Kelp





































Kelp
Temporal range: Lutetian to present[1]


Kelp In Freycinet Tasmania.jpg

Scientific classification
Domain:

Eukaryota

Kingdom:

Chromista

(unranked):

SAR

Superphylum:

Heterokonta

Class:

Phaeophyceae

Order:

Laminariales



Migula, 1909[2]

Families

Akkesiphycaceae
Alariaceae
Chordaceae
Costariaceae
Laminariaceae
Lessoniaceae
Pseudochordaceae



Kelps are large brown algae seaweeds that make up the order Laminariales. There are about 30 different genera.[citation needed]


Kelp grows in "underwater forests" (kelp forests) in shallow oceans, and is thought to have appeared in the Miocene, 23 to 5 million years ago.[3][not in citation given] The organisms require nutrient-rich water with temperatures between 6 and 14 °C (43 and 57 °F). They are known for their high growth rate—the genera Macrocystis and Nereocystis can grow as fast as half a metre a day, ultimately reaching 30 to 80 metres (100 to 260 ft).[4]


Through the 19th century, the word "kelp" was closely associated with seaweeds that could be burned to obtain soda ash (primarily sodium carbonate). The seaweeds used included species from both the orders Laminariales and Fucales. The word "kelp" was also used directly to refer to these processed ashes.[5]




Contents






  • 1 Description


  • 2 Growth and reproduction


  • 3 Kelp forests


  • 4 Commercial uses


    • 4.1 Commercial production


    • 4.2 Renewable energy source




  • 5 In history and culture


  • 6 Conservation


  • 7 Gallery


  • 8 Prominent species


  • 9 Interactions


  • 10 See also


  • 11 References


  • 12 Further reading


  • 13 External links





Description


In most kelp, the thallus (or body) consists of flat or leaf-like structures known as blades. Blades originate from elongated stem-like structures, the stipes. The holdfast, a root-like structure, anchors the kelp to the substrate of the ocean.
Gas-filled bladders (pneumatocysts) form at the base of blades of American species, such as Nereocystis lueteana, (Mert. & Post & Rupr.)[4] to hold the kelp blades close to the surface.




















































































































Seaweed, kelp, raw
Nutritional value per 100 g (3.5 oz)
Energy 180 kJ (43 kcal)
Carbohydrates
9.57 g
Sugars 0.6
Dietary fiber 1.3 g

Fat
0.56 g

Protein
1.68 g

Vitamins
Quantity %DV
Thiamine (B1)

4%
0.05 mg
Riboflavin (B2)

13%
0.15 mg
Niacin (B3)

3%
0.47 mg
Pantothenic acid (B5)

13%
0.642 mg
Folate (B9)

45%
180 μg
Vitamin C
4%
3 mg
Vitamin E
6%
0.87 mg
Vitamin K
63%
66 μg

Minerals
Quantity %DV
Calcium
17%
168 mg
Iron
22%
2.85 mg
Magnesium
34%
121 mg
Manganese
10%
0.2 mg
Phosphorus
6%
42 mg
Potassium
2%
89 mg
Sodium
16%
233 mg
Zinc
13%
1.23 mg




Link to USDA Database entry



  • Units

  • μg = micrograms • mg = milligrams

  • IU = International units



Percentages are roughly approximated using US recommendations for adults.
Source: USDA Nutrient Database


Growth and reproduction


Growth occurs at the base of the meristem, where the blades and stipe meet. Growth may be limited by grazing. Sea urchins, for example, can reduce entire areas to urchin barrens.[6] The kelp life cycle involves a diploid sporophyte and haploid gametophyte stage. The haploid phase begins when the mature organism releases many spores, which then germinate to become male or female gametophytes. Sexual reproduction then results in the beginning of the diploid sporophyte stage, which will develop into a mature individual.


