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Overview
Brief Summary
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Biology
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Description
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Comprehensive Description
Description
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Distribution
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Leewis, R. (2002). Flora en fauna van de zee [Marine flora and fauna]. Veldgids, 16. KNNV Uitgeverij: Utrecht, The Netherlands. ISBN 90-5011-153-X. 320 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1116
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Eneman, E. (1984). Uit het Natuurhistorisch Archief [From the Natural History Archive]. De Strandvlo 4(1): 4-17
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=755
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Müller, Y. (2004). Faune et flore du littoral du Nord, du Pas-de-Calais et de la Belgique: inventaire. [Coastal fauna and flora of the Nord, Pas-de-Calais and Belgium: inventory]. Commission Régionale de Biologie Région Nord Pas-de-Calais: France. 307 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=9269
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Hayward, P.J.; Ryland, J.S. (Ed.) (1990). The marine fauna of the British Isles and North-West Europe: 1. Introduction and protozoans to arthropods. Clarendon Press: Oxford, UK. ISBN 0-19-857356-1. 627 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1
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Zühlke, R.; Alvsvåg, J.; De Boois, I.; Cotter, J.; Ehrich, S.; Ford, A.; Hinz, H.; Jarre-Teichmann, A.; Jennings, S.; Kröncke, I.; Lancaster, J.; Piet, G.; Prince, P. (2001). Epibenthic diversity in the North Sea. Senckenb. Marit. 31(2): 269-281
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1129
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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Christie, H.; Jørgensen, N.M.; Norderhaug, K.M.; Waage-Nielsen, E. (2003). Species distribution and habitat exploitation of fauna associated with kelp (Laminaria hyperborea) along the Norwegian Coast. J. Mar. Biol. Ass. U.K. 83(4): 687-699
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1291
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Backeljau, T. (1986). Lijst van de recente mariene mollusken van België [List of the recent marine molluscs of Belgium]. Koninklijk Belgisch Instituut voor Natuurwetenschappen: Brussels, Belgium. 106 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2
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de Bruyne, R.H. (1991). Schelpen van de Nederlandse kust [Shells of the Dutch coast]. Jeugdbondsuitgeverij/KNNV Uitgeverij: Utrecht, The Netherlands. ISBN 90-5107-017-9. III, 165 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=705
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Trott, T.J. 2004. Cobscook Bay inventory: a historical checklist of marine invertebrates spanning 162 years. Northeastern Naturalist (Special Issue 2): 261 - 324.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=3072
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ILVO epifauna en demersale visdata: epifauna en demersale vismonitoring op het Belgisch deel van de Noordzee sinds 1979
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=132964
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d'Udekem d'Acoz, C. (1990). Notes on some organisms collected between Wenduine and De Haan on 3 March 1990 [Notes sur quelques organismes recueillis entre Wenduine et De Haan le 3 mars 1990]. De Strandvlo 10(3): 74-78
http://www.marinespecies.org/ophiuroidea/aphia.php?p=sourcedetails&id=138631
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Simons, E.; Simons, G.; Corstanje, H. (1988). Report on the beach excursion at Oostduinkerke (Belgium) on 2 November 1988 [Verslag van de strandexcursie te Oostduinkerke op 2 november 1988]. De Strandvlo 8(4): 206-209
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=138809
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Dumoulin, E. (1989). Micromolluscs in sand suppletions from the Goote Bank [Micromollusken uit opgespoten zand afkomstig van de Goote Bank]. De Strandvlo 9(1): 21-31
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=138713
