seeley, 1895: 35 (Mediterranean); Parona, 1898: 38 (Ligurian Sea); Duncker, 1914: 291; de Buen, 1916: 303, figs (Mediterranean coast of Morocco); Landolt, 1947: 353. Centrophorus granulosus — Müller & Henle, 1839: 89, pl. 33 (Sicily, Italy); Barbosa du Bocage & de Brito Capello, 1864: 261 (Portugal); Vinciguerra, 1883: 18 (482) (Gulf of Genoa); Goode & Bean, 1896: 12, pl. 3, fig. 11 (W Atlantic, Mediterranean and adjacent areas); Boutan, 1926: 1 (Algeria); Dieuzeide, 1928a: 15, figs (Algeria); Dieuzeide, 1928b: 1314 (Algeria?); Andr & Canal, 1929: 511 (Algeria); Arcidiacono, 1931: 609 (Gulf of Squillace, Italy); Gruvel, 1931: 74 (State of Syria [Syria, Lebanon, Israel]); Ranzi, 1932: 240 (Naples, Italy); Belloc, 1934: 146, fig. (Western Sahara, Morocco, Canary Islands and Madeira); Ranzi, 1934: 343, 370 (Naples, Italy); Fowler, 1936: 73 (Mediterranean); Fowler, 1941 (in part): 231 (Mediterranean, inc. Italy); Šoljan, 1948: 66, figs (Adriatic Sea); Bigelow et al., 1955: 6 (Gulf of Mexico); Kirinčić & Lepetić, 1955: 24 (southern Adriatic Sea); Tortonese, 1956: 176, figs 94-95 (Italy); Cadenat, 1959: 748, fig. 1b (West Africa); Maurin, 1968: 82 (Morocco to Algeria); Maurin & Bonnet, 1970: 147 (Canary Islands to Cape Verde); Karrer, 1975: 64 (Namibia); Karlovac, 1976: 601, fig. 4 (Adriatic Sea); Guitart, 1979: 67, fig. 46 (Cuba); Bouchet et al., 1982: 577 (Tunisia); Zupanovic & El-Buni, 1982: 111 (Libya); Uyeno et al., 1983: 62, figs (Suriname); Compagno, 1984a: 37, figs (Atlantic and Indo-West Pacific); Gilat & Gelman, 1984: 263 (Levant Sea, Israel); McEachran & Branstetter, 1984: 130, fig. (NE Atlantic and Mediterranean); Muñoz-Chapuli, 1984: 9 (NE Atlantic);? Quéro, 1984: 43, fig.; Capapé, 1985: 97, fig. 1–7 (Eastern Atlantic); Jardas, 1985: 50 (Adriatic Sea); Anon, 1986: 93, fig. 22 (Atlantic Ocean); Bass et al., 1986 (in part): 50, fig. 5.1 (Walvis Bay and Mozambique); Golani, 1986: 23, fig. 2 (Levantine Sea, Israel); Muñoz-Chapuli & Ramos, 1989: 65, figs 1a, 3a, 4b and c, 5a, 6a, 7a (NE Atlantic and Mediterranean); Compagno et al., 1991: 54 (Hondeklip Bay to Namibia); Benli et al., 1993: 133, figs 1 and 2 (Sea of Marmara); Pisanty & Golani, 1995: 388 (Levantine Sea, Israel); Lanfranco, 1996: 6, pl. 4 (Malta); Aldebert, 1997: 284 (Gulf of Lion, France); Guallart, 1998: 1, figs (Balearic Sea); Bello, 1999: 69 (Adriatic Sea); Hernández-Hamón & Núñez, 1998: 107 (Pacific Columbia); Ungaro et al., 1999: 180 (Albania); Capapé et al., 2000: 129 (Languedoc coast, France); Bertrand et al., 2000: 5 (Gibraltar to Aegean Sea, Mediterranean); Golani & Pisanty, 2000: 71 (Levantine Sea, Israel); Baino et al., 2001: 234 (Alboran Island to Aegean Sea, Mediterranean); Guallart & Vicent, 2001: 135, fig. 4 (Balearic Sea, Spain); Bilecenoglu et al., 2002: 16 (Turkey); Schembri et al., 2003: 76, fig. 3c (Malta); McLaughlin & Morrissey, 2004: 481, fig. 3 (Cayman Trench, Jamaica); Moreno García, 2004: 214 (in part, not figs) (Mediterranean Sea); Sion et al., 2004: 155 (Ionian Sea, Greece); Golani, 2005: 11 (Levantine Sea, Israel); Lteif, 2015: 16, figs 9a, 14, (Lebanon); Serena, 2005: 27, figs, pl. I, 8 (Mediterranean Sea); Serét, 2005: 21 (Libya); Bessho, 2006: 28, figs 27–30, 33–35 (Japan, Namibia); Golani et al., 2006: 38, fig. (eastern Mediterranean); Hadjichristophorou, 2006: 163 (Cyprus); Megalofonou & Chatzispyrou, 2006: 67, fig. 4 (Crete, Greece); Mejía-Falla et al., 2007: 116 (Colombia); Psomadakis et al., 2009: 200 (Gulf of Naples, Italy); D’Onghia et al., 2010: 401 (Ionian Sea, Greece); Lipej & Dulĉić, 2010: 10 (Adriatic Sea); Damalas & Vassilopoulou, 2011: 145 (Aegean Sea, Greece); Colloca & Lelli, 2012: 12 (Lebanon); Costa et al., 2012: 7 (Portugal); Guijarro et al., 2012: 89 (Balearic Islands, Spain); Güven et al., 2012: 278 (Antalya Bay, Turkey); Iglésias, 2013: 38, pl. 16 (France and Cape Verde); Carneiro et al., 2014: 13 (Portugal); Farrugio & Soldo, 2014: 33 (Sicily, Italy and Tunisia); Veríssimo et al., 2014: 6 (Gulf of Mexico); Goren & Galil, 2015: 510 (Levant Sea, Israel); Barría et al., 2015a: 226 (Catalan Sea, Spain and Gulf of Lions, France); Barría et al., 2015b: 114 (Catalan Sea, Spain and Gulf of Lions, France); Carpenter & De Angelis, 2016: 1170, figs (Eastern Atlantic); Ramírez-Amaro et al., 2016: 639 (western Mediterranean); Cariani et al., 2017: 5 (Mediterranean);? Haroun et al., 2017: 84 (Egypt); Gajić, 2019: 101, fig. 14 (Croatia, Montenegro and Albania); Bariche & Fricke, 2020: 17, fig. 12 (Lebanon). ? Acanthias nigrescens Nardo, 1860: 70, 96 (Type locality: Venice, Italy). Entoxychirus uyatus — Gill, 1862: 498; Whitley, 1934: 199 (Australia). Acanthias ujatus — Döderlein, 1878: 30 (Sicily, Italy); Döderlein, 1881: 92 (Italy). Centrophorus uyatus — Goode & Bean, 1896: 508; Garman, 1906: 204; Garman, 1913: 9, 196. Squalus uyatus — Garman, 1899: 28. Squalus uyato — Garman, 1906: 204. Centrophorus bragancae Regan, 1906: 438 (Type locality: Cezimbra, Portugal)— Regan, 1908: 53 (coast of Portugal); Strand, 1908: 83. Centrophorus uyato — Fowler, 1936: 72, fig. 21 (Mediterranean and eastern Atlantic); Tortonese, 