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Hoshino, Koichi, Kosaka, Kunpei, Sawada, Kota, Kiyota, Masashi (2022): Identification of the Commercially Important Oreosomatid Fish (Zeiformes: Teleostei) of the Emperor Seamounts, with Comments on Diagnostic Characters of the Species. Species Diversity 27 (1): 1-13, DOI: 10.12782/specdiv.27.1, URL: http://dx.doi.org/10.12782/specdiv.27.1

Unidentified opistognathid. Lissner and Dorsey (1986) observed from a manned submersible a jawfish they were unable to identify at Tanner��� Cortes Bank, southern California., Published as part of Love, Milton S., Bizzarro, Joseph J., Cornthwaite, Maria, Frable, Benjamin W. & Maslenikov, Katherine P., 2021, Checklist of marine and estuarine fishes from the Alaska-Yukon Border, Beaufort Sea, to Cabo San Lucas, Mexico, pp. 1-285 in Zootaxa 5053 (1) on page 150, DOI: 10.11646/zootaxa.5053.1.1, http://zenodo.org/record/5578008, {"references":["Lissner, A. L. & Dorsey, J. H. (1986) Deep-water biological assemblages of a hard-bottom bank-ridge complex of the southern California continental borderland. Bulletin of the Southern California Academy of Sciences, 85, 87 - 101."]}

Zenopsis nebulosa (Temminck & Schlegel, 1845). Mirror Dory. To 70 cm (27.6 in) TL (Roberts et al. 2015). Indo-Pacific (Fricke et al. 2020); western Pacific Ocean north to Peter the Great Bay, Sea of Japan (Kim and Milovankin 2019); central and southern California (Eschmeyer and Herald 1983) to Chile (Peque��o 1989). Off-bottom pelagic (Parin and Pakhorukov 2003). Depth: 30���800 m (100���2,624 ft) (min.: Fitch and Lavenberg 1968; max.: Nakabo in Nakabo 2002). We note that some records of this species may have been confused with the recently described Zenopsis filimentosa Kai and Tashiro, 2019., Published as part of Love, Milton S., Bizzarro, Joseph J., Cornthwaite, Maria, Frable, Benjamin W. & Maslenikov, Katherine P., 2021, Checklist of marine and estuarine fishes from the Alaska-Yukon Border, Beaufort Sea, to Cabo San Lucas, Mexico, pp. 1-285 in Zootaxa 5053 (1) on page 102, DOI: 10.11646/zootaxa.5053.1.1, http://zenodo.org/record/5578008, {"references":["Roberts, C. D., Stewart, A. L. & Struthers, C. D. (Eds.). (2015) The Fishes of New Zealand. Te Papa Press, Wellington.","Fricke, R., Eschmeyer, W. N. & van der Laan, R. (Eds). 2020. Eschmeyer's Catalog of Fishes: Genera, Species, Reference. Available from: http: // researcharchive. calacademy. org / research / ichthyology / catalog / fishcatmain. asp (accessed 17 April 2021).","Kim, L. N. & Milovankin, P. G. (2019) On new finding of mirror dory Zenopsis nebulosa in Peter the Great Bay (Japan Sea). Izvestiya TINRO, 197, 148 - 151 [In Russian.] https: // doi. org / 10.26428 / 1606 - 9919 - 2019 - 197 - 148 - 151","Eschmeyer, W. N. & Herald, E. S. (1983) A Field Guide to Pacific Coast Fishes of North America from the Gulf of Alaska to Baja California. Houghton Mifflin, Boston.","Pequeno R., G. (1989) Peces de Chile lista sistematica revisada y comentada. Revista de Biologia Marina y Oceanografia, 24, 1 - 132.","Fitch, J. E. & Lavenberg, R. J. (1968) Deep-Water Fishes of California. California Natural History Guides, No. 25, University of California Press, Berkeley.","Nakabo, T. (Ed.). (2002) Fishes of Japan with Pictorial Keys to the Species. Tokai University Press, Tokyo."]}

