Macrocystis Explained

Macrocystis is a monospecific genus[1] of kelp (large brown algae) with all species now synonymous with Macrocystis pyrifera. It is commonly known as giant kelp or bladder kelp. This genus contains the largest of all the Phaeophyceae or brown algae. Macrocystis has pneumatocysts at the base of its blades. Sporophytes are perennial and the individual may live for up to three years;[2] stipes/fronds within a whole individual undergo senescence, where each frond may persist for approximately 100 days.[3] The genus is found widely in subtropical, temperate, and sub-Antarctic oceans of the Southern Hemisphere (e.g. Chile, New Zealand, Australia, Falkland Islands, Auckland Islands, South African west coast, etc.) and in the northeast Pacific from Baja California to Sitka, Alaska. Macrocystis is often a major component of temperate kelp forests.

Despite its appearance, it is not a plant; it is a heterokont. Giant kelp is common along the coast of the northeastern Pacific Ocean, from Baja California north to southeast Alaska, and is also found in the southern oceans near South America, South Africa, Australia, and New Zealand. Individual algae may grow to more than 45abbr=offNaNabbr=off long at a rate of as much as 60abbr=onNaNabbr=on per day. Giant kelp grows in dense stands known as kelp forests, which are home to many marine animals that depend on the algae for food or shelter. The primary commercial product obtained from giant kelp is alginate, but humans also harvest this species on a limited basis for use directly as food, as it is rich in iodine, potassium, and other minerals. It can be used in cooking in many of the ways other sea vegetables are used, and particularly serves to add flavor to bean dishes.

Description

Macrocystis is a monospecific genus, the sole species is M. pyrifera. Some individuals are so huge that the thallus may grow to up to 60 m (200 ft).[4] The stipes arise from a holdfast and branch three or four times from near the base. Blades develop at irregular intervals along the stipe.[5] [6] M. pyrifera grows to over 45 m (150 ft) long.[6] [7] The stipes are unbranched and each blade has a gas bladder at its base.[8]

Macrocystis pyrifera is the largest of all algae. The stage of the life cycle that is usually seen is the sporophyte, which is perennial and individuals persist for many years. Individuals may grow to up to 50-1NaN-1 long or more. The kelp often grows even longer than the distance from the bottom to the surface as it will grow in a diagonal direction due to the ocean current pushing against the kelp.[9] The stalks arise from a basal meristem, with as many as 60 stalks in older well protected individuals.[10] Blades develop at irregular intervals along the stipe, with a single pneumatocyst (gas bladder) at the base of each blade.[8] At the base of each stalk is a cluster of blades that lack pneumatocysts, instead they develop small sacks on the blade that release the biflagellated zoospores these are the sporophylls.

The smaller morphs, formerly identified as Macrocystis integrifolia, have deep brown color on flattened rhizomes which are profusely dichotomously branched. Each is attached by branched root-like structures coming out of the sides of the rhizomes. Slender main stipes (about 1cm (00inches) wide to 30m (100feet) long) come from the rhizome which is up to 0.1m (00.3feet) at the widest. Periodically 5cm (02inches) wide and 35cm (14inches) long flattened leaf-like branches derive from the stipe. They have furrowed surfaces and taper gradually, but then have an oval or rounded float where attached to the stipe. The blade-like branches have notched denticulate edges leading to the terminal blade at the tip of the stipe, which is separated by several smaller branches.[11] It grows to only 6m (20feet) long. It is found on intertidal rocks or shallow subtidal rocks along the Pacific coast of North America (British Columbia to California) and South America.[6] [12] In New Zealand M. pyrifera is found in the subtidal zone of southern North Island, the South Island, Chatham, Stewart, Bounty, Antipodes, Auckland and Campbell Islands.[13] The species can be found on rock and on sheltered open coasts.

