Organ pipe coral

The organ pipe coral (Tubipora musica) is an alcyonarian octocoral native to the waters of the Indian Ocean and the central and western regions of the Pacific Ocean.[1] It is the only known species of the genus Tubipora. This species is a soft coral but with a unique, hard skeleton of calcium carbonate that contains many organ pipe-like tubes. On each tube is a series of polyps which each have eight feather-like tentacles. These tentacles are usually extended during the day, but will swiftly withdraw with any sort of disturbance. The skeleton is a bright red color, but is typically obscured by numerous polyps. Because of this, living colonies are typically green, blue, or purple due to the color of the expanded polyps.[2] Colonies are typically dome-shaped and can reach up to 3 meters across,[2][3] while the individual polyps are typically less than 3 mm wide and a few mm long. They are close relatives to other soft coral and sea fans. This species is a popular aquarium coral due to its ease to maintain, as well as higher tolerance compared to most true corals.[4] However, its popularity presents a problem: along with its potential as an aquarium coral, the species' coloration makes it a popular commodity for tourists, leading to a variety of threats to the population.

A living organ pipe coral colony
An organ pipe coral skeleton showing its interconnected pipe and tube structure

Organ pipe coral
Live organ pipe coral
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Cnidaria
Class: Octocorallia
Order: Alcyonacea
Family: Tubiporidae
Genus: Tubipora
Species:
T. musica
Binomial name
Tubipora musica
Synonyms
  • Tubipora purpurea Pallas, 1766

Habitat

Organ pipe corals are restricted to shallow waters, and tend to live in sheltered areas where they eat plankton. Furthermore, it is usually found in habitats ranging from 2 to 20 m in depth.[1][5] Notably, they have been found dominating bedrock and sandy grooves at 8 to 10 m, as well as mid-shelf reefs.[6][5] They are also widely distributed, having been found in the west Pacific, south of Japan, west to Africa's East Coast, as well as throughout the Red Sea.[1] The species prefers good, bright light conditions, as well as medium to strong water currents and well oxygenated water.[1][7] To be successful, they also require sufficient alkalinity and calcium.[4] Colonies of organ pipe corals are interconnected networks, consisting of many pipes and tubes joined together with parallel platforms.[2] Furthermore, the colonies are usually composed of polyps that are all one color, although some large colonies have been found to have a mixture.[2] When this occurs, there are usually obvious sections of specific colors in the colony; different colored polyps do not live interspersed with each other.[2]

Ecology

Organ pipe corals contain polyps that only live in the tops of the colony's tubes.[1] These polyps contain zooxanthellae, which are a symbiotic type of phytoplankton[1] that provide energy for the coral. Furthermore, the polyps also have eight feathery tentacles branching off, which are what give the colony its color.[1] These tentacles allow the corals to capture both prey and organic particles from the surrounding environment.[1] Although the species collects organic particles, also known as DOM (dissolved organic matter), the particles only meet 13% of the metabolic needs of the coral.[8] The corals' skeleton is made of calcium carbonate, and is a deep red color.[1] The coral is also known to interact with other animals, including two recently discovered copepods found in Madagascar.[9]

Colonial behavior

Organ pipe corals exhibit limited colonial behavior. The main action that they can do is reacting as a unified colony when one part of the colony is disturbed.[2] The corals exhibit a through-conducting response when disturbed, with a wave of activity sweeping across each part of a colony.[10] When two or more polyps are touched, others nearby will bend away or retract completely. The corals usually keep activity involving one polyp separate from the rest of the colony, but disturbance of one polyp can still cause the entire colony to retract when necessary. When the polyps retract, they do so in a wave that spreads across the colony away from the place where the coral was disturbed. The corals have been shown to respond to both electrical and mechanical stimulation in this manner. However, colonial behavior beyond this response is likely limited because the corals only have one conduction system.

Full corallum of Tubipora musica.