Allocyttus folletti Myers, 1960. Oxeye Oreo. To 47 cm (18.5 in) TL (Nishida et al. 2016). Honshu, Japan, to Bering Sea and Gulf of Alaska (Mecklenburg et al. 2002), to near Point Arguello (34��36���N, 120��40���W), central California (Personal communication: Scripps Institution of Oceanography Fish Collection, La Jolla, California). Depth: surface to 1,800 m (5,905 ft) (Tokranov et al. 2003). Prejuveniles taken near surface offshore and midocean. Records of Allocyttus verrucosus from California are treated as identical with A. folletti (Mecklenburg et al. 2002)., Published as part of Love, Milton S., Bizzarro, Joseph J., Cornthwaite, Maria, Frable, Benjamin W. & Maslenikov, Katherine P., 2021, Checklist of marine and estuarine fishes from the Alaska-Yukon Border, Beaufort Sea, to Cabo San Lucas, Mexico, pp. 1-285 in Zootaxa 5053 (1) on page 101, DOI: 10.11646/zootaxa.5053.1.1, http://zenodo.org/record/5578008, {"references":["Nishida, K., Murakami, C., Yonezaki, S., Miyamoto, M., Okuda, T. & Kiyota, M. (2016) Prey use by three deep-sea fishes in the Emperor Seamount waters, North Pacific Ocean, as revealed by stomach contents and stable isotope analyses. Environmental Biology of Fishes, 99, 335 - 349. https: // doi. org / 10.1007 / s 10641 - 016 - 0477 - x","Tokranov, A. M. & Orlov, A. M. (2003) On the distribution and biology of roughscale sole Clidoderma asperrimum (Temminck et Schlegel, 1846) in the Pacific waters off the northern Kuril Islands and southeastern Kamchatka. Bulletin of the Sea Fisheries Institute, Issue 2, 67 - 80."]}

This checklist of the Mediterranean fishes of Israel enumerates 469 species which is an addition of 62 species since the previous checklist of 2005. This new checklist includes 58 Condrichthys and 411 Osteicthys species. Most newly-recorded species are of Red Sea origin (Lessepsian migrants)—38 species, 25 species are from previously poorly investigated habitats, mainly deep water, while two species reached the Mediterranean most likely by ballast water and two are aquaculture escapees. The dramatic increase in the number of Lessepsian migrants (an average of 2.5 species per year) is most likely due to the increased water influx between the Red Sea and the Mediterranean, following the recent opening of the new parallel, 72 km, “new canal” and the enlargement of other parts of the Suez Canal.

This paper reports a new record of Zenion hololepis (Goode & Bean, 1896) from Indian waters. The species was collected during an exploratory deep-sea fishery survey onboard FORV Sagar Sampada off the Andaman Islands at a depth of 314 m using a High-Speed Demersal Trawl-Crustacean Version (HSDT-CV) on 25 November 2017. Keywords: Andaman Sea, Deep-Sea, Dwarf dory, Exploratory survey

Zeus faber Linnaeus 1758 ���John dory Taxonomy. First record from Lebanon as Zeus faber, L. by Gruvel (1931: 109); subsequently recorded as Zeus faber Linnaeus 1758 by George et al. (1964: 16); as Zeus faber Linnaeus by Mouneimn�� (1977: 62); as Zeus faber Linnaeus 1758 by Mouneimn�� (2002: 109). Material in collection: AUBM. Distribution. Western Baltic Sea, North Sea, Mediterranean Sea, Sea of Marmara, Black Sea, eastern Atlantic; Indo-West Pacific. Conservation. IUCN: Global (DD: 20 May 2013); Med. (LC: 15 November 2007). Capture and threats: FIB, unknown. Occurrence: Rare. Low priority for conservation action. Non-indigenous species, Published as part of Bariche, Michel & Fricke, Ronald, 2020, The marine ichthyofauna of Lebanon: an annotated checklist, history, biogeography, and conservation status, pp. 1-157 in Zootaxa 4775 (1) on page 116, DOI: 10.11646/zootaxa.4775.1.1, http://zenodo.org/record/3983887, {"references":["Gruvel, A. (1931) Les Etats de Syrie. Richesses marines et fluviales. Exploitation actuelle-Avenir. Societe d'Editions Geographiques, Maritimes et Coloniale, 453 pp.","George, C. J., Athanassiou, V. A. & Boulos, I. (1964) The fishes of the coastal waters of Lebanon. Miscellaneous Papers in the Natural Sciences. The American University of Beirut, 4, 1 - 24.","Mouneimne, N. (1977) Liste des poissons de la cote du Liban (Mediterranee orientale). Cybium, 3 (1), 37 - 66.","Mouneimne, N. (2002) Poissons marins du Liban et de la Mediterranee orientale. INCAM-EU / CNRS Lebanon, Beyrouth, 271 pp."]}

This is an annotated checklist of the marine fish species of Lebanon (Levant coast, eastern Mediterranean). It comprises a total of 367 fish species distributed in 159 families and 27 orders, out of which 70 species are non-indigenous and 28 are recorded for the first time from Lebanon. The checklist includes all names and citations of species found in the literature, as well as references to specimens available in museum collections. It also includes an updated zoogeographic distribution and conservation status for each species. Threats were estimated based on surveys and observations made over the last two decades; broadly categorized conservation actions were also suggested.

