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388 FAO Species Catalogue for Fishery Purposes No. 4, Vol. 2 3. LIST OF NOMI NAL SPECIES The following list gives information (horizontally) in the order (i) the scientific name as it originally appeared, in alphabetical order according to the specific name; (ii) the author(s); (iii) date of publication; and (iv) present allocation. NOMINAL SPECIES PRESENT ALLOCATION ANCISTROCHEIRIDAE Pfeffer, 1912 Enoploteuthis lesueurii d’Orbigny, 1842 Ancistrocheirus lesueurii ARCHITEUTHIDAE Pfeffer, 1900 Architeuthis dux Steenstrup, 1857 Architeuthis dux Megateuthis martensi Hilgendorf, 1880 Architeuthis martensi Mouchezis sanctipauli Velain, 1877 Architeuthis sanctipauli AUSTRALITEUTHIDAE Lu, 2005 Australiteuthis aldrichi Lu, 2005 Australiteuthis aldrichi BATHYTEUTHIDAE Pfeffer, 1900 Bathyteuthis abyssicola Hoyle, 1885 Bathyteuthis abyssicola Bathyteuthis bacidifera Roper, 1968 Bathyteuthis bacidifera Bathyteuthis berryi Roper, 1968 Bathyteuthis berryi BATOTEUTHIDAE Young and Roper, 1968 Batoteuthis skolops Young and Roper, 1968 Batoteuthis skolops BRACHIOTEUTHIDAE Pfeffer, 1908 Brachioteuthis beanii Verrill, 1881 Brachioteuthis beanii Brachioteuthis bowmani Russell, 1909 Brachioteuthis bowmani Brachioteuthis picta Chun, 1910 Brachioteuthis picta Slosarczykovia circumantarctica, Lipinski 2001 Slosarczykovia circumantarctica Slosarczykovia linkovskyi, Lipinski, 2001 Brachioteuthis linkovskyi Tracheloteuthis behni Steenstrup, 1882 Brachioteuthis behnii Tracheloteuthis riisei Steenstrup, 1882 Brachioteuthis riisei CHIROTEUTHIDAE Gray, 1849 Asperoteuthis lui Salcedo-Vargas 1999 Asperoteuthis lui Asperoteuthis mangoldae Young, Vecchione and Roper, 2007 Asperoteuthis mangoldae Chiropsis mega Joubin, 1932 Chiroteuthis mega Chiroteuthis acanthoderma Lu, 1977 Chiroteuthis acanthoderma Chiroteuthis calyx Young, 1972 Chiroteuthis calyx Chiroteuthis imperator Chun, 1908 Chiroteuthis imperator Chiroteuthis joubini, Voss 1967 Chiroteuthis joubini Chiroteuthis picteti Joubin, 1894 Chiroteuthis picteti Chiroteuthis spoeli, Salcedo-Vargas, 1996 Chiroteuthis spoeli Doratopsis exophthalmica Chun, 1908 Planctoteuthis exophthalmica Doratopsis lippula Chun, 1908 Planctoteuthis lippula Loligopsis bonplandi Verany, 1839 Grimalditeuthis bonplandi Loligopsis veranii Ferussac, 1834 Chiroteuthis veranyi Mastigoteuthis levimana Lönnberg, 1896 Planctoteuthis levimana Valbyteuthis danae Joubin, 1931 Planctoteuthis danae Cephalopods of the World 389 NOMINAL SPECIES PRESENT ALLOCATION Valbyteuthis oligobessa Young, 1972 Planctoteuthis oligobessa CHTENOPTERYGIDAE Grimpe, 1922 Chtenopteryx canariensis Salcedo-Vargas and Guerrero-Kommritz, 2000 Chtenopteryx canariensis Chtenopteryx sepioloides Rancurel, 1970 Chtenopteryx sepioloides Sepioteuthis sicula Verany, 1851 Chtenopteryx sicula CRANCHIIDAE Prosch, 1847 Ascocranchia joubini Voss, 1962 Helicocranchia joubini Bathothauma lyromma Chun, 1906 Bathothauma lyromma Belonella borealis Nesis, 1972 Taonius borealis Carymoteuthis oceanica Voss, 1960 Megalocranchia oceanica Cranchia maculata Leach, 1817 Teuthowenia maculata Cranchia (Owenia) megalops Prosch, 1847 Teuthowenia megalops Cranchia scabra Leach, 1817 Cranchia scabra Crystalloteuthis glacialis Chun, 1906 Galiteuthis glacialis Desmoteuthis pellucida Chun, 1910 Teuthowenia pellucida Drechselia danae Joubin, 1931 Leachia danae Egea inermis Joubin, 1933 Egea inermis Galiteuthis armata Joubin, 1898 Galiteuthis armata Galiteuthis phyllura Berry, 1911 Galiteuthis phyllura Helicocranchia pfefferi Massy, 1907 Helicocranchia pfefferi Leachia cyclura Lesueur, 1821 Leachia cyclura Leachia dislocata Young, 1972 Leachia dislocata Leachia reinhardti Steenstrup, 1856 Liocranchia reinhardti Liguriella podophthalma Issel, 1908 Liguriella podophthalma Liocranchia valdiviae Chun 1910 Liocranchia valdiviae