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Migration ( Anglèis )

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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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Morphology ( Anglèis )

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Dorsal spines (total): 0; Dorsal soft rays (total): 13 - 16; Analspines: 0; Analsoft rays: 19 - 22
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Trophic Strategy ( Anglèis )

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Oceanic and mesopelagic, found between 475-1,000 m during the day and between 40-325 m at night (Ref. 4479). Some small juveniles may be non-migratory (Ref. 4775).
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Biology ( Anglèis )

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Oceanic and mesopelagic, found between 475-1,000 m during the day and between 40-325 m at night (Ref. 4479). Some small juveniles may be non-migratory (Ref. 4775).
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Distribution ( Spagneul; Castilian )

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Chile Central
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Comprehensive Description ( Anglèis )

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Lampanyctus festivus

This large myctophid grows to 138 mm (Hulley, 1981); maximum size in the Ocean Acre collections is 110 mm. A bipolar questionably subtropical species, L. festivus is most abundant in the North Atlantic subtropical region (Backus et al., 1977). It is common in the study area, but ranked no higher than twelfth in winter in abundance. The Ocean Acre collections contain 593 specimens; 188 were taken during the paired seasonal cruises, 131 of these in discrete-depth samples, of which 120 were in noncrepuscular tows (Table 23).

DEVELOPMENTAL STAGES.—Postlarvae were 6–23 mm, juveniles 21–65 mm, subadults 63–110 mm, and adult males 85–103 mm. All females larger than 80 mm were examined for reproductive state; none were ripe or nearly ripe. The maximum egg diameter observed was 0.1 mm. The 42 specimens (33–110 mm) that could be sexed were divided equally between males and females. There was no apparent sexual dimorphism.

REPRODUCTIVE CYCLE AND SEASONAL ABUNDANCE.—Lampanyctus festivus probably spawns close to, if not in, the study area. However, until ripe females are taken, the issue is open to question. The parent population apparently spawns over much of the year, with a peak in intensity in winter. The life span is at least two years and probably longer. Abundance was greatest in winter, least in late spring, and intermediate in late summer (Table 92). Postlarvae were most abundant in late spring, juveniles and adults in winter, and subadults in late summer.

Although the lack of ripe females in the Ocean Acre collections casts some doubt on the reproductive status of L. festivus in the study area, the capture of postlarvae and small (less than 25 mm) juveniles suggests that spawning takes place near Bermuda. Young fish were taken over most of the year and probably were present at all times. They were most abundant in late spring and only slightly less abundant in late summer.

In winter recruitment was at a minimum. Very few postlarvae were taken, and most juveniles were larger than 30 mm. Juveniles 30–40 mm dominated the catch. Presumably these represent fish from the previous year's spawning peak. The actual size range of most of the previous year's spawn appears to be 28–57 mm, with few fish larger than 40 mm. The few 63–86 mm specimens taken in late spring probably represent fish two or more years old. The abundance of specimens in excess of 40 mm is too low to note peaks in the size frequency distribution. Size ranges for the various age groups cannot be determined with any certainty.

In late spring postlarvae dominated the small catch, accounting for about 66 percent of the total abundance (Table 92). The relatively low abundance at this season is somewhat puzzling. It probably is due to the relative inefficiency of the 3-m IKMT in sampling postlarvae, which for the most part filter through the net, and specimens larger than about 45 mm. By late summer the abundance of each stage (except postlarvae) increased from its late spring level (Table 92). The increase in juveniles is to be expected, because most postlarvae present in late spring had grown and developed to juveniles. The catch in late spring could be divided into two size groups: recently spawned fish 15–32 mm, and fish larger than 50 mm at least 1.5 years old. Presumably the latter group represented the 28–57 mm fishes of winter at a more advanced age.

VERTICAL DISTRIBUTION.—Depth range by day in winter is 701–850 m with maximum abundance at 701–750 mm, in late spring 51–100 m and 751–800 m (possibly slightly shallower and deeper), and in late summer 501–550 m and 751–1050 m with a maximum at 801–850 m. Vertical range at night in winter is 51–350 m and 851–900 m with maximum abundance at 101–150 m, in late spring 50–150 m and 951–1000 m with a maximum at 50 m, and in late summer 101–300 m and 851–1000 m with a maximum at 251–300 m (Table 93).

Stage and size stratification were evident during the day in late spring and late summer, and by night at each of the three seasons.

During the day only postlarvae were caught above 700 m in late spring and late summer, and deeper than 1000 m in late summer. As a result, mean sizes at those depths were much smaller than those at 751–850 m (Table 93).

At night in winter only juveniles were caught above 150 m and only subadults and adults at 201–350 m. In the upper 200 m size stratification resulted in an increase in the mean and maximum sizes with depth. The only specimen caught at 851–900 m was a 17 mm postlarva. In late spring only postlarvae were taken in the upper 50 m, and the mean size at that depth was much smaller than at other depths. In late summer only postlarvae were caught at 101–150 m and only postlarvae and small juveniles below 850 m. This resulted in smaller mean sizes at those depths than at 151–300 m (Table 93).