The Zeiformes (dories) are mid-water or deep (to 1000 m) marine acanthomorph fishes with a global, circumtropical, and circumtemperate distribution. Some species have a near-worldwide distribution, while others appear to be regional endemics, e.g., near New Zealand. Six families, 16 genera, and 33 species are currently recognized as valid. Relationships among them, however, remain unsettled, especially in light of recent proposals concerning the phylogenetic placement of zeiforms within the Paracanthopterygii rather than allied with beryciforms or percomorphs. The present study uses both morphological and molecular characters to investigate zeiform interrelationships given their revised phylogenetic placement and attendant changes to their close outgroups. Results indicate that revised outgroups affected the phylogenetic conclusions, especially those based on morphology. All analyses recovered monophyletic Zeidae, Cyttidae, and Oreosomatidae. Zeniontidae were recovered as polyphyletic, with the clade Capr...

The Chilean fishes of the order Zeiformes are rare in museum collections, the lack of scientific expeditions to the submarine ridge and the scarcity of new specimens records in Chilean shelves, as well as the lack of biological studies, probably accounts for its apparent rarity. In the last two decades, fishes of the order Zeiformes in Chile have undergone major changes in their taxonomic categories and in the record of new species. In Chile, there are five families, 7 genera and 11 species. They live in benthic and bathypelagic realms and are distributed at depths of 30 to 1500 m. Also, the literature of these species, is scattered, hindering their taxonomic and systematic knowledge, which makes difficult their study and better understanding as a group. It also prevents progress in such important aspects like their phylogenetic relationships, the state of vulnerability of their populations and other biological aspects. In order to contribute to the knowledge and its identification, a bibliographical compilation and a tentative illustrated identification key that unifies all the existing information in a single document, is presented. This may constitute a new tool to contribute to the growing interest in biodiversity studies in the south eastern Pacific Ocean. Normal 0 21 false false false ES X-NONE X-NONE /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Tabla normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin-top:0cm; mso-para-margin-right:0cm; mso-para-margin-bottom:10.0pt; mso-para-margin-left:0cm; line-height:115%; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin;}

Zeiformes Zeidae Zenopsis conchifer (Lowe) Bolbosoma turbinella Corynosoma australe Corynosoma cetaceum

Zeiformes Zeidae Zenopsis conchifer (Lowe) Bolbosoma turbinella Corynosoma australe Corynosoma cetaceum, Published as part of Hern��ndez-Orts, Jes��s S., Kuchta, Roman, Semenas, Liliana, Crespo, Enrique A., Gonz��lez, Ra��l A. & Aznar, Francisco J., 2019, An annotated list of the Acanthocephala from Argentina, pp. 1-64 in Zootaxa 4663 (1) on pages 43-44, DOI: 10.11646/zootaxa.4663.1.1, http://zenodo.org/record/3772372

A detailed list of acanthocephalans from Argentina was generated based on 205 published records. The list includes 52 named and 35 undetermined species of Acanthocephala infecting 6 species of invertebrate (2 amphipods, 3 decapods and 1 insect) and 155 species of vertebrate (one cartilaginous fish, 95 bony fishes, 10 amphibians, 3 reptiles, 13 birds and 33 mammals) host species in the Argentinean territory. The present list contains information on the invertebrate and vertebrate host(s), site of infection, developmental stage and locality(ies) of the acanthocephalans listed and references. For some species of acanthocephalans, information about repositories of the type material, voucher specimens, and DNA sequences of individual taxa are also presented. Finally, a host-Acanthocephala list is also provided. The data compiled revealed considerable gaps in the knowledge of the diversity, taxonomy, distribution, and life cycles of the acanthocephalans from Argentina. Fil: Hernández-Orts, Jesús S.. Universidad Nacional del Comahue. Centro de Investigación Aplicada y Transferencia Tecnológica en Recursos Marinos "Almirante Storni". - Provincia de Río Negro. Ministerio de Agricultura, Ganadería y Pesca. Centro de Investigación Aplicada y Transferencia Tecnológica en Recursos Marinos "Almirante Storni". Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Centro Nacional Patagónico. Centro de Investigación Aplicada y Transferencia Tecnológica en Recursos Marinos "Almirante Storni"; Argentina Fil: Kuchta, Roman. Biology Centre Of The Academy Of Sciences Of The Czech Republic. Institute Of Parasitology. Laboratory Of Fish Protistology; República Checa Fil: Semenas, Liliana. Lab de Parasitologã­a-inibioma (conicet); Argentina Fil: Crespo, Enrique Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Centro Nacional Patagónico. Centro para el Estudio de Sistemas Marinos; Argentina Fil: González, Raul Alberto Candido. Universidad Nacional del Comahue; Argentina Fil: Aznar, Francisco J.. Universidad de Valencia; España

