Seaweed

Seaweed, or macroalgae, refers to thousands of species of macroscopic, multicellular, marine algae. The term includes some types of Rhodophyta (red), Phaeophyta (brown) and Chlorophyta (green) macroalgae. Seaweed species such as kelps provide essential nursery habitat for fisheries and other marine species and thus protect food sources; other species, such as planktonic algae, play a vital role in capturing carbon, producing at least 50% of Earth's oxygen.[3]

Seaweed
Informal group of macroscopic marine algae
Fucus serratus
Scientific classification
Domain: Eukaryota
Seaweeds can be found in the following groups
Ascophyllum nodosum exposed to the sun in Nova Scotia, Canada
Dead man's fingers (Codium fragile) off the Massachusetts coast in the United States
The top of a kelp forest in Otago, New Zealand

Natural seaweed ecosystems are sometimes under threat from human activity. For example, mechanical dredging of kelp destroys the resource and dependent fisheries. Other forces also threaten some seaweed ecosystems; a wasting disease in predators of purple urchins has led to a urchin population surge which destroyed large kelp forest regions off the coast of California.[4]

Humans have a long history of cultivating seaweeds for their uses. In recent years, seaweed farming has become a global agricultural practice, providing food, source material for various chemical uses (such as carrageenan), cattle feeds and fertilizers. Because of their importance in marine ecologies and for absorbing carbon dioxide, recent attention has been on cultivating seaweeds as a potential climate change mitigation strategy for biosequestration of carbon dioxide, alongside other benefits like nutrient pollution reduction, increased habitat for coastal aquatic species, and reducing local ocean acidification.[5] The IPCC Special Report on the Ocean and Cryosphere in a Changing Climate recommends "further research attention" as a mitigation tactic.[6]

Taxonomy

"Seaweed" lacks a formal definition, but seaweed generally lives in the ocean and is visible to the naked eye. The term refers to both flowering plants submerged in the ocean, like eelgrass, as well as larger marine algae. Generally it is one of several groups of multicellular algae: red, green and brown. They lack a common multicellular ancestor, forming a polyphyletic group. In addition, bluegreen algae (Cyanobacteria) are occasionally considered in seaweed literature.[7]

The number of seaweed species is still discussed among scientists, but most likely there are several thousand species of seaweed.[8]

Genera

Claudea elegans tetrasporangia

The following table lists a very few example genera of seaweed.

GenusAlgae
Phylum
Remarks
CaulerpaGreenSubmerged
FucusBrownIn intertidal zones on rocky shores
GracilariaRedCultivated for food
LaminariaBrownAlso known as kelp
8–30 m under water
cultivated for food
MacrocystisBrownGiant kelp
forming floating canopies
MonostromaGreen
PorphyraRedIntertidal zones in temperate climate
Cultivated for food
SargassumBrownPelagic especially in the Sargasso Sea

Anatomy

Seaweed's appearance resembles non-woody terrestrial plants. Its anatomy includes:[9][10]

  • Thallus: algal body
    • Lamina or blade: flattened structure that is somewhat leaf-like
      • Sorus: spore cluster
      • pneumatocyst, air bladder: a flotation-assisting organ on the blade
      • Kelp, float: a flotation-assisting organ between the lamina and stipe
    • Stipe: stem-like structure, may be absent
    • Holdfast: basal structure providing attachment to a substrate
      • Haptera: finger-like extension of the holdfast that anchors to a benthic substrate

The stipe and blade are collectively known as the frond.

Ecology

Seaweed covers this rocky seabed on the east coast of Australia

Two environmental requirements dominate seaweed ecology. These are seawater (or at least brackish water) and light sufficient to support photosynthesis. Another common requirement is an attachment point, and therefore seaweed most commonly inhabits the littoral zone (nearshore waters) and within that zone, on rocky shores more than on sand or shingle. In addition, there are few genera (e.g., Sargassum and Gracilaria) which do not live attached to the sea floor, but float freely.