The parenchymatous thalli are generally covered with a mucilage layer, rather than cuticle.[7]



Kelp forests



Kelp may develop dense forests with high production,[8] biodiversity and ecological function. Along the Norwegian coast these forests cover 5800 km2,[9] and they support large numbers of animals.[10][11] Numerous sessile animals (sponges, bryozoans and ascidians) are found on kelp stipes and mobile invertebrate fauna are found in high densities on epiphytic algae on the kelp stipes and on kelp holdfasts.[12] More than 100,000 mobile invertebrates per square meter are found on kelp stipes and holdfasts in well-developed kelp forests (Christie et al., 2003). While larger invertebrates and in particular sea urchins Strongylocentrotus droebachiensis (O.F. Müller) are important secondary consumers controlling large barren ground areas on the Norwegian coast, they are scarce inside dense kelp forests.[13]



Commercial uses





Alaskan beach kelp


Giant kelp can be harvested fairly easily because of its surface canopy and growth habit of staying in deeper water.


Bongo kelp ash is rich in iodine and alkali. In great amount, kelp ash can be used in soap and glass production. Until the Leblanc process was commercialized in the early 19th century, burning of kelp in Scotland was one of the principal industrial sources of soda ash (predominantly sodium carbonate).[14]Alginate, a kelp-derived carbohydrate, is used to thicken products such as ice cream, jelly, salad dressing, and toothpaste, as well as an ingredient in exotic dog food and in manufactured goods.[citation needed] Alginate powder is also used frequently in general dentistry and orthodontics for making impressions of the upper and lower arches. These impressions are subsequently poured up in stone and the stone models are used in diagnosis and treatment [15]


Kombu (昆布 in Japanese, and 海带 in Chinese, Saccharina japonica and others), several Pacific species of kelp, is a very important ingredient in Chinese, Japanese, and Korean cuisines. Kombu is used to flavor broths and stews (especially dashi), as a savory garnish (tororo konbu) for rice and other dishes, as a vegetable, and a primary ingredient in popular snacks (such as tsukudani). Transparent sheets of kelp (oboro konbu) are used as an edible decorative wrapping for rice and other foods.[16]


Kombu can be used to soften beans during cooking, and to help convert indigestible sugars and thus reduce flatulence.[17]


Because of its high concentration of iodine, brown kelp (Laminaria) has been used to treat goiter, an enlargement of the thyroid gland caused by a lack of iodine, since medieval times.[18]


In 2010, a group of researchers in the University of Newcastle found that a fibrous material called alginate in sea kelp was better at preventing fat absorption than most over-the-counter slimming treatments in laboratory trials. As a food additive, it may be used to reduce fat absorption and thus obesity.[19] Kelp in its natural form has not yet been proven to have such effects.



Commercial production


Commercial production of kelp harvested from its natural habitat took place in Japan for over a century. Many countries today produce and consume laminaria products, but the largest is China. Laminaria japonica, the important commercial seaweed, was first introduced into China in the late 1920s from Hokkaido, Japan. Yet mariculture of this algae on a very large commercial scale was realized in China only in the 1950s. Between the 1950s and the 1980s kelp production in China increased from about 60 to over 250,000 dry weight metric tons annually.



Renewable energy source



Kelp has a high rate of growth and its decay is quite efficient in yielding methane, as well as sugars that can be converted to ethanol. It has been proposed that large open-ocean kelp farms could serve as a source of renewable energy.[20] Unlike some biofuels such as corn ethanol, kelp energy avoids "food vs fuel" issues[citation needed] and does not require irrigation.



In history and culture


Some of the earliest evidence for human use of marine resources, coming from Middle Stone Age sites in South Africa, includes the harvesting of foods such as abalones, limpets, and mussels associated with kelp forest habitats.


