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Longfin Inshore Squid

Doryteuthis (Amerigo) pealeii (Lesueur 1821)

Benefits

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This species of squid is very important to fishing industries throughout the world, including the United States, where a big market exists for this animal in both commercial and recreational fishing. In commercial fishing, Longfin inshore squid are sold to restaurants and other stores. In recreational fishing they serve as bait to catch to fish such as Mahi-mahi, Swordfish, and Marlins (Cadrin 2000, von der Linden et al. 1998).

Loligo pealeii is also used as specimen in neurobiology research. Its neurons, one thousand times larger than their counterparts in humans, have provided scientists ample opportunity to study such things as sodium and potassium ion pumps. The study of these neurons has helped scientists better understand heart disease, cancer, Alzherimer's Disease, and kidney disease (Marine Biological Laboratory, 2000).

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Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Trophic Strategy

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Loligo pealeii is carnivorous. Its diet includes chaetognaths, crustaceans, decapod shrimp, fishes, polychaetes, other squid, and euphausids.

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Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Jerry Kirkhart, Fresno City College
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Distribution

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Loligo pealeii is found from Newfoundland to the Gulf of Venezuela, migrating to different places to spawn. Among other places, these squid migrate to the Cape Cod area during the Spring and are also known as Woods Hole squid because they are studied at the Marine Biological Laboratory in Woods Hole, Massachusetts (Marine Biological Laboratory,2000).

Biogeographic Regions: atlantic ocean (Native )

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Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Jerry Kirkhart, Fresno City College
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Habitat

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This species lives in the waters along the eastern continental shelf of North America, and in the Gulf of Mexico. In comes into shallow waters near shore to lay eggs. (Marine Biological Laboratory, 2000)

Aquatic Biomes: coastal

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Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Jerry Kirkhart, Fresno City College
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Morphology

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These medium-sized squid grow to about 50 cm long. Like all squid, they have ten arms (eight of which are the same length, and one pair used for grabbing prey are longer) and three hearts (two close to their gills) so that they "can pump oxygen to the rest of the body easily." Their speed and maneuverability have earned them the description of "invertebrate athletes" (Squids,2000; Ellis, 34).

Other Physical Features: ectothermic ; bilateral symmetry

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Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Jerry Kirkhart, Fresno City College
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Conservation Status

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This species is vulnerable to overfishing, and the U.S. National Oceanic and Atmospheric Administration's Northeast Fisheries Center has helped establish catch limits to protect the population (Cadrin 2000).

US Federal List: no special status

CITES: no special status

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Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Jerry Kirkhart, Fresno City College
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Reproduction

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Males court females (there is much communication by flashing skin colors), and if accepted by a female, use a modified arm (called a hectocotylus) to transfer a package of sperm called a spermatophore to the female. Females produce packets of about 200 eggs, and stick them to the sea floor in large groups with other females. Sometimes "sneaker" males lurk around the eggmasses, darting in to add their sperm as females lay their eggs. (MBL 2000)

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bibliographic citation
Rodriguez, M. 2001. "Loligo pealeii" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Loligo_pealeii.html
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Martha Rodriguez, Fresno City College
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Jerry Kirkhart, Fresno City College
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Breeding Season

provided by Egg Characteristics and Breeding Season for Woods Hole Species
Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Care of Adults

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
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Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Fertilization and Cleavage

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
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Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Later Stages of Development

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Living Material

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Living Material

provided by Egg Characteristics and Breeding Season for Woods Hole Species
Woods Hole, Maine
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copyright
Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Methods of Observation

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Preparation of Cultures

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Preparation of Slides

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Procuring Gametes

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Special comments

provided by Egg Characteristics and Breeding Season for Woods Hole Species
Woods Hole, Maine