1938: 310 (Mediterranean); Poll 1951: 64, figs 33–34 (Angola and Namibia); Bigelow et al., 1953: 227, fig. 4 (Gulf of Mexico; Nice, Mediterranean Sea); Aksiray, 1954?: 233 (Turkish Seas); Bigelow et al., 1955: 5, 9; Springer & Bullis, 1956: 42 (Gulf of Mexico); Bigelow & Schroeder, 1957: 54, 66, 69, 72, 79–84, fig. 8e (Gulf of Mexico); Springer & Garrick, 1964: 81, 91; Krefft & Tortonese, 1973: 39 (NE Atlantic and Mediterranean); Bass et al., 1976: 31, figs 22, 24E, 24F, pl. 7 (southern Mozambique); Bridger, 1978: 26 (west of Ireland and Britain); Compagno, 1981: 8 [sharks] (Eastern Central Atlantic); Castro, 1983: 54, figs (Gulf of Mexico); Allu et al., 1984: 125 (Namibia); Compagno, 1984a: 45, figs (Atlantic, Indo-West Pacific); Compagno, 1984b: 9 [sharks] (Western Indian Ocean); McEachran & Branstetter, 1984: 132, fig. (NE Atlantic and Mediterranean); Lloris, 1986: 96, fig 24 (Namibia); Turón et al., 1986: 63 (Namibia); Fischer et al., 1987: 823 (Mediterranean); Compagno, 1988b: 603 (Comoro Islands); Compagno et al., 1989: 24, fig. (Hondeklip Bay, South Africa to Namibia);? Clark & Kristof, 1990: 277, fig. 9 (Caribbean); Springer, 1990: 11 (Gulf of Mexico, Mediterranean, and Natal, South Africa); Applegate et al., 1993: 35 (Atlantic Mexican waters); Gomon et al., 1994: 92, 94, figs 30, 31 (southern Australia); Last & Stevens, 1994: 60, figs, pl. 4 (fig. 8.5) (southern Australia); Meriç, 1995: 192 (Sea of Marmara, Turkey); Perry et al., 1995: 139 (Gulf of Mexico); Reiner, 1996: 22, fig. (Cape Verde); Bonfil, 1997: 105 (Veracruz, Mexico); Joseph, 1999: [unpaginated] (Sri Lanka); Cervigón & Alcalá, 1999 (Venezuela); Clarke, 2000: 377 (Rockall Trough, NE Atlantic); Baino et al., 2001: 234 (Alboran Island to Aegean Sea, Mediterranean); Graham et al., 2001: 551 (south-eastern Australia); Yearsley et al., 2001: 35, 360 (southern Australia); Bilecenoglu et al., 2002: 17 (Turkey); Daley et al., 2002: 53 (southern Australia); Ali & Saad, 2003: 58, fig. (Syria); Schembri et al., 2003: 77, fig. 3d (Malta); Serena, 2005: 28, figs, pl. I, 9 (Mediterranean Sea, NE Atlantic, Western Indian, Gulf of Mexico and Taiwan); Meriç et al., 2007: 31 (Turkey); White, 2008: 87, figs (southern Australia); Scacco et al., 2010: 39, fig. 3f (Mediterranean Sea); Castro, 2011: 81, figs 16a-e (north-western Atlantic); Davenport et al.: 2011: 557 (north-western Atlantic, USA); White et al., 2013: 36, fig. 2, 15, 16 (Atlantic); Veríssimo et al., 2014: 6, fig. 5 (Gulf of Mexico); Hipes, 2015: 1, fig. 11 (Gulf of Mexico, USA); Wienerroither et al., 2015: 834, fig. 2 (northern Norway); Farrag, et al., 2016: 481, fig. 2a (Egypt); Driggers et al., 2017: 52 (Gulf of Mexico); Haroun et al., 2017: 84 (Egypt); Lteif et al., 2017: 1491 (Lebanon); Biscoito et al., 2018: 471, fig. 7 (Madeira, Portugal); Carneiro et al., 2019: 36 (Portugal); Ehemann et al., 2019: 4 (Venezuela); Fernando et al., 2019: 231, figs 5e, 18d-f (Mutur, Sri Lanka); Follesa et al., 2019: 85 (Mediterranean); Psomadakis et al., 2019: 162, figs, pl. X (fig. 70) (Myanmar); Iglésias, 2020: 46, pl. 21 (France and Cape Verde); Ebert & Dando, 2021: 217, figs (NE Atlantic and Mediterranean); Kousteni et al., 2021: 1, figs 2 and 3 (Cypriot waters). Centrophorus machiquensis Maul, 1955: 5, figs 13–16 (Type locality: Madeira)— Krefft & Tortonese, 1973: 39 (Madeira); Ali & Saad, 2003: 57, fig. (Syria); Biscoito et al., 2018: 470, fig. 6 (Madeira, Portugal); Almeida & Biscoito, 2019: 99 (Canary Islands and Madeira); Carneiro et al., 2019: 36 (Portugal). Centrophorus ujato — Tortonese, 1956: 178, fig. 96 (Genova, Italy); Bini, 1967: 97, fig. (Italy); Sara, 1968: 1, figs 1–3 (west of Sicily); FAO, 1971: no pagination (Mediterranean Sea). Centrophorus spp. (granulosus group)— Forster et al, 1970 (in part): 388 (Western Indian Ocean). Centrophorus (forme) uyato-machiquensis — Cadenat & Blache, 1981: 58, figs. 36, 37 and 40 (NE Atlantic). Centrophorus spp. — Peyronel et al., 1984: 643 (Bay of Ajaccio, Corsica, France). Centrophorus cf. harrissoni (Undescribed gulper shark #2)— Kiraly et al., 2003: 2 (Puerto Rico, US Virgin Islands, Virginia, North Carolina and Florida Straits to Dry Tortugas). Centrophorus bragance — Hernández-Hamón & Núñez, 1998: 108 (as questionable synonym of C. granulosus). Centrophorus sp. (uyato ?)— Morón et al., 1998: 144 (Beruwela, Sri Lanka). Centrophorus sp. cf. uyato — Saad, et al., 2004: 430 (Syria). ? Centrophorus sp. (non uyato)— Serét, 2005: 21 (Libya). Centrophorus zeehaani White, Ebert & Compagno, 2008: 1, figs 8-10 (Type locality: South Australia)— Last & Stevens, 2009: 68, pl. 9.7, figs (southern Australia); Pethybridge et al., 2010: 1369 (Tasmania and Great Australian Bight, Australia); Pethybridge et al., 2011: 2743 (Tasmania and Victoria, Australia); Graham & Daley, 2011: 583 (southern Australia); Daley et al., 2012: 708 (southern Australia); White et al., 2013: 41 (southern Australia); Daley et al., 2015:127 (southern Australia); Wienerroither et al., 2015: 834, fig. 2 (northern Norway); Bineesh et al., 2016: 461 (Kollam, India). Centrophorus cf. uyato — McLaughlin & Morrissey, 