Nereocystis Explained

Nereocystis (Greek, 'mermaid's bladder') is a monotypic genus of subtidal kelp containing the species Nereocystis luetkeana.[1] Some English names include edible kelp, bull kelp, bullwhip kelp, ribbon kelp, bladder wrack, and variations of these names.[2] Due to the English name, bull kelp can be confused with southern bull kelps, which are found in the Southern Hemisphere.[3] [4] Nereocystis luetkeana forms thick beds on subtidal rocks, and is an important part of kelp forests.

Etymology

The species Nereocystis luetkeana was named (as Fucus luetkeanus) after the German-Russian explorer Fyodor Petrovich Litke (also spelled Lütke) by Mertens. The species was renamed in a description by Postels and Ruprecht.[5]

Description

Nereocystis is a brown macroalgae that derives chemical energy from photosynthesis. Nereocystis in particular, similar to Pelagophycus porra, can be identified by a single large pneumatocyst between the end of its hollow stipe and the blades.[6] Individuals can grow to a maximum of 36m (118feet).[7] Nereocystis has a holdfast of about 40cm (20inches), and a single stipe, topped with a pneumatocyst containing carbon monoxide, from which sprout the numerous (about 30-64) blades. The blades may be up to 4m (13feet) long, and up to 15cm (06inches) wide. It is usually annual, sometimes persisting up to 18 months. Nereocystis is the only kelp which will drop spore patches, so that the right concentration of spores lands near the parent's holdfast.

The thallus of this common canopy-forming kelp has a richly branched holdfast (haptera) and a cylindrical stipe 10–36 m (33–118 ft) long. The stipe terminates in a single, gas-filled pneumatocyst from which many blades grow. Each blade can grow up to 10 m (33 ft) long, and blade growth can reach 15 cm (5.9 in) per day.

Nereocystis grows in areas where Pterygophora californica also inhabits. Bull kelp will often grow on the stipe of Pterygophora, with up anywhere from 10 to 20 individuals of Nereocystis attaching to a single Pterygophora stipe.

Reproduction

Reproduction in Nereocystis is characterized by an alternation of generations. The diploid generation is the recognizable macroscopic sporophyte. During sexual reproduction, reproductive patches (sori) develop on the blades of the sporophyte and drop to the seafloor at maturity.[8] The sori release haploid spores, which become the microscopic gametophytes. The gametophytes produce gametes, and if fertilization occurs, a new sporophyte organism may develop and begin to grow up from the seafloor.[9]

Distribution

The species is common along the Pacific Coast of North America, from Southern California to the Aleutian Islands, Alaska.[10] However, drift individuals disperse with ocean currents further south into northwest Baja California, Mexico.[11] Offshore beds can persist for one or many years, usually in deeper water than Eualaria or Macrocystis, where they co-occur.

This annual kelp grows on rock from the low intertidal to subtidal zones; it prefers semi-exposed habitats or high-current areas. It also does not grow in areas with breaking waves or swells.[6] Its distribution is limited by the requirement of light for photosynthesis, and preference for areas of high water movement where the microscopic gametophyte stage will not be covered by sediment.[12]

Other factors such as salinity, turbidity and water temperature can affect Nereocystis distribution. Nereocystis tends to thrive in temperatures ranging from 5 to 20 degrees Celsius.[13] It is rarely found in environments with high turbidity and low salinity. Nereocystis fails to thrive in areas of reduced salinity, such as brackish estuarine waters, because it has difficulty adjusting to changes in salinity. The increased turbidity of such waters also decreases light available for photosynthesis, limiting its growth. Additionally, disease, competition, and herbivory can affect distribution.