Seaweed occupies various ecological niches. At the surface, they are only wetted by the tops of sea spray, while some species may attach to a substrate several meters deep. In some areas, littoral seaweed colonies can extend miles out to sea. The deepest living seaweed are some species of red algae. Others have adapted to live in tidal rock pools. In this habitat, seaweed must withstand rapidly changing temperature and salinity and occasional drying.[11]

Macroalgae and macroalgal detritus have also been shown to be an important food source for benthic organisms, because macroalgae shed old fronds.[12] These macroalgal fronds tend to be utilized by benthos in the intertidal zone close to the shore.[13][14] Alternatively, pneumatocysts (gas filled “bubbles”) can keep the macroalgae thallus afloat fronds are transported by wind and currents from the coast into the deep ocean.[12] It has been shown that benthic organisms also at several 100 m tend to utilize these macroalgae remnants.[14]

As macroalgae takes up carbon dioxide and release oxygen in the photosynthesis, macroalgae fronds can also contribute to carbon sequestration in the ocean, when the macroalgal fronds drift offshore into the deep ocean basins and sink to the sea floor without being remineralized by organisms.[12] The importance of this process for the Blue Carbon storage is currently discussed among scientists.[15][16][17]

Biogeographic Expansion

Nowadays a number of vectors - e.g., transport on ship hulls, exchanges among shellfish farmers, global warming, opening of trans-oceanic canals - all combine to enhance the transfer of exotic seaweeds to new environments. Since the piercing of the Suez Canal,the situation is particularly acute in the Mediterranean Sea, a 'marine biodiversity hotspot' that now registers over 120 newly introduced seaweed species -the largest number in the world.[18]

Production

As of 2018, the top 10 countries produced 96% of the global total of 2,165,675 metric tons.[19]

Seaweed production
Country metric tons
per year ('000),
cultured+wild
China 699
France 617
United Kingdom 205
Japan 123
Chile 109
Philippines 96
North Korea 71
South Korea 67
Indonesia 47
Norway 41

Farming

Seaweed farming or kelp farming is the practice of cultivating and harvesting seaweed. In its simplest form, it consists of the management of naturally found batches. In its most advanced form, it consists of fully controlling the life cycle of the algae.

The top seven most cultivated seaweed taxa are Eucheuma spp., Kappaphycus alvarezii, Gracilaria spp., Saccharina japonica, Undaria pinnatifida, Pyropia spp., and Sargassum fusiforme. Eucheuma and K. alvarezii are farmed for carrageenan (a gelling agent); Gracilaria is farmed for agar; while the rest are farmed for food. The largest seaweed-producing countries are China, Indonesia, and the Philippines. Other notable producers include South Korea, North Korea, Japan, Malaysia, and Zanzibar (Tanzania).[20] Seaweed farming has frequently been developed as an alternative to improve economic conditions and to reduce fishing pressure and overexploited fisheries.[21]

Global production of farmed aquatic plants, overwhelmingly dominated by seaweeds, grew in output volume from 13.5×10^6 t (13,300,000 long tons; 14,900,000 short tons) in 1995 to just over 30×10^6 t (30,000,000 long tons; 33,000,000 short tons) in 2016.[22] As of 2014, seaweed was 27% of all marine aquaculture.[23] Seaweed farming is a carbon negative crop, with a high potential for climate change mitigation .[23] The IPCC Special Report on the Ocean and Cryosphere in a Changing Climate recommends "further research attention" as a mitigation tactic.[24]

Uses

Seaweed has a variety of uses, for which it is farmed[25] or foraged.[26]

Food

Seaweed is consumed across the world, particularly in East Asia, e.g. Japan, China, Korea, Taiwan and Southeast Asia, e.g. Brunei, Singapore, Thailand, Burma, Cambodia, Vietnam, Indonesia, the Philippines, and Malaysia,[27] as well as in South Africa, Belize, Peru, Chile, the Canadian Maritimes, Scandinavia, South West England,[28] Ireland, Wales, Hawaii and California, and Scotland.

