BIOTIC Species Information for Chorda filum
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Researched by | Nicola White | Data supplied by | MarLIN | ||||||||||||
Refereed by | Dr Stefan Kraan | ||||||||||||||
Taxonomy | |||||||||||||||
Scientific name | Chorda filum | Common name | Sea lace or Dead man's rope | ||||||||||||
MCS Code | ZR345 | Recent Synonyms | Chorda filum var thrix | ||||||||||||
Phylum | Chromophycota | Subphylum | |||||||||||||
Superclass | Class | Phaeophyceae | |||||||||||||
Subclass | Order | Laminariales | |||||||||||||
Suborder | Family | Chordaceae | |||||||||||||
Genus | Chorda | Species | filum | ||||||||||||
Subspecies | |||||||||||||||
Additional Information | Other common names include mermaid's tresses and cat gut. | ||||||||||||||
Taxonomy References | South & Burrows, 1967, Guiry & Nic Dhonncha, 2002, | ||||||||||||||
General Biology | |||||||||||||||
Growth form | Filiform |
Feeding method | Photoautotroph |
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Mobility/Movement | Permanent attachment |
Environmental position | Epifloral |
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Typical food types | Not relevant | Habit | Attached | ||||||||||||
Bioturbator | Not relevant | Flexibility | High (>45 degrees) | ||||||||||||
Fragility | Intermediate | Size | Large(>50cm) | ||||||||||||
Height | Growth Rate | 17 cm/month | |||||||||||||
Adult dispersal potential | None | Dependency | Independent | ||||||||||||
Sociability | Solitary | ||||||||||||||
Toxic/Poisonous? | No | ||||||||||||||
General Biology Additional Information | Chorda filum is a summer annual, falling into decay in the autumn and disappearing during winter. Growth rate is maximal during the summer. The adult frond is a hollow tube, the walls of which are spirally constructed. The frond is frequently inflated with gases in the terminal region. Plants usually grow in clumps. The end of the frond decays continuously and is replaced by growth from a sub-terminal meristem. Hairs are sparse or absent on older plants. | ||||||||||||||
Biology References | South & Burrows, 1967, | ||||||||||||||
Distribution and Habitat | |||||||||||||||
Distribution in Britain & Ireland | All coasts of Britain and Ireland, but rarer in south east England. | ||||||||||||||
Global distribution | See additional information. | ||||||||||||||
Biogeographic range | Not researched | Depth range | Rock pools down to 5m. | ||||||||||||
Migratory | Non-migratory / Resident | ||||||||||||||
Distribution Additional Information | Global distribution Canada (Arctic), Alaska, NW Atlantic from Labrador to New Jersey, Greenland, Iceland, Spitsbergen, Norway, Sweden, Denmark, The Netherlands, Belgium, the Baltic, the Faroes, France, Spain, Portugal, Canary Islands, Greece, China, Japan and south Kurile Islands, NE Pacific and the Bering Strait. Chorda filum occurs in sheltered bays, estuaries, lagoons and sea lochs. It is rarely found on the open coast and is completely absent from exposed shores. The plants occur in clumps on a range of unstable, small objects such as pebbles and shells. It may also be found on sand and detritus but it will not remain for long on this substratum (S. Kraan, pers. comm.). They are also epiphytic on %Zostera marina% and %Fucus vesiculosus%. During stormy weather, plants may be washed to more sheltered locations where they continue development. Chorda filum has considerable tolerance to reduced salinities and extends into river mouths and the Baltic, where it grows at 3.5 psu. However, plants that grow in fully marine conditions cannot withstand immersion in freshwater for 2 hours (Russell, 1985). |
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Substratum preferences | Muddy gravel Pebbles Gravel / shingle Mixed Algae |
Physiographic preferences | Strait / sound Sealoch Ria / Voe Estuary Isolated saline water (Lagoon) Enclosed coast / Embayment |
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Biological zone | Lower Infralittoral Upper Infralittoral Sublittoral Fringe |
Wave exposure | Sheltered Very Sheltered |
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Tidal stream strength/Water flow | Moderately Strong (1-3 kn) Weak (<1 kn) |
Salinity | Low (<18 psu) Reduced (18-30 psu) Full (30-40 psu) Variable (18-40 psu) |
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Habitat Preferences Additional Information | |||||||||||||||
Distribution References | South & Burrows, 1967, Russell, 1985, Norton & South, 1969, Hardy & Guiry, 2003, | ||||||||||||||
Reproduction/Life History | |||||||||||||||
Reproductive type | Alternation of generations |
Developmental mechanism | Spores (sexual / asexual) |
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Reproductive Season | Sporophytes appear on shore Feb-March | Reproductive Location | As adult | ||||||||||||
Reproductive frequency | Annual protracted | Regeneration potential | No | ||||||||||||
Life span | Insufficient information | Age at reproductive maturity | <1 year | ||||||||||||
Generation time | <1 year | Fecundity | Millions of spores | ||||||||||||
Egg/propagule size | Fertilization type | ||||||||||||||
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Reproduction Preferences Additional Information | Chorda filum has a similar life-history to other Laminariales, exhibiting alternation of heteromorphic generations. The species has a macroscopic diploid sporophyte and a microscopic haploid gametophyte. The gametophytes consist of clumps of prostate, branched, filaments approximately 100 micrometres long. Female gametophytes are less branched than male ones and may be distinguished by their larger more densely pigmented cells. The male gametophytes are smaller, paler in colour and more densely branched than the females. Chorda filum exhibits a protracted reproductive period. Visible sporophytes appear on shores between February and mid-March and develop into secondary sporophytes between April and June. The sporophytes are washed away from October to February, leaving behind zoospores or gametophytes. The size of plants is not related to their state of maturity, although the smallest plants to bear sporangia have been observed to be 36.6 cm long. When the meristem becomes indistinct it is likely that fruiting has begun. During the period of fertility the whole plant except the lowermost 5-10 cm, is covered in unilocular sporangia. Experiments on growing Chorda filum in culture have shown that fruiting appears to be endogenously controlled and occurs irrespective of environmental conditions (South & Burrows, 1967). | ||||||||||||||
Reproduction References | South & Burrows, 1967, Fredriksen et al., 1998, |