In 2007, Erlandson et al. suggested that kelp forests around the Pacific Rim may have facilitated the dispersal of anatomically modern humans following a coastal route from Northeast Asia to the Americas. This "kelp highway hypothesis" suggested that highly productive kelp forests supported rich and diverse marine food webs in nearshore waters, including many types of fish, shellfish, birds, marine mammals, and seaweeds that were similar from Japan to California, Erlandson and his colleagues also argued that coastal kelp forests reduced wave energy and provided a linear dispersal corridor entirely at sea level, with few obstacles to maritime peoples. Archaeological evidence from California's Channel Islands confirms that islanders were harvesting kelp forest shellfish and fish beginning as much as 12,000 years ago.


During the Highland Clearances, many Scottish Highlanders were moved on to areas of estates known as crofts, and went to industries such as fishing and kelping (producing soda ash from the ashes of kelp). At least until the 1840s, when there were steep falls in the price of kelp, landlords wanted to create pools of cheap or virtually free labour, supplied by families subsisting in new crofting townships. Kelp collection and processing was a very profitable way of using this labour, and landlords petitioned successfully for legislation designed to stop emigration. But the economic collapse of the kelp industry in northern Scotland led to further emigration, especially to North America.


Natives of the Falkland Islands are sometimes nicknamed "Kelpers".[21][22] This designation is primarily applied by outsiders rather than the natives themselves.


In Chinese slang, "kelp" (simplified Chinese: 海带; traditional Chinese: 海帶; pinyin: hǎi dài), is used to describe an unemployed returnee.[clarification needed] It has negative overtones, implying the person is drifting aimlessly, and is also a homophonic expression (Chinese: 海待; pinyin: hǎidài, literally "sea waiting"). This expression is contrasted with the employed returnee, having a dynamic ability to travel across the ocean: the "sea turtle" (simplified Chinese: 海龟; traditional Chinese: 海龜; pinyin: hǎi gūi) and is also homophonic with another word (simplified Chinese: 海归; traditional Chinese: 海歸; pinyin: hǎi gūi, literally "sea return").



Conservation


Overfishing nearshore ecosystems leads to the degradation of kelp forests. Herbivores are released from their usual population regulation, leading to over-grazing of kelp and other algae. This can quickly result in barren landscapes where only a small number of species can thrive.[23][24] Other major issues that threaten kelp include marine pollution and the quality of water, climate changes and certain invasive species.[25]



Gallery




Prominent species



  • Bull kelp, Nereocystis luetkeana, a northwestern American species. Used by coastal indigenous peoples to create fishing nets.

  • Giant kelp, Macrocystis pyrifera, the largest seaweed. Found in the Pacific coast of North America and South America.


  • Kombu, Saccharina japonica (formerly Laminaria japonica) and others, several edible species of kelp found in Japan.


Species of Laminaria in the British Isles;




  • Laminaria digitata (Hudson) J.V. Lamouroux (Oarweed; Tangle)


  • Laminaria hyperborea (Gunnerus) Foslie (Curvie)


  • Laminaria ochroleuca Bachelot de la Pylaie


  • Laminaria saccharina (Linnaeus) J.V.Lamouroux (sea belt; sugar kelp; sugarwack)


Species of Laminaria worldwide, listing of species at AlgaeBase:[26]




  • Laminaria agardhii (NE. America)


  • Laminaria bongardina Postels et Ruprecht (Bering Sea to California)


  • Laminaria cuneifolia (NE. America)


  • Laminaria dentigera Klellm. (California - America)


  • Laminaria digitata (NE. America)


  • Laminaria ephemera Setchell (Sitka, Alaska, to Monterey County, California - America)


  • Laminaria farlowii Setchell (Santa Cruz, California, to Baja California - America)


  • Laminaria groenlandica (NE. America)


  • Laminaria longicruris (NE. America)


  • Laminaria nigripes (NE. America)


  • Laminaria ontermedia (NE. America)


  • Laminaria pallida Greville ex J. Agardh (South Africa)


  • Laminaria platymeris (NE. America)


  • Laminaria saccharina (Linnaeus) Lamouroux, synonym of Saccharina latissima (north east Atlantic Ocean, Barents Sea south to Galicia - Spain)