Ecology

Nereocystis, like other large, canopy forming kelps, play a crucial role in maintaining the biologically diverse kelp forests in the temperate marine environments where they flourish.[14] Its fast growth and size provide an important habitat not only for the fish and invertebrates that reside in kelp forests, but also for species that use kelp forests as foraging grounds.[15] In bull kelp forests, kelp crabs are important grazers that control the ecosystem by feeding on large canopy kelps such as Nereocystis.[16]

Microbial communities

Nereocystis fosters microbacteria species, affecting the ecology on a microscopic level. These microbial bacteria species foster the growth of seaweed, producing growth-promoting substances.[17] According to studies by Weigel, the microbial communities that grow on Nereocystis are composed mostly of Proteobacteria, Bacteroidetes, Verrucomicrobia, and Planctomycetes. Nereocystis is unique in that it contains a large percentage of Verrucomicrobia, with it composing approximately 10% of microbacteria populations on Nereocystis.[18]

Human effects

Abalone mariculture (the commercial farming and harvest of abalone) and an increasing demand in human consumption have led to a notable and marked increase in Nereocystis extraction. This extraction is done by hand and removes the top two meters of the forest. These first two meters contain bull kelp's pneumatocysts and its reproductive organs, so this method of extraction destroys kelp forests that depend on Nereocystis.[19] Since bull kelp tend to only reproduce once a year, removal of these organs renders Nereocystis unable to reproduce.[20] The tissues of bull kelp are processed and turned into liquid fertilizer as well as food for abalones.

Human uses

Nereocystis was not commercially harvested off the coast of California until around the 1980s. The beginning of this harvest is attributed to the Abalone International company, which was seeking mariculture expansion and efficiency. Kelp harvesters are legally mandated to record every aspect of their harvest, including but not limited to the amount of kelp, the species, and the location where it was taken from. Kelp is currently harvested from the Californian coast, Oregon, Washington, British Columbia, and Alaska.

Human uses of Nereocystis include consumption and agriculture. It is pickled and eaten as a delicacy as well as used for creative purposes. In South Korea, Nereocystis used to make miyeok-guk (Korean kelp soup) weekly by new mothers as it's revered as a blood-cleanser. It is also customary to eat it on one's birthday.

