Overview
Brief Summary
Biology
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Comprehensive Description
Description
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Description
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Distribution
Distribution
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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Distribution
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Leewis, R. (2002). Flora en fauna van de zee [Marine flora and fauna]. Veldgids, 16. KNNV Uitgeverij: Utrecht, The Netherlands. ISBN 90-5011-153-X. 320 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1116
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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Vandendriessche, S.; Degraer, S.; Vincx, M. (2003). Drijvende wieren als habitat voor macrofauna aan de Belgische kust [Floating seaweeds as habitat for macrofauna at the Belgian coast]. De Strandvlo 23(2): 50-57
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1670
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Davoult, D.; Dewarumez, J.-M.; Luczak, C.; Migné, A. (1999). Nouvelles signalisations d'espèces benthiques sur les côtes françaises de la Manche orientale et de la Mer du Nord [New reports of benthic species from the french coasts of the eastern English Channel and the North Sea]. Cah. Biol. Mar. 40(2): 121-127
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1260
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Annys, A. (1984). Verslag excursie naar Sas van Goes (Ned.) op 9 oktober 1983 [Report on the excursion to Sas van Goes (Netherlands), 9 October 1983]. De Strandvlo 4(1): 18-19
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=757
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Herkül, K.; Kotta, J.; Kotta, I. (2006). Distribution and population characteristics of the alien talitrid amphipod Orchestia cavimana in relation to environmental conditions in the Northeastern Baltic Sea. Helgol. Mar. Res. 60(2): 121-126.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=9802
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Reise, K.; Olenin, S.; Thieltges, D.W. (2006). Are aliens threatening European aquatic coastal ecosystems?. Helgol. Mar. Res. 60(2): 77-83
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=9796
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Coppejans, E. (1998). Flora van de Noord-Franse en Belgische zeewieren [Marine algae of northern France and Belgium]. Nationale Plantentuin van België: Meise, Belgium. ISBN 90-72619-41-2. 462 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1236
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Sheridan, S.; Massin, C. (1998). Guide de la faune et flore sous-marine de Zelande. Commission Scientifique LIFRAS. 320 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1191
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De Blauwe, H. (2000c). Riemwiervoetjes en hun begroeiing [Seaweed haptera and their overgrowth]. De Strandvlo 20(3): 130-137
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1163
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Simons, E.; Simons, G.; Corstanje, H. (1988). Report on the beach excursion at Oostduinkerke (Belgium) on 2 November 1988 [Verslag van de strandexcursie te Oostduinkerke op 2 november 1988]. De Strandvlo 8(4): 206-209
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=138809
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Kerckhof, F. (1990). An invasion of the Purple Jellyfish, Pelagia noctiluca (Forskal, 1775), along the Belgian coast [Een invasie van de Parelkwal Pelagia noctiluca (Forskal, 1775) langs de Belgische kust]. De Strandvlo 10(4): 101-109
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=138626
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Vanhaelen, M.-Th. (1990). Observations at Koksijde and Oostduinkerke after the heavy winter storms of 26-27 February and 1-2 March 1990 [Waarnemingen te Koksijde en Oostduinkerke na de zware winterstormen van 26-27 februari en 1-2 maart 1990]. De Strandvlo 10(4): 88-92
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=138623
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Guiry, M.D. (2001). Macroalgae of Rhodophycota, Phaeophycota, Chlorophycota, and two genera of Xanthophycota, in: Costello, M.J. et al. (Ed.) (2001). European register of marine species: a check-list of the marine species in Europe and a bibliography of guides to their identification. Collection Patrimoines Naturels, 50: pp. 20-38
http://www.marbef.org/data/aphia.php?p=sourcedetails&id=1366
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Herkül, K.; Kotta, J.; Kotta, I. (2006). Invasion history and distribution of the semi-terrestrial invasive amphipod Orchestia cavimana in the Estonian coastal sea, in: Ojaveer, H.; Kotta, J. (Ed.) (2006). Alien invasive species in the north-eastern Baltic Sea: population dynamics and ecological impacts. Estonian Marine Institute Report Series, 14: pp. 23-30.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=9784
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MEDIN (2011). UK checklist of marine species derived from the applications Marine Recorder and UNICORN, version 1.0.