References

  • Broors, W. K., 1880. The development of the squid Loligo pealii (Lesueur). Anniv. Mem. Boston Soc. Nat. Hist., 1880, pp. 1-22.
  • Drew, G. A., 1911. Sexual activities of the squid, Loligo pealii (Les.). I. Copulation, egglaying and fertilization. J. Morph., 22: 327-359.
  • Drew, G. A., 1919. Sexual activities of the squid Loligo pealii (Les.). Ii. The spermatophore; its structure, ejaculation and formation. J. Morph., 32: 379-435.
  • Hoadley, L., 1930. Polocyte formation and the cleavage of the polar body in Loligo and Chaetopterus. Biol. Bull., 58: 256-264.
  • Korschelt, E., 1892. Beitrage zur Entwicklungsgeschichte der Cephalopoden. I. Die Entstehung des Darmkanals und Nervensystems in Beziehung zur Keimblatterfrage. Festschrift R. Leuckart, S. 347-373.
  • Korschelt, E., 1936. Cephalopoden. In: Vergleichende Entwicklungsgeschichte der Tiere, Gustav Fischer, Jenz, Bd. 2, S. 968-1009.
  • Naef, A., 1928. Die Cephalopoden, Bd. 2, Embryologie. Fauna und Flora des Golfes von Neapel, 35: 1-347.
  • Portmann, A., 1926. Der embryonale Blutkreislauf und die Dotterresorption bei Loligo vulgaris. Zeitschr. f. Morph. u. Okol. d. Tiere, 5: 406-423.
  • Portmann, A., and A. M. Bidder, 1928. Yolk-absorption in Loligo and the function of the embryonic liver and pancreas. Quart. J. Micr. Sci., 72: 301-324.
  • Ranzi, S., 1931a. Duplicitas cruciata in embrioni di Cefalopodi. Pubbl. Staz. Zool., Napoli, 11: 86-103.
  • Ranzi, S., 1931b. Sviluppo di parti isolate di embrioni di Cefalopodi. (Analisi sperimentale dell'embriogenesi.) Pubbl. Staz. Zool., Napoli, 11: 104-146.
  • Ranzi, S., 1937. Ricerche sulfa fisiologia dell'embrione dei Ce&lopodi. Pont. Acad. Scient., Acta, 1: 43-49.
  • Spek, J., 1934. Die bipolare Differenzierung des Cephalopoden- und des Prosobranchiereies. Arch. f. Entw., 131: 362-372.
  • Watase, S., 1891. Studies on Cephalopods. I. Cleavage of the ovum. J. Morph., 4: 247-302.
  • Williams, L. W., 1910. The anatomy of the common squid, Loligo pealii, Lesueur. E. J. Brill, Leiden, Holland, pp. 1-92.

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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

The Spermatophore

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

The Unfertilized Ovum

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Woods Hole, Maine
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Donald P. Costello and Catherine Henley
bibliographic citation
Costello, D.P. and C. Henley (1971). Methods for obtaining and handling marine eggs and embryos. Marine Biological Laboratory, Woods Hole, MA (Second Edition)
author
Costello, D.P.
author
C. Henley

Diagnostic Description

provided by FAO species catalogs
Mantle long, moderately slender, cylindrical, the posterior end bluntly pointed. Eyes not unusually large, diameter of externally visible eyeball 8 to 18% of mantle length, and diameter of dissected lens 2 to 6% of mantle length. Fins rhomboidal, their sides nearly straight. Left ventral arm IV hectocotylized in mature males by modification of the distal third to fourth of arm, but the modification does not extend to arm tip; fewer than 12 of the suckers in dorsal row usually smaller than half the size of their counterparts in the ventral row; bases or pedicels of some of the modified suckers rounded, narrowly triangular. Gladius long, rather wide, feather-shaped, ratio of greatest width of vane of gladius to greatest width of rachis 2.7 to 3.7 in females, 2.4 to 2.9 in males; edge of vane curved (sometimes straight in males), thin, rarely ribbed.

References

  • Cohen, (1976, systematics)
  • McMahon & Summers, (1971, temperature effect on development rate)
  • Rathjen, Hixon & Hanlon, (1979, fishery)
  • Roper, (1978, Species Identification Sheets, western central Atlantic, fishing area 31)
  • Serchuk & Rathjen, (1974, abundance in relation to temperature)
  • Summers, (1968, 1971, growth and size distribution)
  • Tibbets, (1977, fishery)
  • Tomiyama & Hibiya, (1978)

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FAO Species catalogue VOL. 3. Cephalopods of the world An Annotated and Illustrated Catalogue of Species of Interest to FisheriesClyde F.E. Roper Michael J. Sweeney Cornelia E. Nauen 1984. FAO Fisheries Synopsis No. 125, Volume 3
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Food and Agriculture Organization of the UN
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Distribution

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Western Atlantic: 5° N to 50° N, including Gulf of Mexico and Caribbean Sea.
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FAO Species catalogue VOL. 3. Cephalopods of the world An Annotated and Illustrated Catalogue of Species of Interest to FisheriesClyde F.E. Roper Michael J. Sweeney Cornelia E. Nauen 1984. FAO Fisheries Synopsis No. 125, Volume 3
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Size

