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7. Index of Scientific and Vernacular Names
Cephalopods of the World 249 7. INDEX OF SCIENTIFIC AND VERNACULAR NAMES Explanation of the System Italics : Valid scientific names (double entry by genera and species) Italics : Synonyms, misidentifications and subspecies (double entry by genera and species) ROMAN : Family names ROMAN : Scientific names of divisions, classes, subclasses, orders, suborders and subfamilies Roman : FAO names Roman : Local names 250 FAO Species Catalogue for Fishery Purposes No. 4, Vol. 1 A B Acanthosepion pageorum .....................118 Babbunedda ................................184 Acanthosepion whitleyana ....................128 bandensis, Sepia ..........................72, 138 aculeata, Sepia ............................63–64 bartletti, Blandosepia ........................138 acuminata, Sepia..........................97,137 bartletti, Sepia ............................72,138 adami, Sepia ................................137 bartramii, Ommastrephes .......................18 adhaesa, Solitosepia plangon ..................109 bathyalis, Sepia ..............................138 affinis, Sepia ...............................130 Bathypolypus sponsalis........................191 affinis, Sepiola.......................158–159, 177 Bathyteuthis .................................. 3 African cuttlefish..............................73 baxteri, Blandosepia .........................138 Ajia-kouika .................................. 115 baxteri, Sepia.............................72,138 albatrossae, Euprymna ........................181 belauensis, Nautilus .....................51,53–54 -
Austrorossia Antillensis (Voss, 1955) Fig
192 FAO Species Catalogue for Fishery Purposes No. 4, Vol. 1 Austrorossia antillensis (Voss, 1955) Fig. 273 Rossia antillensis Voss, 1955, Bulletin of Marine Science of the Gulf and Caribbean, 5(2): 86 [type locality: Cuba]. Frequent Synonyms: None. Misidentifications: None. FAO Names: En – Antilles bobtail squid; Fr – Sépiole mignonne; Sp – Globito antillano. tentacular club dorsal view Fig. 273 Austrorossia antillensis Diagnostic Features: Body soft, fleshy. Males mature at smaller sizes and do not grow as large as females. Mantle oval, short, saccular. Dorsal mantle free from head (not fused to head). Fins wide; ovate; short, do not exceed length of mantle anteriorly or posteriorly. Head slightly broader than mantle; eyes large. Male and female arms moderate length. Non-hectocotylized arm sucker arrangement same in both sexes: arm suckers biserial, suckers sparsely arranged; median arm suckers enlarged in males; larger than female arm suckers. Hectocotylus present, both dorsal arms modified: ventrolateral edge of proximal oral surface of hectocotylized arms bordered by swollen glandular crest, inner edge of which forms a deep furrow; glandular crest extends over sucker rows 3 to 8. Club slightly recurved, short; sucker-bearing face convex; tentacular club not expanded, same width as stalk; with 30 to 40 suckers in transverse rows; all suckers of similar minute size; swimming keel of club extends slightly proximal to carpus. Anal flaps well developed. Epirenal bodies and anal pads absent. Ink sac well developed. Colour: Pinkish brown, with scattered dark purple chromatophores; fins pigmented the same as the mantle; dorsal pigmentation extends to ventral surface of fins. Size: Up to 90 mm mantle length. -
Ommastrephidae 199
click for previous page Decapodiformes: Ommastrephidae 199 OMMASTREPHIDAE Flying squids iagnostic characters: Medium- to Dlarge-sized squids. Funnel locking appara- tus with a T-shaped groove. Paralarvae with fused tentacles. Arms with biserial suckers. Four rows of suckers on tentacular clubs (club dactylus with 8 sucker series in Illex). Hooks never present hooks never on arms or clubs. One of the ventral pair of arms present usually hectocotylized in males. Buccal connec- tives attach to dorsal borders of ventral arms. Gladius distinctive, slender. funnel locking apparatus with Habitat, biology, and fisheries: Oceanic and T-shaped groove neritic. This is one of the most widely distributed and conspicuous families of squids in the world. Most species are exploited commercially. Todarodes