BIOTIC Species Information for Scoloplos armiger
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Researched by | Lizzie Tyler | Data supplied by | University of Sheffield | ||||||||||||
Refereed by | This information is not refereed. | ||||||||||||||
Taxonomy | |||||||||||||||
Scientific name | Scoloplos armiger | Common name | A polychaete worm | ||||||||||||
MCS Code | P672 | Recent Synonyms | None | ||||||||||||
Phylum | Annelida | Subphylum | |||||||||||||
Superclass | Class | Polychaeta | |||||||||||||
Subclass | Order | Orbiniida | |||||||||||||
Suborder | Family | Orbiniidae | |||||||||||||
Genus | Scoloplos | Species | armiger | ||||||||||||
Subspecies | |||||||||||||||
Additional Information | None entered | ||||||||||||||
Taxonomy References | Fish & Fish, 1996, Hayward et al., 1996, Hayward & Ryland, 1995b, Fauchald, 1977, | ||||||||||||||
General Biology | |||||||||||||||
Growth form | Vermiform segmented |
Feeding method | Surface deposit feeder Sub-surface deposit feeder |
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Mobility/Movement | Burrower |
Environmental position | Infaunal |
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Typical food types | Insufficient information | Habit | Burrow dwelling | ||||||||||||
Bioturbator | Diffusive mixing | Flexibility | High (>45 degrees) | ||||||||||||
Fragility | Fragile | Size | Medium(11-20 cm) | ||||||||||||
Height | Not relevant | Growth Rate | Insufficient information | ||||||||||||
Adult dispersal potential | 100-1000m | Dependency | Independent | ||||||||||||
Sociability | Solitary | ||||||||||||||
Toxic/Poisonous? | No | ||||||||||||||
General Biology Additional Information | Gibbs (1968) described the worm as 'extremely fragile'. Up to 12 cm in length (Fish & Fish, 1996). Worms roam through burrow system down to 15 cm depth. Do not usually appear at sediment surface (Kruse et al., 2004). | ||||||||||||||
Biology References | Kruse et al., 2003, Kruse et al., 2004, Gibbs, 1968, Hayward & Ryland, 1990, Julie Bremner, unpub data, | ||||||||||||||
Distribution and Habitat | |||||||||||||||
Distribution in Britain & Ireland | Widely distributed in NW Europe and Britain on lower shore and in sublittoral (Fish & Fish, 1996), | ||||||||||||||
Global distribution | Found from the Arctic and north west Europe to the Indian Ocean, the Pacific and the Antarctic. | ||||||||||||||
Biogeographic range | Not researched | Depth range | |||||||||||||
Migratory | Non-migratory / Resident | ||||||||||||||
Distribution Additional Information | None entered | ||||||||||||||
Substratum preferences | Coarse clean sand Fine clean sand Muddy sand |
Physiographic preferences | |||||||||||||
Biological zone | Wave exposure | ||||||||||||||
Tidal stream strength/Water flow | Salinity | ||||||||||||||
Habitat Preferences Additional Information | None entered | ||||||||||||||
Distribution References | Fish & Fish, 1996, Hayward et al., 1996, Hayward & Ryland, 1995b, Rasmussen, 1973, Hayward & Ryland, 1990, Julie Bremner, unpub data, | ||||||||||||||
Reproduction/Life History | |||||||||||||||
Reproductive type | Gonochoristic |
Developmental mechanism | Lecithotrophic Direct Development |
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Reproductive Season | Insufficient information | Reproductive Location | See additional information | ||||||||||||
Reproductive frequency | Annual episodic | Regeneration potential | No | ||||||||||||
Life span | 3-5 years | Age at reproductive maturity | 1-2 years | ||||||||||||
Generation time | Insufficient information | Fecundity | |||||||||||||
Egg/propagule size | Fertilization type | Insufficient information | |||||||||||||
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Reproduction Preferences Additional Information | Two types of development reported. A holobenthic type that crawls out from a cocoon fixed on the substrate and burrows immediately, usually associated with intertidal populations in North Sea region and adjacent waters and a pelagic larvae associated with subtidal populations (Kruse et al., 2003; Kruse et al., 2004). In Isle of Sylt, North Sea, egg cocoons found on intertidal flats between Feb-April (Kruse et al., 2004). Spawning varies with location. In North Sea, main spawn March, secondary (pelagic) spawn from offshore in Oct (Kruse et al., 2004). At Whitstable, spawned four times in one year, main late Feb-April (Gibbs, 1968). 600-1920 / m² Oosterschelde (Coosen et al., 1994), 800 / m² at Whitstable (Gibbs, 1968). | ||||||||||||||
Reproduction References | Kruse et al., 2003, Kruse et al., 2004, Coosen et al., 1994, Gibbs, 1968, Eckert, 2003, Julie Bremner, unpub data, Bartolomaeus, 1998, |