Sea anemone

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Sea anemones
A selection of sea anemones,
painted by Giacomo Merculiano, 1893
Scientific classification e
Kingdom: Animalia
Phylum: Cnidaria
Class: Anthozoa
Subclass: Hexacorallia
Order: Actiniaria
46 families

Sea anemones are a group of water-dwelling, predatory animals of the order Actiniaria. They are named for the anemone, a terrestrial flower. Sea anemones are classified in the phylum Cnidaria, class Anthozoa, subclass Hexacorallia.[1] Anthozoa often have large polyps that allow for digestion of larger prey and also lack a medusa stage.[2] As cnidarians, sea anemones are related to corals, jellyfish, tube-dwelling anemones, and Hydra.

Many sea anemones form symbiotic relationships with single-celled dinoflagellates, whether zooxanthellae or zoochlorellae, that live within their cells.

The global trade in marine ornamentals for aquariums is rapidly expanding, and threatens sea anemone populations as the trade depends on collection from the wild, and the animals grow and reproduce relatively slowly.[citation needed]


Sea Anemone Anatomy.
1. Tentacles 2. Mouth 3. Retracting muscles 4. Gonads 5. Acontial filaments 6. Pedal disk 7. Ostium 8. Coelenteron 9. Sphincter muscle 10. Mesentery 11. Column 12. Pharynx
The 49th plate from Ernst Haeckel's Kunstformen der Natur, 1904, showing various sea anemones classified as Actiniae

A sea anemone is a sessile polyp attached at the bottom to the surface beneath it by an adhesive foot, called a basal disc, with a column-shaped body ending in an oral disc. Most are from 1.8 to 3 cm (0.71 to 1.18 in) in diameter, but anemones as small as 4 mm (0.16 in) or as large as nearly 2 m (6.6 ft) are known.[3] They can have from a few tens to a few hundred tentacles.

A few species are pelagic and are not attached to the bottom; instead, they have a gas chamber within the pedal disc, allowing them to float upside down in the water.[4]

The mouth, also the anus of the sea anemone, is in the middle of the oral disc surrounded by tentacles armed with many cnidocytes, cells that are both defensive and used to capture prey. Cnidocytes contain stinging nematocysts, capsule-like organelles capable of everting suddenly, giving the phylum Cnidaria its name.[5] Each nematocyst contains a small venom vesicle filled with actinotoxins, an inner filament, and an external sensory hair. A touch to the hair mechanically triggers a cell explosion, which launches a harpoon-like structure that attaches to the organism that triggered it, and injects a dose of venom in the flesh of the aggressor or prey. This gives the anemone its characteristic sticky feeling. The sea anemone eats small fish and shrimp.

The venom is a mix of toxins, including neurotoxins, that paralyzes the prey so the anemone can move it to the mouth for digestion inside the gastrovascular cavity. Actinotoxins are highly toxic to prey species of fish and crustaceans. However, Amphiprioninae (clownfish), small banded fish in various colors, are not affected by their host anemone's sting and shelter themselves from predators among its tentacles.[6] Several other species have similar adaptions and are also unaffected (see Symbiotic relationships). Most sea anemones are harmless to humans, but a few highly toxic species (notably Actinodendron, Phyllodiscus and Stichodactyla) have caused severe injuries and are potentially lethal.[7]

Digestive system

A gastrovascular cavity functions as a stomach and possesses a single opening to the outside, which operates as both a mouth and anus. Waste and undigested matter is excreted through this opening, which can be described as an incomplete gut. The mouth is typically slit-like in shape, and bears a groove at one or both ends. The groove, termed a siphonophore, is ciliated, and helps to circulate water through the gastrovascular cavity.[4] Some anemones feed on small particles, which are caught with the aid of a mucus secretion and moving currents that are set up by the tentacles. Most sea anemones are predacious, immobilizing their prey with the aid of their nematocysts.[8]

The mouth opens into a flattened pharynx. This consists of an in-folding of the body wall, and is therefore lined by the animal's epidermis. The pharynx typically runs for about two-thirds the length of the body before opening into the gastrovascular cavity that fills the remainder of the body.

The gastrovascular cavity itself is divided into a number of chambers by mesenteries radiating inwards from the body wall. Some of the mesenteries form complete partitions with a free edge at the base of the pharynx, where they connect, but others reach only partway across. The mesenteries are usually found in multiples of twelve, and are symmetrically arranged around the central pharynx. They have stomach lining on both sides, separated by a thin layer of mesoglea, and includes filaments of tissue specialised for secreting digestive enzymes. In some species, these filaments extend below the lower margin of the mesentery, hanging free in the gastrovascular cavity as acontial filaments.[4]

Nerve system

Striped colonial anemone

A primitive nervous system, without centralization, coordinates the processes involved in maintaining homeostasis, as well as biochemical and physical responses to various stimuli. No specialized sense organs are present.