Gim (김, Korea), nori (海苔, Japan) and zicai (紫菜, China) are sheets of dried Porphyra used in soups, sushi or onigiri (rice balls). Chondrus crispus ('Irish moss' or carrageenan moss) is used in food additives, along with Kappaphycus and Gigartinoid seaweed. Porphyra is used in Wales to make laverbread (sometimes with oat flour). In northern Belize, seaweed is mixed with milk, nutmeg, cinnamon and vanilla to make "dulce" ("sweet").

Alginate, agar and carrageenan are gelatinous seaweed products collectively known as hydrocolloids or phycocolloids. Hydrocolloids are food additives.[29] The food industry exploits their gelling, water-retention, emulsifying and other physical properties. Agar is used in foods such as confectionery, meat and poultry products, desserts and beverages and moulded foods. Carrageenan is used in salad dressings and sauces, dietetic foods, and as a preservative in meat and fish, dairy items and baked goods.

Medicine and herbs

Seaweed-covered rocks in the United Kingdom
Seaweed on rocks on Long Island

Alginates are used in wound dressings (see alginate dressing), and dental moulds. In microbiology, agar is used as a culture medium. Carrageenans, alginates and agaroses, with other macroalgal polysaccharides, have biomedicine applications. Delisea pulchra may interfere with bacterial colonization.[30] Sulfated saccharides from red and green algae inhibit some DNA and RNA-enveloped viruses.[31]

Seaweed extract is used in some diet pills.[32] Other seaweed pills exploit the same effect as gastric banding, expanding in the stomach to make the stomach feel more full.[33][34]

Climate change

"Ocean afforestation” is a proposal for farming seaweed for carbon removal.[35][36] After harvesting the seaweed decomposes into biogas, (60% methane and 40% carbon dioxide) in an anaerobic digester. The methane can be used as a biofuel, while the carbon dioxide can be stored to keep it from the atmosphere. Seaweed grows quickly and takes no space on land. Afforesting 9% of the ocean could sequester 53 billion tons of carbon dioxide annually (annual emissions are about 40 billion tons).[37]

The approach requires efficient techniques for growing and harvesting, efficient gas separation, and carbon capture and storage. The Advanced Research Projects Agency for Energy has a $22 million program called Macroalgae Research Inspiring Novel Energy Resources (MARINER) supporting innovations that could aid a seaweed industry.[37]

Other uses

Other seaweed may be used as fertilizer, compost for landscaping, or to combat beach erosion through burial in beach dunes.[38]

Seaweed is under consideration as a potential source of bioethanol.[39][40]

Seaweed is lifted out of the top of algae scrubber/cultivator, to be discarded or used as food, fertilizer, or skin care

Alginates are used in industrial products such as paper coatings, adhesives, dyes, gels, explosives and in processes such as paper sizing, textile printing, hydro-mulching and drilling. Seaweed is an ingredient in toothpaste, cosmetics and paints. Seaweed is used for the production of bio yarn (a textile).[41]

Several of these resources can be obtained from seaweed through biorefining.

Seaweed collecting is the process of collecting, drying and pressing seaweed. It was a popular pastime in the Victorian era and remains a hobby today. In some emerging countries, Seaweed is harvested daily to support communities.

Women in Tanzania grow "Mwani" (seaweed in Swahili). The farms are made up of little sticks in neat rows in the warm, shallow water. Once they harvest the seaweed, it is used for many purposes: food, cosmetics, fabric, etc.

Seaweed is sometimes used to build roofs on houses on Læsø in Denmark[42]

Seaweeds are used as animal feeds. They have long been grazed by sheep, horses and cattle in Northern Europe. They are valued for fish production.[43] Adding seaweed to livestock feed can substantially reduce methane emissions from cattle.[44]

Health risks

Rotting seaweed is a potent source of hydrogen sulfide, a highly toxic gas, and has been implicated in some incidents of apparent hydrogen-sulphide poisoning.[45] It can cause vomiting and diarrhea.