2005: 1185, figs 2, 3 (Cayman Trench, Jamaica); Veríssimo et al., 2014: 7 (Gulf of Mexico); Serena et al., 2020: 502, 509 (Mediterranean); Bellodi et al., 2022: 2 (Mediterranean Sea). Centrophorus zeehani — Daley et al., 2012: fig. 2 (misspelling; southern Australia); Bineesh et al., 2016: 466 (misspelling; Kollam, India). Centrophorus ‘uyato’ — White et al., 2017: 86 (Eastern Atlantic); Almeida & Biscoito, 2019: 100 (Mediterranean Sea, Canary Islands and Madeira). Centrophorus cf. granulosus — Follesa et al., 2019: 85 (Mediterranean); FAO, 2018: unpaginated, fig. (Mediterranean Sea). ? Centrophorus granulosus — Parenti, 2019: 102 (Sicily). Material examined. Neotype: BMNH 2021.10.4.1 (eviscerated; GenBank accession ON167716), female 983 mm TL, between Gorgona and Capraia islands, Ligurian Sea, 43°19.8′ N, 9°56.1′ E, 180 m, 20 Dec. 2012. Other specimens: Australia: AMS I 44310 –001 (paratype of Centrophorus zeehaani; GenBank accession ON167706), adult male 826 mm TL, southwest of Coffin Bay, South Australia, 35°14′ S, 134°29′ E, 360–600 m, 28 July 2005; CSIRO CA 4104, adult male 843 mm TL, east of Gabo Island, Victoria, 37°40′ S, 150°15′ E, 504–508 m, 4 May 1984; CSIRO H 866–02, immature male 456 mm TL, CSIRO H 867–01, female 439 mm TL, east of Jervis Bay, New South Wales, 34°58′ S, 151°09′ E, 490–576 m, 10 Sep. 1986; CSIRO H 2268–02, adult male 800 mm TL, west of Bunbury, Western Australia, 33°03′ S, 114°25′ E, 701 m, 10 Feb. 1989; CSIRO H 6307–01 (skeletal parts), female 1027 mm TL, 12 July 2004, east of Flinders Island, Tasmania, ~ 40° S, ~ 149° E, 350–430 m; CSIRO H 6309–01 (skeletal parts; GenBank accession ON167708), adult male 865 mm TL, CSIRO H 6309–02 (skeletal parts), adult male 876 mm TL, CSIRO H 6309–04 (skeletal parts), adult male 906 mm TL, east of Flinders Island, Tasmania, ~ 40° S, ~ 149° E, 400–450 m, 1 Aug. 2004; CSIRO H 6310–04 (skeletal parts), female 970 mm TL, northeast of Flinders Island, Tasmania, 39°04′ S, 148°39′ E, 500–680 m, 24 Jul. 1986; CSIRO H 6311–01 (skeletal parts), female 655 mm TL, east of St. Helens, Tasmania, 41°27′ S, 148°44′ E, 850–860 m, 5 Jun. 1987; CSIRO H 6500-02, adult male 862 mm TL, east of Flinders Island, Tasmania, 40°15′ S, 148°45′ E, 329–512 m, 21 Aug. 2003; CSIRO H 6503–02 (skeletal parts), female 991 mm TL, CSIRO H 6503–03 (skeletal parts; GenBank accession ON167709), female 1023 mm TL, CSIRO H 6503–04 (skeletal parts; GenBank accession ON167710), female 987 mm TL, CSIRO H 6503–05 (skeletal parts), female 957 mm TL, northeast of Flinders Island, Tasmania, 39°20′ S, 148°45′ E, 370–420 m, 7 Apr. 2003; CSIRO H 6504–02, adult male 854 mm TL, CSIRO H 6504–03, female 817 mm TL, CSIRO H 6504–04, juvenile male 666 mm TL, CSIRO H 6504–05, adult male 861 mm TL, east of Jervis Bay, New South Wales, 35°12′ S, 150°58′ E, 320–500 m, July to Aug. 2003; CSIRO H 6628–01 (paratype of Centrophorus zeehaani), immature male 506 mm TL, CSIRO H 6628–02 (paratype of Centrophorus zeehaani; GenBank accession ON167705), immature male 645 mm TL, CSIRO H 6628–03 (paratype of Centrophorus zeehaani), adult male 875 mm TL, CSIRO H 6628–04 (paratype of Centrophorus zeehaani), adult male 910 mm TL, CSIRO H 6628–05 (holotype of Centrophorus zeehaani), adult male 893 mm TL, CSIRO H 6628–06 (paratype of Centrophorus zeehaani), adult male 852 mm TL, CSIRO H 6628–07 (paratype of Centrophorus zeehaani), adult male 906 mm TL, NMV A 29736 –001 (paratype of Centrophorus zeehaani), adult male 820 mm TL, southwest of Coffin Bay, South Australia, 35°14′ S, 134°29′ E, 360–600 m, 28 July 2005; CSIRO unreg. (DB 02/181), Great Australian Bight, adult male 857 mm TL; CSIRO unreg. (LJVC 880517), female 840 mm TL, unknown location; PMH095-11 (jaws only), female 104 cm TL, Albany, Western Australia. Eastern Atlantic (including Mediterranean): AMNH 78267, female 922 mm TL, AMNH 78269, female 937 mm TL, AMNH 78271, female 1016 mm TL, AMNH 78273, adult male 872 mm TL, AMNH 78277, adult male 895 mm TL, AMNH 78279, adult male 890 mm TL, between Tenerife and Gran Canaria, Canary Islands, Spain, 3 Oct. 1986; AMNH 78280, female 996 mm TL, AMNH 78282, female 1059 mm TL, AMNH 78283, female 1056 mm TL, AMNH 78284, adult male 832 mm TL, AMNH 78285, female 921 mm TL, AMNH 78286, female 1004 mm TL, AMNH 78291, female 1034 mm TL, AMNH 78292, female 980 mm TL, AMNH 78294, adult male 891 mm TL, between Tenerife and Gran Canaria, Canary Islands, Spain, 4 Oct. 1986; BMNH 1862.4.22.29, female 449 mm TL, Madeira, Portugal; BMNH 1864.7.18.1, female 894 mm TL, Madeira, Portugal; BMNH 1904.11.30.9- 10 (2 specimens), female 1036 mm TL, adult male 888 mm TL, west of Faro, Portugal, 662 m depth; BMNH 1904.11.30.11 (paralectotype of Centrophorus bragancae), juvenile male 488 mm TL, off Sesimbra, Portugal, 841 m depth; BMNH 1904.11.30.12 (lectotype of Centrophorus bragancae), female 467.5 mm TL, off Sesimbra, Portugal, 505 m depth; BMNH 2013.9.20.34, female 875 mm TL, BMNH 2013.9.20.35, female 930 mm TL, BMNH 2013.9.20.36, female 935 mm TL, BMNH 2013.9.20.37, female 731 mm TL, BMNH 2013.9.20.38, adult male 843 mm TL, BMNH 2013.9.20.39, adult