Threats and human interaction

Organ pipe coral is listed as a near threatened species, with over 50% of the population being lost in the past 10 years.[1][11] It has become popular with dealers, hobbyists, the medical community, and tourists over the years; this is because of its ability to be easily kept in aquariums, its high medical and scientific value, as well as its use in jewelry and other commodities.[1][4][12][13][14] Due to its popularity, it is also illegally harvested and smuggled, with one report showing that it is one of the fifteen most traded corals in the world.[15][1] Observed colonies frequently show signs of being harvested and collected, providing a visual example of how the population is under intense pressure from overharvesting.[1] Subsequently, the most flourishing colonies are often found in areas with strong waves, likely due to the difficulty of collecting them in these areas.[1] Because of these problems, scientists are calling for increased protection for organ pipe corals, ranging from protected areas to awareness campaigns, as well as investigating the potential for farming these corals.[1]

References

  1. Ammar, Mohammed S. A. (2005-05-26). "An alarming threat to the red organ pipe coral Tubipora musica and suggested solutions". Ecological Research. 20 (5): 529–535. doi:10.1007/s11284-005-0064-7. ISSN 0912-3814. S2CID 44760888.
  2. ANDERSON, PETER A. V. (June 1976). "The electrophysiology of the organ-pipe coral, Tubipora musica". The Biological Bulletin. 150 (3): 337–347. doi:10.2307/1540676. ISSN 0006-3185. JSTOR 1540676. PMID 8160.
  3. Felix., Spiro, Baruch (1971). Ultrastructure and chemistry of the skeleton of Tubipora musica Linné. OCLC 633208230.{{cite book}}: CS1 maint: multiple names: authors list (link)
  4. Tullock, John (2001). Natural reef aquariums : simplified approaches to creating living saltwater microcosms. TFH-Microcosm. ISBN 1-890087-00-9. OCLC 1011858098.
  5. Fabricius, Katharina (2001). Soft corals and sea fans : a comprehensive guide to the tropical shallow water genera of the central-west Pacific, the Indian Ocean and the Red Sea. Australian Institute of Marine Science. OCLC 679405393.
  6. Pinca, S (2002). Biodiversity, ecology and conservation study in Rongelab. pp. 84–100.
  7. Borneman, Eric (2009). Aquarium corals : selection, husbandry, and natural history. Microcosm Ltd. ISBN 978-1-890087-47-0. OCLC 1058717796.
  8. Sorokin, YI (1991). "Biomass, metabolic rates and feeding of some common reef zoantharians and octocorals". Marine and Freshwater Research. 42 (6): 729. doi:10.1071/mf9910729. ISSN 1323-1650.
  9. Kim, Il‐Hoi (January 2004). "Two new species of siphonostomatoid copepods (crustacea) associated with the stoloniferan coraltubipora musica(Linnaeus) from Madagascar". Korean Journal of Biological Sciences. 8 (3): 187–196. doi:10.1080/12265071.2004.9647750. ISSN 1226-5071. S2CID 85434417.
  10. Adrian., Horridge, George (1957). The co-ordination of the protective retraction of coral polyps. Royal Society. OCLC 253743344.{{cite book}}: CS1 maint: multiple names: authors list (link)
  11. Programme., International Union for Conservation of Nature and Natural Resources. Red List (2000). IUCN red list of threatened species. IUCN. ISBN 2-00-123407-4. OCLC 46824197.
  12. Duh, Chang-Yih; Chen, Kuan-Jen; El-Gamal, Ali Ali H.; Dai, Chang-Feng (November 2001). "Sesquiterpenes from the Formosan StoloniferTubiporamusica". Journal of Natural Products. 64 (11): 1430–1433. doi:10.1021/np010228f. ISSN 0163-3864. PMID 11720526.
  13. BLAY, G.; CARDONA, L.; GARCIA, B.; PEDRO, J. R.; SANCHEZ, J. J. (2010-08-04). "ChemInform Abstract: Stereoselective Synthesis of 8,12-Furanoeudesmanes from Santonin. Absolute Stereochemistry of Natural Furanoeudesma-1,3-diene and Tubipofurane". ChemInform. 27 (39): no. doi:10.1002/chin.199639215. ISSN 0931-7597.
  14. Karacan, Ipek; Gunduz, Oguzhan; Ozyegin, L. Sevgi; Gökce, Hasan; Ben-Nissan, Besim; Akyol, Sibel; Oktar, Faik N. (2017-11-07). "The natural nano-bioceramic powder production from organ pipe red coral (Tubipora musica) by a simple chemical conversion method". Journal of the Australian Ceramic Society. 54 (2): 317–329. doi:10.1007/s41779-017-0156-1. ISSN 2510-1560. S2CID 104106934.
  15. Green, G, ed. (1999). WCMC biodiversity series no. 10. The global trade in corals. Cambridge, UK: World Conservation.
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