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De Maersschalck, V. (2004). An inventory of the macrofauna of the Sluice Dock at Oostende: contribution to an integrated management [Een inventarisatie van de macrofauna van de Spuikom te Oostende: bijdrage tot een geïntegreerd beheer]. MSc Thesis. Universiteit Gent, Vakgroep Biologie: Gent, Belgium. 71, tables, figures pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=133008
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Gofas, S.; Le Renard, J.; Bouchet, P. (2001). Mollusca, 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. 180-213
http://www.marinespecies.org/mollusca/aphia.php?p=sourcedetails&id=1364
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Billiau, R. (2002). Reuzenstranding van verse (levende) wijde mantels Aequipecten opercularis (L., 1758) te De Panne op 8 en 9 november 1999 [Mass stranding of fresh (living) Queen scallop Aequipecten opercularis (L., 1758) at De Panne on 8 and 9 November 1999]. De Strandvlo 22(3-4): 99-102
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1088
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Leloup, E. (1952). Contributions à l'étude de la faune belge: 19. Observation sur la crevette grise au large de la côte belge en 1949 [Contribution to the study on the Belgian fauna: 19. Observation on the brown shrimp along the Belgian coast in 1949]. Med. K. Belg. Inst. Nat. Wet. 18(1): 1-28
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1648
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Ziegelmeier, E. (1966). Die Schnecken (Gastropoda Prosobranchia) der deutsche Meeresgebiete und brackigen Küstengewässer [The Gastropoda Prosobranchia from the German seas and brackish coastal waters]. Helgol. Wiss. Meeresunters. 13: 1-66 [Subsequent publication]
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1678
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Adam, W.; Leloup, E. (1934). Sur la présence du gastéropode Crepidula fornicata (Linné, 1758) sur la côte belge [Occurrence of the gastropod Crepidula fornicata (Linneaus, 1758) at the Belgian coast]. Bull. Mus. royal d'Hist. Nat. Belg./Med. Kon. Natuurhist. Mus. Belg. 10(45): 1-6
http://www.marinespecies.org/mollusca/aphia.php?p=sourcedetails&id=1250
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Natural Geography in Shore Areas (NaGISA) database, compiled by Ann Knowlton.
http://www.marinespecies.org/arms/aphia.php?p=sourcedetails&id=145467
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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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Guiry, M.D. & Guiry, G.M. (2011). Species.ie version 1.0 World-wide electronic publication, National University of Ireland, Galway (version of 15 March 2010).
http://www.marinespecies.org/ascidiacea/aphia.php?p=sourcedetails&id=149068
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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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Miller, Roberta. 2011. The St. Anne de Bellevue Arctic Biological Station Collection In Museum collection database, Fisheries and Oceans Canada digital collections, Maurice Lamontagne Institute, Quebec
http://www.marinespecies.org/asteroidea/aphia.php?p=sourcedetails&id=150285
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Bossé, L., B. Sainte-Marie et J. Fournier (1996). Les invertébrés des fonds meubles et la biogéographie du fjord du Saguenay. Rapp. tech. can. sci. halieut. aquat. 2 132: vii + 45 p.
http://www.marinespecies.org/asteroidea/aphia.php?p=sourcedetails&id=153966
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Préfontaine, G. & P. Brunel. 1962. Liste d'invertébrés marins recueillis dans l'estuaire du Saint-Laurent de 1929 à 1934. Naturaliste Canadien, Quebec 89(8-9):237-263, fig. 1.
http://www.marinespecies.org/ascidiacea/aphia.php?p=sourcedetails&id=109070
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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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Geographic Range
The waved whelk, or common northern whelk, can be found in the North Atlantic along the coastline of North America from New Jersey northward, the coastline of Greenland, the coastline of Europe from France northward, the coastlines of Norway, the British Isles, Iceland, and the coastlines of some islands in the Arctic Ocean (George and George 1979, Grzimek 1972, Ghiselin 2000).