male 865 mm TL, northeast Atlantic; CSIRO H 7471-01 (GenBank accession ON167715), adult male 853 mm TL, east of Corsica, France, 42°05.8′ N, 9°44.5′ E, 550–565 m, 30 May 2012; CSIRO H 7472-01, juvenile male 440 mm TL, southeast of Corsica, France, 41°47.9′ N, 9°30.5′ E, 466–480 m, 31 May 2012; ERB 1288, male 770 mm TL, Concarneau fish-market, France, 9 Sep. 2000; ERB 0763, male, 850 mm TL, Concarneau, France, 13 May 2009; HUJ 10885, female 760 mm TL, Hadera, Israel, 13 Sep. 1982; HUJ 11339, adult male 796 mm TL, Haifa Bay, Israel, 1 Mar. 1983; HUJ 17029, female 476 mm TL, Haifa, Israel, 16 Mar. 1983; HUMZ 151304, juvenile male 578 mm TL; HUMZ 151306, female 978 mm TL, Namibia; HUJ 21135 (GenBank accession ON167718), female 753 mm TL, Haifa fishing port, Israel, 29 July 2013; MNHN-IC 1905- 0568, juvenile male 454 mm TL, Portugal, 460 m depth, June 1903; MNHN-IC 1969-0269, juvenile male 499 mm TL, southwest of Monrovia, Liberia, 6°08′ N, 10°56′ W, 400 m depth, 27 Apr. 1964; MNHN-IC 0000-1224, female 537 mm TL, Naples, Italy; MNHN-IC 2005-0169, adult male 892 mm TL, west of Ireland, 28 Apr. 2005; NMW 15009, female 889 mm TL, Nice; NMW 63020, adult male 880 mm TL, Nice, France, 1902, Published as part of White, William T., Guallart, Javier, Ebert, David A., Naylor, Gavin J. P., Mo, Ana Veríssi-, Cotton, Charles F., Harris, Mark, Serena, Fabrizio & Iglésias, Samuel P., 2022, Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3 - Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history, pp. 1-51 in Zootaxa 5155 (1) on pages 15-41, DOI: 10.11646/zootaxa.5155.1.1, http://zenodo.org/record/6669082, {"references": ["Rafinesque, C. S. (1810) Caratteri di alcuni nuovi generi e nuove specie di animali e piante della Sicilia, con varie osservazioni sopra i medisimi. Sanfilippo, Palermo, 1, 3 - 69. https: // doi. org / 10.5962 / bhl. title. 104418", "Cuvier, G. (1818) Dictionnaire des sciences naturelles, dans lequel on traite meithodiquement des diffeirens e \u02c6 tres de la nature, consideireis soit en eux-me \u02c6 mes, d'apreIs l'eitat actuel de nos connoissances, soit relativement aI l'utilitei qu'en peuvent retirer la meidecine, l'agriculture, le commerce et les artes. 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(1984) Les poissons de mer des peches Francaises. Jacques Grancher, Paris.", "Capape, C. (1985) Nouvelle description de Centrophorus granulosus (Schneider, 1801) (Pisces, Squalidae). Donnees sur la biologie de la reproduction et le pecim alimentaire des pecimens des cotes tunisiennes. Bulletin de l'Institut National Scientifique et Technique d'Oceanographie et de Peche de Salommbo, 12, 97 - 141.", "Jardas, I. (1985) Pregled riba (sensu lato) Jadranskog mora (Cyclostomata, Selachii, Osteichthyes) s obzirom na taksonomiju I utvrdeni broj. Biosistematika, 11, 45 - 74.", "Anon. (1986) Monografiias de zoologiia marina. Volume 1. Instituto de Ciencias del Mar, Barcelona, Consejo Superior de Investigaciones Cientiificas, Madrid.", "Bass, A. J., Compagno, L. J. V. & Heemstra, P. C. (1986) Family no. 5: Squalidae, pp. 49 - 62. In: Smith, M. M. & Heemstra, P. C. (eds). Smith's Sea fishes. Berlin: Springer-Verlag.", "Golani, D. (1986) On deep-water sharks caught off the Mediterranean coast of Israel. Israel Journal of Zoology, 34, 23 - 31.", "Munoz-Chapuli, R. & Ramos, F. (1989) Review of the Centrophorus sharks (Elasmobranchii, Squalidae) of the eastern Atlantic. Cybium, 13, 65 - 81.", "Compagno, L. J. V., Ebert, D. A. & Cowley, P. A. (1991) Distribution of offshore demersal cartilaginous fish (class Chondrichthyes) off the west coast of southern Africa, with notes on their systematics. South African Journal of Marine Science, 11, 43 - 139. https: // doi. org / 10.2989 / 025776191784287664", "Benli, H. A., Cihangir, B. & Bizsel, K. C. (1993) A new record for the Sea of Marmara; (Family: Squalidae) Centrophorus granulosus (Bloch & Schneider, 1801). Doda, Turkish Journal Of Zoology, 17, 133 - 135.", "Pisanty, S. & Golani, D. (1995) Vertical distribution of demersal fish on the continental slope of Israel (Eastern Mediterranean). In: Armantrout, N. B. (Ed.), Condition of the world's aquatic habitats. Proceedings of the World Fisheries Congress, Theme 1. Oxford & IBH Publishing Co. Pvt. Ltd, New Delhi.", "Lanfranco, G. G. (1996) The fish around Malta (Central Mediterranean). Progress Press Co. Ltd. (Malta), 132 pp.", "Aldebert, Y. (1997) Demersal resources of the Gulf of Lions (NW Mediterranean). Impact of exploitation on fish diversity. Vie et Milieu - Life and Environment, 47, 275 - 284.", "Guallart, J. (1998) Contribucion al conocimiento de la biologia y la taxonomia del tiburon batial Centrophorus granulosus (Bloch y Schneider, 1801) (Elasmobranchii, Squalidae) en el mar balear (Mediterraneo Occidental). PhD Thesis. Universitat de Valencia, Valencia, 291 pp.", "Bello, G. (1999) The chondrichthyans of the Adriatic Sea. Acta Adriatica, 40, 65 - 76. https: // doi. org / 10.1093 / mollus / 65.2.233", "Hernandez-Hamon, H. & Nunez, S. R. (1998) Nuevo registro para el caribe sur Colombiano del tiburon quelvacho Centrophorus granulosus (Schneider) (Pisces: Centrophoridae). Boletin de Investigaciones Marinas y Costeras, 27, 107 - 112. https: // doi. org / 10.25268 / bimc. invemar. 