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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus |
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Ulva intestinalis Linnaeus (detailed information)
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Species Details
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Class: |
Ulvophyceae |
Genus: |
Ulva Linnaeus |
Species: |
Ulva intestinalis |
Authority: |
Linnaeus |
Description: |
Ulva intestinalis is a conspicuous bright grass-green seaweed, consisting of inflated irregularly constricted, tubular fronds that grow from a small discoid base. Fronds are typically unbranched. Fronds may be 10-30 cm or more in length and 6-18 mm in diameter, the tips of which are usually rounded. Like other members of the genus, Ulva intestinalis is a summer annual, decaying and forming masses of bleached white fronds towards the end of the season. Link for (Pereira, 2010) Handbook Guide Original publication: Linnaeus, C. (1753). Species plantarum, exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas. Vol. 2 pp. [i], 561-1200, [1-30, index], [i, err.]. Holmiae [Stockholm]: Impensis Laurentii Salvii.
Download PDF from Algaebase
Original description: Download PDF from Algaebase |
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Name History |
Adjective (Latin), relating to or found in the intestines
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Biogeography |
More or less globally distributed: entire Atlantic, Mediterranean, Caribbean, NE and NW Pacific, Idian Ocean, Australasia, Antarctica. |
Life Cycle |
Digenetic, isomorphic alternation of generations (sporophytes and gametophytes). Species of the genus Ulva are rapidly growing opportunists, favoured by the frequency and speed of their reproduction. The short lived plants reach maturity at a certain stage of development rather than relying on an environmental trigger. Ulva intestinalis can be found in reproductive condition at all times of the year, but maximum development and reproduction occur during the summer months especially towards the northern end of the distribution of the species (Burrows, 1991). The life history consists of an isomorphic (indistinguishable except for the type of reproductive bodies produced) alternation between haploid gametophytic and diploid sporophytic generations, but can be modified by environmental conditions (Burrows, 1959; Moss & Marsland, 1976; Reed & Russell, 1978). McArthur & Moss (1979) examined the process of gametogenesis and gamete structure using scanning and transmission electron microscopy. The haploid gametophytes of Ulva produce enormous numbers of biflagellate motile gametes which cluster and fuse to produce a sporophyte (diploid zygote). The sporophyte matures and produces by meiosis large numbers of quadriflagellate zoospores that mature as gametophytes, and the cycle is repeated. Both gametes and spores may be released in such quantities into rock pools or slack water that the water mass is coloured green (Little & Kitching, 1996). Together spores and gametes are termed 'swarmers'. Swarmers are often released in relation to tidal cycles, with the release being triggered by the incoming tide as it wets the thallus. However, the degree of release is usually related to the stage of the spring/neap tidal cycle, so allowing regular periodicity and synchronization of reproduction (Little & Kitching, 1996). Christie & Evans (1962) found that swarmer release of Ulva intestinalis (as Enteromorpha intestinalis) from the Menai Straits, Wales, peaked just before the highest tides of each neap-spring cycle. Mobility of swarmers belonging to Ulva intestinalis (as Enteromorpha intestinalis) can be maintained for as long as 8 days (Jones & Babb, 1968). Algae such as Ulva intestinalis tend to have large dispersal shadows, with propagules being found far from the nearest adult plants, e.g. 35 km (Amsler & Searles, 1980) |
Uses and compounds |
Communesins, exhibiting cytotoxic activity against the cultured P-388 lymphocytic leukemia cells, were isolated from the mycelium of a strain of Penicillium species stuck on the marine alga Ulva intestinalis (= Enteromorpha intestinalis) (Numata et al., 1993). Penostatins (Takahashi et al., 1996; Iwamoto et al., 1999) have been isolated from a strain of Penicillium species originally separated from the marine alga Ulva intestinalis (= Enteromorpha intestinalis) (Ulvaceae). The compounds A–C and E exhibited a significant cytotoxicity against cultured P388 cell line (Iwamoto et al., 1999; Takahashi et al., 1996). Penostatins were isolated from a strain of Penicillum originally separated from the marine alga Ulva intestinalis (= Enteromorpha intestinalis) (Ulvaceae). All the compounds exhibit significant cytotoxicity against cultured cells (Iwamoto et al., 1998). |
References |
Braune, W. (2008). Meeresalgen. Ein Farbbildführer zu den verbreiteten benthischen Grün- Braun- und Rotalgen der Weltmeere. pp. [1]-596, 266 pls. Ruggell: A.R.G. Gantner Verlag. Brodie, J., Maggs, C.A. & John, D.M. (2007). Green seaweeds of Britain and Ireland. pp. [i-v], vi-xii, 1-242, 101 figs. London: British Phycological Society. Dawes, C.J. & Mathieson, A.C. (2008). The seaweeds of Florida. pp. [i]- viii, [1]-591, [592], pls I-LI. Gainesville, Florida: University Press of Florida. Hayden, H.S. & Waaland, J.R. (2004). A molecular systematic study of Ulva (Ulvaceae, Ulvales) from the northeast Pacific. Phycologia 43: 364-382. Hayden, H.S., Blomster, J., Maggs, C.A., Silva, P.C., Stanhope, M.J. & Waaland, J.R. (2003). Linnaeus was right all along: Ulva and Enteromorpha are not distinct genera. European Journal of Phycology 38: 277-294. Lindeberg, M.R. & Lindstrom, S.C. (2010). Field guide to the seaweeds of Alaska. pp. [i-]iii-iv, 1-188, numerous col. photographs. Fairbanks: Alaska Sea Grant College Program. Loiseaux-de Goër, S. & Noailles, M.-C. (2008). Algues de Roscoff. pp. [1]-215, col. figs. Roscoff: Editions de la Station Biologique de Roscoff. Norris, J.N. (2010). Marine algae of the Northern Gulf of California: Chlorophyta and Phaeophyceae. Smithsonian Contributions to Botany 94: i-x, 1-276. Pedroche, F.F., Silva, P.C., Aguilar-Rosas, L.E., Dreckmann, K.M. & Aguilar-Rosas, R. (2005). Catálogo de las algas marinas bentónicas del Pacífico de México. I. Chlorophycota. pp. i-viii, 17-146. Ensenada, México: Universidad Autónoma de Baja California. Skelton, P.A. & South, G.R. (2007). The benthic marine algae of the Samoan Archipelago, South Pacific, with emphasis on the Apia District. Nova Hedwigia Beihefte 132: 1-350 |

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Habitat: |
In sheltered as well as exposed locations, on boulders, breakwaters and piers, in pools, also epiphytically. From the upper littoral (also supralittoral) poolls into the subtidal. |
Common names: |
In Portuguese: Alface-do-mar In English: Gut weed, Gut laver, Hollow Green Weed. |
Type information: |
Type locality: Woolwich, London, England? (Hayden et al. 2003: 289). Lectotype: Dillenius (1742: pl. 9: fig. 7) (epitype) OXF (Yoshida 1998 Notes: Blomster et al. (1999) select a lectotype (epitype) of Dillenius (1742: pl. 9: fig. 7); see also Hayden et al. (2003: 289). Type locality: 'in Mari omni' (South & Skelton, 2003). |
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1975 specimens in MACOI collections
2293 bibliographic references
2839 occurrence records
6322 images
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