Biogeographic Regions: arctic ocean (Native ); atlantic ocean (Native )
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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
United States
Origin: Native
Regularity: Regularly occurring
Currently: Present
Confidence: Confident
Type of Residency: Year-round
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Range
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Physical Description
Morphology
Physical Description
The marbled body of the whelk is encased in a calcified shell, which ranges from 6-10 cm in length. The shell is spiraled, and lacks the nacreous surface layer of some other gastropods. The body is composed of three basic parts: the foot, the head, and a visceral mass. The foot extends from the shell next to the head and is used for locomotion and grasping prey or a substrate when feeding on algae. The head includes a mouth, from which the radula, an elongated tongue-like apparatus bearing three central teeth and two rows of transverse teeth, is extended for feeding. There are also two cephalic tentacles which have some tactile sensation. These tentacles and the osphradia, a structure that does not emerge from the shell but is positioned at the end of a siphon pointing in the direction of the current, have chemoreceptors which aid in scavenging. Whelks are either male or female, with gonads positioned deep within the shell behind the body because of the torsion of the spiral shell. Males of the species have a penis for sperm transfer (George and George 1979, Grzimek 1972, Brusca 1990).
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Ecology
Habitat
Waved whelks occupy coastlines within the range described above from the tide level to 180 meters depth. They live in the mud and sand of these areas on the ocean floor (Ghiselin 2000, George-George 1979, Grzimek 1972, Anderson 1988).
Aquatic Biomes: coastal
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Natural Geography in Shore Areas (NaGISA) database, compiled by Ann Knowlton.
http://www.marinespecies.org/arms/aphia.php?p=sourcedetails&id=145467
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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 650 samples.
Environmental ranges
Depth range (m): -2.2 - 549
Temperature range (°C): -0.262 - 12.552
Nitrate (umol/L): 0.660 - 22.184
Salinity (PPS): 22.343 - 35.343
Oxygen (ml/l): 3.835 - 8.193
Phosphate (umol/l): 0.064 - 1.647
Silicate (umol/l): 0.987 - 17.288
Graphical representation
Depth range (m): -2.2 - 549
Temperature range (°C): -0.262 - 12.552
Nitrate (umol/L): 0.660 - 22.184
Salinity (PPS): 22.343 - 35.343
Oxygen (ml/l): 3.835 - 8.193
Phosphate (umol/l): 0.064 - 1.647
Silicate (umol/l): 0.987 - 17.288
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Stellwagen Bank Benthic Community
The species associated with this article partially comprise the benthic community of Stellwagen Bank, an undersea gravel and sand deposit stretching between Cape Cod and Cape Ann off the coast of Massachusetts. Protected since 1993 as part of the Stellwagen Bank National Marine Sanctuary, the bank is known primarily for whale-watching and commercial fishing of cod, lobster, hake, and other species (Eldredge 1993).
The benthic community of Stellwagen Bank is diverse and varied, depending largely on the grain size of the substrate. Sessile organisms such as bryozoans, ascidians, tunicates, sponges, and tube worms prefer gravelly and rocky bottoms, while burrowing worms, burrowing anemones, and many mollusks prefer sand or mud surfaces (NOAA 2010). Macroalgae, such as kelps, are exceedingly rare in the area — most biogenic structure along the bottom is provided by sponges, cnidarians, and worms. The dominant phyla of the regional benthos are Annelida, Mollusca, Arthropoda, and Echinodermata (NOAA 2010).
Ecologically, the Stellwagen Bank benthos contributes a number of functions to the wider ecosystem. Biogenic structure provided by sessile benthic organisms is critical for the survivorship of juveniles of many fish species, including flounders, hake, and Atlantic cod. The benthic community includes a greater than average proportion of detritivores — many crabs and filter-feeding mollusks — recycling debris which descends from the water column above (NOAA 2010). Finally, the organisms of the sea-bed are an important source of food for many free-swimming organisms. Creatures as large as the hump-backed whale rely on the benthos for food — either catching organisms off the surface or, in the whale’s case, stirring up and feeding on organisms which burrow in sandy bottoms (Hain et al 1995).
As a U.S. National Marine Sanctuary, Stellwagen Bank is nominally protected from dredging, dumping, major external sources of pollution, and extraction of mammals, birds or reptiles (Eldredge 1993). The benthic habitat remains threatened, however, by destructive trawling practices. Trawl nets are often weighted in order that they be held against the bottom, flattening soft surfaces, destroying biogenic structure, and killing large numbers of benthic organisms. There is also occasional threat from contaminated sediments dredged from Boston harbor and deposited elsewhere in the region (NOAA 2010). The region benefits from close observation by NOAA and the Woods Hole Oceanographic Institute, however, and NOAA did not feel the need to make any special recommendations for the preservation of benthic communities in their 2010 Management Plan and Environmental Assessment.