Loligo pavo Lesueur, 1821 Taonius pavo Megalocranchia maxima Pfeffer, 1884 Megalocranchia maxima Megalocranchia papillata Voss, 1960 Helicocranchia papillata Mesonychoteuthis hamiltoni Robson, 1925 Mesonychoteuthis hamiltoni Pyrgopsis atlantica Degner, 1925 Leachia atlantica Pyrgopsis lemur Berry, 1920 Leachia lemur Sandalops melancholicus Chun, 1906 Sandalops melancholicus Taonidium pacificum Robson, 1948 Galiteuthis pacifica Taonius suhmi Hoyle, 1886 Galiteuthis suhmi Toxeuma belone Chun, 1906 Taonius belone Zygaenopsis pacifica Issel, 1908 Leachia pacifica CYCLOTEUTHIDAE Naef, 1923 Cycloteuthis akimushkini Filippova, 1968 Cycloteuthis akimushkini Cycloteuthis sirventi Joubin, 1919 Cycloteuthis sirventi Discoteuthis discus Young and Roper, 1969 Discoteuthis discus Discoteuthis laciniosa Young and Roper, 1969 Discoteuthis laciniosa 390 FAO Species Catalogue for Fishery Purposes No. 4, Vol. 2 NOMINAL SPECIES PRESENT ALLOCATION ENOPLOTEUTHIDAE Pfeffer, 1900 Abralia (Micrabralia) affinis Pfeffer, 1912 Abraliopsis affinis Abralia andamanica Goodrich, 1896 Abralia andamanica Abralia astrolineata Berry, 1914 Abralia astrolineata Abralia astrostricta Berry, 1909 Abralia astrostricta Abralia fasciolata Tsuchiya, 1991 Abralia fasciolata Abralia gilchristi Robson, 1924 Abralia gilchristi Abralia grimpei Voss, 1959 Abralia grimpei Abralia heminuchalis Burgess, 1992 Abralia heminuchalis Abralia lineata Goodrich, 1896 Abraliopsis lineata Abralia marisarabica Okutani, 1983 Abralia marisarabica Abralia multihamata Sasaki, 1929 Abralia multihamata Abralia omiae Hidaka and Kubodera, 2000 Abralia omiae Abralia redfieldi Voss, 1955 Abralia redfieldi Abralia renschi Grimpe, 1931 Abralia renschi Abralia robsoni Grimpe, 1931 Abralia robsoni Abralia siedleckyi Lipinski, 1983 Abralia siedleckyi Abralia similis Okutani and Tsuchiya, 1987 Abralia similis Abralia spaercki Grimpe, 1931 Abralia spaercki Abralia steindachneri Weindl, 1912 Abralia steindachneri Abralia trigonura Berry, 1913 Abralia trigonura Abraliopsis atlantica Nesis, 1982 Abraliopsis atlantica Abraliopsis chuni Nesis, 1982 Abraliopsis chuni Abraliopsis falco Young, 1972 Abraliopsis falco Abraliopsis felis McGowan and Okutani, 1968 Abraliopsis felis Abraliopsis pacificus Tsuchiya and Okutani, 1990 Abraliopsis pacificus Abraliopsis scintillans Berry, 1911 Watasenia scintillans Abraliopsis tui Riddell, 1985 Abraliopsis tui Enoploteuthis anapsis Roper, 1964 Enoploteuthis anapsis Enoploteuthis chunii Ishikawa, 1914 Enoploteuthis chunii Enoploteuthis dubia Adam, 1960 Abralia dubia Enoploteuthis galaxias Berry, 1918 Enoploteuthis galaxias Enoploteuthis higginsi Burgess, 1982 Enoploteuthis higginsi Enoploteuthis hoylei Pfeffer, 1884 Abraliopsis hoylei Enoploteuthis jonesi Burgess, 1982 Enoploteuthis jonesi Enoploteuthis leptura magnoceani Nesis, 1982 Enoploteuthis leptura magnoceani Enoploteuthis migrato Burgess, 1982 Enoploteuthis obliqua Enoploteuthis migratory Rancurel, 1970 Enoploteuthis reticulata Enoploteuthis octolineata Burgess, 1982 Enoploteuthis octolineata Enoploteuthis semilineata Alexeyev, 1994 Enoploteuthis semilineata Enoploteuthis veranyi Rüppel, 1844 Abralia veranyi Cephalopods of the World 391 NOMINAL SPECIES PRESENT ALLOCATION Loligo lepturo Leach, 1817 Enoploteuthis leptura leptura Onychoteuthis armatus Quoy and Gaimard, 1832 Abralia armata Onychoteuthis morisi Verany, 1839 Abraliopsis morisii GONATIDAE Hoyle, 1886 Berryteuthis magister nipponensis Okutani and Kubodera, 1987 Berryteuthis magister nipponensis Berryteuthis magister shevtsovi Katugin, 2000 Berryteuthis magister shevtsovi Eogonatus tinro Nesis, 1972 Eogonatus tinro Gonatopisis okutanii Nesis, 1972 Gonatopisis okutanii Gonatopsis borealis Sasaki, 1923 Gonatopsis borealis Gonatopsis japonicus Okiyama, 1969 Gonatopsis japonicus Gonatopsis makko Okutani and Nemoto, 1964 Gonatopsis