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Trophic Strategy

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Usually occurs at depths of around 300 m (Ref. 26335). Mesopelagic (Ref. 5951).
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Pascualita Sa-a
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Morphology

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Dorsal spines (total): 0; Dorsal soft rays (total): 10 - 13; Analspines: 0; Analsoft rays: 21 - 23
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Migration

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Oceanodromous. Migrating within oceans typically between spawning and different feeding areas, as tunas do. Migrations should be cyclical and predictable and cover more than 100 km.
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Diagnostic Description

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Mature males with 6-8 supracaudal luminous structures; mature females with 3-6 infracaudal luminous patches.
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Biology

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Oceanic, found between 425-1,000 m during the day with maximum abundance at 425-650 m (Ref. 4479). Nyctoepipelagic from the surface to 175 m (Ref. 4479).
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Comprehensive Description

provided by Smithsonian Contributions to Zoology
Gonichthys cocco

Although this medium-size lanternfish grows to 60 mm, the maximum size in the Ocean Acre collections was 45 mm, with very few exceeding 40 mm. According to Backus et al. (1977), G. cocco is a questionably tropical-subtropical species that is not found in the Caribbean Sea. Near Bermuda it is an “abundant” lanternfish. It is the most abundant one that comes to the surface at night, and ranks among the ten most abundant lanternfish at all three seasons. About 95 percent of all specimens caught were from night neuston samples. Of the 1326 specimens caught, 1112 were taken during the paired seasonal cruises, 1057 of these from surface samples. Discrete-depth samples made with the 3-m Isaccs-Kidd midwater trawl during the paired seasonal cruises accounted for only 35 specimens.

DEVELOPMENTAL STAGES.—Postlarvae were 5–15 mm, juveniles 13–32 mm, subadults 26–45 mm, and adults 34–44 mm. Most juveniles 13–20 mm have slender thread-like gonads and could not be sexed. Several fish larger than 40 mm that were categorized as subadults apparently were spent adults. Adult females contained eggs as large as 0.45 mm, but most eggs were 0.25–0.35 mm in diameter. Subadult and adult males had supracaudal luminescent glands and subadult and adult females infracaudal glands. There was no sexual dimorphism in size.

REPRODUCTIVE CYCLE AND SEASONAL ABUNDANCE.—Gonichthys cocco has a one-year life cycle, with very few, if any, individuals surviving much beyond a year. Spawning occurs from winter to early summer, with a peak in winter or early spring. Abundance was greatest in late spring (Table 61), when G. cocco was the fourth most abundant lanternfish, and juveniles were most abundant. Subadults and adults were most abundant in winter.

The winter catch was dominated by juveniles, but subadults and adults were at their yearly high in abundance. Spawning evidently was low over late summer and fall, as most winter juveniles were 20–30 mm, and transformation occurs at about 14 mm (Taaning, 1918). By late spring much of the winter population had matured, spawned, and died, resulting in a decrease in abundance of subadults and adults and an increase in juveniles; in late spring most juveniles were 18–21 mm. Subadults and adults (small juveniles of the winter) would spawn and die by late summer. As a result of postspawning mortality, the older stages virtually were absent at that season (Table 61), and most fish were 20 mm or smaller. This suggests that few fish live more than one year.

Abundance most likely was underestimated both in late spring and late summer, as several 8 mm postlarvae were taken, and fish less than 10 mm probably were not adequately sampled by the nets. In winter small juveniles (16–20 mm) were at a minimum and subadults and adults at a maximum. Continuing mortality in the recruit class should have resulted in a decrease in total abundance from late summer to winter but, because of the underestimation of the late summer population, no significant change was apparent (Table 61).

SEX RATIOS.—The sexes probably are equally abundant at all seasons. Total female-to-male sex ratios were 1.0:1 in winter and 1.3:1 at the other two seasons; only the difference in late spring differed significantly from equality (Table 62). Most of the difference in late spring was due to juveniles, of which about half could be sexed. Adult females outnumbered adult males in winter and late spring, and juveniles and subadults showed no consistent trend in numerical dominance of either sex. None of the sex ratios for individual stages differed significantly from equality.


