Overview
Comprehensive Description
Biology
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Fernholm, B. 1998 Hagfish systematics. p. 33-44. In J.M. Jørgensen, J.P. Lomholt, R.E. Weber and H. Malte (eds.) The biology of hagfishes. Chapman & Hall, London. 578 p. (Ref. 31276)
http://www.fishbase.org/references/FBRefSummary.php?id=31276&speccode=54060
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Description
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Distribution
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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van der Land, J.; Costello, M.J.; Bailly, N.; Eschmeyer, W.N.; Froese, R. (2001). Pisces - Agnatha, in: Costello, M.J. et al. (Ed.) (2001). European register of marine species: a check-list of the marine species in Europe and a bibliography of guides to their identification. Collection Patrimoines Naturels, 50: pp. 358
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1409
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Nozères C., Archambault D., Chouinard P.-M., Gauthier J., Miller R., Parent E., Schwab P., Savard L., and Dutil J.-D. 2010. Identification guide for marine fishes of the estuary and northern Gulf of St. Lawrence and sampling protocols used during trawl surveys between 2004 and 2008. Can. Tech. Rep. Fish. Aquat. Sci. 2866: xi + 243 p
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=145051
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MEDIN (2011). UK checklist of marine species derived from the applications Marine Recorder and UNICORN, version 1.0.
http://www.marinespecies.org/asteroidea/aphia.php?p=sourcedetails&id=149081
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Ramos, M. (ed.). 2010. IBERFAUNA. The Iberian Fauna Databank
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=149024
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Siferd, Tim. 2010. Central and Arctic multi-species stock assessment surveys. In OBIS Canada Digital Collections. Bedford Institute of Oceanography, Dartmouth, Nova Scotia. OBIS Canada Ver1
http://www.marinespecies.org/ophiuroidea/aphia.php?p=sourcedetails&id=155140
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Miller, Roberta. 2012. The museum collection database, Fisheries and Oceans Canada digital collections, Maurice Lamontagne Institute, Quebec
http://www.marinespecies.org/asteroidea/aphia.php?p=sourcedetails&id=163928
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Dyntaxa (2013) Swedish Taxonomic Database. Accessed at www.dyntaxa.se [15-01-2013].
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=165516
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Fernholm, B. 1998 Hagfish systematics. p. 33-44. In J.M. Jørgensen, J.P. Lomholt, R.E. Weber and H. Malte (eds.) The biology of hagfishes. Chapman & Hall, London. 578 p. (Ref. 31276)
http://www.fishbase.org/references/FBRefSummary.php?id=31276&speccode=54060
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Range Description
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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National Distribution
Canada
Origin: Native
Regularity: Regularly occurring
Currently: Present
Confidence: Confident
Type of Residency: Year-round
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- Bigelow, H. B., and Schroeder. W.C.,1953; Fernholm, B.,1998.
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Physical Description
Size
- Bigelow, H. B., and Schroeder. W.C.,1953; Fernholm, B.,1998.
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Diagnostic Description
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Bigelow, H.B. and W.C. Schroeder 1948 Cyclostomes. p. 29-58. In J. Tee-Van, C.M. Breder, S.F. Hildebrand, A.E. Parr and W.C. Schroeder (eds.) Fishes of the Western North Atlantic. Part one. Lancelets, cyclostomes, sharks. Sears Foundation for Marine Research, Yale University, New Haven. 576 p. (Ref. 34302)
http://www.fishbase.org/references/FBRefSummary.php?id=34302&speccode=2513
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Ecology
Habitat
Environment
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Fernholm, B. 1998 Hagfish systematics. p. 33-44. In J.M. Jørgensen, J.P. Lomholt, R.E. Weber and H. Malte (eds.) The biology of hagfishes. Chapman & Hall, London. 578 p. (Ref. 31276)
http://www.fishbase.org/references/FBRefSummary.php?id=31276&speccode=54060
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Habitat and Ecology
This species is found on muddy bottoms where they hide in the mud. Slime is utilized for defence and it feeds chiefly on dead and dying fish of varying species by boring into the body and consuming viscera and musculature. The species is chiefly nocturnal. Its eggs are few in number about 19-30 mm and large (20-25 mm), the horny shell has a cluster of anchor-tipped filaments at each end. The copulatory organ is absent in this species. The gonads of hagfishes are situated in the peritoneal cavity. The ovary is found in the anterior portion of the gonad, and the testis is found in the posterior part. The animal becomes female if the cranial part of the gonad develops or male if the caudal part undergoes differentiation. If none develops, then the animal becomes sterile. If both anterior and posterior parts develop, then the animal becomes a functional hermaphrodite. However, hermaphroditism being characterised as functional needs to be validated by more reproduction studies (Patzner 1998).