Cyttomimus affinis Weber 1913 —False dory Status at New Ireland. New record, based on NTUM material (1 specimen, St. CP 4419-7, northeast of New Hanover). Distribution and habitat. New Ireland: 1.—General distribution: antiequatorial in western Pacific: South China Sea to southern Japan; northern Australia and Papua New Guina to New Caledonia. Bathydemersal, 200– 366 m depth. Marine., Published as part of Andréfouët, Serge, Chen, Wei-Jen, Kinch, Jeff, Mana, Ralph, Russell, Barry C., Tully, Dean & White, William T., 2019, Checklist of the marine and estuarine fishes of New Ireland Province, Papua New Guinea, western Pacific Ocean, with 810 new records, pp. 1-360 in Zootaxa 4588 (1) on page 88, DOI: 10.11646/zootaxa.4588.1.1, http://zenodo.org/record/2988163

Zenopsis nebulosa (Temminck & Schlegel 1845) —Mirror dory Status at New Ireland. New record, based on NTUM 12429 (1 specimen, 177.5 mm TL, St. CP 4255-16, 11.2 km northwest of Kavieng). Distribution and habitat. New Ireland: 2.—General distribution: antitropical in southeastern Indian Ocean and western Pacific: Japan, Hawaiian Islands, California (U.S.A.); southern Australia, Chesterfield Islands (New Caledonia), New Zealand region. Benthopelagic, 30–800 m depth. Marine., Published as part of Andréfouët, Serge, Chen, Wei-Jen, Kinch, Jeff, Mana, Ralph, Russell, Barry C., Tully, Dean & White, William T., 2019, Checklist of the marine and estuarine fishes of New Ireland Province, Papua New Guinea, western Pacific Ocean, with 810 new records, pp. 1-360 in Zootaxa 4588 (1) on page 88, DOI: 10.11646/zootaxa.4588.1.1, http://zenodo.org/record/2988163

Zenion japonicum Kamohara 1934 —Japanese dory (Fig. 32) Status at New Ireland. New record, based on NTUM material (2 specimens, St. CP 4420-15, CP4420-20, northeast of New Hanover; 2 specimens, St. CP 4421-12-13, northeast of New Hanover; 2 specimens, St. CP 4437- 11-12, northeast of New Hanover; 1 specimen, St. CP 4438-18, northeast of New Hanover; 3 specimens, St. CP 4446-15-17, north of New Hanover; 1 specimen, St. CP 4498-6, north of New Hanover). Distribution and habitat. New Ireland: 1.—General distribution: Pacific Ocean: South China Sea east to Chile, north to southern Japan, south to northern Australia. Bathydemersal, 200–1000 m depth. Marine., Published as part of Andréfouët, Serge, Chen, Wei-Jen, Kinch, Jeff, Mana, Ralph, Russell, Barry C., Tully, Dean & White, William T., 2019, Checklist of the marine and estuarine fishes of New Ireland Province, Papua New Guinea, western Pacific Ocean, with 810 new records, pp. 1-360 in Zootaxa 4588 (1) on page 88, DOI: 10.11646/zootaxa.4588.1.1, http://zenodo.org/record/2988163

Andréfouët, Serge, Chen, Wei-Jen, Kinch, Jeff, Mana, Ralph, Russell, Barry C., Tully, Dean, White, William T. (2019): Checklist of the marine and estuarine fishes of New Ireland Province, Papua New Guinea, western Pacific Ocean, with 810 new records. Zootaxa 4588 (1): 1-360, DOI: https://doi.org/10.11646/zootaxa.4588.1.1

Family † Bajaichthyidae Bannikov & Sorbini 2014 † Bajaichthyidae Bannikov & Sorbini in Bannikov 2014b: 625 (family) † Bajaichthys Sorbini 1983, Published as part of Laan, Richard Van Der, 2018, Family-group names of fossil fishes, pp. 1-167 in European Journal of Taxonomy 466 on page 71, DOI: 10.5852/ejt.2018.466, http://zenodo.org/record/5557557, {"references":["Bannikov A. F. 2014 b. A new genus of the family Palaeocentrotidae (Teleostei, Lampridiformes) from the Oligocene of the Northern Caucasus and comments on other fossil Veliferoidei. Paleontological Journal 48 (6): 624 - 632. [Also in Russian Paleontologicheskii Zhurnal 48 (6): 50 - 58.] https: // doi. org / 10.1134 / S 0031030114060021"]}