VERTICAL DISTRIBUTION.—Diurnal catches in each season were poor; only 19 fish were taken in all daytime discrete-depth samples combined. The combined seasonal day discrete-depth samples give a depth range of 501–1000 m, with no apparent depth preference (Table 63). Gonichthys cocco probably was well dispersed vertically by day at all seasons, as all positive samples contained 3 or fewer fish. One specimen, a probable contaminant, was taken at the surface by day in late spring.

A dramatic concentration takes place at night. More than 95 percent of the nocturnal catch in each season came from the surface (Table 63). In winter fish also were taken at 101–200 m and at 751–900 m, in late spring a single specimen was taken at 51–100 m, and in late summer one fish each was taken at 1–50 m and 851–900 m.

Only fish smaller than 20 mm were taken below 750 m day or night at all seasons (Table 63). Because day catches in each season contained mostly one developmental stage and night catches were mostly from the surface, little can be said concerning stage stratification.

Although most migrants were found at or close to the surface, at each season migrants also were taken well below the surface. These individuals were most abundant in winter, when juveniles, subadults, and adults all were taken at 101–200 m (Table 63). In late spring and late summer only a single migrant juvenile was taken well below the surface (at 90 m and 33 m, respectively).

Apparently, regular migratory behavior is assumed at about 16–19 mm. Larger sizes were all migrators, and a few 16–19 mm juveniles were taken at day depths by night in winter and late summer. Nonmigrants accounted for about 2 percent of the winter night catch, and less than 1 percent of that in late summer.

Migrations could not be traced in any season due to poor diurnal and evening crepuscular catches. In late summer one fish was taken at 501–550 m between 2.3 and 1.3 hours before sunset and another at 101–150 m between 1.5 and 0.5 hours before sunset. Surface waters were occupied 1.5 hours or less after sunset in each season. In late spring fish were taken at the surface between 1.5 to 0.5 hours before sunrise, and in late summer samples taken up to 45 minutes before sunrise were negative. Samples were not taken within 1.75 hours of sunrise in winter. Table 64 gives the catch rate (specimens/hour) for selected times for the five cruises during which neuston samples were taken.

PATCHINESS.—Significant patchiness was indicated at the surface by night in each season. Table 64 shows the great variation in catch rates even when samples taken from the same times on different days are combined. Examination of individual samples revealed even greater variation. Sequential samples often had catch rates that differed by a factor of 2 or more. Additionally, on several occasions negative samples were interspersed amongst several positive samples.

A significant CD also was obtained for late spring day surface samples. However, this was due to the capture of a single fish, a probable contaminant. This obviously is not indicative of a patchy distribution even if the capture is a valid record for G. cocco.

NIGHT: DAY CATCH RATIOS.—Night catches were consistently larger than those of day, with ratios of 13.6:1 in winter 70.3:1 in late spring, and 9.9:1 in late summer (Table 65). The large night catches must be due, at least partially, to the great constriction of the vertical range at that time, Net avoidance is the obvious explanation for the virtual absence of this species from daytime samples; its effect at night cannot be evaluated.
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bibliographic citation
Gibbs, Robert H., Jr. and Krueger, William H. 1987. "Biology of midwater fishes of the Bermuda Ocean Acre." Smithsonian Contributions to Zoology. 1-187. https://doi.org/10.5479/si.00810282.452

Gonichthys cocco ( Catalan; Valencian )

provided by wikipedia CA

Gonichthys cocco és una espècie de peix de la família dels mictòfids i de l'ordre dels mictofiformes.[5]

Morfologia

Depredadors

A les Illes Açores és depredat per Beryx splendens i Phycis phycis.[8][9]

Hàbitat

És un peix marí i d'aigües profundes que viu entre 0-1.000 m de fondària.[6]