Life cycle

The macroscopic sporophyte has many specialized blades growing near the holdfast. These blades bear various sori containing sporangia, which release haploid spores, which will grow into microscopic female and male gametophytes. These gametophytes, after reaching the appropriate substrata, grow mitotically to eventually produce gametes.[14]

Females release their eggs (oogonia) along with a pheromone, the lamoxirene.[15] [16] This compound triggers sperm release by males. The Macrocystis sperm consists of biflagellate non-synthetic antherozoids, which find their way to the oogonia following the lamoxirene. The egg is then fertilized to form the zygote, which, through mitosis, begins growth.

Macrocystis integrifolia is found on intertidal rocks or shallow subtidal rocks along the Pacific coast of North America from British Columbia to California.[17] [18] It prefers water about 7m (23feet) to 10m (30feet) deep and exposed to the open sea and normal salinities, yet sheltered from full wave action.[19]

Macrocystis integrifolia alternates heteromorphic phases from a macroscopic sporophyte to dioecious microscopic gametophytes. It has been studied as a plant fertilizer, increasing bean yields up to 24% and chemical studies indicate presence of phytohormone-like substances.[20]

Growth

Macrocystis pyrifera is one of the fastest-growing organisms on Earth.[21] [22] They can grow at a rate of 600NaN0 a day to reach over 45abbr=onNaNabbr=on long in one growing season.[6] [23] [24]

Juvenile giant kelp grow directly upon their parent female gametophyte. To establish itself, a young kelp produces one or two primary blades, and begins a rudimentary holdfast, which serves to anchor the plant to the rocky bottom. As the kelp grows, additional blades develop from the growing tip, while the holdfast enlarges and may entirely cover the rock to which it is attached.

Growth occurs with lengthening of the stipe (central stalk), and splitting of the blades. At the growing tip is a single blade, at the base of which develop small gas bladders along one side. As the bladders and stipe grow, small tears develop in the attached blade. Once the tears have completed, each bladder supports a single separate blade along the stipe, with the bladders and their blades attached at irregular intervals.[5] [25]

Ecology

See main article: article and Kelp forest. Macrocystis typically grow forming extensive beds, large "floating canopies", on rocky substrata between the low intertidal.[6] [14] It was harvested by barges which used large blades to harvest up to 300 tons a day along the coast of California.[26]

Macrocystis pyrifera is found in North America (Alaska to California), South America, South Africa, New Zealand, and southern Australia.[27] It thrives in cooler waters where the ocean water temperature remains mostly below 70F.[24] The species is also found near Tristan da Cunha in the Mid-South Atlantic Ocean.

Where the bottom is rocky and affords places for it to anchor, giant kelp forms extensive kelp beds with large "floating canopies".[6] When present in large numbers, giant kelp forms kelp forests that are home to many marine species that depend upon the kelp directly for food and shelter, or indirectly as a hunting ground for prey. Both the large size of the kelp and the large number of individuals significantly alter the availability of light, the flow of ocean currents, and the chemistry of the ocean water in the area where they grow.[28]

In high-density populations, giant kelp individuals compete with other individuals of the species for space and resources. Giant kelp may also compete with Pterygophora californica in these circumstances.[29] [30]

Where surface waters are poor in nutrients, nitrogen in the form of amino acids is translocated up the stipe through sieve elements that very much resemble the phloem of vascular plants.[28] [9] Translocation of nutrients along the stipe may be as rapid as 60cm (20inches) per hour.[25] Most translocation occurs to move carbon-rich photosynthate, and typically transfers material from mature regions to actively growing regions where the machinery of photosynthesis is not yet fully in place. Translocation also moves nutrients downward from light-exposed surface fronds to sporophylls (reproductive fronds) at the base of the kelp, where there is little light and thus little photosynthesis to produce food.