Family †Caproberycidae Patterson 1967 †Caproberycinae Patterson 1967: 88 (subfamily) † Caproberyx Regan 1911 †Alloberycinae Gayet 1982a: 28 (subfamily) † Alloberyx Gaudant 1969 † Stichocentridae Gayet 1982a: 32 (family) † Stichocentrus Patterson 1967 [name only, published after 1960, not available, Art. 13.1.1] † Stichocentridae Gayet 1982b: 99 (family) † Stichocentrus Patterson 1967, Published as part of Laan, Richard Van Der, 2018, Family-group names of fossil fishes, pp. 1-167 in European Journal of Taxonomy 466 on page 74, DOI: 10.5852/ejt.2018.466, http://zenodo.org/record/5557557, {"references":["Patterson C. 1967. New Cretaceous berycoid fishes from the Lebanon. Bulletin of the British Museum (Natural History), Geology 14 (3): 67 - 109. Available from https: // www. biodiversitylibrary. org / page / 36368748 [accessed 17 Jul. 2018].","Regan C. T. 1911. The anatomy and classification of the teleostean fishes of the orders Berycomorphi and Xenoberyces. Annals and Magazine of Natural History (series 8) 7 (37): 1 - 9. https: // doi. org / 10.1080 / 00222931108692901","Gayet M. 1982 a. Essai de definition des relations phylogenetiques des Holocentroidea nov. et des Trachichthyoidea nov. (Pisces, Acanthopterygii, Beryciformes). Bulletin du Museum national d'histoire naturelle, Section C, Sciences de la Terre, paleontologie, geologie, mineralogie (serie 4) 4 (1 - 2): 21 - 41. Available from http: // bibliotheques. mnhn. fr / EXPLOITATION / infodoc / ged / viewportalpublished. ashx? eid = IFD _ FICJOINT _ BMCTE _ S 004 _ 1982 _ T 004 _ N 001 _ 1 [accessed 16 Sep. 2018].","Gayet M. 1982 b. Etude anatomique et systematique des acanthopterygiens du Senonien de Sahel-Alma (Liban). Palaeontographia Italica 72: 98 - 136."]}

Family † Cretazeidae Tyler, Bronzi & Ghiandoni 2000 † Cretazeidae Tyler, Bronzi & Ghiandoni 2000: 12 (family) † Cretazeus Tyler, Bronzi & Ghiandoni 2000, Published as part of Laan, Richard Van Der, 2018, Family-group names of fossil fishes, pp. 1-167 in European Journal of Taxonomy 466 on page 72, DOI: 10.5852/ejt.2018.466, http://zenodo.org/record/5557557, {"references":["Tyler J. C., Bronzi P. & Ghiandoni A. 2000. The Cretaceous fishes of Nardo 11 °: A new genus and species of Zeiformes, Cretazeus rinaldii, the earliest record for the order. Bollettino del Museo Civico di Storia Naturale di Verona, Geologia Paleontologia Preistoria 24: 11 - 28."]}

Family Parazenidae McAllister 1968 †Isozenidae Schwarzhans 1996: 427 (family) † Isozen Schwarzhans 2010 [no valid type genus, not available, Art. 11.7.1.1; also name only, published after 1960, not available, Art. 13.1.1], Published as part of Laan, Richard Van Der, 2018, Family-group names of fossil fishes, pp. 1-167 in European Journal of Taxonomy 466 on page 72, DOI: 10.5852/ejt.2018.466, http://zenodo.org/record/5557557, {"references":["Schwarzhans W. 1996. Otoliths from the Maastrichtian of Bavaria and their evolutionary significance. In: Arratia G. & Viohl G. (eds) Mesozoic Fishes Systematics and Paleoecology, Proceedings of the International Meeting Eichstatt 1993: 417 - 431. Verlag Dr. Friedrich Pfeil, Munich."]}

The collection of the Museu Oceanográfico D. Carlos I is a historical specimen, instrument, and document collection that has been housed at the Aquário Vasco da Gama since 1935. The collection is largely the result of several scientific campaigns conducted by Dom Carlos de Bragança between 1896 and 1907. Specifically, the ichthyological collection consists of 675 surviving catalogue records of specimens caught, acquired or offered to D. Carlos I between 1892 to 1907, and includes the type specimen for Odontaspisnasutus Bragança, 1904 (junior synonym of Mitsukurinaowstoni Jordan, 1898), along with several specimens of deep sea species. All specimens were captured in coastal Portuguese waters, and were preserved in alcohol, formalin, or mounted.

In addition to the series of documents that we have been publishing on the "Atlas of Teleostei Otoliths for the Southeastern-Southern Brazilian region", in this volume we present the results of species of the orders Atheriniformes (1 species), Beloniformes (5), Beryciformes (2), Zeiformes (2), Syngnathiformes (2), Scorpaeniformes (9) and Tetraodontiformes (6). Features, measurements and indices were analyzed according to methodology used in anterior series. Three otoliths of each species have been illustrated and photographed whenever possible. The frequency of occurrence of each characteristic was calculated by total length classes (TL), and differences within and among classes have been analyzed applying the multiple χ2 test (significance 0.05). Resumo Em adição à série de documentos que estamos publicando sobre o "Atlas de Otólitos para os peixes Teleósteos da região Sudeste-Sul do Brasil", neste volume apresentamos os resultados obtidos para espécies das ordens Atheriniformes (1 espécie), Beloniformes (5), Beryciformes (2), Zeiformes (2), Syngnathiformes (2), Scorpaeniformes (9) e Tetraodontiformes (6). Foram analisadas as feições, medidas e índices usualmente empregados conforme metodologia apresentada nas séries anteriores. Três otólitos de cada espécie foram desenhados e fotografados, sempre que possível. A frequência de ocorrência de cada característica por classe de comprimento total foi calculada (CT) e as diferenças dentro de cada classe e entre classes foram analisadas aplicando teste χ2 múltiplo (significância 0,05).