  • Laminaria setchellii Silva (Aleutian Islands, Alaska to Baja California America)


  • Laminaria sinclairii (Harvey ex Hooker f. ex Harvey) Farlow, Anderson et Eaton (Hope Island, British Columbia to Los Angeles, California - America)


  • Laminaria solidungula (NE. America)


  • Laminaria stenophylla (NE. America)





Costaria costata, five-ribbed kelp


Other species in the Laminariales that may be considered as kelp:




  • Alaria marginata Post. & Rupr. (Alaska and California - America)


  • Costaria costata (C.Ag.) Saunders (Japan; Alaska, California - America)


  • Ecklonia brevipes J. Agardh (Australia; New Zealand)


  • Ecklonia maxima (Osbeck) Papenfuss (South Africa)


  • Ecklonia radiata (C.Agardh) J. Agardh (Australia; Tasmania; New Zealand; South Africa)


  • Eisenia arborea Aresch. (Vancouver Island, British Columbia, Montrey, Santa Catalina Island, California - America)


  • Egregia menziesii (Turn.) Aresch.

  • Hedophyllum sessile (C.Ag.) Setch (Alaska, California - America)


  • Macrocystis angustifolia Bory (Australia; Tasmania and South Africa)


  • Pleurophycus gardneri Setch. & Saund. (Alaska, California - America)


  • Pterygophora californica Rupr. (Vancouver Island, British Columbia to Bahia del Ropsario, Baja California and California - America)


Non-Laminariales species that may be considered as kelp:




  • Durvillea antarctica, Fucales (New Zealand, South America, and Australia)


  • Durvillea willana, Fucales (New Zealand)


  • Durvillaea potatorum (Labillardière) Areschoug, Fucales (Tasmania; Australia)



Interactions


Some animals are named after the kelp, either because they inhabit the same habitat as kelp or because they feed on kelp. These include:




  • Northern kelp crab (Pugettia producta) and graceful kelp crab (Pugettia gracilis), Pacific coast of North America.


  • Kelpfish (blenny) (e.g., Heterosticbus rostratus, genus Gibbonsia), Pacific coast of North America.


  • Kelp goose (kelp hen) (Chloephaga hybrida), South America and the Falkland Islands


  • Kelp pigeon (sheathbill) (Chionis alba and Chionis minor), Antarctic



See also



  • Bladder wrack

  • Blue carbon

  • Durvillea

  • Wrack zone



References





  1. ^ William Miller, III (13 October 2011). Trace Fossils: Concepts, Problems, Prospects: Chapter 13 "Zoophycos and the Role of Type Specimens in Ichnotaxonomy by Davide Olivero. Elsevier. pp. 224–226. ISBN 978-0-08-047535-6. Retrieved 1 April 2013..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}


  2. ^ Migula, W. (1909). Kryptogamen-Flora von Deutschland, Deutsch-Österreich und der Schweiz. Band II. Algen. 2. Teil. Rhodophyceae, Phaeophyceae, Characeae. Gera: Verlag Friedriech von Zezschwitz. pp. i–iv, 1–382, 122 (41 col.) pls.


  3. ^ Macrocystis Evolution


  4. ^ ab Thomas, D. 2002. Seaweeds. The Natural History Museum, London, p. 15.
    ISBN 0-565-09175-1



  5. ^ "Kelp," in Oxford English Dictionary (Second Edition). Oxford University Press, 1989. Retrieved 1 December 2006


  6. ^ Norderhaug, KM., Christie, H. 2009. Sea urchin grazing and kelp re-vegetation in the NE Atlantic. Marine Biology Research 5: 515-528. Estuarine, Coastal and Shelf Science 95: 135-144


  7. ^ Fritsch, F. E. (1945). Structure and Reproduction of the Algae, Volume 2. Cambridge University Press. p. 226. ISBN 9780521050425. OCLC 223742770.


