AquaNISInformation system on aquatic non-indigenous and cryptogenic species |
Species | Colpomenia peregrina [WoRMS] | |
Authority | Sauvageau, 1927 References (not structured): Sauvageau C (1927) Sur le Colpomenia sinuosa Derb. et Sol.. Bulletin de la Station Biologique d'Arachon 24: 309-355, 8 figs |
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Family | Scytosiphonaceae | |
Order | Ectocarpales | |
Class | Phaeophyceae | |
Phylum | Ochrophyta | |
Synonym (?) | Colpomenia sinuosa var. peregrina (Sauvageau, 1927) References (not structured): Sauvageau C (1927) Sur le Colpomenia sinuosa Derb. et Sol.. Bulletin de la Station Biologique d'Arachon 24: 309-355, 8 figs Comments: This name is currently regarded as a taxonomic synonym of Colpomenia peregrina Sauvageau. |
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Sub-species level (?) | Not entered |
Native origin (?) | Ocean: Pacific --> Ocean region: NE Pacific References (not structured): Minchin D (2001) Biodiversity and marine invaders. In Marine Biodiversity in Ireland and Adjacent Waters. (Appendix) Proceedings of a Conferernce 26 - 27 April 2001, Ulster Museum. publication no.8 Farnham FW (1980) Systematics association by Academic Press. The shore enviroment (vol. 2: Ecosystems, chapter 14), pp 878-890 Comments: Colpomenia peregrina occurs naturally in the Pacific Ocean. It was introduced to France with with juvenile Crassostrea virginica from the Pacific coast of North America. |
Life form / Life stage (?) |
References (not structured): Clayton MN (1979) The life history and sexual reproduction of Colpomenia peregrina (Scytosiphonaceae, Phaeophyta) in Australia. British Phycological Journal 14: 1-1 Kogame K, Yamagishi Y (1997) The life history and phenology of Colpomenia peregrina (Scytosiphonales, Phaeophyceae) from Japan. Phycologia: September 1997, Vol. 36, No. 5, pp. 337-344. Botanica Marina. Volume 41, Issue 1-6, Pages 217–222, ISSN (Online) 1437-4323, ISSN (Print) 0006-8055, DOI: 10.1515/botm.1998.41.1-6.217, //1998 Fletcher RL (1987) Seaweeds of the British Isles. Volume 3 Fucophyceae (Phaeophyceae) Part 1. British Museum (Natural History), London. ISBN 0-565-00992-3 Vandermeulen H (1986) Growth of Colpomenia peregrina (Phaeophyceae) in culture: effects of salinity, temperature and daylength. Journal of Phycology 22: 138-144. Vandermeulen H, DeWreede RE (1987) Analysis of a population of Colpomenia peregrina in British Columbia: relationships with environment and primary substrate. Japanese Journal of Phycology 35: 91-98. Comments: Colpomenia peregrina occurs on rock, other seaweeds and shells. The species is usually epiphytic, growing on a variety of seaweeds in mid-tide rockpools and down to the sub-littoral region. It thrives in sheltered areas. It has flagellated spores and gametes (named as eggs, because there is no other option for them) |
Sociability / Life stage (?) |
References (not structured): Clayton MN (1979) The life history and sexual reproduction of Colpomenia peregrina (Scytosiphonaceae, Phaeophyta) in Australia. British Phycological Journal 14: 1-10 Kazuhiro Kogame and Yukimasa Yamagishi and (1997) The life history and phenology of Colpomenia peregrina (Scytosiphonales, Phaeophyceae) from Japan. Phycologia: September 1997, Vol. 36, No. 5, pp. 337-344. Botanica Marina. Volume 41, Issue 1-6, Pages 217–222, ISSN (Online) 1437-4323, ISSN (Print) 0006-8055, DOI: 10.1515/botm.1998.41.1-6.217, //1998 Fletcher, R.L. 1987. Seaweeds of the British Isles. Volume 3 Fucophyceae (Phaeophyceae) Part 1. British Museum (Natural History), London. ISBN 0-565-00992-3 Vandermeulen, H. & DeWreede, R.E. (1987). Analysis of a population of Colpomenia peregrina in British Columbia: relationships with environment and primary substrate. Japanese Journal of Phycology 35: 91-98. Comments: It appears in scattered clusters, rarely solitary. |