pacificus makes up the bulk of the squid landings in Japan (up to 600 000 t annually) and may comprise at least 1/2 the annual world catch of cephalopods.In various parts of the West- ern Central Atlantic, 6 species of ommastrephids currently are fished commercially or for bait, or have a potential for exploitation. Ommastrephids are powerful swimmers and some species form large schools. Some neritic species exhibit strong seasonal migrations, wherein they occur in huge numbers in inshore waters where they are accessable to fisheries activities. The large size of most species (commonly 30 to 50 cm total length and up to 120 cm total length) and the heavily mus- cled structure, make them ideal for human con- ventral view sumption. Similar families occurring in the area Onychoteuthidae: tentacular clubs with claw-like hooks; funnel locking apparatus a simple, straight groove. -
Evolution of the Hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and Description of Four New Genera
European Journal of Taxonomy 655: 1–53 ISSN 2118-9773 https://doi.org/10.5852/ejt.2020.655 www.europeanjournaloftaxonomy.eu 2020 · Bello G. This work is licensed under a Creative Commons Attribution License (CC BY 4.0). Monograph urn:lsid:zoobank.org:pub:0042EFAE-2E4F-444B-AFB9-E321D16116E8 Evolution of the hectocotylus in Sepiolinae (Cephalopoda: Sepiolidae) and description of four new genera Giambattista BELLO Arion, Via Colombo 34, 70042 Mola di Bari, Italy. [email protected] urn:lsid:zoobank.org:author:31A50D6F-5126-48D1-B630-FBEDA63944D9 …it is impossible to doubt that the [hectocotylized] arm is thereby adapted to some particular purpose, […] because its transformation occurs in so great a number of species of the class, and bears its peculiar characters in each natural genus. Japetus Steenstrup (1857) Abstract. The subfamily Sepiolinae (Mollusca: Cephalopoda: Sepiolidae), currently containing the genera Sepiola Leach, 1817, Euprymna Steenstrup, 1887, Inioteuthis Verrill, 1881, Rondeletiola Naef, 1921 and Sepietta Naef, 1912, is characterized by the hectocotylization of the left dorsal arm, i.e., its transformation into a copulatory organ thanks to modifications of sucker/pedicel elements. The hectocotylus morphology varies to a great extent across genera and species. In particular, one to several pedicels in its proximal third lose their sucker and become highly and diversely modified in shape to constitute a copulatory apparatus. An evolutionary gradient was observed in the copulatory apparatus morphology, from the simple modification into a papilla of just one pedicel from the third element of the ventral sucker row (some nominal species of Euprymna) to a quite complex structure involving several variously modified pedicels from both the ventral and dorsal sucker rows (Inioteuthis). -
Canada's Arctic Marine Atlas
Lincoln Sea Hall Basin MARINE ATLAS ARCTIC CANADA’S GREENLAND Ellesmere Island Kane Basin Nares Strait N nd ansen Sou s d Axel n Sve Heiberg rdr a up Island l Ch ann North CANADA’S s el I Pea Water ry Ch a h nnel Massey t Sou Baffin e Amund nd ISR Boundary b Ringnes Bay Ellef Norwegian Coburg Island Grise Fiord a Ringnes Bay Island ARCTIC MARINE z Island EEZ Boundary Prince i Borden ARCTIC l Island Gustaf E Adolf Sea Maclea Jones n Str OCEAN n ait Sound ATLANTIC e Mackenzie Pe Ball nn antyn King Island y S e trait e S u trait it Devon Wel ATLAS Stra OCEAN Q Prince l Island Clyde River Queens in Bylot Patrick Hazen Byam gt Channel o Island Martin n Island Ch tr. Channel an Pond Inlet S Bathurst nel Qikiqtarjuaq liam A Island Eclipse ust Lancaster Sound in Cornwallis Sound Hecla Ch Fitzwil Island and an Griper nel ait Bay r Resolute t Melville Barrow Strait Arctic Bay S et P l Island r i Kel l n e c n e n Somerset Pangnirtung EEZ Boundary a R M'Clure Strait h Island e C g Baffin Island Brodeur y e r r n Peninsula t a P I Cumberland n Peel Sound l e Sound Viscount Stefansson t Melville Island Sound Prince Labrador of Wales Igloolik Prince Sea it Island Charles ra Hadley Bay Banks St s Island le a Island W Hall Beach f Beaufort o M'Clintock Gulf of Iqaluit e c n Frobisher Bay i Channel Resolution r Boothia Boothia Sea P Island Sachs Franklin Peninsula Committee Foxe Harbour Strait Bay Melville Peninsula Basin Kimmirut Taloyoak N UNAT Minto Inlet Victoria SIA VUT Makkovik Ulukhaktok Kugaaruk Foxe Island Hopedale Liverpool Amundsen Victoria King -