Distribució geogràfica

Es troba a l'Atlàntic oriental (des de Portugal fins a Libèria, i des d'Angola fins a Sud-àfrica),[10] la Mediterrània oriental[11] i l'Atlàntic occidental.[6][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26]

Referències

  1. Gistel, J. 1850. (Títol incert). Isis (Munic) v. 5: 71.
  2. BioLib (anglès)
  3. Cocco, A., 1829. Su di alcuni nuovi pesci de' mari di Messina. Giornale di Scienze Lettere e Arti per La Sicilia Anno 7, v. 26 (núm. 77): 138-147.
  4. «Gonichthys cocco». Catalogue of Life. (anglès) (anglès)
  5. The Taxonomicon (anglès)
  6. 6,0 6,1 6,2 FishBase (anglès)
  7. Hulley, P.A., 1990. Myctophidae. p. 398-467. A J.C. Quero, J.C. Hureau, C. Karrer, A. Post i L. Saldanha (eds.) Check-list of the fishes of the eastern tropical Atlantic (CLOFETA). JNICT, Lisboa; SEI; París; i UNESCO, París. Vol. 1.
  8. Gomes, T.M., E. Sola, M.P. Grós, G. Menezes i M.R. Pinho, 1998. Trophic relationships and feeding habits of demersal fishes from the Azores: importance to multispecies assessment. ICES C.M. 1998/O: 7.
  9. FishBase (anglès)
  10. Bianchi, G., K.E. Carpenter, J.-P. Roux, F.J. Molloy, D. Boyer i H.J. Boyer, 1993. FAO species identification field guide for fishery purposes. The living marine resources of Namibia. FAO, Roma, Itàlia. 250 p.
  11. Quignard, J.-P. i J.A. Tomasini, 2000. Mediterranean fish biodiversity. Biol. Mar. Mediterr. 7(3):1-66.
  12. Bekker, V.E., T.N. Belyanina, N.I. Kashkin I K.N. Nesis, 1982. Mesopelagic fish and cephalopoda from the four regions of the North Atlantic (from collections of the 31st study cruise of the research vessel Akademik Kurchatov). J. Ichthyol. 22(4):19-25.
  13. Bertolini, F., U. D'Ancona, E. Padoa Montalenti, S. Ranzi, L. Sanzo, A. Sparta, E. Tortonese I M. Vialli, 1956. Uova, larve e stadi giovanili di Teleostei. Fauna Flora Golfo Napoli Monogr. 38:1-1064.
  14. Bilecenoglu, M., E. Taskavak S. Mater i M. Kaya, 2002. Checklist of the marine fishes of Turkey. Zootaxa (113):1-194.
  15. Boltachev, A.R., 1987. Species structure of Myctophidae communities from some Atlantic regions. J. Ichthyol. 27(5):51-59.
  16. Brito, A., 1991. Catálogo de los peces de las Islas Canarias. Francisco Lemus, La Laguna, Illes Canàries, Espanya. 230 p.
  17. Chen, S., 2002. Fauna Sinica. Ostichthyes. Myctophiformes, Cetomimiformes, Osteoglossiformes. Science Press, Beijing. 349 p.
  18. Chirichigno, N.F., 1974. Clave para identificar los peces marinos del Perú. Inf. Inst. Mar Perú (44):387 p.
  19. Claro, R., 1994. Características generales de la ictiofauna. p. 55-70. A R. Claro (ed.) Ecología de los peces marinos de Cuba. Instituto de Oceanología Academia de Ciencias de Cuba i Centro de Investigaciones de Quintana Roo.
  20. Claro, R. i L.R. Parenti, 2001. The marine ichthyofauna of Cuba. p. 21-57. A Claro, R., K.C. Lindeman i L.R. Parenti (eds) Ecology of the marine fishes of Cuba. Smithsonian Institution Press, Washington i Londres. 253p.
  21. Costa, F., 1991. Atlante dei pesci dei mari italiani. Gruppo Ugo Mursia Editore S.p.A. Milà, Itàlia. 438 p.
  22. Papasissi, C., 1989. A contribution to the study of the biology of the ichthyoplankton in the Gulf of Kissamos (N.W. Crete, Greece). Tesi. 300 p.
  23. Reiner, F., 1996. Catálogo dos peixes do Arquipélago de Cabo Verde. Publicações avulsas do IPIMAR Núm. 2. 339 p.
  24. Santos, R.S., F.M. Porteiro i J.P. Barreiros, 1997. Marine fishes of the Azores: annotated checklist and bibliography. Bulletin of the University of Azores. Supplement 1. 244 p.
  25. Scott, W.B. i M.G. Scott, 1988. Atlantic fishes of Canada. Can. Bull. Fish. Aquat. Sci. 219: 731 p.
  26. Tinker, S.W., 1978. Fishes of Hawaii, a handbook of the marine fishes of Hawaii and the Central Pacific Ocean. Hawaiian Service Inc., Honolulu. 568 p.