Systems
- Marine
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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Water temperature and chemistry ranges based on 4413 samples.
Environmental ranges
Depth range (m): -9 - 1044
Temperature range (°C): -0.070 - 22.025
Nitrate (umol/L): 1.402 - 23.955
Salinity (PPS): 27.525 - 36.240
Oxygen (ml/l): 3.207 - 7.862
Phosphate (umol/l): 0.253 - 1.806
Silicate (umol/l): 0.987 - 25.595
Graphical representation
Depth range (m): -9 - 1044
Temperature range (°C): -0.070 - 22.025
Nitrate (umol/L): 1.402 - 23.955
Salinity (PPS): 27.525 - 36.240
Oxygen (ml/l): 3.207 - 7.862
Phosphate (umol/l): 0.253 - 1.806
Silicate (umol/l): 0.987 - 25.595
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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From 40 to 1200 meters.
Habitat: demersal. Found on muddy bottom. Feeds chiefly on dead and dying fish of varying species by boring into the body and consuming viscera and musculature. Chiefly nocturnal. Its eggs are few in number about 19-30 and large (20-25 mm), the horny shell has a cluster of anchor-tipped filaments at each end.
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- Bigelow, H. B., and Schroeder. W.C.,1953; Fernholm, B.,1998.
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Migration
Non-Migrant: No. All populations of this species make significant seasonal migrations.
Locally Migrant: No. No populations of this species make local extended movements (generally less than 200 km) at particular times of the year (e.g., to breeding or wintering grounds, to hibernation sites).
Locally Migrant: No. No populations of this species make annual migrations of over 200 km.
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Trophic Strategy
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Fernholm, B. 1998 Hagfish systematics. p. 33-44. In J.M. Jørgensen, J.P. Lomholt, R.E. Weber and H. Malte (eds.) The biology of hagfishes. Chapman & Hall, London. 578 p. (Ref. 31276)
http://www.fishbase.org/references/FBRefSummary.php?id=31276&speccode=54060
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- Bigelow, H. B., and Schroeder. W.C.,1953; Fernholm, B.,1998.
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Life History and Behavior
Life Cycle
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Patzner, R.A. 1998 Gonads and reproduction in hagfishes. p. 378-395. In J.M. Jørgensen, J.P. Lomholt, R.E. Weber and H. Malte (eds.) The biology of hagfishes. Chapman & Hall, London. 578 p. (Ref. 51361)
http://www.fishbase.org/references/FBRefSummary.php?id=51361&speccode=54060
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Reproduction
- Bigelow, H. B., and Schroeder. W.C.,1953; Fernholm, B.,1998.
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Evolution and Systematics
Functional Adaptations
Functional adaptation
Glands of hagfish protect it from predators by secreting a complex material of fibers and rapid water-absorbing slime.
"Hagfishes are known for producing large volumes of slime when stressed. Their slime is believed to act as a defence mechanism against gill-breathing predators, as it has been shown to reduce water flow over the gills of fish. Hagfish slime is composed of two interacting components, slime thread skeins and mucin vesicles, which are both released from glands along the ventrolateral length of the animal. Each slime gland is surrounded by striated muscle and a connective tissue capsule, and contains large numbers of gland thread cells and gland mucous cells. Gland thread cells contain skeins of tightly coiled polymers rich in intermediate filaments, while gland mucous cells produce vesicles containing mucins, a class of glycoproteins. Both cell types rupture partially as they pass through the slime gland duct, causing each to lose its plasma membrane, and releasing both thread skeins and mucin vesicles into the external environment. The mucin vesicles are released by holocrine secretion rather than the more typical mechanism of mucus secretion through fusion of vesicles with the membrane of the mucous cell and release of mucin granules by exocytosis. In this way, the mucin vesicles remain intact until they come into contact with seawater in the external environment.