The so-called "stinging seaweed" Microcoleus lyngbyaceus is a filamentous cyanobacteria which contains toxins including lyngbyatoxin-a and debromoaplysiatoxin. Direct skin contact can cause seaweed dermatitis characterized by painful, burning lesions that last for days.[1][46]

Threats

Bacterial disease ice-ice infects Kappaphycus (red seaweed), turning its branches white. The disease caused heavy crop losses in the Philippines, Tanzania and Mozambique.[37]

Sea urchin barrens have replaced kelp forests in multiple areas. They are “almost immune to starvation”. Lifespans can exceed 50 years. When stressed by hunger, their jaws and teeth enlarge, and they form "fronts" and hunt for food collectively.[37]

See also

  • Algaculture  Aquaculture involving the farming of algae
  • Seaweed fertilizer
  • Algae fuel  Use of algae as a source of energy rich oils
  • Edible seaweed  Algae that can be eaten and used for culinary purposes
    • Aonori  Type of edible green seaweed
    • Cochayuyo  Species of seaweed, a form of kelp used as a vegetable in Chile
    • Hijiki  Species of seaweed
    • Kombu  Edible kelp
    • Limu
    • Mozuku  Species of seaweed
    • Nori  Edible seaweed species of the red algae genus Pyropia
    • Ogonori  Genus of seaweeds
    • Wakame  Species of seaweed
  • Marine permaculture
  • Sea lettuce  Genus of seaweeds
  • Seaweed cultivator
  • Seaweed dermatitis  Species of bacterium
  • Seaweed toxins