Family Oreosomatidae Neocyttus helgae (Holt & Byrne, 1908) ���False boarfish (Fig. 21) One specimen was caught at depths between 1,410 and 1,427 m. Biometry and meristic: 119 mm TL; 100 mm SL; HL: 35.0; PO: 9.0; POL: 7.0; ED: 19.0; IOW: 12.0; PD: 45.0; LD: 50.0; PA: 48.0; LA: 37.0; PP: 40.0; PV: 39.0; LP: 15.0; LV: 15.0; H: 51.0; D: VII+ 33; A: IV+ 31; P: 19; V: I+ 6; Gr: 5 + 18; SLL: 80. Habitat and Distribution: bathypelagic species along the outer continental shelf insular slope and seamounts, strongly associated with habitats of high currents, ripple marks, slopes, reefs of rocks and gorgonians, at depths from 850 to 1,700 m. Northeastern Atlantic, from Iceland to Madeira and northwestern Atlantic. Vulnerability: DD (IUCN), HV (FishBase)., Published as part of Ba��on, Rafael, Arronte, Juan Carlos, Rodriguez-Cabello, Cristina, Pi��eiro, Carmen-Gloria, Punzon, Antonio & Serrano, Alberto, 2016, Commented checklist of marine fishes from the Galicia Bank seamount (NW Spain), pp. 293-333 in Zootaxa 4067 (3) on page 320, DOI: 10.11646/zootaxa.4067.3.2, http://zenodo.org/record/256670

Family Oreosomatidae Neocyttus helgae (Holt & Byrne, 1908) —False boarfish (Fig. 21) One specimen was caught at depths between 1,410 and 1,427 m. Biometry and meristic: 119 mm TL; 100 mm SL; HL: 35.0; PO: 9.0; POL: 7.0; ED: 19.0; IOW: 12.0; PD: 45.0; LD: 50.0; PA: 48.0; LA: 37.0; PP: 40.0; PV: 39.0; LP: 15.0; LV: 15.0; H: 51.0; D: VII+ 33; A: IV+ 31; P: 19; V: I+ 6; Gr: 5 + 18; SLL: 80. Habitat and Distribution: bathypelagic species along the outer continental shelf insular slope and seamounts, strongly associated with habitats of high currents, ripple marks, slopes, reefs of rocks and gorgonians, at depths from 850 to 1,700 m. Northeastern Atlantic, from Iceland to Madeira and northwestern Atlantic. Vulnerability: DD (IUCN), HV (FishBase).

A commented checklist containing 139 species of marine fishes recorded at the Galician Bank seamount is presented. The list is based on nine prospecting and research surveys carried out from 1980 to 2011 with different fishing gears. The ichthyofauna list is diversified in 2 superclasses, 3 classes, 20 orders, 62 families and 113 genera. The largest family is Macrouridae, with 9 species, followed by Moridae, Stomiidae and Sternoptychidae with 7 species each. The trachichthyd Hoplostethus mediterraneus and the morid Lepidion lepidion were the most abundant species. Biogeographically, the Atlantic group, with 113 species (81.3%) is the best represented, followed by the Lusitanian one with 17 species (12.2%). Data on species abundance, as number of individuals caught, size and depth are reported. Habitat, distribution and vulnerability status are commented. Moreover, biometric data and meristic counts are also reported for several species. The results obtained showing a high fish biodiversity and a sensible number of threatened species, strongly support the future declaration of the Galicia Bank as a Marine Protected Area., SI