Rossia Macrosoma (Delle Chiaie, 1830) Fig
Cephalopods of the World 183 3.2.2 Subfamily ROSSIINAE Appellöf, 1898 Rossia macrosoma (Delle Chiaie, 1830) Fig. 261 Sepiola macrosoma Delle Chiaie, 1830, Memoire sulla storia e notomia degli Animali senza vertebre del Regno di Napoli. 4 volumes, atlas. Napoli, pl. 17 [type locality: Tyrrhenian Sea]. Frequent Synonyms: Sepiola macrosoma Delle Chiaie, 1829. Misidentifications: None. FAO Names: En – Stout bobtail squid; Fr – Sépiole melon; Sp – Globito robusto. tentacular club arm dorsal view Fig. 261 Rossia macrosoma Diagnostic Features: Body smooth, soft. Males mature at smaller sizes and do not grow as large as females. Mantle dome-shaped. Dorsal mantle free from head (not fused to head). Nuchal cartilage oval, broad. Fins short, do not exceed length of mantle anteriorly or posteriorly. Arm webs broad between arms III and IV. Non-hectocotylized arm sucker arrangement same in both sexes: arm suckers biserial basally, tetraserial medially and distally. Dorsal and ventral sucker rows of arms II to IV of males enlarged; ventral marginal rows of arms II and III with 1 to 3 greatly enlarged suckers basally (diameter 8 to 11% mantle length); dorsal and ventral marginal sucker rows of arms II to IV with more than 10 enlarged suckers (diameter 4 to 7% mantle length); suckers on median rows in males smaller than female arm suckers in size. Hectocotylus present; both dorsal arms modified: ventrolateral edge of proximal oral surface of hectocotylized arms bordered by swollen glandular crest, inner edge of which forms a deep furrow; glandular crest extends over entire arm length; suckers decrease in size from proximal to distal end of arms; biserial proximally, tetraserial distally (marginal and medial suckers similar in size, smaller than on rest of arm); arms with deep median furrow and with transversely grooved ridges. -
Reproductive Strategies in Female Polar and Deep-Sea Bobtail Squid Genera Rossia and Neorossia (Cephalopoda: Sepiolidae)
Polar Biol (2008) 31:1499–1507 DOI 10.1007/s00300-008-0490-4 ORIGINAL PAPER Reproductive strategies in female polar and deep-sea bobtail squid genera Rossia and Neorossia (Cephalopoda: Sepiolidae) V. V. Laptikhovsky · Ch. M. Nigmatullin · H. J. T. Hoving · B. Onsoy · A. Salman · K. Zumholz · G. A. Shevtsov Received: 7 April 2008 / Revised: 18 June 2008 / Accepted: 30 June 2008 / Published online: 18 July 2008 © Springer-Verlag 2008 Abstract Female reproductive features have been investi- Introduction gated in Wve polar and deep-sea bobtail squid genera Rossia and Neorossia (R. macrosoma, R. moelleri, R. paciWca, CuttleWsh of the family Sepiolidae, commonly known as N.c. caroli and N.c. jeannae). These species are character- “bobtail squid”, inhabit tropical, temperate and polar waters ized by asynchronous ovary maturation, very large eggs of all oceans. The family has three subfamilies including (>10% ML), fecundity of several hundred oocytes, very the oceanic and pelagic Heteroteuthinae and the benthic high reproductive output, and continuous spawning with Sepiolinae and Rossiinae which inhabit continental shelf low batch fecundity. This adaptive complex of reproductive and slope waters. Sepiolinae are common on tropical and traits evolved in these small animals as an optimum strat- temperate shelves and on the upper part of the continental egy for polar and deep-water habitats. slope (down to depths of about 400 m). Rossiinae are gen- erally associated with cold water. They occur on polar Keywords Neorossia · Rossia · Spawning · shelves and in deep seas between 200 and 2,000 m, usually Reproduction · Polar · Deep-sea deeper than 500 m, though not south of the Antarctic Polar Front (Reid and Jereb 2005). -
Phylum: Mollusca Class: Cephalopoda