"The mature slime is formed when exudate released from the hagfish contacts convectively mixing seawater. Agitation during mixing causes the thread skeins to uncoil to lengths of 10–17 cm, providing a large surface area to which the mucins released from the ruptured vesicles can attach. The fully formed slime is a complex network capable of confining seawater to channels between the slime threads and ruptured mucins like a fine sieve. The interaction between the thread skeins and ruptured mucins is critical for the production of the mature slime." (Herr et al. 2010:1092; citations removed from quote)
"When agitated, Atlantic hagfish (Myxine glutinosa) produce large quantities of slime that consists of hydrated bundles of protein filaments and membrane-bound mucin vesicles from numerous slime glands. When the slime exudate contacts seawater, the thread bundles unravel and the mucin vesicles swell and rupture. Little is known about the mechanisms of vesicle rupture in seawater and stabilization within the gland, although it is believed that the vesicle membrane is permeable to most ions except polyvalent anions. We hypothesized that the most abundant compounds within the slime gland exudate have a stabilizing effect on the mucin vesicles. To test this hypothesis, we measured the chemical composition of the fluid component of hagfish slime exudate and conducted functional assays with these solutes to test their ability to keep the vesicles in a condensed state. We found K+ concentrations that were elevated relative to plasma, and Na+, Cl– and Ca2+ concentrations that were considerably lower. Our analysis also revealed high levels of methylamines such as trimethylamine oxide (TMAO), betaine and dimethylglycine, which had a combined concentration of 388 mmol l–1 in the glandular fluid. In vitro rupture assays demonstrated that both TMAO and betaine had a significant effect on rupture, but neither was capable of completely abolishing mucin swelling and rupture, even at high concentrations. This suggests that some other mechanism such as the chemical microenvironment within gland mucous cells, or hydrostatic pressure is responsible for stabilization of the vesicles within the gland." (Herr et al. 2010:1092)
"Hagfishes are benthic marine protovertebrates that secrete copious quantities of slime when threatened. The slime originates as a two-component glandular exudate comprised of coiled bundles of cytoskeletal intermediate filaments (thread skeins) and mucin vesicles. Holocrine secretion of the slime into seawater results in the rapid deployment of both fibrous and mucin components, resulting in about a liter of dilute slime. Deployment of the thread skeins involves their unraveling in a fraction of a second from a 150 µm-long ellipsoid bundle to a thread that is 100x longer. We hypothesized that thread skein deployment requires both vigorous hydrodynamic mixing and the presence of mucin vesicles, both of which are required for whole slime deployment. Here we provide evidence that mixing and mucin vesicles are indeed crucial for skein unraveling. Specifically, we show that mucin vesicles mixed into seawater swell and elongate into high-aspect ratio mucin strands that attach to the thread skeins, transmit hydrodynamic forces to them and effect their unraveling by loading them in tension. Our discovery of mucin strands in hagfish slime not only provides a mechanism for the rapid deployment of thread skeins in vivo, it also helps explain how hagfish slime is able to trap such impressive volumes of seawater via viscous entrainment. We believe that the deployment of thread skeins via their interaction with shear-elongated mucins represents a unique mechanism in biology and may lead to novel technologies for transmitting hydrodynamic forces to microscale particles that would typically be immune to such forces." (Winegard & Fudge 2010:1235)
Learn more about this functional adaptation.
- Downer, J. 2002. Weird Nature: An Astonishing Exploration of Nature's Strangest Behavior. Ontario: Firefly Books.
- Herr JE; Weingard TM; O'Donnell MJ; Yancey PH; Judge DS. 2010. Stabilization and swelling of hagfish slime mucin vesicles. Journal of Experimental Biology. 213(7): 1092-1099.
- Winegard TM; Fudge DS. 2010. Deployment of hagfish slime thread skeins requires the transmission of mixing forces via mucin strands. Journal of Experimental Biology. 213(8): 1235-1240.
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Myxine glutinosa
There are 3 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Download FASTA File
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Statistics of barcoding coverage: Myxine glutinosa
Public Records: 6
Specimens with Barcodes: 15
Species With Barcodes: 1
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Contributor/s
Justification
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Trends
Population
Population Trend
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Threats
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IUCN 2006 2006 IUCN red list of threatened species. www.iucnredlist.org. Downloaded July 2006.
http://www.fishbase.org/references/FBRefSummary.php?id=57073
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In the Gulf of Maine (GOM), Atlantic hagfish are caught using modified 55-gallon plastic barrels, called hagfish pots, attached to sinking line and buoys. Typically 20-40 traps are deployed in a string for a small commercial vessel and 80-200 traps for larger vessels (NEFSC 2003). A series of funnelled holes in the side of the barrel allow hagfish to enter the baited pot but doesn’t allow them to escape. Several rows of 3/8” holes allow smaller animals to escape the traps.
Reporting of Atlantic hagfish landings is presently not required by law and fishery data are therefore incomplete. Atlantic hagfish landings first appear in the NEFSC commercial database in 1993 with a reported landing of approximately 500 metric tons. Annual reported landings during 1994-2000 ranged between 1,100 and 3,000 metric tons with a peak in 2000 (Keith 2006).