Species

Initially, 17 species were described within the genus Macrocystis.[31] In 1874, Hooker, following blade morphology, put them all under the same taxon, Macrocystis pyrifera.[32] In modern times, the large number of species were re-classified based on the holdfast morphology, which distinguished three species (M. angustifolia, M. integrifolia, and M. pyrifera) and on blade morphology, which added a fourth species (M. laevis) in 1986.[33] In 2009 and 2010, however, two studies that used both morphological[34] and molecular[1] assessments demonstrate that Macrocystis is monospecific (as M. pyrifera), which is currently accepted by the phycological community (see AlgaeBase).[35]

Morphs

Although Macrocystis is a monospecific genus, some split it into the four morphs, or sub-species, described below, following pre-2010 taxonomy:[36] [37]

Distribution

Macrocystis is distributed along the eastern Pacific coast from Alaska to Mexico and from Peru and along the Argentinian coast as well as in Australia, New Zealand, South Africa and most sub-Antarctic islands to 60°S.[14]

Aquaculture

Macrocystis pyrifera has been utilized for many years as a food source;[40] it also contains many compounds such as iodine, potassium, other minerals vitamins and carbohydrates and thus has also been used as a dietary supplement.[41] [42] In the beginning of the 20th century California kelp beds were harvested as a source for soda ash.[43] [44] With commercial interest increasing significantly during the 1970s and the 1980s this was primarily due to the production of alginates, and also for biomass production for animal feed due to the energy crisis during that period.[45] [44] However the commercial production of M. pyrifera never became reality. With the end of the energy crisis and the decline in prices of alginates, the research into farming Macrocystis also declined.

The demand for M. pyrifera is increasing due to the newfound uses of these plants such as fertilizers, cultivation for bioremediation purposes, abalone and sea urchin feed. There is current research going into utilizing M. pyrifera as feed for other aquaculture species such as shrimps.[46] Recently, M. pyrifera has been examined as a possible feedstock for conversion into ethanol for biofuel use.[47]

Conservation

In recent years, the kelp forests have decreased dramatically throughout Japan, Chile, Korea, Australia and North America.[48] Harvesting of kelp as a food source and other uses may be the least concerning aspect to its depletion. In the Northwest Pacific kelp forests in waters near large population centres may be most affected by the sewer/stormwater discharge.[49]

The natural phenomenon known as El Niño cycles warm, tropical water from the South Pacific to Northern waters. This has been known to kill off M. pyrifera, due to its need for cold waters it would usually find in the North Pacific Ocean.[50] In California, El Niño also brought along a population bloom of purple sea urchins which feed on the giant kelp.[51]

Tasmania

Off the coast of Tasmania, kelp forests have been significantly affected by several factors, including warming waters, shifting of the East Australian current (EAC), and invasion of long-spine sea urchins. Locals have noticed significant effects on the population of abalone, a food source for the Aboriginal Tasmanians for thousands of years. These changes have also affected the oyster farming industry. By saving oysters that have survived disease outbreaks, they have been able to continue their way of life.[52] It was estimated that by 2019, 95 per cent of the giant kelp forests along Tasmania's east coast had been lost within just a few decades. Some of this loss was attributed by locals to the harvesting of the forests by Alginates Australia, which opened its factory near Triabunna in 1963, shutting down operations 10 years later as uneconomical. However, expert in marine ecosystems Craig Johnson says that the loss of the forests "is almost certainly the result of climate change". Water temperatures along the east coast of Tasmania have been rising at nearly four times the average rate globally. The EAC brings warmer waters, which are also nutrient-poor compared to the previously usual cold water around the coast. Common kelp (Ecklonia radiata) is better at nitrogen storage than giant kelp, so has been taking over the areas formerly occupied by giant kelp.[53]

Macrocystis pyrifera has become Australia’s first federally-listed endangered marine community.[53] [54] Scientists and conservationists are continuously looking into ways to restore the once heavily populated species to its original state. Methods include artificial reefs, reducing numbers of purple sea urchins in overpopulated areas, and planting roots along the ocean floor.[48] Scientists had built 28 artificial reefs off Maria Island by 2019, and were hopeful of bringing the kelp forests back.[55]

