BIOTIC Species Information for Funiculina quadrangularis
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| Click here to view the MarLIN Key Information Review for Funiculina quadrangularis | |||||||||||||||
| Researched by | Olwen Ager | Data supplied by | MarLIN | ||||||||||||
| Refereed by | This information is not refereed. | ||||||||||||||
| Taxonomy | |||||||||||||||
| Scientific name | Funiculina quadrangularis | Common name | The tall sea pen | ||||||||||||
| MCS Code | D615 | Recent Synonyms | None | ||||||||||||
| Phylum | Cnidaria | Subphylum | |||||||||||||
| Superclass | Anthozoa | Class | Octocorallia | ||||||||||||
| Subclass | Order | Pennatulacea | |||||||||||||
| Suborder | Family | Funiculinidae | |||||||||||||
| Genus | Funiculina | Species | quadrangularis | ||||||||||||
| Subspecies | |||||||||||||||
| Additional Information | |||||||||||||||
| Taxonomy References | Howson & Picton, 1997, Hayward & Ryland, 1995b, Manuel, 1988, Hayward et al., 1996, | ||||||||||||||
| General Biology | |||||||||||||||
| Growth form | Pinnate |
Feeding method | Passive suspension feeder |
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| Mobility/Movement | Temporary attachment |
Environmental position | Epibenthic Epifaunal |
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| Typical food types | Plankton and organic particles | Habit | Attached | ||||||||||||
| Bioturbator | Not relevant | Flexibility | Low (10-45 degrees) | ||||||||||||
| Fragility | Intermediate | Size | Large(>50cm) | ||||||||||||
| Height | Up to ca 2 m | Growth Rate | Insufficient information | ||||||||||||
| Adult dispersal potential | No information found | Dependency | Independent | ||||||||||||
| Sociability | Colonial | ||||||||||||||
| Toxic/Poisonous? | No | ||||||||||||||
| General Biology Additional Information | Flexibility Eno et al. (1996) found that the tall sea pen bends away from lobster creels dropped on of them in a passive response to the pressure wave travelling ahead of the pot. Associated species The deep-water brittlestar, Asteronyx loveni, which has been recorded sporadically from the west coast of Scotland (Hughes, 1998b), is known to use its arms to cling to Funiculina quadrangularis (Fujita & Ohta, 1988). |
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| Biology References | Eno et al., 1996, Hughes, 1998(b), Jones et al., 2000, Fujita & Ohta, 1988, | ||||||||||||||
| Distribution and Habitat | |||||||||||||||
| Distribution in Britain & Ireland | West and north coasts of Ireland and Scotland. | ||||||||||||||
| Global distribution | Funiculina quadrangularis occurs in the North Atlantic and Mediterranean. It has been recorded in New Zealand (Manuel, 1988) and Japan (Fujita & Ohta, 1988). | ||||||||||||||
| Biogeographic range | Not researched | Depth range | 20-2000m | ||||||||||||
| Migratory | Non-migratory / Resident | ||||||||||||||
| Distribution Additional Information | |||||||||||||||
| Substratum preferences | Mud Muddy sand |
Physiographic preferences | Open coast Sealoch |
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| Biological zone | Upper Circalittoral Lower Circalittoral |
Wave exposure | Sheltered Very Sheltered Extremely Sheltered Ultra Sheltered |
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| Tidal stream strength/Water flow | Weak (<1 kn) Very Weak (negligible) |
Salinity | Full (30-40 psu) |
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| Habitat Preferences Additional Information | |||||||||||||||
| Distribution References | Hayward & Ryland, 1995b, Manuel, 1988, Hayward et al., 1996, Hughes, 1998(b), Fujita & Ohta, 1988, | ||||||||||||||
| Reproduction/Life History | |||||||||||||||
| Reproductive type | Gonochoristic |
Developmental mechanism | Insufficient information |
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| Reproductive Season | Insufficient information | Reproductive Location | Insufficient information | ||||||||||||
| Reproductive frequency | Insufficient information | Regeneration potential | No | ||||||||||||
| Life span | See additional information | Age at reproductive maturity | See additional information | ||||||||||||
| Generation time | See additional information | Fecundity | Insufficient information | ||||||||||||
| Egg/propagule size | Insufficient information | Fertilization type | Insufficient information | ||||||||||||
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| Reproduction Preferences Additional Information |
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| Reproduction References | Hughes, 1998(b), Birkeland, 1974, | ||||||||||||||