- Eldredge, Maureen. 1993. Stellwagen Bank: New England’s first sanctuary. Oceanus 36:72.
- Hain JHW, Ellis SL, Kenney RD, Clapham PJ, Gray BK, Weinrich MT, Babb IG. 1995. Apparent bottom feeding by humpback-whales on Stellwagen Bank. Marine Mammal Science 11, 4:464-479.
- National Oceanographic & Atmospheric Administration. 2010. Stellwagen Bank National Marine Sanctary Final Management Plan and Environmental Assessment. “Section IV: Resource States” pp. 51-143. http://stellwagen.noaa.gov/management/fmp/pdfs/sbnms_fmp2010_lo.pdf
- National Oceanographic & Atmospheric Administration. 2010. Stellwagen Bank National Marine Sanctary Final Management Plan and Environmental Assessment. “Appendix J: Preliminary Species List for the SBNMS” pp. 370-381. http://stellwagen.noaa.gov/management/fmp/pdfs/sbnms_fmp2010_lo.pdf
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Trophic Strategy
Food Habits
The waved whelk is a carnivore, and feeds on crabs, polychaete worms, bivalves, and dead organisms. Water enters the siphon which is pointed in the direction of the current and the osphridia's chemoreceptors detect for prey. The whelk moves to the prey using its foot, and uses it to grasp the shell in the case of a crab or bivalve. The radula is extended from the mouth and if the prey has a shell, the radula's teeth are used to drill a beveled hole through which the radula can extract the body matter. Radular teeth of whelks are solid and do not contain poison as in the case of cones, but the tongue may confer a secreted acidic mucus to the shell that is being bored. Digestion is primarily extracellular and takes place within a digestive gland at the end of a long esophagus that empties into a stomach (Anderson 1988, Alexander 1979, Brusca 1990, Ghiselin 2000).
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Life History and Behavior
Reproduction
Sexes are separate, and the male has a penis which transfers sperm to the female, where internal fertilization occurs. There are two types of sperm produced by the male whelk. The first is the viable euspermatozoa, which are the functional gametes that will unite with the egg in the reproductive tract of the female. Accompanying these are paraspermatozoa, which have multiple external tails and help to control and assist in the movement of the viable sperm, as well as provide them with nutrients. After fertilized eggs emerge from the oviduct, they are coated in mucus and approximately 1000 are contained in a flexible capsule. These capsules are then released into piles. Of the 1000 eggs in a capsule, only about 10 undergo full development, the rest providing nutrition. Snails hatch from these capsules fully developed (Anderson 1988, Grzimek 1972).
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Buccinum undatum
There is 1 barcode sequence available from BOLD and GenBank. Below is the 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. Other sequences that do not yet meet barcode criteria may also be available.
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Download FASTA File
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Statistics of barcoding coverage: Buccinum undatum
Public Records: 1
Specimens with Barcodes: 5
Species With Barcodes: 1
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Conservation
Conservation Status
The northern whelk is found readily in along the coasts of its geographic range in large numbers, especially in North America, probably due in part to its excellent and complex reproductive adaptations (Anderson 1988, Ghiselin 2000, U.S. Fish and Wildlife 2000, Sea World Education Dep. 2000).
US Federal List: no special status
CITES: no special status
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National NatureServe Conservation Status
United States
Rounded National Status Rank: NNR - Unranked
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Status
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Threats
Management
Conservation
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Relevance to Humans and Ecosystems
Benefits
Economic Importance for Humans: Positive
On the coast of North America fishermen often use the body of the whelk without the shell as bait for cod. In the past fishermen have been known to use the egg capsule of the whelk as "sea soap" to clean their hands. In Europe and Scandinavia the waved whelk serves as a food source for humans. We also receive the indirect benefit of the scavenging habits of the whelk in the disposal of carrion on the ocean floor (Grzinek 1972, Brusca 1990).