The muscles and nerves are much simpler than those of most other animals, although more specialised than in other cnidarians, such as corals. Cells in the outer layer (epidermis) and the inner layer (gastrodermis) have microfilaments that group into contractile fibers. These fibers are not true muscles because they are not freely suspended in the body cavity as they are in more developed animals. Longitudinal fibres are found in the tentacles and oral disc, and also within the mesenteries, where they can contract the whole length of the body. Circular fibers are found in the body wall and, in some species, around the oral disc, allowing the animal to retract its tentacles into a protective sphincter.[4]

Since the anemone lacks a skeleton, the contractile cells pull against the gastrovascular cavity, which acts as a hydrostatic skeleton. The anemone stabilizes itself by shutting its mouth, which keeps the gastrovascular cavity at a constant volume, making it more rigid. Although generally sessile, sea anemones are capable of slow movements using their pedal disc, or of swimming, using either their tentacles or by flexing their bodies.


Brooding anemone (Epiactis prolifera) with developing young

Unlike other cnidarians, anemones (and other anthozoans) entirely lack the free-swimming medusal stage of their lifecycle; the polyp produces eggs and sperm, and the fertilized egg develops into a planula that develops directly into another polyp.

Anemones tend to stay in the same spot until conditions become unsuitable (prolonged dryness, for example), or a predator attacks them. In that case, anemones can release themselves from the substrate and use flexing motions to swim to a new location. Most sea anemones attach temporarily to submerged objects; a few thrust themselves into the sand or live in burrows; a few are parasitic on other marine organisms,[8] and some have symbiotic relationships with hermit crabs.

The sexes in sea anemones are separate in some species, while other species are protandric hermaphrodites. The brooding anemone (Epiactis prolifera) is gynodioecious, starting life as a female and later becoming hermaphroditic, so that populations consist of females and hermpaphrodites, and all females are fertilized by hermaphrodites. The gonads are strips of tissue within the mesenteries. Both sexual and asexual reproduction can occur. In sexual reproduction, males release sperm to stimulate females to release eggs, and fertilization occurs. Anemones eject eggs and sperm through the mouth. The fertilized egg develops into a planula, which settles and grows into a single polyp.

Anemones can also reproduce asexually, by budding or in some cases by binary fission, when the polyp separates into two halves. Some species can also reproduce by pedal laceration. In this process, a ring of material breaks off from the pedal disc at the base of the column which then fragments, the pieces regenerating into new individuals.[9] The sea anemone Aiptasia diaphana displays sexual plasticity. Thus asexually produced clones derived form a single founder individual can contain both male and female individuals (ramets).[10] When eggs and sperm (gametes) are formed, they can produce zygotes derived from “selfing” (within the founding clone) or out-crossing, that then develop into swimming planula larvae.


The sea anemone has an oral disk, which the organism uses to capture prey. The anemone attaches to the substrate using the basal disk at its posterior end. Others also burrow into weaker objects. Some species attach to kelp while others are free-swimming.

Symbiotic relationships

Although not plants and therefore incapable of photosynthesis themselves, many sea anemones form an important facultative symbiotic relationship with certain single-celled algae species that reside in the animals' gastrodermal cells. These algae may be either zooxanthellae, zoochlorellae or both. The sea anemone benefits from the products of the algae's photosynthesis, namely oxygen and food in the form of glycerol, glucose and alanine; the algae in turn are assured a reliable exposure to sunlight and protection from micro-feeders, which the sea anemones actively maintain. The algae also benefit by being protected by the sea anemone's stinging cells, nematocysts, reducing the likelihood of being eaten by herbivores.

Several species of fish and invertebrates live in symbiotic or commensal relationships with sea anemones, most famously the clownfish, but also certain cardinalfish (such as Banggai cardinalfish), juvenile threespot dascyllus,[11] Bucchich's (or anemone) goby,[12] juvenile painted greenling,[13] various crabs (such as Inachus phalangium, Mithraculus cinctimanus and Neopetrolisthes), shrimp (such as certain Alpheus, Lebbeus, Periclimenes and Thor),[14] opossum shrimp (such as Heteromysis and Leptomysis),[15] and various marine snails.[16][17][18]

Two of the more unusual relationships are those between certain anemones (such as Adamsia, Calliactis and Neoaiptasia) and hermit crabs or snails, and Bundeopsis or Triactis anemones and Lybia boxing crabs. In the former, the anemones live on the shell of the hermit crab or snail.[14][16][17][18] In the latter, the small anemones are carried in the claws of the boxing crab.[14][19]


Most species inhabit tropical reefs, although there are species adapted to relatively cold waters, intertidal reefs, and sand/kelp environments.