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Maximum mantle length 50 cm in males, approximately 40 cm in females off the southern New England States of the USA; common length in catches ranges between 10 and 20 cm. Maturity is attained at about 15 cm in males and 13 or 14 cm in females.
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FAO Species catalogue VOL. 3. Cephalopods of the world An Annotated and Illustrated Catalogue of Species of Interest to FisheriesClyde F.E. Roper Michael J. Sweeney Cornelia E. Nauen 1984. FAO Fisheries Synopsis No. 125, Volume 3
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Brief Summary

provided by FAO species catalogs
A neritic speciesoccurring over the continental shelf and upper slope from the surface down to about 400 m depth,but rare or absent around islands.Optimum water temperatures for this species fluctuate between 10 and 14° C. Adults are demersal in daytime but disperse into the water column and many appear at the surface (in summer or in warm waters) at night. Longfin squid are known to effect seasonal migrations. They overwinter in dense concentrations in offshore areas at depths between 100 and 200 m, and move thereafter to the nearshore feeding and spawning areas where they are found from late spring through fall. Mature squids are encountered almost throughout the year, but two peak spawning periods generally are observed: the first and more important in spring, and the second, less intense, in late summer and fall, this leading to the differentiation of multiple cohorts each year. Eggs are laid in gelatinous, finger-like strands, many of which are attached together in large masses ("sea mops") to solid substrates (i.e. rocks, shells, shipwrecks) in depths between 10 and 250 m. The eggs hatch after approximately 27 days (at temperatures at 12 to 18° C) or after 11 days (at 21.5 to 23° C) (McMahon & Summers (1971). Planktonic larvae and juveniles are abundant in surface waters and resemble adults in appearance (no metamorphosis). Squid originating from the spring spawn reach maturity in summer of the following year (after about 14 months, while individuals hatched in early autumn will spawn only in spring of the second successive year, at about 20 months of age. This overcrossing of the life-cycles of two life successive groups of hatchlings is a phenomenon also observed in other squid and cuttlefish species. Postspawning mortality is very high, particularly in females, a fact that is reflected in the smaller maximum size of females.Longfin squid prey on euphausids, fishes and other squids. Cannibalism is common.The species is in turn preyed upon by yellowfin tuna (Thunnus albacares ), toothed whales and other pelagic predators.
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bibliographic citation
FAO Species catalogue VOL. 3. Cephalopods of the world An Annotated and Illustrated Catalogue of Species of Interest to FisheriesClyde F.E. Roper Michael J. Sweeney Cornelia E. Nauen 1984. FAO Fisheries Synopsis No. 125, Volume 3
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Food and Agriculture Organization of the UN
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Benefits

provided by FAO species catalogs
Longfin squid was formerly taken only as bycatch to the shrimp and scale-fish trawl fishery, but in recent years an international fishery was developed, specifically for this species. The world catch of longfin squid fluctuated irregularly between about 10 700 t in 1978 and 23 600 t in 1980. In 1981 catches were back on the 1978 level. This can be explained by the absence of Spanish and Mexican vessels from Fishing Area 21 (northwestern Atlantic) where almost the entire catch is taken. The major exploiting countries are Japan, Italy and USA (FAO, 1983). Fishing operations are most intensive from November to March along the outer continental shelf of the New England and mid-Atlantic states where the overwintering stock is exploited. The identified longfin squid catch from the Gulf of Mexico and the Caribbean in 1981 was reported as only 40 t but it is suspected that this species accounts for part of the catch identified as Loligo spp. which amounted to almost 1 600 t in the same year (FAO, 1983). The flesh of longfin squid is of excellent quality and marketed fresh and frozen.The total catch reported for this species to FAO for 1999 was 18 749 t. The countries with the largest catches were USA (18 749 t).
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FAO Species catalogue VOL. 3. Cephalopods of the world An Annotated and Illustrated Catalogue of Species of Interest to FisheriesClyde F.E. Roper Michael J. Sweeney Cornelia E. Nauen 1984. FAO Fisheries Synopsis No. 125, Volume 3
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Food and Agriculture Organization of the UN
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Longfin inshore squid

provided by wikipedia EN

The longfin inshore squid (Doryteuthis pealeii) is a species of squid of the family Loliginidae.

Description

This species of squid is often seen with a reddish hue, but like many types of squid can manipulate its color, varying from a deep red to a soft pink. The dorsal mantle length of some males can reach up to 50 cm, although most squid commercially harvested are smaller than 30 cm long. This species exhibits sexual dimorphism, with most males growing faster and reaching larger sizes than females.