PHYLUM: MOLLUSCA CLASS: CEPHALOPODA Authors Rob Leslie1 and Marek Lipinski2 Citation Leslie RW and Lipinski MR. 2018. Phylum Mollusca – Class Cephalopoda In: Atkinson LJ and Sink KJ (eds) Field Guide to the Ofshore Marine Invertebrates of South Africa, Malachite Marketing and Media, Pretoria, pp. 321-391. 1 South African Department of Agriculture, Forestry and Fisheries, Cape Town 2 Ichthyology Department, Rhodes University, Grahamstown, South Africa 321 Phylum: MOLLUSCA Class: Cephalopoda Argonauts, octopods, cuttlefish and squids Introduction to the Class Cephalopoda Cephalopods are among the most complex and The relative length of the arm pairs, an important advanced invertebrates. They are distinguished from identiication character, is generally expressed as the rest of the Phylum Mollusca by the presence an arm formula, listing the arms from longest to of circumoral (around the mouth) appendages shortest pair: e.g. III≥II>IV>I indicates that the two commonly referred to as arms and tentacles. lateral arm pairs (Arms II and III) are of similar length Cephalopods irst appeared in the Upper Cambrian, and are longer than the ventral pair (Arms IV). The over 500 million years ago, but most of those dorsal pair (Arms I) is the shortest. ancestral lineages went extinct. Only the nautiluses (Subclass Nautiloidea) survived past the Silurian (400 Order Vampyromorpha (Vampire squids) million years ago) and are today represented by only This order contains a single species. Body sac-like, two surviving genera. All other living cephalopods black, gelatinous with one pair (two in juveniles) of belong to the Subclass Coleoidea that irst appeared paddle-like ins on mantle and a pair of large light in the late Palaeozoic (400-350 million years ago). -
Description of Key Species Groups in the East Marine Region
Australian Museum Description of Key Species Groups in the East Marine Region Final Report – September 2007 1 Table of Contents Acronyms........................................................................................................................................ 3 List of Images ................................................................................................................................. 4 Acknowledgements ....................................................................................................................... 5 1 Introduction............................................................................................................................ 6 2 Corals (Scleractinia)............................................................................................................ 12 3 Crustacea ............................................................................................................................. 24 4 Demersal Teleost Fish ........................................................................................................ 54 5 Echinodermata..................................................................................................................... 66 6 Marine Snakes ..................................................................................................................... 80 7 Marine Turtles...................................................................................................................... 95 8 Molluscs ............................................................................................................................ -
Recent Cephalopoda Primary Types
Ver. 2 March 2017 RECENT CEPHALOPOD PRIMARY TYPE SPECIMENS: A SEARCHING TOOL Compiled by Michael J. Sweeney Introduction. This document was first initiated for my personal use as a means to easily find data associated with the ever growing number of Recent cephalopod primary types. (Secondary types (paratypes, etc) are not included due to the large number of specimens involved.) With the excellent resources of the National Museum of Natural History, Smithsonian Institution and the help of many colleagues, it grew in size and became a resource to share with others. Along the way, several papers were published that addressed some of the problems that were impeding research in cephalopod taxonomy. A common theme in each paper was the need to locate and examine types when publishing taxonomic descriptions; see Voss (1977:575), Okutani (2005:46), Norman and Hochberg (2005b:147). These publications gave me the impetus to revive the project and make it readily available. I would like to thank the many individuals who assisted me with their time and knowledge, especially Clyde Roper, Mike Vecchione, Eric Hochberg and Mandy Reid. Purpose. This document should be used as an aid for finding the location of types, type names, data, and their publication citation. It is not to be used as an authority in itself or to be cited as such. The lists below will change over time as more research is published and ambiguous names are resolved. It is only a search aid and data from this document should be independently verified prior to publication. My hope is that this document will make research easier and faster for the user. -
