BIOTIC Species Information for Maja squinado
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Researched by | Emily Wilson | Data supplied by | MarLIN | ||||||||||||
Refereed by | This information is not refereed. | ||||||||||||||
Taxonomy | |||||||||||||||
Scientific name | Maja squinado | Common name | Common spider crab | ||||||||||||
MCS Code | S1515 | Recent Synonyms | None | ||||||||||||
Phylum | Crustacea | Subphylum | |||||||||||||
Superclass | Class | Eumalacostraca | |||||||||||||
Subclass | Eucarida | Order | Decapoda | ||||||||||||
Suborder | Pleocyemata | Family | Majidae | ||||||||||||
Genus | Maja | Species | squinado | ||||||||||||
Subspecies | |||||||||||||||
Additional Information | |||||||||||||||
Taxonomy References | Howson & Picton, 1997, Hayward & Ryland, 1995b, Hayward et al., 1996, Ingle, 1980, | ||||||||||||||
General Biology | |||||||||||||||
Growth form | Articulate |
Feeding method | Omnivore Scavenger Predator |
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Mobility/Movement | Crawler |
Environmental position | Epibenthic |
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Typical food types | Habit | Free living | |||||||||||||
Bioturbator | Flexibility | None (< 10 degrees) | |||||||||||||
Fragility | Fragile | Size | Medium(11-20 cm) | ||||||||||||
Height | Insufficient information | Growth Rate | Insufficient information | ||||||||||||
Adult dispersal potential | >10km | Dependency | Independent | ||||||||||||
Sociability | Solitary | ||||||||||||||
Toxic/Poisonous? | No | ||||||||||||||
General Biology Additional Information | Up to 22.5 cm carapace length (Ingle, 1997). Although solitary, forms aggregated 'mounds' of individuals in late summer / autumn (Fish & Fish, 1996). | ||||||||||||||
Biology References | Fish & Fish, 1996, Ingle, 1997, | ||||||||||||||
Distribution and Habitat | |||||||||||||||
Distribution in Britain & Ireland | West and south-west coasts of Britain. It is at its northern limit in the UK. | ||||||||||||||
Global distribution | NE Atlantic from Ireland to Guinea (W Africa) and Med to 150 m (Ingle, 1997). | ||||||||||||||
Biogeographic range | Not researched | Depth range | Down to ca 75 m. | ||||||||||||
Migratory | Insufficient information | ||||||||||||||
Distribution Additional Information | |||||||||||||||
Substratum preferences | Bedrock Coarse clean sand Fine clean sand |
Physiographic preferences | Insufficient information |
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Biological zone | Insufficient information |
Wave exposure | Insufficient information |
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Tidal stream strength/Water flow | Insufficient information |
Salinity | Insufficient information |
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Habitat Preferences Additional Information | Found on rocky sandy bottoms. Usually inhabits weed covered substrata or sandy / shingly substrata where weeds occur (Ingle, 1997). | ||||||||||||||
Distribution References | Hayward & Ryland, 1995b, Hayward et al., 1996, NBN, 2002, JNCC, 1999, Picton & Costello, 1998, Hardy & Guiry, 2003, Morton, 1994, Ingle, 1997, | ||||||||||||||
Reproduction/Life History | |||||||||||||||
Reproductive type | Gonochoristic |
Developmental mechanism | Planktotrophic |
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Reproductive Season | Summer - Autumn | Reproductive Location | As adult | ||||||||||||
Reproductive frequency | Annual protracted | Regeneration potential | No | ||||||||||||
Life span | Insufficient information | Age at reproductive maturity | 1-2 years | ||||||||||||
Generation time | Insufficient information | Fecundity | 156,000 (Hartnoll, 1963) | ||||||||||||
Egg/propagule size | Insufficient information | Fertilization type | Internal | ||||||||||||
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Reproduction Preferences Additional Information | Maturity 2 years in the Med (Hines et al., 1995). Main breeding season in south-west England between July - September (Lebour, 1927) and March - Sept in Ireland (Rodhouse, 1984). NE Atlantic in general, females bear eggs between March and October (Ingle, 1997). Time taken to reach the megalopa stage was reported to take ca 1 week in the laboratory (Lebour, 1927). In the Ría de Arousa, Spain, Maja squinado were reported to have moved up to 10.7 km within one month (González-Gurriarán & Freire, 1994). González-Gurriarán et al., (1993) estimated females to produce at least three consecutive broods during the yearly cycle. This is possible due to the storage of sperm which allows consecutive broods without the need for copulation before spawning (González-Gurriarán et al., 1996). In the UK and Ireland, only one brood is produced per yearly cycle (Rodhouse, 1984). In this species, the crabs do not moult again after becoming sexually mature i.e. the terminal moult is the pubertal moult. | ||||||||||||||
Reproduction References | González-Gurriarán & Freire, 1994, González-Gurriarán et al, 1996, Rodhouse, 1984, Lebour, 1927, Ingle, 1997, Hartnoll, 1963, |