Development apparently begins in the upper layers, and transformation takes place at relatively great depths. Postlarvae taken in the upper 120 m are 6–11 mm; those taken at 851–1050 m are 19–23 mm. Four juveniles 21–25 mm (two each day and night) were taken at 901–1000 m. Migrations apparently start at about 25 mm, the size of smallest juvenile size taken in the upper 250 m at night (Table 93).

PATCHINESS.—A patchy distribution was indicated at the depth of maximum abundance by day in each season. Juveniles accounted for all or most of the catch at these depths (Table 93). There was no indication of patchiness at night at any season.

NIGHT: DAY CATCH RATIOS.—Night-to-day catch ratios including interpolated values are 0.6:1 in winter, 3.4:1 in late spring, and 0.4:1 in late summer. Juveniles accounted for most of the diel differences in the catch in winter and late summer, and postlarvae for most of the difference in late spring (Table 94).

The greater catches by day in winter and late summer probably were due to the tendency of juveniles to form aggregations, resulting in large catches when such aggregations were encountered by the net.

In late spring the catch of postlarvae at night accounted for nearly all of the difference between day and night catches. The depth at which most postlarvae were taken at night (50 m) was not sampled during the day. Samples made during the day at 27 m (two samples) and 55 m (one sample) failed to take postlarval L. festivus. In any case, abundance was low.
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sitassion bibliogràfica
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

Lampanyctus festivus ( Catalan; Valensian )

fornì da wikipedia CA

Lampanyctus festivus és una espècie de peix de la família dels mictòfids i de l'ordre dels mictofiformes.

Morfologia

Depredadors

És depredat per Stenella attenuata i, a les Illes Açores, per Beryx decadactylus, Beryx splendens i Phycis phycis.[6]

Hàbitat

És un peix marí i d'aigües profundes que viu entre 40-1.052 m de fondària.[4]

Distribució geogràfica

Es troba a l'Atlàntic,[7][8][9] l'Índic i el Pacífic (Japó,[10] Austràlia,[11] Nova Zelanda[12] i Xile).[13][4][14][15][16]

Referències

  1. Bonaparte C. L., 1840. Iconografia della fauna italica per le quattro classi degli animali vertebrati. Tomo III. Pesci. Roma. Iconografia, v. 3. Fasc. 27-29, puntata 136-154.
  2. BioLib (anglès)
  3. «Lampanyctus festivus». Catalogue of Life. (anglès) (anglès)
  4. 4,0 4,1 4,2 FishBase (anglès)
  5. 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.
  6. FishBase (anglès)
  7. 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.
  8. Boltachev, A.R., 1987. Species structure of Myctophidae communities from some Atlantic regions. J. Ichthyol. 27(5):51-59.
  9. 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.
  10. Masuda, H., K. Amaoka, C. Araga, T. Uyeno i T. Yoshino, 1984. The fishes of the Japanese Archipelago. Vol. 1. Tokai University Press, Tòquio, Japó. 437 p.
  11. Paxton, J.R., D.F. Hoese, G.R. Allen i J.E. Hanley, 1989. Pisces. Petromyzontidae to Carangidae. Zoological Catalogue of Australia, Vol. 7. Australian Government Publishing Service, Canberra, 665 p.
  12. Paulin, C., A. Stewart, C. Roberts i P. McMillan, 1989. New Zealand fish: a complete guide. National Museum of New Zealand Miscellaneous Series Núm. 19. xiv+279 p.
  13. Pequeño, G., 1989. Peces de Chile. Lista sistemática revisada y comentada. Rev. Biol. Mar., Valparaiso 24(2):1-132.
  14. Chen, S., 2002. Fauna Sinica. Ostichthyes. Myctophiformes, Cetomimiformes, Osteoglossiformes. Science Press, Beijing. 349 p.
  15. Hoese, D.F., D.J. Bray, J.R. Paxton i G.R. Allen, 2006. Fishes. A Beasley, O.L. i A. Wells (eds.) Zoological Catalogue of Australia. Volum 35. ABRS & CSIRO Publishing: Australia Part 1, pp. xxiv 1-670; Part 2, pp. xxi 671-1472; Part 3, pp. xxi 1473-2178.
  16. Young, J.W., T.D. Lamb i R.W. Bradford, 1996. Distribution and community structure of midwater fishes in relation to the subtropical convergence off eastern Tasmania, Australia. Mar. Biol. 126(4):571-584.


Bibliografia

  • Eschmeyer, William N.: Genera of Recent Fishes. California Academy of Sciences. San Francisco, Califòrnia, Estats Units. iii + 697. ISBN 0-940228-23-8 (1990).
  • 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.
  • 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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Lampanyctus festivus: Brief Summary ( Catalan; Valensian )

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Lampanyctus festivus és una espècie de peix de la família dels mictòfids i de l'ordre dels mictofiformes.