Further reading

External links

Notes and References

  1. Fisher. K. Martone. P.T.. 20391876. Field Study of Growth and Calcification Rates of Three Species of Articulated Coralline Algae in British Columbia, Canada. Biological Bulletin. April 2014. 226. 2. 121–130. 24797094. 10.1086/bblv226n2p121.
  2. Book: Angier, Bradford . Bradford Angier . Field Guide to Medicinal Wild Plants . 1978 . Stackpole Books . Harrisburg, Pa. . 978-0-8117-2076-2 . 156.
  3. Cheshire. A.C.. Hallam. N.. 83670142. 2009. Morphological Differences in the Southern Bull-Kelp (Durvillaea potatorum) throughout South-Eastern Australia. Botanica Marina. 32. 3. 191–198. 10.1515/botm.1989.32.3.191.
  4. Fraser. C.I.. Winter. D.J.. Spencer. H.G.. Waters. J.M.. 2010. Multigene phylogeny of the southern bull-kelp genus Durvillaea (Phaeophyceae: Fucales). Molecular Phylogenetics and Evolution. 57. 3. 1301–11. 10.1016/j.ympev.2010.10.011. 20971197.
  5. Book: Marine Algae of California. Science. 101. 2617. 188–92. Isabella A.. Abbott. Abbott. Isabella. George J.. Hollenberg. 1 August 1992. 22 February 2018. Google Books. 1945Sci...101..188S. 10.1126/science.101.2617.188. 17750419. 9780804721523.
  6. FOREMAN, R. E. (1970). Physiology, Ecology, And Development Of The Brown Alga, Nereocystis Luetkeana (mertens) P. & R (Order No. 7109813). Available from ProQuest Dissertations & Theses Global. (302503381).
  7. Bringloe . Trevor T. . Starko . Samuel . Wade . Rachael M. . Vieira . Christophe . Kawai . Hiroshi . De Clerck . Olivier . Cock . J. Mark . Coelho . Susana M. . Destombe . Christophe . Valero . Myriam . Neiva . João . Pearson . Gareth A. . Faugeron . Sylvain . Serrão . Ester A. . Verbruggen . Heroen . 2020-07-03 . Phylogeny and Evolution of the Brown Algae . Critical Reviews in Plant Sciences . 39 . 4 . 281–321 . 10.1080/07352689.2020.1787679 . 221469037 . 0735-2689. free .
  8. Amsler . Charles D. . Neushul . Michael . 1989-01-01 . Diel periodicity of spore release from the kelp Nereocystis luetkeana (Mertens) Postels et Ruprecht . Journal of Experimental Marine Biology and Ecology . en . 134 . 2 . 117–127 . 10.1016/0022-0981(90)90104-K . 0022-0981.
  9. Dayton . Paul K. . 1985 . Ecology of Kelp Communities . Annual Review of Ecology and Systematics . 16 . 215–245 . 10.1146/annurev.es.16.110185.001243 . 2097048 . 0066-4162.
  10. Schoch . G. Carl . Chenelot . Héloïse . 2004 . The Role of Estuarine Hydrodynamics in the Distribution of Kelp Forests in Kachemak Bay, Alaska . Journal of Coastal Research . 10045 . 179–194 . 10.2112/SI45-179.1 . 25737077 . 6906851 . 0749-0208.
  11. Bushing WW (1994) Biogeographical and ecological implications of kelp rafting as a dispersal vector for marine invertebrates. In: Halvorson W, Maender G (eds) Proceedings of the Fourth California Islands Symposium: Update on the Status of Resources, March 22–25, 1994. Santa Barbara Museum of Natural History, Santa Barbara, CA
  12. Schiel . David R. . Wood . Spencer A. . Dunmore . Robyn A. . Taylor . David I. . April 2006 . Sediment on rocky intertidal reefs: Effects on early post-settlement stages of habitat-forming seaweeds . Journal of Experimental Marine Biology and Ecology . en . 331 . 2 . 158–172 . 10.1016/j.jembe.2005.10.015.
  13. Web site: Springer . Yuri . Hays . Cynthia . Carr . Mark . Mackey . Megan . Bloeser . Jennifer . March 2007 . Ecology and Management of the Bull Kelp, Nereocystis Luetkeana .
  14. Wheeler, W. N., and Druehl, L. D. (1986). Seasonal growth and productivity of Macrocystis integrifolia in British Columbia, Canada. Mar. Biol. 90, 181–186. doi: 10.1007/BF00569125
  15. Calvert EL, Siddon CE, Stekoll MS (in prep). Direct and Indirect Effects of Kelp Beds in Structuring Fish and Invertebrate Assemblages in Southeastern Alaska.
  16. Dobkowski, Katie. “The Role of Kelp Crabs as Consumers in Bull Kelp Forests—Evidence from Laboratory Feeding Trials and Field Enclosures.” PeerJ, PeerJ Inc., 1 May 2017
  17. Ravindra Pal Singh, C.R.K. Reddy, Seaweed–microbial interactions: key functions of seaweed-associated bacteria, FEMS Microbiology Ecology, Volume 88, Issue 2, April 2014
  18. Weigel, Brooke L., et al. “Successional Dynamics and Seascape-Level Patterns of Microbial Communities on the Canopy-Forming Kelps Nereocystis luetkeana and Macrocystis pyrifera.” Frontiers in Microbiology, vol. 10, 2019.
  19. Hansen GI, Mumford TF (1995) 1994/1995 Regulations for Seaweed Harvesting on the West Coast of North America.
  20. Springer, Yuri; Hays, Cynthia; Carr, Mark; Mackey, Megan; Bloeser, Jennifer (March 2007). "Ecology and Management of the Bull Kelp, Nereocystis Luetkeana" (PDF).