References

  1. https://www.cabdirect.org/cabdirect/abstract/19822902103 "Escharotic stomatitis caused by the "stinging seaweed" Microcoleus lyngbyaceus (formerly Lyngbya majuscula): case report and literature review"
  2. James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
  3. "How much oxygen comes from the ocean?". National Ocean Service. National Oceanic and Atmospheric Administration. Retrieved 23 November 2021.
  4. "California's crashing kelp forest". phys.org. Retrieved 2021-02-24.
  5. Duarte, Carlos M.; Wu, Jiaping; Xiao, Xi; Bruhn, Annette; Krause-Jensen, Dorte (2017). "Can Seaweed Farming Play a Role in Climate Change Mitigation and Adaptation?". Frontiers in Marine Science. 4. doi:10.3389/fmars.2017.00100. ISSN 2296-7745.
  6. Bindoff, N. L.; Cheung, W. W. L.; Kairo, J. G.; Arístegui, J.; et al. (2019). "Chapter 5: Changing Ocean, Marine Ecosystems, and Dependent Communities" (PDF). IPCC Special Report on the Ocean and Cryosphere in a Changing Climate. pp. 447–587.
  7. Lobban, Christopher S.; Harrison, Paul J. (1994). "Morphology, life histories, and morphogenesis". Seaweed Ecology and Physiology: 1–68. doi:10.1017/CBO9780511626210.002. ISBN 9780521408974.
  8. Townsend, David W. (March 2012). Oceanography and Marine Biology: An Introduction to Marine Science. Oxford University Press Inc. ISBN 9780878936021.
  9. "seaweed menu". www.easterncapescubadiving.co.za. Retrieved 2019-04-28.
  10. "The Science of Seaweeds". American Scientist. 2017-02-06. Retrieved 2022-06-02.
  11. Lewis, J. R. 1964. The Ecology of Rocky Shores. The English Universities Press Ltd.
  12. Krause-Jensen, Dorte; Duarte, Carlos (2016). "Substantial role of macroalgae in marine carbon sequestration". Nature Geoscience. 9 (10): 737–742. Bibcode:2016NatGe...9..737K. doi:10.1038/ngeo2790..
  13. Dunton, K. H.; Schell, D. M. (1987). "Dependence of consumers on macroalgal (Laminaria solidungula) carbon in an arctic kelp community: δ13C evidence". Marine Biology. 93 (4): 615–625. doi:10.1007/BF00392799. S2CID 84714929.
  14. Renaud, Paul E.; Løkken, Therese S.; Jørgensen, Lis L.; Berge, Jørgen; Johnson, Beverly J. (June 2015). "Macroalgal detritus and food-web subsidies along an Arctic fjord depth-gradient". Front. Mar. Sci. 2. doi:10.3389/fmars.2015.00031. S2CID 10417856.
  15. Watanabe, Kenta; Yoshida, Goro; Hori, Masakazu; Umezawa, Yu; Moki, Hirotada; Kuwae, Tomohiro (May 2020). "Macroalgal metabolism and lateral carbon flows can create significant carbon sinks". Biogeosciences. 17 (9): 2425–2440. Bibcode:2020BGeo...17.2425W. doi:10.5194/bg-17-2425-2020. Retrieved September 21, 2020.
  16. Krause-Jensen, Dorte; Lavery, Paul; Serrano, Oscar; Marbà, Núria; Masque, Pere; Duarte, Carlos M. (June 2018). "Sequestration of macroalgal carbon: the elephant in the Blue Carbon room". The Royal Society Publishing. 14 (6). doi:10.1098/rsbl.2018.0236. PMC 6030603. PMID 29925564.
  17. Ortega, Alejandra; Geraldi, Nathan R.; Alam, Intikhab; Kamau, Allan A.; Acinas, Silvia G; Logares, Ramiro; Gasol, Josep M; Massana, Ramon; Krause-Jensen, Dorte; Duarte, Carlos M (2019). "Important contribution of macroalgae to oceanic carbon sequestration". Nature Geoscience. 12 (9): 748–754. Bibcode:2019NatGe..12..748O. doi:10.1038/s41561-019-0421-8. hdl:10754/656768. S2CID 199448971.
  18. Briand, Frederic, ed. (2015). CIESM Atlas of Exotic Species in the Mediterranean. Volume 4. Macrophytes. CIESM, Paris, Monaco. p. 364. ISBN 9789299000342.
  19. "Volume of seaweed production ranked by country". surialink.seaplant.net. Archived from the original on 2020-08-13. Retrieved 2019-04-28.
  20. Buschmann, Alejandro H.; Camus, Carolina; Infante, Javier; Neori, Amir; Israel, Álvaro; Hernández-González, María C.; Pereda, Sandra V.; Gomez-Pinchetti, Juan Luis; Golberg, Alexander; Tadmor-Shalev, Niva; Critchley, Alan T. (2 October 2017). "Seaweed production: overview of the global state of exploitation, farming and emerging research activity". European Journal of Phycology. 52 (4): 391–406. doi:10.1080/09670262.2017.1365175. ISSN 0967-0262. S2CID 53640917.
  21. Ask, E.I (1990). Cottonii and Spinosum Cultivation Handbook. Philippines: FMC BioPolymer Corporation. p. 52.
  22. In brief, The State of World Fisheries and Aquaculture, 2018 (PDF). Food and Agriculture Organization. 2018.