Bibliografia

  • Anònim, 2001. Base de dades de la col·lecció de peixos del National Museum of Natural History (Smithsonian Institution). Smithsonian Institution - Division of Fishes.
  • Anònim, 2002. Base de dades de la col·lecció de peixos del Museu Americà d'Història Natural. Museu Americà d'Història Natural, Central Park West, NY 10024-5192 (Estats Units).
  • Becker, V. E., 1964: Slendertailed myctophids (genera Loweina, Tarletonbeania, Gonichthys and Centrobranchus) of the Pacific and Indian oceans. Systematics and distribution. A: Fishes of the Pacific and Indian oceans. Trudy Instituta okeanologii im. P.P. Shirshova v. 73: 10-75 (en rus, amb resum en anglès).
  • Eschmeyer, William N., ed. 1998. Catalog of Fishes. Special Publication of the Center for Biodiversity Research and Information, núm. 1, vol. 1-3. California Academy of Sciences. San Francisco, Califòrnia, Estats Units. ISBN 0-940228-47-5.
  • Helfman, G., B. Collette i D. Facey: The diversity of fishes. Blackwell Science, Malden, Massachusetts (Estats Units), 1997.
  • Hopkins, T.L., T.T. Sutton i T.M. Lancraft, 1996. The trophic structure and predation impact of a low latitude midwater fish assemblage. Prog. Oceanog. 38:205-239.
  • Hulley, P.A., 1984. Myctophidae. p. 429-483. A P.J.P. Whitehead, M.-L. Bauchot, J.-C. Hureau, J. Nielsen i E. Tortonese (eds.). Fishes of the north-eastern Atlantic and the Mediterranean. UNESCO, París, França. Vol. 1.
  • Moyle, P. i J. Cech.: Fishes: An Introduction to Ichthyology, 4a edició, Upper Saddle River, Nova Jersey, Estats Units: Prentice-Hall. Any 2000.
  • Nelson, J.: Fishes of the World, 3a edició. Nova York, Estats Units: John Wiley and Sons. Any 1994.
  • Paxton, J.R., 1979. Nominal genera and species of lanternfishes (Family Myctophidae). Contrib. Sci. Natur. Hist. Mus. Los Angeles County, 322:1-28.
  • Paxton, J.R. i P.A. Hulley, 1999. Myctophidae. Lanternfishes. p. 1957-1964. A K.E. Carpenter i V.H. Niem (eds.) FAO species identification guide for fishery purposes. The living marine resources of the WCP. Vol. 3. Batoid fishes, chimaeras and bony fishes part 1 (Elopidae to Linophrynidae). FAO, Roma, Itàlia.
  • Riede, K., 2004. Global register of migratory species - from global to regional scales. Final Report of the R&D-Projekt 808 05 081. Federal Agency for Nature Conservation, Bonn, Alemanya. 329 p.
  • Wheeler, A.: The World Encyclopedia of Fishes, 2a edició, Londres: Macdonald. Any 1985.