Acanthomorpha (spiny-rayed fishes) is a clade of teleosts that includes more than 15, 000 extant species. Their deep phylogenetic intrarelationships, first reconstructed using morphological characters, have been extensively revised with molecular data. Moreover, the deep branches of the acanthomorph tree are still largely unresolved, with strong disagreement between studies. Here, we review the historical propositions for acanthomorph deep intrarelationships and attempt to resolve their earliest branching patterns using a new morphological data matrix compiling and revising characters from previous studies. The taxon sampling we use constitutes a first attempt to test all previous hypotheses (molecular and morphological alike) with morphological data only. Our sampling also includes Late Cretaceous fossil taxa, which yield new character state combinations that are absent in extant taxa. Analysis of the complete morphological data matrix yields a new topology that shows remarkable congruence with the well-supported molecular results. Lampridiformes (oarfishes and allies) are the sister to all other acanthomorphs. Gadiformes (cods and allies) and Zeiformes (dories) form a clade with Percopsiformes (trout-perches) and the enigmatic Polymixia (beardfish) and Stylephorus (tube-eye). Ophidiiformes (cusk-eels and allies) and Batrachoidiformes (toadfishes) are nested within Percomorpha, the clade that includes most of modern acanthomorph diversity. These results provide morphological synapomorphies and independent corroboration of clades previously only recovered from molecular data, thereby suggesting the emergence of a congruent picture of acanthomorph deep intrarelationships. Fossil taxa play a critical role in achieving this congruence, since a very different topology is found when they are excluded from the analysis.

Between October and August 1999 five cruises were made on board of R/V Ancón, across the Colombian Caribbean slope, from Punta Estrella (Guajira), near the Venezuelan border, to Cabo Tiburón (Chocó), near the Panamá border. Eighty trawls were made between 200 and 500 m depth with a semi-balloon net. Twelve new records of fishes for the Colombian Caribbean in the orders Beryciformes, Zeiformes, Perciformes and Tetraodontiformes were collected. Plectranthias garrupellus (Serranidae), Benthodesmus tenuis and B. simonyi (Trichiuridae) are new records for the Caribbean; Diplospinnus multistriatus family (Gempylidae) is a new record for the southern Caribbean.

Nakabo T., Bray D.J. and Yamada U. 2006. A new species of Zenopsis (Zeiformes: Zeidae) from the South China Sea, East China Sea and off Western Australia. Memoirs of Museum Victoria 63(1): 91–96. Zenopsis stabilispinosa sp. nov. is described from the South China Sea, East China Sea and off Western Australia. It differs from other species of Zenopsis in having the third anal-fi n spine fused to its pterygiophore, seven dorsal-fi n spines, a short pelvic fi n in adults, and 32 (13+19) vertebrae. A key to the species of Zenopsis is provided.

Family Cyttidae Günther 1860 Cyttina Günther 1860:356, 393 [ref. 1963] (group) Cyttus, Published as part of Laan, Richard Van Der, Eschmeyer, William N. & Fricke, Ronald, 2014, Family-group names of Recent fishes, pp. 1-230 in Zootaxa 3882 (2) on page 79, DOI: 10.11646/zootaxa.3882.1.1, http://zenodo.org/record/7047777, {"references":["Gunther, A. (1860) Catalogue of the fishes in the British Museum. Catalogue of the acanthopterygian fishes in the collection of the British Museum. Squamipinnes, Cirrhitidae, Triglidae, Trachinidae, Sciaenidae, Polynemidae, Sphyraenidae, Trichiuridae, Scombridae, Carangidae, Xiphiidae, Volume 2. British Museum, London, xxi + 548 pp. [13 October, ref. 1963] http: // dx. doi. org / 10.5962 / bhl. title. 8321"]}

Laan, Richard Van Der, Eschmeyer, William N., Fricke, Ronald (2014): Family-group names of Recent fishes. Zootaxa 3882 (2): 1-230, DOI: http://dx.doi.org/10.11646/zootaxa.3882.1.1, URL: http://dx.doi.org/10.11646/zootaxa.3882.1.1

Subfamily Macrurocyttinae Myers 1960 Macrurocyttidae Myers & Storey 1956:19 [ref. 32831] (family) Macrurocyttus [genus inferred from the stem, Article 11.7.1.1; unavailable publication] Macrurocyttidae Myers 1960:90 [ref. 9580] (family) Macrurocyttus, Published as part of Laan, Richard Van Der, Eschmeyer, William N. & Fricke, Ronald, 2014, Family-group names of Recent fishes, pp. 1-230 in Zootaxa 3882 (2) on page 79, DOI: 10.11646/zootaxa.3882.1.1, http://zenodo.org/record/7047777, {"references":["Myers, G. S. (1960) A new zeomorph fish of the family Oreosomatidae from the coast of California, with notes on the family. Stanford Ichthyological Bulletin, 7 (4), 89 - 98. [ref. 9580]","Myers, G. S. & Storey, M. H. (1956) Curatorial practices in zoological research collections 2. System followed in filing specimens of Recent fishes in the natural history museum of Stanford University. Circular Number 6 of the Natural History Museum of Stanford University, i-viii + 1 - 44 [originally compiled in December 1939, emended 1939 - 1956; on the cover of the Circular: \" They are not generally available or for sale \"; work not published according to ICZN Article 8.1] [October, ref. 32831]"]}