1998.27.0.336", "Ungaro, N., Marano, C. A., Marsan, R., Martino, M., Marzano, M. C., Strippoli, G. & Vlora, A. (1999) Analysis of demersal species assemblages from trawl surveys in the South Adriatic Sea. Aquatic Living Resources, 12, 177 - 185. https: // doi. org / 10.1016 / S 0990 - 7440 (00) 88469 - 7", "Capape, C., Tomasini, J. A. & Quignard, J. P. (2000) The pleurotremate elasmobranchs from the Languedoc coast (southern France): biological and demographic observations. Vie et Milieu - Life and Environment, 50, 123 - 133.", "Golani, D. & Pisanty, S. (2000) Biological aspects of the Gulper shark, Centrophorus granulosus (Bloch and Schneider, 1801), from the Mediterranean coast of Israel. Acta Adriatica, 41, 71 - 78.", "Guallart, J. & Vicent, J. J. (2001) Changes in composition during embryo development of the gulper shark, Centrophorus granulosus (Elasmobranchii, Centrophoridae): an assessment of maternal-embryonic nutritional relationships. Environmental Biology of Fishes, 61, 135 - 150. https: // doi. org / 10.1023 / A: 1011080429625", "Bilecenoglu, M., Taskavak, E., Mater, S. & Kaya, M. (2002). Checklist of the marine fishes of Turkey. Zootaxa, 113 (1), 1 - 194. https: // doi. org / 10.11646 / zootaxa. 113.1.1", "Schembri, T., Fergusson, I. K. & Schembri, P. J. (2003) Revision of the records of shark and ray species from the Maltese Islands (Chordata: Chondrichthyes). The Central Mediterranean Naturalist, 4, 71 - 104.", "McLaughlin, D. M. & Morrissey, J. F. (2004) New records of elasmobranchs from the Cayman Trench, Jamaica. Bulletin of Marine Science, 75, 481 - 485.", "Sion, L., Bozzano, A., D'Onghia, G., Capezzuto, F. & Panza, M. (2004) Chondrichthyes species in deep waters of the Mediterranean Sea. Scientia Marina, 68 (Suppl. 3), 153 - 162. https: // doi. org / 10.3989 / scimar. 2004.68 s 3153", "Golani, D. (2005) Checklist of the Mediterranean fishes of Israel. Zootaxa, 947 (1), 1 - 90. https: // doi. org / 10.11646 / zootaxa. 947.1.1", "Lteif, M. (2015) Biology, distribution and diversity of cartilaginous fish species along the Lebanese coast, eastern Mediterranean. Universite de Perpignan via Domitia, France, 262 pp.", "Serena, F. (2005) Field identification guide to the sharks and rays of the Mediterranean and Black Sea. FAO Species Identification Guide for Fishery Purposes. FAO, Rome.", "Seret, B. (2005) Chondrichthyan fishes of Libya: proposal for a research programme. United Nations Environment Programme, Mediterranean Action Plan, Regional Activity Centre for Specially Protected Areas, Tunisia, 31 pp.", "Bessho, M. (2006) Taxonomic revision of the genus Centrophorus (Centrophoriformes: Centrophoridae) in Japanese waters. Unpublished Masters Thesis, Graduate School of Fisheries Science, Hokkaido University, 85 pp.", "Golani, D., Ozturk, B. & Basuta, N. (2006) Fishes of the eastern Mediterranean. Turkish Marine Research Foundation, Istanbul, Turkey, 260 pp.", "Hadjichristophorou, M. (2006) Chondrichthyes in Cyprus. In: Basusta, N., Keskin, C., Serena, F. & Seret, B. (Eds.), The proceedings of the workshop on Mediterranean cartilaginous fish with emphasis on Southern and Eastern Mediterranean. Turkish Marine Research Foundation, Istanbul-Turkey.", "Megalofonou, P. & Chatzispyrou, A. (2006) Sexual maturity and feeding of the gulper shark, Centrophorus granulosus, from the eastern Mediterranean Sea. Cybium, 30, 67 - 74. https: // doi. org / 10.26028 / cybium / 2006 - 304 supp- 009", "Mejia-Falla, P. A., Navia, A. F., Mejia-Ladino, L. M., Acero, A. P. & Rubio, E. A. (2007) Tiburones y rayas de Colombia (Pisces: Elasmobranchii): lista actualizada, revisada y comentada. Boletin de Investigaciones Marinas y Costeras, 36, 111 - 149.", "Psomadakis, P. N., Maio, N. & Vacchi, M. (2009) The chondrichthyan biodiversity in the Gulf of Naples (SW Italy, Tyrrhenian Sea): an historical overview. Cybium, 33, 199 - 209. https: // doi. org / 10.26028 / cybium / 2009 - 333 - 003", "D'Onghia, G., Maiorano, P., Sion, L., Giove, A., Capezzuto, F., Carlucci, R. & Tursi, A. (2010) Effects of deep-water coral banks on the abundance and size structure of the megafauna in the Mediterranean Sea. Deep Sea Research Part II Topical Studies in Oceanography, 57, 397 - 411. https: // doi. org / 10.1016 / j. dsr 2.2009.08.022", "Lipej, L. & Dulcic, J. (2010) Checklist of the Adriatic Sea fishes. Zootaxa, 2589 (1), 1 - 92. https: // doi. org / 10.11646 / zootaxa. 2589.1.1", "Damalas, D. & Vassilopoulou, V. (2011) Chondrichthyan by-catch and discards in the demersal trawl fishery of the central Aegean Sea (Eastern Mediterranean). Fisheries Research, 108, 142 - 152. https: // doi. org / 10.1016 / j. fishres. 2010.12.012", "Colloca, F. & Lelli, S. (2012) Report of the FAO EastMed support to the fishing trials carried out off the South Lebanese Coast. EastMed Technical Documents 14. FAO, Rome, 38 pp.", "Costa, F. O., Landi, M., Martins, R., Costa, M. H., Costa, M. E., Carneiro, M., Alves, M.