See also

Further reading

External links

Notes and References

  1. Macaya . Erasmo C. . Zuccarello . Giuseppe C. . DNA barcoding and genetic divergence in the Giant Kelp Macrocystis (Laminariales). . Journal of Phycology . August 2010 . 46 . 4 . 736–742 . 10.1111/j.1529-8817.2010.00845.x. 84033275 .
  2. W.J. North (1971) The biology of giant kelp beds.
  3. G.E. Rodriguez, A. Rassweiler, D.C. Reed, & S.J. Holbrook (2013) The importance of progressive senescence in the biomass dynamics of giant kelp (Macrocystis pyrifera). Ecology, 94(8), 1848-1858.
  4. C. van den Hoek, D.G. Mann and H.M. Jahns (1995) Algae An Introduction to Phycology. Cambridge University Press, Cambridge.
  5. Mondragon, Jennifer and Mondragon, Jeff (2003) Seaweeds of the Pacific Coast. Sea Challengers, Monterey, California.
  6. I.A. Abbott and G.J. Hollenberg (1976) Marine Algae of California. Stanford University Press, California.
  7. A.B. Cribb (1953) Macrocystis pyrifera (L.) Ag. in Tasmanian waters Australian Journal of Marine and Freshwater Research, Vol 5, issue 1.
  8. [Joanna M. Kain|Kain, J M]
  9. Hoek, C van den; D G Mann & H M Jahns. (1995) Algae: An Introduction to Phycology. Cambridge: Cambridge University Press.
  10. Web site: Biology of the Macrocystis resource in North America. 2021-01-27. www.fao.org.
  11. http://www.racerocks.com/racerock/algae/ryanmurphy/macrocystis.htm Phylum: Phaeophyta, Class: Phaeophyceae, Order: Laminariales, Family: Lessoniaceae, Macrocystis integrifolia (Bory)
  12. [AlgaeBase]
  13. Book: Nelson, W. A.. New Zealand seaweeds : an illustrated guide. Te Papa Press. 2013. 9780987668813. Wellington, New Zealand. 100. 841897290.
  14. M.H. Graham, J.A. Vásquez and A.H. Buschmann (2007) Global ecology of the giant kelp Macrocystis: From ecotypes to ecosystems. Oceanography and Marine Biology: An Annual Review 45: 39-88.
  15. I. Maier, D.G. Müller, G. Gassman, W. Boland and L. Jaenicke (1987) Sexual pheromones and related egg secretions in Laminariales (Phaeophyta). Zeitschrift Naturforschung Section C Biosciences 42: 948–954.
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  18. http://ucjeps.berkeley.edu/guide/brown61.html Macrocystis integrifolia Bory
  19. http://www.racerocks.com/racerock/eco/taxalab/bio2002/macrocystisi.htm The Race Rocks Taxonomy, Macrocystis integrifolia
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  21. Fenner, Bob The Brown Algae
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  26. Smith, G.M. 1955. Cryptogamic Botany. Volume 1. Algae and Fungi. McGraw-Hill Book Company, Inc.
  27. [AlgaeBase]
  28. Lobban, C S & P J Harrison. (1994) Seaweed Ecology and Physiology. Cambridge: Cambridge University Press.
  29. Reed, D C. (1990) "The effects of variable settlement and early competition on patterns of kelp recruitment." Ecology 71:776-787.
  30. Reed, D C, M Neushul, & A W Ebeling. (1991) "Role of settlement density on gametophyte growth and reproduction in the kelps Pterygophora californica and Macrocystis pyrifera (Phaeophyceae)." Journal of Phycology 27:361-366.
  31. W.J. North (1971) Review of Macrocystis biology. In Biology of Economic Algae, I. Akatsuka (ed.). Hague: Academic Publishing, 447–527.
  32. J.D. Hooker (1874) The Botany of the Antarctic Voyage of H.M. Discovery Ships Erebus and Terror. I. Flora Antarctica. London: Reeve Brothers.
  33. C.H. Hay (1986) A new species of Macrocystis C. Ag. (Phaeophyta) from Marion Island, southern Indian Ocean. Phycologia 25: 241–252.