makko Gonatopsis octopedatus Sasaki, 1920 Gonatopsis octopedatus Gonatus anonychus Pearcy and Voss, 1963 Berryteuthis anonychus Gonatus antarcticus Lönnberg, 1898 Gonatus antarcticus Gonatus berryi Naef, 1923 Gonatus berryi Gonatus californiensis Young, 1972 Gonatus californiensis Gonatus madokai Kubodera and Okutani, 1977 Gonatus madokai Gonatus magister Berry, 1913 Berryteuthis magister Gonatus onyx Young, 1972 Gonatus onyx Gonatus oregonensis Jefferts, 1985 Gonatus oregonensis Gonatus pyros Young, 1972 Gonatus pyros Gonatus steenstrupi Kristensen, 1981 Gonatus steenstrupi Gonatus ursabrunae Jefferts, 1985 Gonatus ursabrunae Onychoteuthis fabricii Lichtenstein, 1818 Gonatus fabricii Onychoteuthis kamtschatica Middendorff, 1849 Gonatus kamtschaticus HISTIOTEUTHIDAE Verrill, 1881 Calliteuthis celetaria celetaria Voss, 1960 Histioteuthis celetaria celetaria Calliteuthis celetaria pacifica Voss, 1962 Histioteuthis celetaria pacifica Calliteuthis corona Voss and Voss, 1962 Histioteuthis corona corona Calliteuthis (Meleagroteuthis) heteropsis Berry, 1913 Histioteuthis heteropsis Calliteuthis inermis Taki, 1964 Histioteuthis corona inermis Calliteuthis meleagroteuthis Chun, 1910 Histioteuthis meleagroteuthis Calliteuthis miranda Berry, 1918 Histioteuthis miranda Calliteuthis reversa Verrill, 1880 Histioteuthis reversa Cranchia bonnellii Ferussac, 1834 Histioteuthis bonnellii Histiopsis atlantica Hoyle, 1885 Histioteuthis atlantica Histiopsis hoylei Goodrich, 1896 Histioteuthis hoylei Histiothauma oceani Robson, 1948 Histioteuthis oceani Histioteuthis corona berryi Voss, 1969 Histioteuthis corona berryi Histioteuthis corona cerasina Nesis, 1971 Histioteuthis corona cerasina Histioteuthis eltaninae Voss, 1969 Histioteuthis eltaninae 392 FAO Species Catalogue for Fishery Purposes No. 4, Vol. 2 NOMINAL SPECIES PRESENT ALLOCATION Histioteuthis macrohista Voss, 1969 Histioteuthis macrohista Stigmatoteuthis
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    Notes MARINE MAMMAL SCIENCE, 00(00): 00–00 (Month 2018) VC 2018 Society for Marine Mammalogy DOI: 10.1111/mms.12507 Stomach contents and diel diving behavior of melon-headed whales (Peponocephala electra) in Hawaiian waters 1 KRISTI L. WEST, Department of Human Nutrition, Food and Animal Science, College of Tropical Agriculture and Human Resources, Agricultural Sciences 216, 1955 East-West Road, University of Hawai‘i at Manoa, Honolulu, Hawai‘i 96822, U.S.A.; WILLIAM A. WALKER, Marine Mammal Laboratory, National Marine Fisheries Service, NOAA, 7600 Sand Point Way N.E., Seattle, Washington 98115, U.S.A.; ROBIN W. BAIRD,DANIEL L. WEBSTER, and GREGORY S. SCHORR, Cascadia Research Collective, 218 1=2 W. 4th Avenue, Olympia, Washington 98501, U.S.A. Knowledge of the diet and diving behavior of a species is crucial for understand- ing its behavior and ecology, and also has relevance to assessing the impact of poten- tial changes in behavior or spatial use. Assessing diet for many species of cetaceans is difficult, given that most foraging occurs far below the surface and that stomach contents of stranded animals are rarely available. Very little information on food habits or the diving behavior of melon-headed whales (Peponocephala electra)isavail- able from any region of the world. Although there is a paucity of knowledge on melon-headed whales, more is known about them in Hawaiian waters than anywhere else in the world (Aschettino et al. 2012, Woodworth et al. 2012, Baird 2016). In Hawai‘i, two populations of melon-headed whales are recognized, a Hawaiian Islands population estimated to be close to 5,000 individuals that travels offshore and among the islands, and a smaller, inshore population estimated to be about 450 individuals that is found off Hawai‘i Island and known as the Kohala resident population (Aschettino 2010, Aschettino et al.