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Gonichthys cocco: Brief Summary ( Catalan; Valencian )

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Gonichthys cocco és una espècie de peix de la família dels mictòfids i de l'ordre dels mictofiformes.

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Gonichthys cocco

provided by wikipedia EN

Gonichthys cocco, often called the Cocco's lanternfish, is a species of oceanodromous lanternfish.[2]

Distribution and habitat

It lives in the Eastern and Western Atlantic, near areas like Portugal, Liberia, Angola, South Africa, Brazil, and the eastern Mediterranean. It is found from depths from 0 to 1,450 m (0 to 4,757 ft) below the surface, usually at 425 to 650 m (1,394 to 2,133 ft) below the surface. During the day it is in waters from 425 to 1,000 m (1,394 to 3,281 ft) deep,[2] and can be up to 200 m (660 ft) deep at night to feed.[3]

Description

G. cocco can reach a length of up to 6 cm (2.4 in). It has 10 to 13 dorsal soft rays, and 21 to 23 anal soft rays. Mature males have 6 to 8 supracaudal luminous structures, while mature females only have 3 to 6.[2]

Conservation

It has no threats; its distribution overlaps with several marine protected areas, and its population is stable, and is listed as Least Concern by the IUCN Red List.[4]

Taxonomy

G. cocco is one of four species in its genus. The other three are Gonichthys barnesi, Gonichthys tenuiculus, and Gonichthys venetus.[5]

Synonymised names

Placed by the WoRMS.[6]

  • Alysia loricata Lowe, 1839
  • Gonichthys coccoi Cocco, 1829 (misspelling)
  • Myctophum coccoi Cocco, 1829 (misspelling)
  • Myctophum hians Richardson, 1845
  • Rhinoscopelus cocco Cocco, 1829
  • Rhinoscopelus coccoi Cocco, 1829 (misspelling)
  • Scopelus cocco Cocco, 1829
  • Scopelus coccoi Günther, 1864
  • Scopelus gracile Lütken, 1892
  • Scopelus gracilis Lütken, 1892
  • Scopelus jagorii Peters, 1859 (synonym)

References

  1. ^ Hulley, P. (2015). "Gonichthys cocco". IUCN Red List of Threatened Species. 2015: e.T198616A15603135. doi:10.2305/IUCN.UK.2015-4.RLTS.T198616A15603135.en. Retrieved 20 November 2021.
  2. ^ a b c "Gonichthys cocco summary page". FishBase. Retrieved 2019-04-07.
  3. ^ "The IUCN Red List of Threatened Species". IUCN Red List of Threatened Species. Retrieved 2019-04-07.
  4. ^ "The IUCN Red List of Threatened Species". IUCN Red List of Threatened Species. Retrieved 2019-04-07.
  5. ^ "ADW: Gonichthys: CLASSIFICATION". animaldiversity.org. Retrieved 2019-04-07.
  6. ^ "WoRMS - World Register of Marine Species - Gonichthys cocco (Cocco, 1829)". www.marinespecies.org. Retrieved 2019-04-07.
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Gonichthys cocco: Brief Summary

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Gonichthys cocco, often called the Cocco's lanternfish, is a species of oceanodromous lanternfish.

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Gonichthys cocco ( Spanish; Castilian )

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El pez-linterna de cocco (Gonichthys cocco),[1][2]​ es una especie de pez marino de la familia de los mictófidos o peces linterna.[3]

Morfología

Su longitud cuando alcanza la madurez es de unos 4 cm y la longitud máxima descrita es de 6'0 cm, sin espinas en las aletas, con más radios blandos en la aleta anal que en la aleta dorsal.[1]​ Son luminiscentes, con hileras de fotóforos a lo largo de su cuerpo, teniendo el macho adulto entre 6 y 8 fotóforos supracaudales mientras que la hembra tiene 3 a 6 fotóforos infracaudales.[1]