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30. Distribution and comments on the morphology of Centroscymnus owstonii Garman, 1906 (Squaliformes: Somniosidae), with focus on its occurrence in the Indian Ocean
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Weigmann, Simon, Vaz, Diego F. B., White, William T., de Carvalho, Marcelo R., and Thiel, Ralf
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- 2016
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31. Aetomylaeus caeruleofasciatus, a new species of eagle ray (Myliobatiformes: Myliobatidae) from northern Australia and New Guinea
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White, William T., Last, Peter R., and Baje, Leontine
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- 2016
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32. Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3—Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
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WHITE, WILLIAM T., primary, GUALLART, JAVIER, additional, EBERT, DAVID A., additional, NAYLOR, GAVIN J.P., additional, VERÍSSIMO, ANA, additional, COTTON, CHARLES F., additional, HARRIS, MARK, additional, SERENA, FABRIZIO, additional, and IGLÉSIAS, SAMUEL P., additional
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- 2022
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33. Market surveys and social media provide confirmation of the endangered giant freshwater whipray Urogymnus polylepis in Myanmar
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Grant, Michael I., primary, Bicknell, Anthony W. J., additional, Htut, Thaung, additional, Maung, Antt, additional, Maung, Thu, additional, Myo Myo, Khin, additional, Rein, Thu, additional, San, Min Khan, additional, White, William T., additional, Ya, Kyaw Zay, additional, and Mizrahi, Meira, additional
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- 2022
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34. Redescription of Scymnodon ichiharai Yano and Tanaka 1984 (Squaliformes: Somniosidae) from the western North Pacific, with comments on the definition of somniosid genera
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White, William T., Vaz, Diego F. B., Ho, Hsuan-Ching, Ebert, David A., de Carvalho, Marcelo R., Corrigan, Shannon, Rochel, Elisabeth, de Carvalho, Murilo, Tanaka, Sho, and Naylor, Gavin J. P.
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- 2015
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35. Integrated Taxonomy Revealed Genetic Differences in Morphologically Similar and Non-Sympatric Scoliodon macrorhynchos and S. laticaudus
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Lim, Kean Chong, primary, White, William T., additional, Then, Amy Y. H., additional, Naylor, Gavin J. P., additional, Arunrugstichai, Sirachai, additional, and Loh, Kar-Hoe, additional
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- 2022
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36. Dietary overlap of carcharhinid sharks in the Gulf of Papua
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Baje, Leontine, primary, Chin, Andrew, additional, White, William T., additional, and Simpfendorfer, Colin A., additional
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- 2022
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37. Habitat Works: How Partnerships and Habitat Improvement have Restored Quail Populations in the 2C Quail Focus Area
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Metcalf, E. Lee, primary, Emmerich, Beth A., additional, and White, William T., additional
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- 2022
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38. Landowner Cooperative Key to Success in the Bee Ridge Quail Focus Area
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Pinkowski, John A., primary, Emmerich, Beth A., additional, and White, William T., additional
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- 2022
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39. Biogeographical structure and affinities of the marine demersal ichthyofauna of Australia
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Last, Peter R., White, William T., Gledhill, Daniel C., Pogonoski, John J., Lyne, Vince, and Bax, Nic J.
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- 2011
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40. Long-term shifts in abundance and distribution of a temperate fish fauna: a response to climate change and fishing practices
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Last, Peter R., White, William T., Gledhill, Daniel C., Hobday, Alistair J., Brown, Rebecca, Edgar, Graham J., and Pecl, Gretta
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- 2011
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41. Civil Rights Directory: 1981 Clearinghouse Publication 15. Revised.
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Commission on Civil Rights, Washington, DC. and White, William T.