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Wikipedia
Buccinum undatum
Buccinum undatum, known as the common whelk, is a large edible marine gastropod in the family Buccinidae, the "true whelks".
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Distribution
This species is a familiar part of the marine fauna of the Northern Atlantic and is found on the shores of the United Kingdom, France, Norway, Iceland, some Arctic islands, and North America as far south as New Jersey. They prefer colder temperatures, and cannot survive at temperatures above 29°C.[1]
Habitat
This species is mainly found on soft bottoms in the sublittoral zone, and occasionally on the littoral fringe, where it is sometimes found alive at low tide. It does not adapt well to life in the intertidal zone, due to its intolerance for low salinities. If exposed to air, it may crawl from its shell, risking desiccation.[1]
Shell
This species' solid shell is very pale. In life, the shell is covered in a yellowish-brown periostracum.
The shell surface has a sculpture of vertical, wavy folds (hence the name undatum, which means wavy). The wavy folds are crossed by numerous incised spiral lines, some of which are paired. The aperture of the shell is broadly oval and tapers to a siphonal canal. The number of shell whorls is seven or eight.
The maximum height of the shell is 10 cm and the maximum width is 6 cm.
The animal emits a thin and copious slime.[2]
Trophic connections
This species of whelk feeds on live bivalves, and are, in turn, preyed upon by several fish (cod, dogfish, etc.) and crustaceans.[1] They may benefit from seastar feeding, by eating the extracted bivalve remains abandoned by the seastar.[3]
Parasites
Larval stages of Stephanostomum baccatum were found in the digestive gland of Buccinum undatum.[4]
As a food item
Buccinum undatum is eaten widely. Some believe they are best cooked by boiling in sea water.[citation needed] There is a strong fishery on many shores around the world. They are trapped in pots using dogfish and brown crab as bait.[5]
Ecology and population decline
Disappearing or diminishing populations of whelks have been observed since the early 1970s, especially in the North Sea and the Wadden Sea. Additionally, vast beds of empty shells have been discovered where no living whelks are present. Imposex, the occurrence of male gonads on female whelks, has been detected since the early 1990s, and is thought to be a product of the shipping industry.[1] Specifically, TBT has been shown to reduce viability of whelk populations.[6]
References
- ^ a b c d Ten Hallers-Tjabbes, C.C., Everaarts, J.M., Mensink, B.P., & Boon, J.P. (1996) The Decline of the North Sea Whelk (Buccinum undatum L.) Between 1970 and 1990: A Natural or Human-Induced Event? 17:1-3. pp. 333-43. Marine Ecology.
- ^ G.W. Tryon, Systematic Conchology vol. I, Philadelphia, 1882
- ^ Himmelman, J.H. and Hamel, J.-R. (1993) Diet, behaviour and reproduction of the whelk Buccinum undatum in the northern Gulf of St. Lawrence, eastern Canada. 116:3. pp. 423-430. Marine Biology.
- ^ Sommerville C. (1978). "The histopathology of Stephanochasmus baccatus Nicoll, 1907 in the digestive gland of Buccinum undatum (L.)". Journal of Fish Diseases 1(3): 219-232. doi:10.1111/j.1365-2761.1978.tb00024.x.
- ^ Fahy, E. (2001) Conflict between two inshore fisheries: for whelk (Buccinum undatum) and brown crab (Cancer pagurus), in the southwest Irish Sea. 465: 73-83. Hydrobiologia.
- ^ Mensink, B.P., Everaarts, J.M., Kralt, H., ten Hallers-Tjabbes, C.C., & Boon, J.P. (1996) Tributyltin exposure in early life stages induces the development of male sexual characteristics in the common whelk, Buccinum undatum. 42: 1-4. pp. 151-154. Marine Environmental Research.
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