5.4. Cephalopods in the Canary Current Large Marine Ecosystem
Cephalopods in the Canary Current Large Marine Ecosystem Item Type Report Section Authors Rocha, Francisco; Cheikh, Inejih Publisher IOC-UNESCO Download date 28/09/2021 07:33:13 Link to Item http://hdl.handle.net/1834/9192 5.4. Cephalopods in the Canary Current Large Marine Ecosystem For bibliographic purposes, this article should be cited as: Rocha, F. and Cheikh, I. 2015. Cephalopods in the Canary Current Large Marine Ecosystem. In: Oceanographic and biological features in the Canary Current Large Marine Ecosystem. Valdés, L. and Déniz‐González, I. (eds). IOC‐ UNESCO, Paris. IOC Technical Series, No. 115, pp. 245‐255. URI: http://hdl.handle.net/1834/9192. The publication should be cited as follows: Valdés, L. and Déniz‐González, I. (eds). 2015. Oceanographic and biological features in the Canary Current Large Marine Ecosystem. IOC‐UNESCO, Paris. IOC Technical Series, No. 115: 383 pp. URI: http://hdl.handle.net/1834/9135. The report Oceanographic and biological features in the Canary Current Large Marine Ecosystem and its separate parts are available on‐line at: http://www.unesco.org/new/en/ioc/ts115. The bibliography of the entire publication is listed in alphabetical order on pages 351‐379. The bibliography cited in this particular article was extracted from the full bibliography and is listed in alphabetical order at the end of this offprint, in unnumbered pages. ABSTRACT This work presents a brief review of cephalopod fauna found in the Canary Current Large Marine Ecosystem waters in terms of biodiversity, ecology and fisheries. This large marine ecosystem presents 139 cephalopod species, including high commercial value groups (Ommastrephids, Loliginids, Octopods and Sepiids), corresponding to a transitional zone between different Atlantic zoogeographic provinces where tropical, temperate and cold water cephalopod species mix. -
Family SEPIOLIDAE Leach, 1817
Cephalopods of the World 153 3.2 Family SEPIOLIDAE Leach, 1817 by Amanda Reid and Patrizia Jereb Sepiolidae Leach, 1817, Synopsis of the Orders, Families and Genera of the Class Cephalopoda, In: Leach and Nodder, The Zoological Miscellany, 3(30):137–141. FAO Names: En – Bobtail squids; Fr – Sépioles; Sp – Globitos, Sepietas, Sepiolas, Sepiolinas. Diagnostic Features: Mantle broad, oval; posterior mantle margin rounded. Dorsal mantle fused to head, or free from head. Mantle cavity divided by thin septum. Fins wide; rounded, semicircular, or kidney-shaped, with pronounced anterior lobes, or ‘earlets’; attached about midway along mantle; fin attachment short, fin length exceeds attachment length. Head slightly broader than, or as wide as, mantle. Large eyes covered by corneal membranes. Mantle-locking cartilage simple, linear. Arms short; protective membranes absent in both sexes. Webs between arms III and IV envelop tentacle bases on outside only, without forming sac. Hectocotylus present: left dorsal arm, both dorsal arms, or dorsolateral arms modified. Tentacles retractable, each bears a well defined club. Only the left oviduct is developed. Eggs large, development direct. Internal gladius present, rudimentary, chitinous, or absent. Size: Small, up to 80 mm, rarely 100 mm, mantle length. Habitat and Biology: Benthic or neritic. Represented in tropical, temperate and subpolar waters of all oceans. Interest to Fisheries: Separate statistics are not reported for this group, but many species are utilized locally as food even though not commercially exploited. The flesh is generally very tasty though difficult to preserve. Currently of low commercial value; in some areas of their distribution catches are very abundant and the resource is valued as a delicacy (i.e.