- Abstract
This is the Civil Rights Directory for 1981 published by the United States Commission on Civil Rights. It lists relevant federal, state and local agencies, private and women's organizations, research institutions, and other miscellaneous organizations related to Civil Rights. The directory provides a description of each listed organization and the services it offers. The addresses and the areas served by these agencies are also included. (APM)
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- 1981
42. Dasyatidae Jordan & Gilbert 1879
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Dasyatidae ,Myliobatiformes ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Family Dasyatidae Dasyatidae (stingrays) are the dominant group of rays in the coastal tropical Indo-West Pacific. While stingray taxonomy is problematic, recent revisions have vastly improved knowledge of this family (Last et al. 2016a). Dasyatidae are amongst the most commonly landed ray groups in Bangladesh, with high demand for consumption and accessories (Last et al. 2016a; Haque et al. 2018). This report identified seven species of Dasyatidae rays in addition to the 24 species previously reported in Bangladesh (Roy et al. 2015)., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 213, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Last, P., Naylor, G., Seret, B., White, W., de Carvalho, M. & Stehmann, M. (2016 a) Rays of the World. CSIRO publishing, Melbourne, ix + 790 pp.","Haque, A. B., Biswas, A. & Latifa, G. A. (2018) Observations of shark and ray products in the processing centres of Bangladesh, trade in CITES species and conservation need. TRAFFIC Bulletin, 30 (1), 6 - 14.","Roy, B. J., Singha, N. K., Rhaman, M. G. & Ali, A. H. M. H. (2015) Status and recorded of sharks and rays in the Bay of Bengal of Bangladesh Region. Brazilian Journal of Biological Sciences, 2 (4), 343 - 367."]}
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- 2021
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43. Narcinidae T.N.Gill 1862
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Myliobatiformes ,Narcinidae ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Family Narcinidae One specimen of Narcine was recorded which appears to be consistent with N. sp. of Psomadakis et al. (2020). This appeared to be morphologically similar to N. brevilabiata and N. atzi. Further specimens are required to confirm the species identification therefore this species is tentatively identified as Narcine sp. (Figure 14). (sensu Psomadakis et al. 2020)., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 224, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Psomadakis, P., Thein, H., Russell, B. C. & Tun, M. T. (2020) Field identification guide to the living marine resources of Myanmar. FAO species identification guide for fishery purposes. FAO, Rome, 840 pp."]}
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- 2021
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44. Neotrygon Castelnau 1873
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Dasyatidae ,Myliobatiformes ,Neotrygon ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Genus Neotrygon The Neotrygon kuhlii species complex has recently been expanded (Last et al. 2016). These taxonomic revisions, however, did not consider Bay of Bengal specimens in detail. To date, two species have been recorded from Bangladesh; N. indica and N. kuhlii (Haque et al. 2019a; Hoq et al. 2011). In this present study, a total of 649 specimens were examined, and five sampled for genetic analysis. Morphological differences were observed, including the dorsal coloration and tail banding. Several specimens were most consistent with N. caeruleopunctata, but have been preliminarily identified as N. cf. caeruleopunctata (Figure 5) due to possible genetic differences in the Bay of Bengal specimens. It is likely that previous records of N. kuhlii represent this species, with N. kuhlii now considered to occur only from the Solomon Islands, and adjacent island groups (Last et al. 2016a). All genetically sampled specimens were labelled as Neotrygon Bay of Bengal variants., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 218, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Haque, A. B., Das, S. A. & Biswas, A. R. (2019 a) DNA analysis of elasmobranch products originating from Bangladesh reveals unregulated elasmobranch fishery and trade on species of global conservation concern. PloS one, 14 (9), e 0222273. https: // doi. org / 10.1371 / journal. pone. 0222273","Hoq, M. E., Haroon, A. Y. & Hussain, M. G. (2011) Shark fisheries in the Bay of Bengal, Bangladesh: Status and potentialities. Support to Sustainable Management of the BOBLME Project, Bangladesh Fisheries Research Institute, 76 pp.","Last, P., Naylor, G., Seret, B., White, W., de Carvalho, M. & Stehmann, M. (2016 a) Rays of the World. CSIRO publishing, Melbourne, ix + 790 pp."]}
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- 2021
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45. Telatrygon Last, Naylor & Manjaji-Matsumoto 2016
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Dasyatidae ,Myliobatiformes ,Animalia ,Biodiversity ,Telatrygon ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Genus Telatrygon Three specimens of a sharp-snouted stingray were preliminarily identified as Telatrygon crozieri,based on morphology. Samples were not obtained for genetic analysis and so further work is needed to confirm the identification and to distinguish T. crozieri from the recently described T. biasa recorded from Indonesia (Last et al. 2016d)., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 221, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Last, P. R., White, W. T. & Naylor, G. (2016 d) Three new stingrays (Myliobatiformes: Dasyatidae) from the Indo-West Pacific. Zootaxa, 4147 (4), 377 - 402. https: // doi. org / 10.11646 / zootaxa. 4147.4.2"]}
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- 2021
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46. Mobulidae Gill 1893
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Myliobatiformes ,Mobulidae ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Family Mobulidae Two species of Mobula have previously been recorded from Bangladesh; Mobula mobular and M. kuhlii ( Hoq et al. 2011; Roy et al. 2014a ). In this study, M. birostris, M. tarapacana, M. eregoodoo and M. thurstoni (Figure 13) were recorded following examination of 97 mobulid specimens. Genetic analysis confirmed species identification for M. tarapacana, M. kuhlii and M. mobular, and the presence of either M. alfredi or M. birostris, but the NADH2 sequences alone cannot distinguish between these two species due to overlapping sequence polymorphism (G. Naylor, unpubl. data). This study confirms the presence of at least six mobulid species in Bangladesh; M. alfredi or M. birostris, M. eregoodoo, M. kuhlii, M. mobular, M. tarapacana and M. thurstoni where M. thurstoni has been reported for the first time with possible presence of M. alfredi., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 223, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Hoq, M. E., Haroon, A. Y. & Hussain, M. G. (2011) Shark fisheries in the Bay of Bengal, Bangladesh: Status and potentialities. Support to Sustainable Management of the BOBLME Project, Bangladesh Fisheries Research Institute, 76 pp.","Roy, B. J., Alam, M. F., Rhaman, M. G., Singha, N. K. & Akhtar, A. (2014 a) Landing trends, species composition and percentage composition of Sharks and Rays in Chittagong and Cox's Bazar, Bangladesh. Global Journal of Science Frontier Research, 14, 070403 - 079999."]}
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- 2021
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47. Triakidae J.E.Gray 1851
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Myliobatiformes ,Animalia ,Biodiversity ,Chordata ,Triakidae ,Taxonomy ,Elasmobranchii - Abstract