Reproductive frequency (?) | Semelparous References (not structured): Parson MJ (1982)"Colpomenia (Endlicher) Derbes et Solier (Phaeophyta) in New Zealand." New Zealand Journal of Botany Vol. 20: 289-301. Clayton MN (1979) The life history and sexual reproduction of Colpomenia peregrina (Scytosiphonaceae, Phaeophyta) in Australia. British Phycological Journal 14: 1-10. Kogame K, Yamagishi Y (1997) The life history and phenology of Colpomenia peregrina (Scytosiphonales, Phaeophyceae) from Japan. Phycologia: September 1997, Vol. 36, No. 5, pp. 337-344 Comments: At maturity the rows of loculi of the plurilocular reproductive organs appear to be free from each other and the contents of these rows are released sequentially from the top to the bottom. Usually part of the side walls of the plurilocular reproductive organs remain on the basal cortical cell. The paraphyses elongate at the same time as the plurilocular reproductive organs and usually protrude a little from the surface of the sorus. The paraphyses remain above the cortex after the plurilocular reproductive organs have disintergrated. In C. peregrina secondary plurilocular reproductive organs have been seen developing between the upstanding paraphyses; the basal mother cells of the old reproductive organs proliferate to produce a second set of plurilocular reproductive organs. |
Reproductive type (?) | Sexual References: Clayton MN (1979) The life history and sexual reproduction of Colpomenia peregrina (Scytosiphonaceae, Phaeophyta) in Australia. British Phycological Journal 14: 1-10. Kogame K, Yamagishi Y (1997) The life history and phenology of Colpomenia peregrina (Scytosiphonales, Phaeophyceae) from Japan. Phycologia: September 1997, Vol. 36, No. 5, pp. 337-344 Botanica Marina. Volume 41, Issue 1-6, Pages 217–222, ISSN (Online) 1437-4323, ISSN (Print) 0006-8055, DOI: 10.1515/botm.1998.41.1-6.217, //1998 Comments: Gametophytes occur in late winter, they are dioecious and reproduction is anisogamous. The zygotes, female gametes, and the majority of male gametes develop into filamentous sporophytes bearing unilocular sporangia. Zoosporcs from the sporophyte generatiorts mostly give rise to saccate C. peregrina. Cultured strains derived from wild C. peregrina differ in their reproductive potential. Sporophyte generations were only found in strains derived from parthenogametes or zygotes. Several other strains produced saccate progeny, irrespective of the culture conditions. The evidence that such strains may be asexually reproducing, "morphological" gametophytes is discussed. |
Developmental trait (?) | Unknown References: Clayton MN (1979) The life history and sexual reproduction of Colpomenia peregrina (Scytosiphonaceae, Phaeophyta) in Australia. British Phycological Journal 14: 1-1 Kogame K, Yamagishi Y (1997) The life history and phenology of Colpomenia peregrina (Scytosiphonales, Phaeophyceae) from Japan. Phycologia: September 1997, Vol. 36, No. 5, pp. 337-344. Botanica Marina. Volume 41, Issue 1-6, Pages 217–222, ISSN (Online) 1437-4323, ISSN (Print) 0006-8055, DOI: 10.1515/botm.1998.41.1-6.217, //1998 Fletcher RL (1987) Seaweeds of the British Isles. Volume 3 Fucophyceae (Phaeophyceae) Part 1. British Museum (Natural History), London. ISBN 0-565-00992-3 Vandermeulen H (1986) Growth of Colpomenia peregrina (Phaeophyceae) in culture: effects of salinity, temperature and daylength. Journal of Phycology 22: 138-144. Vandermeulen H, DeWreede RE (1987) Analysis of a population of Colpomenia peregrina in British Columbia: relationships with environment and primary substrate. Japanese Journal of Phycology 35: 91-98. Comments: They reproduce by means of flagellated spores and gametes. |
Characteristic feeding method / Life stage (?) |