Reported commercial hagfish trips ranged from 94 trips in 1994 to 863 trips in 1996 and averaged slightly above 400 trips per year during 1994-2000. Landings during 2001 to 2005 have ranged from 700-1,300 metric tons per year. Trips targeting Atlantic hagfish declined after 2001, averaging 253 per year (Keith 2006) NMFS Logbook database indicated that the number of vessels in the hagfish fishery peaked at 23 vessels in 1996 and 22 vessels in 2000 (Keith 2006). Since 2000 there has been a steady decline of vessels reporting landings, with only six vessels reporting in 2005.
A data collection program has been proposed for Atlantic Hagfish by NMFS requiring seafood dealers to acquire permits and report on the purchase of hagfish made from commercial fishing vessels to aid in the future management of this species (Federal Register 2006, Keith 2006).
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Management
Conservation Actions
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Relevance to Humans and Ecosystems
Benefits
Importance
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Muus, B. and P. Dahlström 1978 Meeresfische der Ostsee, der Nordsee, des Atlantiks. BLV Verlagsgesellschaft, München. 244 p. (Ref. 4645)
http://www.fishbase.org/references/FBRefSummary.php?id=4645&speccode=23
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Wikipedia
Myxine glutinosa
Myxine glutinosa, known as the Atlantic hagfish in North America, and often simply as the hagfish in Europe, is a species of jawless fish of the genus Myxine.
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Distribution
The distribution of Myxine glutinosa in the eastern Atlantic Ocean extends from the western Mediterranean Sea and Portugal to the North Sea, Skagerrak, Kattegat and the Varanger Fjord.[1] It is also found in the western Atlantic Ocean from Baffin Island, Canada south to North Carolina.[2] A related species, the Gulf hagfish (Eptatretus springeri), occurs in the Gulf of Mexico.[3]
Description
The Atlantic hagfish may grow up to 2.5 feet (0.76 m) long, with no eyes and no jaws; its star-shaped mouth is surrounded by 6 barbels.[2] There is a single gill slit on each side of the eel-like body.[2] It has a total of 88–102 pores from which it can exude a slimy mucus.[1]
Ecology
Hagfish such as M. glutinosa feed on the carcasses of fishes, which they bore into through any available opening.[1][2]
Trivia
Following a public poll in 1982, it was voted to be the national fish of Norway with over 4000 votes, beating the second place ( Atlantic Cod ) by a large margin, as that only got 2,552 votes. [4]
References
| External identifiers for Myxine glutinosa | |
|---|---|
| Encyclopedia of Life | 207930 |
| ITIS | 159772 |
| NCBI | 7769 |
| WoRMS | 101170 |
| Also found in: FishBase | |
- ^ a b c P. J. P. Whitehead, M.-L. Bauchot, J.-C. Hureau, J. Nielsen & E. Tortonese, ed. (1984/1986). "Hagfish (Myxine glutinosa)". Fishes of the NE Atlantic and the Mediterranean. http://species-identification.org/species.php?species_group=fnam&id=945.
- ^ a b c d Michael Filisky & Roger Tory Peterson (1998). "Atlantic Hagfish". Peterson First Guide to Fishes of North America (2nd ed.). Houghton Mifflin Harcourt. p. 10. ISBN 978-0-395-91179-2. http://books.google.co.uk/books?id=Lr-5YlYlWhkC&pg=PA10.
- ^ Edwin S. Iversen & Renate H. Skinner (2006). "Atlantic hagfish Myxine glutinosa". Dangerous Sea Life of the West Atlantic, Caribbean, and Gulf of Mexico: A Guide for Accident Prevention and First Aid. Pineapple Press. p. 72. ISBN 978-1-56164-370-7. http://books.google.co.uk/books?id=MqyPjacQHFoC&pg=PA72.
- ^ Friis, R. (1982): «Slimåler» raser mot NRK/torsken, VG, s. 33, 15. november 1982
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Names and Taxonomy
Taxonomy
Comments: This species, as previously recognized, is assumed to occur across the North Atlantic Ocean, but Wisner and McMillan (1995) provided diagnostic characters to distinguish a western Atlantic species, Myxine limosa Girard, 1859, and an eastern Atlantic species. However, the results of Martini, Lesser and Heiser (1998) did not support a clean division between North Atlantic populations of M. glutinosa, and they recommended "that until and unless molecular data indicate otherwise, the species name M. glutinosa be retained as encompassing both eastern and western North Atlantic populations" (Nelson et al. 2004).
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