  23. Duarte, Carlos M.; Wu, Jiaping; Xiao, Xi; Bruhn, Annette; Krause-Jensen, Dorte (2017). "Can Seaweed Farming Play a Role in Climate Change Mitigation and Adaptation?". Frontiers in Marine Science. 4. doi:10.3389/fmars.2017.00100. ISSN 2296-7745.
  24. Bindoff, N. L.; Cheung, W. W. L.; Kairo, J. G.; Arístegui, J.; et al. (2019). "Chapter 5: Changing Ocean, Marine Ecosystems, and Dependent Communities" (PDF). IPCC Special Report on the Ocean and Cryosphere in a Changing Climate. pp. 447–587.
  25. "Seaweed farmers get better prices if united". Sun.Star. 2008-06-19. Archived from the original on 2008-09-09. Retrieved 2008-07-16.
  26. "Springtime's foraging treats". The Guardian. London. 2007-01-06. Retrieved 2008-07-16.
  27. Mohammad, Salma (4 Jan 2020). "Application of seaweed (Kappaphycus alvarezii) in Malaysian food products". International Food Research Journal. 26: 1677–1687.
  28. "Devon Family Friendly – Tasty Seaweed Recipe – Honest!". BBC. 2005-05-25. Retrieved 2012-06-28.
  29. Round F. E. 1962 The Biology of the Algae. Edward Arnold Ltd.
  30. Francesca Cappitelli; Claudia Sorlini (2008). "Microorganisms attack synthetic polymers in items representing our cultural heritage". Applied and Environmental Microbiology. 74 (3): 564–569. Bibcode:2008ApEnM..74..564C. doi:10.1128/AEM.01768-07. PMC 2227722. PMID 18065627.
  31. Kazłowski B.; Chiu Y. H.; Kazłowska K.; Pan C. L.; Wu C. J. (August 2012). "Prevention of Japanese encephalitis virus infections by low-degree-polymerisation sulfated saccharides from Gracilaria sp. and Monostroma nitidum". Food Chem. 133 (3): 866–74. doi:10.1016/j.foodchem.2012.01.106.
  32. Maeda, Hayato; Hosokawa, Masashi; Sashima, Tokutake; Funayama, Katsura; Miyashita, Kazuo (2005-07-01). "Fucoxanthin from edible seaweed, Undaria pinnatifida, shows antiobesity effect through UCP1 expression in white adipose tissues". Biochemical and Biophysical Research Communications. 332 (2): 392–397. doi:10.1016/j.bbrc.2005.05.002. ISSN 0006-291X. PMID 15896707.
  33. "New Seaweed Pill Works Like Gastric Banding". Fox News. 25 March 2015.
  34. Elena Gorgan (6 January 2009). "Appesat, the Seaweed Diet Pill that Expands in the Stomach". softpedia.
  35. Duarte, Carlos M.; Wu, Jiaping; Xiao, Xi; Bruhn, Annette; Krause-Jensen, Dorte (2017). "Can Seaweed Farming Play a Role in Climate Change Mitigation and Adaptation?". Frontiers in Marine Science. 4: 100. doi:10.3389/fmars.2017.00100. ISSN 2296-7745.
  36. Woody, Todd (2019-08-29). "Forests of seaweed can help climate change—without risk of fire". National Geographic. Retrieved 2021-11-15.{{cite web}}: CS1 maint: url-status (link)
  37. Buck, Holly Jean (April 23, 2019). "The desperate race to cool the ocean before it's too late". MIT Technology Review. Retrieved 2019-04-28.
  38. Rodriguez, Ihosvani (April 11, 2012). "Seaweed invading South Florida beaches in large numbers". South Florida Sun-Sentinel. Retrieved 2012-04-11.
  39. "Seaweed Power: Ireland Taps New Energy Source". alotofyada.blogspot.co.uk. 2008-06-24. Retrieved 9 April 2018.
  40. Chen, Huihui; Zhou, Dong; Luo, Gang; Zhang, Shicheng; Chen, Jianmin (2015). "Macroalgae for biofuels production: Progress and perspectives". Renewable and Sustainable Energy Reviews. 47: 427–437. doi:10.1016/j.rser.2015.03.086.
  41. "The promise of Bioyarn from AlgiKnit". MaterialDriven.
  42. "Seaweed Thatch". naturalhomes.org. Retrieved 9 April 2018.
  43. Heuzé V., Tran G., Giger-Reverdin S., Lessire M., Lebas F., 2017. Seaweeds (marine macroalgae). Feedipedia, a programme by INRA, CIRAD, AFZ and FAO. https://www.feedipedia.org/node/78 Last updated on May 29, 2017, 16:46
  44. "Seaweed shown to reduce 99% methane from cattle". irishtimes.com. Retrieved 9 April 2018.
  45. "Algues vertes: la famille du chauffeur décédé porte plainte contre X" AFP, retrieved 2010-04-22 (in French)
  46. Werner, K. A.; Marquart, L.; Norton, S. A. (2012). "Lyngbya dermatitis (toxic seaweed dermatitis)". International Journal of Dermatology. 51 (1): 59–62. doi:10.1111/j.1365-4632.2011.05042.x. PMID 21790555. S2CID 22375739.

Further reading

  • Christian Wiencke, Kai Bischof (ed.)(2012). Seaweed Biology: Novel Insights into Ecophysiology, Ecology & Utilization. Springer. ISBN 978-3-642-28450-2 (print); ISBN 978-3-642-28451-9 (eBook).
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.