http://www.marinespecies.org/asteroidea/aphia.php?p=sourcedetails&id=149081
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Guiry, M.D. & Guiry, G.M. (2011). Species.ie version 1.0 World-wide electronic publication, National University of Ireland, Galway (version of 15 March 2010).
http://www.marinespecies.org/ascidiacea/aphia.php?p=sourcedetails&id=149068
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Kedra, M. (2010). A Checklist of marine species occurring in Polish marine waters, compiled in the framework of the PESI EU FP7 project.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=149084
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Range
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Physical Description
Diagnostic Description
Morphology
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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Ecology
Habitat
Habitat
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North-West Atlantic Ocean species (NWARMS)
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=2901
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Water temperature and chemistry ranges based on 31 samples.
Environmental ranges
Depth range (m): 0 - 23.77
Temperature range (°C): 11.471 - 12.348
Nitrate (umol/L): 4.729 - 7.121
Salinity (PPS): 35.035 - 35.363
Oxygen (ml/l): 6.069 - 6.339
Phosphate (umol/l): 0.336 - 0.439
Silicate (umol/l): 2.315 - 3.388
Graphical representation
Depth range (m): 0 - 23.77
Temperature range (°C): 11.471 - 12.348
Nitrate (umol/L): 4.729 - 7.121
Salinity (PPS): 35.035 - 35.363
Oxygen (ml/l): 6.069 - 6.339
Phosphate (umol/l): 0.336 - 0.439
Silicate (umol/l): 2.315 - 3.388
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Environmental ranges
Depth range (m): 0 - 0
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Environmental ranges
Depth range (m): 0 - 0
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Habitat
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Habitat
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Associations
Associations
Foodplant / saprobe
Lulworthia salina is saprobic on very old, worn thallus stump of Fucus vesiculosus
Remarks: Other: uncertain
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Molecular Biology and Genetics
Molecular Biology
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Barcode data: Fucus vesiculosus
There are 14 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Download FASTA File
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Statistics of barcoding coverage: Fucus vesiculosus
Public Records: 14
Species: 14
Species With Barcodes: 1
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Conservation
Conservation Status
Threats
Management
Conservation
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Wikipedia
Fucus vesiculosus
Fucus vesiculosus, known by the common name bladder wrack or bladderwrack, is a seaweed found on the coasts of the North Sea, the western Baltic Sea, and the Atlantic and Pacific Oceans, also known by the common names black tang, rockweed, bladder fucus, sea oak, black tany, cut weed, dyers fucus, red fucus, and rock wrack. It was the original source of iodine, discovered in 1811, and was used extensively to treat goitre, a swelling of the thyroid gland related to iodine deficiency.