  • Environmental Effects on Cephalopod Population Dynamics: Implications for Management of Fisheries

    Environmental Effects on Cephalopod Population Dynamics: Implications for Management of Fisheries

    Advances in Cephalopod Science:Biology, Ecology, Cultivation and Fisheries,Vol 67 (2014) Provided for non-commercial research and educational use only. Not for reproduction, distribution or commercial use. This chapter was originally published in the book Advances in Marine Biology, Vol. 67 published by Elsevier, and the attached copy is provided by Elsevier for the author's benefit and for the benefit of the author's institution, for non-commercial research and educational use including without limitation use in instruction at your institution, sending it to specific colleagues who know you, and providing a copy to your institution’s administrator. All other uses, reproduction and distribution, including without limitation commercial reprints, selling or licensing copies or access, or posting on open internet sites, your personal or institution’s website or repository, are prohibited. For exceptions, permission may be sought for such use through Elsevier's permissions site at: http://www.elsevier.com/locate/permissionusematerial From: Paul G.K. Rodhouse, Graham J. Pierce, Owen C. Nichols, Warwick H.H. Sauer, Alexander I. Arkhipkin, Vladimir V. Laptikhovsky, Marek R. Lipiński, Jorge E. Ramos, Michaël Gras, Hideaki Kidokoro, Kazuhiro Sadayasu, João Pereira, Evgenia Lefkaditou, Cristina Pita, Maria Gasalla, Manuel Haimovici, Mitsuo Sakai and Nicola Downey. Environmental Effects on Cephalopod Population Dynamics: Implications for Management of Fisheries. In Erica A.G. Vidal, editor: Advances in Marine Biology, Vol. 67, Oxford: United Kingdom, 2014, pp. 99-233. ISBN: 978-0-12-800287-2 © Copyright 2014 Elsevier Ltd. Academic Press Advances in CephalopodAuthor's Science:Biology, personal Ecology, copy Cultivation and Fisheries,Vol 67 (2014) CHAPTER TWO Environmental Effects on Cephalopod Population Dynamics: Implications for Management of Fisheries Paul G.K.
  • Vertical Distribution Patterns of Cephalopods in the Northern Gulf of Mexico

    Vertical Distribution Patterns of Cephalopods in the Northern Gulf of Mexico

    fmars-07-00047 February 20, 2020 Time: 15:34 # 1 ORIGINAL RESEARCH published: 21 February 2020 doi: 10.3389/fmars.2020.00047 Vertical Distribution Patterns of Cephalopods in the Northern Gulf of Mexico Heather Judkins1* and Michael Vecchione2 1 Department of Biological Sciences, University of South Florida St. Petersburg, St. Petersburg, FL, United States, 2 NMFS National Systematics Laboratory, National Museum of Natural History, Smithsonian Institution, Washington, DC, United States Cephalopods are important in midwater ecosystems of the Gulf of Mexico (GOM) as both predator and prey. Vertical distribution and migration patterns (both diel and ontogenic) are not known for the majority of deep-water cephalopods. These varying patterns are of interest as they have the potential to contribute to the movement of large amounts of nutrients and contaminants through the water column during diel migrations. This can be of particular importance if the migration traverses a discrete layer with particular properties, as happened with the deep-water oil plume located between 1000 and 1400 m during the Deepwater Horizon (DWH) oil spill. Two recent studies focusing on the deep-water column of the GOM [2011 Offshore Nekton Sampling and Edited by: Jose Angel Alvarez Perez, Analysis Program (ONSAP) and 2015–2018 Deep Pelagic Nekton Dynamics of the Gulf Universidade do Vale do Itajaí, Brazil of Mexico (DEEPEND)] program, produced a combined dataset of over 12,500 midwater Reviewed by: cephalopod records for the northern GOM region. We summarize vertical distribution Helena Passeri Lavrado, 2 Federal University of Rio de Janeiro, patterns of cephalopods from the cruises that utilized a 10 m Multiple Opening/Closing Brazil Net and Environmental Sensing System (MOC10).