  8. ^ Abdullah, M.I., Fredriksen, S., 2004. Production, respiration and exudation of dissolved organic matter by the kelp Laminaria hyperborea along the west coast of Norway. Journal of the Marine Biological Association of the UK 84: 887.


  9. ^ Rinde, E., 2009. Dokumentasjon av modellerte marine Naturtyper i DNs Naturbase. Førstegenerasjonsmodeller til kommunenes startpakker for kartlegging av marine naturtyper 2007. NIVA report, 32 pp.


  10. ^ Christie, H., Jørgensen, N.M., Norderhaug, K.M., Waage-Nielsen, E., 2003. Species distribution and habitat exploitation of fauna associated with kelp (Laminaria hyperborea) along the Norwegian coast. Journal of the Marine Biological Association of the UK 83, 687-699.


  11. ^ Jørgensen, N.M., Christie, H., 2003. Follow me @radd.michyy and lowk3y.nadine l Diurnal, horizontal and vertical dispersal of kelp associated fauna. Hydrobiologia 50, 69-76.


  12. ^ Norderhaug, K.M., Christie, H., Rinde, E., 2002. Colonisation of kelp imitations by epiphyte and holdfast fauna; a study of mobility patterns. Marine Biology 141, 965-973.


  13. ^ Norderhaug, K.M., Christie, H., 2009. Sea urchin grazing and kelp re-vegetation in the NE Atlantic. Marine Biology Research 5, 515-528.


  14. ^ Clow, Archibald; Clow, Nan L. (1952). Chemical Revolution. Ayer Co Pub. pp. 65–90. ISBN 978-0-8369-1909-7. OCLC 243798097.


  15. ^ Powers, John M. Powers. Craig's Restorative Dental Materials, 12th Edition. C.V. Mosby, 022006. p. 270


  16. ^ Kazuko, Emi: Japanese Cooking, p. 78, Hermes House, 2002, p. 78.
    ISBN 0-681-32327-2



  17. ^ Graimes, Nicola: The Best-Ever Vegetarian Cookbook, Barnes & Noble Books, 1999, p. 59.
    ISBN 0-7607-1740-0



  18. ^ Iodine Helps Kelp Fight Free Radicals and May Aid Humans, Too Newswise, Retrieved on July 8, 2008.


  19. ^ "Is Seaweed The Answer To A Dieter's Prayer?". Sky News. March 22, 2010. Archived from the original on March 25, 2010. Retrieved March 23, 2010.


  20. ^ Christiansen, Ryan C. (2008-10-31). "British report: Use kelp to produce energy". Biomassmagazine.com. Retrieved 2013-02-12.


  21. ^ [1] allwords.com definition for "Kelper",


  22. ^ [2] dictionary.com definition for "Kelper"


  23. ^ Dayton, P.K. 1985a. Ecology of kelp communities. Annual Review of Ecology and Systematics 16: 215-245.


  24. ^ Sala, E., C.F. Bourdouresque and M. Harmelin-Vivien. 1998. Fishing, trophic cascades, and the structure of algal assemblages: evaluation of an old but untested paradigm. Oikos 82: 425-439.


  25. ^ Planet, Team (2012-01-12). "Green Glossary: Kelp Forests: Other Marine Life: Animal Planet". Animals.howstuffworks.com. Archived from the original on 2012-10-24. Retrieved 2013-02-12.


  26. ^ AlgaeBase Laminariales




Further reading



  • Druehl, L.D. 1988. Cultivated edible kelp. in Algae and Human Affairs. Lembi, C.A. and Waaland, J.R. (Editors) 1988.
    ISBN 0 521 32115 8.

  • Erlandson, J.M., M.H. Graham, B.J. Bourque, D. Corbett, J.A. Estes, & R.S. Steneck. 2007. The Kelp Highway hypothesis: marine ecology, the coastal migration theory, and the peopling of the Americas. Journal of Island and Coastal Archaeology 2:161-174.



External links




  • Media related to Laminariales at Wikimedia Commons


  • Data related to Laminariales at Wikispecies










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