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Description
The fronds of F. vesiculosus have a prominent midrib and almost spherical air bladders which are usually paired but may be absent in young plants. The margin is smooth and the frond is dichotomously branched. It is sometimes confused with Fucus spiralis with which it hybridises.[1]
Distribution
Fucus vesiculosus is one of the most common algae on the shores of the British Isles.[2] It has been recorded from the Atlantic shores of Europe, Northern Russia, the Baltic Sea, Greenland, Azores, Canary Islands, Morocco and Madeira.[3][4] It is also found on the Atlantic coast of North America from Ellesmere Island, Hudson Bay to North Carolina.[5]
Ecology
The species is especially common on sheltered shores from the middle littoral to lower intertidal levels.[5] It is rare on exposed shores where any specimens may be short, stunted and without the air vesicles.[6] F. vesiculosus supports few colonial organisms but provides a canopy and shelter for the tube worm Spirorbis spirorbis, herbivorous isopods, such as Idotea and surface grazing snails such as Littorina obtusata.[1] Phlorotannins in Fucus vesiculosus act as chemical defences against the marine herbivorous snail Littorina littorea.[7]
Biology
Plants of F. vesiculosus are dioecious. Gametes are generally released into the seawater under calm conditions and the eggs are fertilised externally to produce a zygote.[1] Eggs are fertilised shortly after being released from the receptacle. A study on the coast of Maine showed that there was 100% fertilisation at both exposed and sheltered sites.[1] Continuously submerged populations in the Baltic Sea are very responsive to turbulent conditions. High fertilisation success is achieved because the gametes are only released when water velocities are low.[8]
Consumption
Primary chemical constituents of this plant include mucilage, algin, mannitol, beta-carotene, zeaxanthin, iodine, bromine, potassium, volatile oils, and many other minerals. The main use of bladder wrack (and other types of seaweed) in herbal medicine is as a source of iodine, an essential nutrient for the thyroid gland. Bladder wrack has been used in the treatment of underactive thyroid glands (hypothyroidism) and goitre.[9]
Bladder wrack has been shown to help women with abnormal menstrual cycling patterns and menstrual-related disease histories.[10] Doses of 700 to 1400 mg/day were found to increase the menstrual cycle lengths, decrease the days of menstruation per cycle, and decrease the serum levels of 17B-estradiol while was later carried out and showed similar effects.[11]
See also
References
- ^ a b c d Marine Life Information Network
- ^ F. G. Hardy & M. D. Guiry (2003). A Check-list and Atlas of the Seaweeds of Britain and Ireland. London: British Phycological Society. ISBN 0-9527115-1-6. http://seaweed.ucg.ie/check-list/check-list.pdf.
- ^ M. D. Guiry & Wendy Guiry (January 12, 2007). "Fucus vesiculosus Linnaeus". AlgaeBase. National University of Ireland, Galway. http://www.algaebase.org/speciesdetail.lasso?species_id=87&sk=0&from=results. Retrieved April 22, 2012.
- ^ Charlotta A. Nygård & Matthew J. Dring (2008). "Influence of salinity, temperature, dissolved inorganic carbon and nutrient concentration on the photosynthesis and growth of Fucus vesiculosus from the Baltic an Irish Seas". European Journal of Phycology 43 (3): 253–262. doi:10.1080/09670260802172627.
- ^ a b W. R. Taylor (1957). Marine Algae of the Northeastern Coast of North America. University of Michigan, Ann Arbor. ISBN 0-472-04904-6.
- ^ C. S. Lobban & P. J. Harrison (1994). Seaweed Ecology and Physiology. Cambridge University Press, Cambridge. ISBN 0-521-40897-0.
- ^ J. A. Geiselman & O. J. McConnell (1981). "Polyphenols in brown algae Fucus vesiculosus and Ascophyllum nodosum: chemical defenses against the marine herbivorous snail, Littorina littorea". Journal of Chemical Ecology 7 (6): 1115–1133. doi:10.1007/BF00987632.
- ^ E. A. Serrao, G. Pearson, L. Kautsky & S. H. Brawley (1996). "Successful external fertilization in turbulent environments". Proceedings of the National Academy of Sciences 93 (11): 5286–5290. Bibcode 1996PNAS...93.5286S. PMC 39237. PMID 11607682. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=39237.
- ^ P. R. Bradley (1992). British Herbal Compendium. 1. Bournemouth, England: British Herbal Medicine Association. ISBN 0-903032-09-0.
- ^ Christine F. Skibola (2004). "The effect of Fucus vesiculosus, an edible brown seaweed, upon menstrual cycle length and hormonal status in three pre-menopausal women: a case report". BMC Complementary and Alternative Medicine 4: 10. doi:10.1186/1472-6882-4-10. PMC 514561. PMID 15294021. http://www.biomedcentral.com/1472-6882/4/10.
- ^ Christine F. Skibola, John D. Curry, Catherine VandeVoort, Alan Conley & Martyn T. Smith (2005). "Brown kelp modulates endocrine hormones in female Sprague–Dawley rats and in human luteinized granulosa cells". Journal of Nutrition 135 (2): 296–300. PMID 15671230. http://jn.nutrition.org/cgi/pmidlookup?view=long&pmid=15671230.
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