References (not structured): Matta JL, Chapman DJ (1991) Photosynthetic responses and daily carbon balance of Colpomenia peregrina: seasonal variations and differences between intertidal and subtidal populations. Marine Biology, Berlin 108(2): 303-313. Vandermeulen H (1986)Growth of Colpomenia peregrina (Phaeophyceae) in culture: effects of salinity, temperature and daylength. Journal of Phycology 22: 138-144 Oates BR (1985)Photosynthesis and amelioration of desiccation in the intertidal saccate alga Colpomenia peregrina. Marine Biology, Berlin 89: 109-119 Fletcher RL (1987) Seaweeds of the British Isles. Volume 3 Fucophyceae (Phaeophyceae) Part 1. British Museum (Natural History), London. ISBN 0-565-00992-3 Comments: Colpomenia peregrina belongs to brown algae, and they belong to Heterokontophyta, a eukaryotic group of organisms distinguished most prominently by having chloroplasts surrounded by four membranes. |
Mobility / Life stage (?) |
References (not structured): Vandermeulen H (1986)Growth of Colpomenia peregrina (Phaeophyceae) in culture: effects of salinity, temperature and daylength. Journal of Phycology 22: 138-144. Kogame K, Yamagishi Y (1997) The life history and phenology of Colpomenia peregrina (Scytosiphonales, Phaeophyceae) from Japan. Phycologia: September 1997, Vol. 36, No. 5, pp. 337-344. Fletcher RL (1987) Seaweeds of the British Isles. Volume 3 Fucophyceae (Phaeophyceae) Part 1. British Museum (Natural History), London. ISBN 0-565-00992-3 Vandermeulen H,DeWreede RE (1987) Analysis of a population of Colpomenia peregrina in British Columbia: relationships with environment and primary substrate. Japanese Journal of Phycology 35: 91-98. Comments: Attached by rhizoidal filaments to rock at the base. They reproduce by means of flagellated spores and gametes. |
Salinity tolerance range (?) | Venice system: 6. Polymixohaline [18-30psu] References: Paavola MA, Olenin E, Leppakoski (2005) Are invasive species most successful in habitats of low native species richness across European brackish water seas? Estuarine, Coastal and Shelf Science, 64: 738-750. |
Habitat modifying ability potential (?) | Autogenic ecosystem engineers |
Toxicity / Life stage (?) | Not relevant References: Hopkins CCE (2001) Actual and potential effects of introduced marine organisms in Norwegian waters, including Svalbard Research report 2001-1 Directorate for Nature Management Theresa Wiesemeier KJa G P "No Evidence for the Induction of Brown Algal Chemical Defense by the Phytohormones Jasmonic Acid and Methyl Jasmonate " Journal of Chemical Ecology Volume 34, Number 12: 1523-1531 Comments: It has negligible effects on the environment. It was tested the hypothesis that JA or related metabolites play a role in induced brown algal defense. Quantification of oxylipins with a detection limit around 20 ng g−1 algal tissue did not reveal the presence of JA in Colpomenia peregrina. |
Bioaccumulation association (?) | Unknown |
Known human health impact? | Known References: Rocha, C. P., Pacheco, D., Cotas, J., Marques, J. C., Pereira, L., Gonçalves, A. M. 2021. Seaweeds as valuable sources of essential fatty acids for human nutrition. International Journal of Environmental Research and Public Health, 18(9), 4968. Comments: C. peregrina known forn utritional value, harvested in the Atlantic Ocean showed a diverse lipidic profile. |
Known economic impact? | Known References: Green, L. A., Mathieson, A. C., Neefus, C. D., Traggis, H. M., Dawes, C. J. 2012. Southern expansion of the brown alga Colpomenia peregrina Sauvageau (Scytosiphonales) in the Northwest Atlantic Ocean. Botanica Marina, 55(6), pp. 643-647. Comments: The introduction of C. peregrina to France caused significant economic losses to the oyster industry. |
Known measurable environmental impact? | Known References: Green, L. A., Mathieson, A. C., Neefus, C. D., Traggis, H. M., Dawes, C. J. 2012. Southern expansion of the brown alga Colpomenia peregrina Sauvageau (Scytosiphonales) in the Northwest Atlantic Ocean. Botanica Marina, 55(6), pp. 643-647. Comments: C. sinuosa causing significant damage to the oyster industry when older attached thalli became buoyant and often displaced shellfish. |
Included in the Target Species list? | No References: HELCOM, 2009. Alien Species and Ballast Water [PDF]. Available at: (https://archive.iwlearn.net/helcom.fi/stc/files/shipping/Table_2_Alienspecies_%20lists_2009.pdf) |
Last update by | Sandra Gečaitė, 2024-07-09 |