Distribución y hábitat

Es un pez marino bati-pelágico de aguas profundas, oceanódromo,[4]​ que habita en un rango de profundidad entre 0 y 1000 metros, aunque normalmente está entre 425 y 650 m de profundidad durante el día, con migraciones nocturnas a la zona superficial del océano.[1]​ Se distribuye por todo el norte del océano Atlántico, así como por la totalida del mar Mediterráneo y el mar Caribe.[1]

Referencias

  1. a b c d e Hulley, P.A. (1990). «Myctophidae». p. 398-467. En J.C. Quero, J.C. Hureau, C. Karrer, A. Post y L. Saldanha (eds.) Check-list of the fishes of the eastern tropical Atlantic (CLOFETA). JNICT, Lisboa; SEI; París; y UNESCO, París. Vol. 1.
  2. "Gonichthys cocco". En FishBase (Rainer Froese y Daniel Pauly, eds.). Consultada en noviembre de 2015. N.p.: FishBase, 2015.
  3. "Myctophidae". En FishBase (Rainer Froese y Daniel Pauly, eds.). Consultada en octubre de 2015. N.p.: FishBase, 2015.
  4. Riede, K. (2004). «Global register of migratory species - from global to regional scales». Final Report of the R&D-Projekt 808 05 081. Federal Agency for Nature Conservation, Bonn, Alemania. 329 p.

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Gonichthys cocco: Brief Summary ( Spanish; Castilian )

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El pez-linterna de cocco (Gonichthys cocco),​​ es una especie de pez marino de la familia de los mictófidos o peces linterna.​

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Gonichthys cocco ( Basque )

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Gonichthys cocco Gonichthys generoko animalia da. Arrainen barruko Myctophidae familian sailkatzen da.

Banaketa

Erreferentziak

  1. Froese, Rainer & Pauly, Daniel ed. (2006), Gonichthys cocco FishBase webgunean. 2006ko apirilaren bertsioa.

Ikus, gainera

(RLQ=window.RLQ||[]).push(function(){mw.log.warn("Gadget "ErrefAurrebista" was not loaded. Please migrate it to use ResourceLoader. See u003Chttps://eu.wikipedia.org/wiki/Berezi:Gadgetaku003E.");});
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Gonichthys cocco: Brief Summary ( Basque )

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Gonichthys cocco Gonichthys generoko animalia da. Arrainen barruko Myctophidae familian sailkatzen da.

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Gonichthys cocco ( Italian )

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Il pesce lanterna nasuto (Gonichthys cocco) è un pesce abissale della famiglia Myctophidae.

Distribuzione e habitat

È una specie pelagica di profondità, di giorno si trattiene tra i 300 ed i 600 metri di profondità mentre la notte sale a quote meno elevate. È stato trovato tra la superficie (rarissimamente) ed i 4000 metri.
Vive nel mar Mediterraneo, dove è più comune nel settore orientale, e nell'Oceano Atlantico, nei settori tropicali e temperati caldi.

Descrizione

Si tratta di uno dei pochi pesci lanterna che si possono riconoscere anche con caratteri diversi dalla disposizione dei fotofori, infatti ha una sagoma caratteristica a causa del peduncolo caudale sottile e lungo, che contrasta con il corpo, che invece è alto e molto compresso lateralmente. L'occhio è grande ed anche la bocca, orizzontale. Il muso sporge con una prominenza appuntita. Le squame sono grandi e ben visibili ma molto caduche. La pinna anale è più lunga della pinna dorsale. I caratteri dei fotofori rivestono una certa importanza anche per accertare la classificazione di questa specie (per la nomenclatura dei fotofori vedi la voce Myctophidae): è presente un unico POL e due Prc, PLO alla base della pinna pettorale, gli AO della serie anteriore sono da 4 ad 8. Esiste il dimorfismo sessuale (nei fotofori), nel maschio sono presenti 7 Gs, nelle femmine 4-6 Gi.
Il colore è grigio acciaio sul dorso ed argentato sul ventre.
Misura al massimo 6 cm.