Specimen with tentacles outstretched
The gladius of a longfin inshore squid

Distribution

The longfin inshore squid is found in the North Atlantic, schooling in continental shelf and slope waters from Newfoundland to the Gulf of Venezuela. It is commercially exploited, especially in the range from the Southern Georges Bank to Cape Hatteras. The population makes seasonal migrations that appear to be related to bottom water temperatures; they move offshore during late autumn to overwinter along the edge of the continental shelf and return inshore during the spring and early summer (MAFMC 1998).

Diet

"The diet of the longfin inshore squid changes with size; small immature individuals feed on planktonic organisms while larger individuals feed on crustaceans and small fish. Studies have shown that juveniles feed on euphausiids and arrow worms, while older individuals feed mostly on small crabs, but also on polychaetes and shrimp. Adults feed on fish (clupeids, myctophids) and squid larvae/juveniles, and those larger than 16 cm feed on fish and squid. Fish species preyed on by longfin inshore squid include silver hake, mackerel, herring, menhaden, sand lance, bay anchovy, weakfish, and silversides. Maurer and Bowman (1985) discovered a difference in inshore/offshore diet: in offshore waters in the spring, the diet is composed of crustaceans (mainly euphausiids) and fish; in inshore waters in the fall, the diet is composed almost exclusively of fish; and in offshore waters in the fall, the diet is composed of fish and squid. Cannibalism is observed in individuals larger than 5 cm."[2]

Predators

Many pelagic and demersal fish species, as well as marine mammals and diving birds, prey upon juvenile and adult longfin inshore squid. Marine mammal predators include longfin pilot whales and common dolphins. Fish predators include striped bass, bluefish, sea bass, mackerel, cod, haddock, pollock, silver hake, red hake, sea raven, spiny dogfish, angel shark, goosefish, dogfish, mako shark, blue marlin and flounder. These squid do have ways of evading predators too. They have a very complex way of swimming called jet propulsion. The fin stroke plus the propulsion creates a very unique way of swimming in the ocean. This can help squid get away from predators more efficiently. [3]

Reproduction

The longfin inshore squid spawns year-round and lives for less than one year. "Eggs are demersal. Enclosed in a gelatinous capsule containing up to 200 eggs. Each female lays 20-30 capsules. Fecundity ranges from 950–15,900 eggs per female. Laid in masses made up of hundreds of egg capsules from different females."[2] Individuals hatched in summer generally grow more rapidly than those hatched in winter due to the warmer temperature of the water. The lifespan of a typical specimen is normally less than one year.

Research

This species is a model organism in neuroscience and it was used by Andrew Huxley and Alan Hodgkin in their studies on axons. Its axon is the largest axon known to science.[4] They are also used for research on replicating their camouflage abilities due to the chromatophores in their skin, which reflect a different color depending on the angle at which the light is hitting them. A dead longfin can show a colourful display with its chromatophores by connecting its axons to a music player.[5][6][7]

References

  1. ^ a b Julian Finn (2016). "Doryteuthis (Amerigo) pealeii (Lesueur, 1821)". World Register of Marine Species. Flanders Marine Institute. Retrieved 23 February 2018.
  2. ^ a b NOAA Longfin Inshore Squid, Loligo pealeii, Life History and Habitat Characteristics retrieved: Dec. 26, 2012
  3. ^ Anderson, Erik, and M. Edwin Demont. “The Locomotory Function of the Fins in the Squid Loligo Pealei.” Marine and Freshwater Behaviour and Physiology, vol. 38, no. 3, 2005, pp. 169–89, https://doi.org/10.1080/10236240500230765.
  4. ^ Hellier, Jennifer L. (2014). The Brain, the Nervous System, and Their Diseases. ABC-Clio. p. 532. ISBN 9781610693387.
  5. ^ Gage, Greg. "Insane in the Chromatophores" Youtube video Vimeo video Backyard Brains, 23 August 2012. Retrieved: 2 September 2012.
  6. ^ "MBL Scientists Discover Nerves Control Iridescence in Squid’s Remarkable “Electric Skin”" Marine Biological Laboratory, 24 August 2012. Retrieved: 2 September 2012.
  7. ^ Kenney, Diane. "Insanely Popular: MBL Squid Research/Rap Video Goes Viral" Marine Biological Laboratory, 31 August 2012. Retrieved: 2 September 2012.
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Longfin inshore squid: Brief Summary

provided by wikipedia EN

The longfin inshore squid (Doryteuthis pealeii) is a species of squid of the family Loliginidae.

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