Subfamily Parazeninae McAllister 1968 Parazenidae Greenwood, Rosen, Weitzman & Myers 1966:398 [ref. 26856] (family) Parazen [name only, published after 1960, not available, Article 13.1.1] Parazenidae McAllister 1968:109 [ref. 26854] (family) Parazen [name only, but bibliographic reference to the description by Mead 1957:236 [ref. 33068] Article 13.1.2; family name sometimes seen as Parasenidae], Published as part of Laan, Richard Van Der, Eschmeyer, William N. & Fricke, Ronald, 2014, Family-group names of Recent fishes, pp. 1-230 in Zootaxa 3882 (2) on page 79, DOI: 10.11646/zootaxa.3882.1.1, http://zenodo.org/record/7047777, {"references":["McAllister, D. E. (1968) The evolution of branchiostegals and associated opercular, gular, and hyoid bones and the classification of teleostome fishes, living and fossil (Biological Series No. 77). Bulletin National Museum of Canada, 221, 1 - 239. [ref. 26854]","Greenwood, P. H., Rosen, D. E., Weitzman, S. H. & Myers, G. S. (1966) Phyletic studies of teleostean fishes, with a provisional classification of living forms. Bulletin of the American Museum of Natural History, 131 (4), 341 - 455. [ref. 26856] http: // digitallibrary. amnh. org / dspace / handle / 2246 / 1678","Mead, G. W. (1957) An Atlantic record of the zeoid fish Parazen pacificus. Copeia, 1957 (3), 235 - 237. [26 August, ref. 33068] http: // dx. doi. org / 10.2307 / 1439374"]}

Tyler, J. C. & Santini, F. (2005). A phylogeny of the fossil and extant zeiform-like fishes, Upper Cretaceous to Recent, with comments on the putative zeomorph clade (Acanthomorpha). —Zoological Scripta, **, ***–***. A phylogenetic hypothesis based on 107 morphological characters is proposed for a data set of 43 taxa. Thirty-three are extant and belong to the orders Zeiformes (20 taxa), Caproiformes (2), Tetraodontiformes (2), Beryciformes (3), Stephanoberyciformes (3) and Perciformes (3). Ten are fossil taxa previously assigned to the Zeiformes (3), Caproiformes (1), Tetraodontiformes (2), Perciformes (1), and to two extinct Eocene families, the Sorbinipercidae (2) and the Zorzinichthyidae (1). This analysis indicates the existence of a previously undocumented clade formed by the families Sorbinipercidae + Zorzinichthyidae that may be related to the tetraodontiforms. It also shows that two uppermost Palaeocene species, Archaeozeus skamolensis and Protozeus kuehnei, sequentially represent the two most basal lineages of zeiforms, whereas the most ancient known zeiform, the Upper Cretaceous Cretazeus rinaldii, belongs within the clade of extant species in a polytomy with many other zeiform lineages. A reduced data set of 25 mostly zeiform taxa, after the removal of most outgroups, shows at least weak support for Cretazeus being nested deeply within the extant zeiforms; such a placement would indicate that at least six lineages of zeiforms were present during the Upper Cretaceous, and survived the Cretaceous/Tertiary (K/T) extinction to radiate in Cenozoic seas.

SYNOPSIS. The evolution of feeding mechanisms in the ray-finned fishes (Actinopterygii) is a compelling example of transformation in a musculoskeletal complex involving multiple skeletal elements and numerous muscles that power skull motion. Biomechanical models of jaw force and skull kinetics aid our understanding of these complex systems and enable broad comparison of feeding mechanics across taxa. Mechanical models characterize how muscles move skeletal elements by pulling bones around points of rotation in lever mechanisms, or by transmitting force through skeletal elements connected in a linkage. Previous work has focused on the feeding biomechanics of several lineages of fishes, but a broader survey of skull function in the context of quantitative models has not been attempted. This study begins such a survey by examining the diversity of mechanical design of the oral jaws in 35 species of ray-finned fishes with three main objectives: (1) analyze lower jaw lever models in a broad phylogenetic range of taxa, (2) identify the origin and evolutionary patterns of change in the linkage systems that power maxillary rotation and upper jaw protrusion, and (3) analyze patterns of change in feeding design in the context of actinopterygian phylogeny. The mandibular lever is present in virtually all actinopterygians, and the diversity in lower jaw closing force transmission capacity, with mechanical advantage ranging from 0.04 to 0.68, has important functional consequences. A four-bar linkage for maxillary rotation arose in the Amiiformes and persists in various forms in many teleost species. Novel mechanisms for upper jaw protrusion based on this linkage for maxillary rotation have evolved independently at least five times in teleosts. The widespread anterior jaws linkage for jaw protrusion in percomorph fishes arose initially in Zeiformes and subsequently radiated into a wide range of premaxillary protrusion capabilities.