Biologia

Nonostante sia una specie che vive a profondità accessibili non si trova quasi mai spiaggiata sulle rive dello Stretto di Messina, come invece fanno moltissimi altri pesci abissali, anche della stessa famiglia. Si nutre di piccoli organismi zooplanctonici.

Pesca

Del tutto occasionale con reti a strascico. Importanza economica nulla.

Bibliografia

  • Tortonese E. Osteichthyes, Calderini, 1975
  • Costa F. Atlante dei pesci dei mari italiani Mursia, 1991 ISBN 8842510033

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Gonichthys cocco: Brief Summary ( Italian )

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Il pesce lanterna nasuto (Gonichthys cocco) è un pesce abissale della famiglia Myctophidae.

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Gonichthys cocco ( Dutch; Flemish )

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Vissen

Gonichthys cocco is een straalvinnige vissensoort uit de familie van de lantaarnvissen (Myctophidae).[1] De wetenschappelijke naam van de soort werd in 1829 gepubliceerd door Cocco.

Synoniemen

  • Alysia loricata Lowe, 1839
  • Myctophum hians Richardson, 1845
  • Scopelus jagorii Peters, 1859
  • Scopelus gracilis Lütken, 1892[2]
Bronnen, noten en/of referenties
  1. (en) Gonichthys cocco. FishBase. Ed. Ranier Froese and Daniel Pauly. 10 2011 version. N.p.: FishBase, 2011.
  2. Lütken, C.F. (1892). Spolia atlantica. Scopelini Musei Zoologici Hauniensis. Bidrag til Kundskab om det aabne Havs Laxesild eller Scopeliner. Det Kongelige Danske videnskabernes Selskabs Skrifter. Naturvidenskabelig og mathematiske Afdeling ser. 6, 7: 255
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Gonichthys cocco: Brief Summary ( Dutch; Flemish )

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Gonichthys cocco is een straalvinnige vissensoort uit de familie van de lantaarnvissen (Myctophidae). De wetenschappelijke naam van de soort werd in 1829 gepubliceerd door Cocco.

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柯氏星灯鱼 ( Chinese )

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二名法 Gonichthys coccoi
Cocco, 1829[1]

柯氏星灯鱼学名Gonichthys coccoi)为輻鰭魚綱燈籠魚目灯笼鱼科星灯鱼属鱼类。分布于大西洋印度洋太平洋以及海等,常生活于广泛生活在热带和亚热带海洋,屬深海魚類,棲息深度0-1000公尺,體長可達6公分。该物种的模式产地在意大利的墨西拿。[1]

参考文献

  1. ^ 1.0 1.1 中国科学院动物研究所. 柯氏星灯鱼. 中国动物物种编目数据库. 中国科学院微生物研究所. [2009-04-11]. (原始内容存档于2016-03-05).

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柯氏星灯鱼: Brief Summary ( Chinese )

provided by wikipedia 中文维基百科

柯氏星灯鱼(学名:Gonichthys coccoi)为輻鰭魚綱燈籠魚目灯笼鱼科星灯鱼属鱼类。分布于大西洋印度洋太平洋以及海等,常生活于广泛生活在热带和亚热带海洋,屬深海魚類,棲息深度0-1000公尺,體長可達6公分。该物种的模式产地在意大利的墨西拿。

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Distribution

provided by World Register of Marine Species
Western Atlantic: about 50°N, east of 40°W or south of the slope water region west of 40°W to about Brazil (absent over the minimum region off Brazil and lower abundance in the South Sargasso Sea)

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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Nyctoepipelagic species, migrates from daytime depth of 500- 1000 m to between 0- 175 m at night.

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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nektonic

Reference

North-West Atlantic Ocean species (NWARMS)

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Habitat

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Known from seamounts and knolls

Reference

Stocks, K. 2009. Seamounts Online: an online information system for seamount biology. Version 2009-1. World Wide Web electronic publication.

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