BIOTIC Species Information for Echinus esculentus
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Researched by | Dr Harvey Tyler-Walters and Lizzie Tyler | Data supplied by | MarLIN and University of Sheffield | ||||||||||||
Refereed by | This information is not refereed. | ||||||||||||||
Taxonomy | |||||||||||||||
Scientific name | Echinus esculentus | Common name | Edible sea urchin | ||||||||||||
MCS Code | ZB198 | Recent Synonyms | None | ||||||||||||
Phylum | Echinodermata | Subphylum | Echinozoa | ||||||||||||
Superclass | Class | Echinoidea | |||||||||||||
Subclass | Order | Echinoida | |||||||||||||
Suborder | Family | Echinidae | |||||||||||||
Genus | Echinus | Species | esculentus | ||||||||||||
Subspecies | |||||||||||||||
Additional Information | The genus Echinus is derived from the Greek 'echinos' meaning 'a hedgehog'. An omnivorous grazer feeding on seaweeds (e.g. Laminaria spp. sporelings), Bryozoa, barnacles and other encrusting invertebrates. Size range varies depending on age and locality, e.g. c. 4 cm at 1 year, 4-7 cm at 2 years, 7 -9 cm at 3 years and 9-11 cm at 4 years. This species may hybridize with Echinus acutus if sympatric. | ||||||||||||||
Taxonomy References | Hayward & Ryland, 1995b, Howson & Picton, 1997, Mortensen, 1927, Fish & Fish, 1996, Hyman, 1955, Nichols, 1969, | ||||||||||||||
General Biology | |||||||||||||||
Growth form | Globose |
Feeding method | Grazer (grains/particles) Grazer (fronds/blades) Grazer (surface/substratum) |
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Mobility/Movement | Crawler |
Environmental position | Epifaunal |
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Typical food types | Recorded feeding on; worms, barnacles (e.g. Balanus spp.), hydroids, tunicates, bryozoans (e.g. Membranipora spp.), macroalgae (e.g. Laminaria spp.), bottom material and detritus (reviewed by Lawrence 1975). | Habit | Free living | ||||||||||||
Bioturbator | Not relevant | Flexibility | None (< 10 degrees) | ||||||||||||
Fragility | Fragile | Size | Medium(11-20 cm) | ||||||||||||
Height | Growth Rate | See additional information | |||||||||||||
Adult dispersal potential | 1km-10km | Dependency | Independent | ||||||||||||
Sociability | Gregarious | ||||||||||||||
Toxic/Poisonous? | No | ||||||||||||||
General Biology Additional Information | Growth rates are variable depending on time of larval settlement, food availability, water temperature and age. Growth rates vary with locality although there is evidence to suggest that largest specimens are found in the south west (Nichols 1979). Growth rates based on growth lines in skeletal plates are probably underestimates (Gage 1992a & b). In the UK population growth is continuous in the first year after metamorphosis and considerably faster than adults in their 2nd year. In adults maximal growth occurs in a few months in spring and early summer but mature adults are slow growing. Comely & Ansell (1988) recorded 28 invertebrate species associated with Echinus esculentus from the west cost of Scotland near Oban. These included the parasites Echinomermella grayi and Euonyx chelatus mentioned above and in additional; 4 species of commensal polychaetes, a copepod and 10 amphipod species. The polychaete Adyte assimilis and the copepod Pseudoanthessius liber were regular commensals amongst the spines. Hyman (1955) states that Echinus esculentus is often infested with parasitic copepods e.g. Asterocheres echinola. | ||||||||||||||
Biology References | Hayward & Ryland, 1995b, Mortensen, 1927, Fish & Fish, 1996, Lawrence, 1975, MacBride, 1903, Kozloff & Westervelt, 1990, Comely & Ansell, 1988, Hyman, 1955, Gage, 1992(a), Gage, 1992(b), Nichols, 1979, Nichols, 1969, Emson & Moore, 1998, MacBride, 1914, Nichols, 1984, Boolootian, 1966, Birkett et al., 1998b, Hayward & Ryland, 1990, Julie Bremner, unpub data, Mortensen, 1927, Rees & Dare, 1993, | ||||||||||||||
Distribution and Habitat | |||||||||||||||
Distribution in Britain & Ireland | Common on most coasts of the British Isles but absent from most of east coast of England, the eastern English Channel and some parts of north Wales. | ||||||||||||||
Global distribution | Abundant in the N.E. Atlantic from Iceland, north to Finmark, Norway and south to Portugal. Absent from the Mediterranean. | ||||||||||||||
Biogeographic range | Not researched | Depth range | 0 - 1200 m | ||||||||||||
Migratory | Non-migratory / Resident | ||||||||||||||
Distribution Additional Information | No text entered | ||||||||||||||
Substratum preferences | Bedrock Large to very large boulders Small boulders Artificial (e.g. metal/wood/concrete) Rockpools Under boulders Caves Crevices / fissures Overhangs |
Physiographic preferences | Open coast Strait / sound Sealoch Ria / Voe Enclosed coast / Embayment |
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Biological zone | Sublittoral Fringe Upper Infralittoral Lower Infralittoral Upper Circalittoral Lower Circalittoral |
Wave exposure | Exposed Moderately Exposed Sheltered |
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Tidal stream strength/Water flow | Moderately Strong (1-3 kn) |
Salinity | Full (30-40 psu) |
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Habitat Preferences Additional Information | |||||||||||||||
Distribution References | Hayward & Ryland, 1995b, Mortensen, 1927, Fish & Fish, 1996, Hyman, 1955, Nichols, 1979, Nichols, 1969, Nichols, 1984, JNCC, 1999, Picton & Costello, 1998, NBN, 2002, Hayward & Ryland, 1990, Julie Bremner, unpub data, | ||||||||||||||
Reproduction/Life History | |||||||||||||||
Reproductive type | Gonochoristic |
Developmental mechanism | Planktotrophic |
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Reproductive Season | Spring | Reproductive Location | Water column | ||||||||||||
Reproductive frequency | Annual episodic | Regeneration potential | No | ||||||||||||
Life span | 6-10 years | Age at reproductive maturity | 1-2 years | ||||||||||||
Generation time | 1-2 years | Fecundity | 20000000 | ||||||||||||
Egg/propagule size | Fertilization type | External | |||||||||||||
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Reproduction Preferences Additional Information |
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Reproduction References | Lawrence, 1975, MacBride, 1903, Hyman, 1955, Gage, 1992(a), Gage, 1992(b), Nichols, 1979, Nichols, 1969, Emson & Moore, 1998, MacBride, 1914, Nichols, 1984, Lang & Mann, 1978, Bishop, 1985, Boolootian, 1966, Bishop & Earll, 1984, Todd et al., 1996, Julie Bremner, unpub data, Rees & Dare, 1993, |