  34. Demes . Kyle W. . Graham . Michael H. . Suskiewicz . Thew S. . Phenotypic plasticity reconciles incongruous molecular and morphological taxonomies: the Giant Kelp, Macrocystis (Laminariales, Phaeophyceae), is a monospecific genus. . Journal of Phycology . December 2009 . 45 . 6 . 1266–1269 . 10.1111/j.1529-8817.2009.00752.x . 27032582. 29176127 .
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  36. Demes . Kyle W. . Graham . Michael H. . Suskiewicz . Thew S. . Phenotypic Plasticity Reconciles Incongruous Molecular and Morphological Taxonomies: The Giant Kelp, Macrocystis (Laminariales, Phaeophyceae), is a Monospecific Genus1 . December 2009 . Journal of Phycology . en . 45 . 6 . 1266–1269 . 10.1111/j.1529-8817.2009.00752.x. 27032582 . 29176127 .
  37. Demes, K.W, Graham, M.H. & Suskiewicz, T.S. (2009). Phenotypic plasticity reconciles incongruous molecular and morphological taxonomies: the giant kelp, Macrocystis (Laminariales, Phaeophyceae), is a monospecific genus (note). Journal of Phycology 45(6): 1266-1269.
  38. M. Neushul (1971) The biology of giant kelp beds (Macrocystis) inCalifornia: the species of Macrocystis. Nova Hedwigia 32: 211–22.
  39. J.M. Huisman (2000) Marine Plants of Australia. University of Western Australia Press.
  40. Gutierrez, A., Correa, T., Muñoz, V., Santibañez, A., Marcos, R., Cáceres, C., et al. (2006). Farming of the Giant Kelp Macrocystis Pyrifera in Southern Chile for Development of Novel Food Products. Journal of Applied Phycology, 18(3), 259-267.
  41. Bushing, William W (2000) Giant Bladder Kelp .
  42. Connor, Judith & Charles Baxter. (1989) Kelp Forests. Monterey, California: Monterey Bay Aquarium.
  43. Abbott, I. A. (1996). Ethnobotany of seaweeds: clues to uses of seaweeds. Hydrobiologia, 326-327(1), 15-20.
  44. Druehl LD, Baird R, Lindwall A, Lloyd KE, Pakula S (1988) Longline cultivation of some Laminareaceae in British Columbia. Aquacult. Fish Management 19, 253–263.
  45. Neushul M (1987) Energy from marine biomass: The historicalrecord. In: Bird KT, Benson PH (eds), Seaweed Cultivation for Renewable Resources, Elsevier Science Publishers, Amsterdam, 1–37.
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  47. Wargacki, A.J., Leonard, E., Win, M.N., Regitsky, D.D., Santos, C.N.S., et al. (2012). An engineered microbial platform for direct biofuel production from brown macroalgae. Science, 335(1), 308-313.
  48. Web site: Scientists Work to Save Disappearing Kelp Forests. VOA. 2016-04-20.
  49. Filbee-Dexter. K. Scheibling. Re. 2014-01-09. Sea urchin barrens as alternative stable states of collapsed kelp ecosystems. Marine Ecology Progress Series. en. 495. 1–25. 10.3354/meps10573. 2014MEPS..495....1F. 0171-8630. free.
  50. Book: Advances in Ecological Research. 1987-11-05. Academic Press. 9780080567013. en.
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  52. Web site: Warming has dire effects in oceans 1/19/2020. Star Tribune. 2020-01-19.
  53. Web site: Kean . Zoe . These giant kelp forests were a boon for Tasmania's economy in the 60s and 70s. Now they're all but gone . ABC News . 27 February 2021 . 28 February 2021.
  54. Web site: Department of the Environment, Commonwealth of Australia. Threatened Ecological Community Profile — Giant Kelp Marine Forests of South East Australia. 2021-07-29. www.environment.gov.au. en.
  55. Web site: MacDonald . Lucy . Scientists in race to save giant kelp off Tasmanian coast . ABC News . . 5 February 2019 . 28 February 2021.