Family Triakidae Three houndshark species have been previously recorded from Bangladesh, i.e. Mustelus manazo, M. mosis and Iago garricki (Hoq et al. 2011; Habib et al. 2020).A total of 31 specimens of a second species of the Iago omanensis complex (which includes the poorly defined I. mangalorensis, if considered valid (Sen et al. 2020; Weigmann 2016; Maduna & Bester-van der Merwe 2017)) were recorded in this study. There is a possibility the recorded Iago sp. could be a new species to science as two separate species (Iago sp. A and Iago sp. B) have been theorised to be present in the Indian waters (Bineesh et al. 2017). This species is tentatively identified as Iago cf. omanensis (Figure 18) pending further taxonomic investigation. It brings the total number of triakid species in Bangladesh to four, with the taxonomy of the Mustelus species in this region being investigated by one of the authors (WW)., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 226, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Hoq, M. E., Haroon, A. Y. & Hussain, M. G. (2011) Shark fisheries in the Bay of Bengal, Bangladesh: Status and potentialities. Support to Sustainable Management of the BOBLME Project, Bangladesh Fisheries Research Institute, 76 pp.","Habib, K. A., Neogi, A. K., Nahar, N., Oh, J., Lee, Y. H. & Kim, C. G. (2020) An overview of fishes of the Sundarbans, Bangladesh and their present conservation status. Journal of Threatened Taxa, 12 (1), 15154 - 15172. https: // doi. org / 10.11609 / jott. 4893.12.1.15154 - 15172","Sen, S., Dash, G., Valappil, A. K., Kizhakudan, S. J. & Chakraborty, R. (2020) Occurrences of Intersexual Hound Sharks, Iago cf. omanensis (Triakidae: Carcharhiniformes) from North-western Bay of Bengal. Thalassas: An International Journal of Marine Sciences, 36, 525 - 534. https: // doi. org / 10.1007 / s 41208 - 020 - 00220 - 0","Weigmann, S. (2016) Annotated checklist of the living sharks, batoids and chimaeras (Chondrichthyes) of the world, with a focus on biogeographical diversity. Journal of Fish Biology, 88 (3), 837 - 1037. https: // doi. org / 10.1111 / jfb. 12874","Maduna, S. N. & Bester-van der Merwe, A. E. (2017) Molecular research on the systematically challenging smoothhound shark genus Mustelus: a synthesis of the past 30 years. African Journal of Marine Science, 39 (4), 373 - 387. https: // doi. org / 10.2989 / 1814232 X. 2017.1394365","Bineesh, K. K., Gopalakrishnan, A., Akhilesh, K. V., Sajeela, K. A., Abdussamad, E. M., Pillai, N. G. K., Basheer, V. S., Jena, J. K. & Ward, R. D. (2017) DNA barcoding reveals species composition of sharks and rays in the Indian commercial fishery. Mitochondrial Dna Part A, 28 (4), 458 - 472. https: // doi. org / 10.3109 / 19401736.2015.1137900"]}
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- 2021
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48. Pastinachus Ruppell in Ruppell 1828
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Dasyatidae ,Myliobatiformes ,Pastinachus ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Genus Pastinachus The current study confirmed two Pastinachus ater (Figure 7) specimens in Bangladesh and 18 specimens of Pastinachus solocirostris (Figure 8). It is assumed that, P. ater has been previously reported from Bangladesh as P. sephen (Roy et al. 2015), though a recent taxonomic study found that P. sephen is only found in the Western Indian Ocean (Red Sea to Pakistan) (Last & Manjaji-Matsumoto 2010). However, four specimens were morphologically very close to P. sephen and referred to as P. cf. sephen (Figure 9) needing further taxonomic work. We also recorded two specimens of a third species of Pastinachus, which are morphologically consistent with P. gracilicaudus. Further taxonomic examination is required, however, as differences were found between the NADH2 sequences of the Bangladesh as compared to Borneo specimens. This species is tentatively referred to as Pastinachus cf. gracilicaudus (Figure 10)., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 219, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Roy, B. J., Singha, N. K., Rhaman, M. G. & Ali, A. H. M. H. (2015) Status and recorded of sharks and rays in the Bay of Bengal of Bangladesh Region. Brazilian Journal of Biological Sciences, 2 (4), 343 - 367.","Last, P. R. & Manjaji-Matsumoto, B. M. (2010) Description of a new stingray, Pastinachus gracilicaudus sp. nov. (Elasmobranchii: Myliobatiformes), based on material from the Indo - Malay Archipelago. In: Last, P. R., White, W. T. & Pogonoski, J. J. (Eds.), Descriptions of New Sharks and Rays from Borneo. CSIRO Marine and Atmospheric Research Paper 032. CSIRO Marine and Atmospheric Research, Hobart, pp. 115 - 127."]}
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- 2021
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49. Rhinobatidae Bonaparte 1835
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Myliobatiformes ,Rhinobatidae ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii - Abstract
Family Rhinobatidae Rhinobatos ranongensis (Figure 15), which was recently described from the Bay of Bengal and Arabian sea (Last et al. 2019), was recorded from> 300 specimens from a single site. With the record of this Rhinobatos species, a total of at least eight species of Rhinopristiformes, including giant guitarfish (Glaucostegidae), guitarfish (Rhinobatidae) and wedgefish (Rhinidae), have been confirmed in the territorial waters of Bangladesh (Haque in review). Although not a new record, one specimen from one site and one genetic sample collected from the processed meat of an unknown species was confirmed to be Rhinobatos lionotus representing the first verified report from Bangladesh., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 225, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Last, P. R., Seret, B. & Naylor, G. J. (2019) Description of Rhinobatos ranongensis sp. nov. (Rhinopristiformes: Rhinobatidae) from the Andaman Sea and Bay of Bengal with a review of its northern Indian Ocean congeners. Zootaxa, 4576 (2), 257 - 287. https: // doi. org / 10.11646 / zootaxa. 4576.2.3"]}
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- 2021
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50. Urogymnus J.P.Muller & Henle 1837
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Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti, and Hossain, Nazia
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Dasyatidae ,Myliobatiformes ,Animalia ,Biodiversity ,Chordata ,Taxonomy ,Elasmobranchii ,Urogymnus - Abstract
Genus Urogymnus Urogymnus granulatus (Figure 11) was reported for the first time from Bangladesh, based on three specimens from one study site. NADH2 sequence analysis from one of the three specimens supported this identification. This confirms that four species of Urogymnus occur in Bangladeshi waters; U. asperrimus, U. granulatus (likely previously misidentified as U. Africana) ( Hoq et al. 2011; Roy et al. 2015), U. lobistoma and U. polylepis, especially around mangrove areas in the southwestern region. Urogymnus polylepis (Figure 12) has been recorded in news articles but has not yet been added to checklists. Hence, while this is not considered a new record for Bangladesh, it is the first verified record from 52 specimens., Published as part of Haque, Alifa Bintha, White, William T., Cavanagh, Rachel D., Biswas, Aparna Riti & Hossain, Nazia, 2021, New records of elasmobranchs in the Bay of Bengal, Bangladesh: further taxonomic research is essential, pp. 211-230 in Zootaxa 5027 (2) on page 223, DOI: 10.11646/zootaxa.5027.2.4, http://zenodo.org/record/5448230, {"references":["Hoq, M. E., Haroon, A. Y. & Hussain, M. G. (2011) Shark fisheries in the Bay of Bengal, Bangladesh: Status and potentialities. Support to Sustainable Management of the BOBLME Project, Bangladesh Fisheries Research Institute, 76 pp.","Roy, B. J., Singha, N. K., Rhaman, M. G. & Ali, A. H. M. H. (2015) Status and recorded of sharks and rays in the Bay of Bengal of Bangladesh Region. Brazilian Journal of Biological Sciences, 2 (4), 343 - 367."]}
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- 2021
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