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Lampanyctus festivus ( Anglèis )

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Lampanyctus festivus is a species of lanternfish.[1][2][3][4] It is found in the Atlantic, Indian, and Pacific Oceans.[1][2][4] It is a mesopelagic fish that undertakes diel vertical migration.[1] It grows to about 14 cm (5.5 in) standard length.[2] It is an important component in the diet of forkbeard Phycis phycis off the Azores.[5]

References

  1. ^ a b c d Hulley, P. (2015). "Lampanyctus festivus". IUCN Red List of Threatened Species. 2015: e.T15599067A15603795. doi:10.2305/IUCN.UK.2015-4.RLTS.T15599067A15603795.en. Retrieved 20 November 2021.
  2. ^ a b c d Froese, Rainer; Pauly, Daniel (eds.) (2019). "Lampanyctus festivus" in FishBase. February 2019 version.
  3. ^ Bailly N, ed. (2019). "Lampanyctus festivus Tåning, 1928". FishBase. World Register of Marine Species. Retrieved 8 July 2019.
  4. ^ a b Eschmeyer, William N.; Fricke, Ron & van der Laan, Richard (eds.). "Lampanyctus festivus". Catalog of Fishes. California Academy of Sciences. Retrieved 8 July 2019.
  5. ^ Morato, Telmo; Solà, Encarnacion; Grós, Maria P. & Menezes, Gui M. (1999). "Diets of forkbeard (Phycis phycis) and conger eel (Conger conger) off the Azores during spring of 1996 and 1997" (PDF). Arquipélago – Life and Marine Sciences. 17A: 51–64. hdl:10400.3/211.
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Lampanyctus festivus: Brief Summary ( Anglèis )

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Lampanyctus festivus is a species of lanternfish. It is found in the Atlantic, Indian, and Pacific Oceans. It is a mesopelagic fish that undertakes diel vertical migration. It grows to about 14 cm (5.5 in) standard length. It is an important component in the diet of forkbeard Phycis phycis off the Azores.

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Lampanyctus festivus ( Basch )

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Lampanyctus festivus Lampanyctus generoko animalia da. Arrainen barruko Myctophidae familian sailkatzen da.

Banaketa

Erreferentziak

  1. Froese, Rainer & Pauly, Daniel ed. (2006), Lampanyctus festivus 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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Lampanyctus festivus: Brief Summary ( Basch )

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Lampanyctus festivus Lampanyctus generoko animalia da. Arrainen barruko Myctophidae familian sailkatzen da.

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Lampanyctus festivus ( olandèis; flamand )

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Vissen

Lampanyctus festivus is een straalvinnige vissensoort uit de familie van lantaarnvissen (Myctophidae).[1] De wetenschappelijke naam van de soort is voor het eerst geldig gepubliceerd in 1928 door Tåning.

Bronnen, noten en/of referenties
  1. (en) Lampanyctus festivus. FishBase. Ed. Ranier Froese and Daniel Pauly. 10 2011 version. N.p.: FishBase, 2011.
Geplaatst op:
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Dit artikel is een beginnetje over biologie. U wordt uitgenodigd om op bewerken te klikken om uw kennis aan dit artikel toe te voegen. Beginnetje
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雜色珍燈魚 ( cinèis )

fornì da wikipedia 中文维基百科
二名法 Lampanyctus festivus
Tåning, 1928

雜色珍灯鱼学名Lampanyctus festivus)为輻鰭魚綱燈籠魚目灯笼鱼科的其中一。分布于全球三大洋海域,為深海魚類,棲息深度40-1052公尺,體長可達13.8公分。

参考文献

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 src= 維基物種中有關雜色珍灯鱼的數據

小作品圖示这是一篇與灯笼鱼目相關的小作品。你可以通过编辑或修订扩充其内容。
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雜色珍燈魚: Brief Summary ( cinèis )

fornì da wikipedia 中文维基百科

雜色珍灯鱼(学名:Lampanyctus festivus)为輻鰭魚綱燈籠魚目灯笼鱼科的其中一。分布于全球三大洋海域,為深海魚類,棲息深度40-1052公尺,體長可達13.8公分。

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Distribution ( Anglèis )

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Atlantic Ocean: north to about 40°N, with isolates to 50°N and from about 13°S to the subtropical convergence

Arferiment

North-West Atlantic Ocean species (NWARMS)

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Habitat ( Anglèis )

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oceanic and mesopelagic, found between 475-1,000 m during the day and between 40-325 m at night

Arferiment

North-West Atlantic Ocean species (NWARMS)

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Habitat ( Anglèis )

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nektonic

Arferiment

North-West Atlantic Ocean species (NWARMS)

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Habitat ( Anglèis )

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Known from seamounts and knolls

Arferiment

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

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