Actinodendron sp.

The global trade of marine ornamentals has been a rapidly expanding industry involving numerous countries worldwide. In the early 1980s, the estimated value of imported marine fish and invertebrates was US$24–40 million annually.[20] Current estimates place that value at US$200–330 million,[21] with the United States accounting for 80% of the industry imports.[22] Despite advances and the expansion of aquaculture, postlarval capture and rearing, the majority of marine ornamentals are collected in the wild as adults or juveniles.[23]

Anemones are susceptible to overexploitation due to their long lifespans, slower relative growth rates, and lower reproductive rates than their resident fish, which are also affected because they settle exclusively and are restricted to specific host sea anemones. The demand for these organisms is reflected in fishermen's catch records, which document the value they are paid per catch, and on average sea anemones were valued at five times the average value of anemonefish, and 10 times the value of the most abundant anemonefish, and in fact only made up 4.1% of the total value of the catch.

Aquarium fishing activities significantly impact the populations of anemones and anemonefish by drastically reducing the densities of each in exploited areas,[23] and could also negatively impact anemone shrimp, and any organisms obligately associated with sea anemones. Anemonefish can survive alone in captivity, as has been shown by multiple research efforts.[24][25]

In southern Italy and southwestern Spain, the anemone Anemonia sulcata is consumed as a delicacy.[26] The whole animal is marinated in vinegar, then coated in a tempura-like batter and deep-fried in olive oil. They are similar in appearance and texture to croquettes, but have an intense seafood taste.

Fossil record

Most Actiniaria do not form hard parts that can be recognized as fossils, but a few do exist; Mackenzia, from the Middle Cambrian Burgess Shale of Canada, is the oldest fossil identified as a sea anemone.


Rodriguez et al. proposed a new classification for the Actiniaria based on extensive DNA results.[27]

Suborders and Superfamilies included in Actiniaria are:

The relationships of higher-level taxa in Carlgren’s[28] classification are re-interpreted as follows:

Carlgren taxon Phylogenetic result
Protantheae Sister to Boloceroidaria
Ptychodacteae Polyphyletic because its members are not recovered as sister taxa; clustered with members of former Endomyaria
Endocoelantheae Sister to athenarian family Edwardsiidae; together these clades are re-classified as suborder Anenthemonae
Nynantheae Polyphyletic because of the relationship between Edwardsiidae and Endocoelantheae and because members of Protantheae and Ptychodacteae are recovered as sister to its members
Boloceroidaria Boloceroides mcmurrichi and Bunodeopsis nested among acontiate taxa; B. daphneae apart from other Actiniaria
Athenaria Polyphyletic: families formerly in this suborder distributed across tree as sister to former members of Endomyaria, Acontiaria, and Endocoelantheae
Thenaria Boloceroidaria, Protantheae, Ptychodacteae, and most Athenaria nest within this group
Endomyaria Paraphyletic: includes Pychodacteae and some Athenaria
Mesomyaria Polyphyletic: one clade at base of Nynantheae, other lineages are associated with former members of Acontiaria
Acontiaria Paraphyletic; includes several lineages formerly in Mesomyaria and Athenaria, plus Boloceroidaria and Protantheae

See also


  1. Daly, Marymegan; Brugler, Mercer R.; Cartwright, Paulyn; Collins, Allen G.; Dawson, Michael N.; Fautin, Daphne G.; France, Scott C.; McFadden, Catherine S.; Opresko, Dennis M.; Rodriguez, Estefania; Romano, Sandra L.; Stake, Joel L. (2007). "The phylum Cnidaria: A review of phylogenetic patterns and diversity 300 years after Linnaeus" (PDF). Zootaxa. 1668: 127–182. ISSN 1175-5334.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  2. Castro, Peter; Huber, Michael E. (2010). Marine Biology. New York: McGraw-Hill. p. 121.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  3. "Sea Anemones – info and games". Retrieved November 20, 2010.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  4. 4.0 4.1 4.2 4.3 Barnes, Robert D. (1982). Invertebrate Zoology. Philadelphia, PA: Holt-Saunders International. pp. 150–157. ISBN 0-03-056747-5.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  5. Campbell, N.; Reece, J. (2002). Biology (6th ed.). San Francisco: Pearson Education. ISBN 978-0-8053-0009-3.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  6. "Fagatele Bay NMS: Clownfish and Sea Anemone". National Marine Sanctuaries. January 12, 2006. Retrieved November 20, 2010.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  7. Mizuno, Masashi; Ito, Yasuhiko; Morgan, B. Paul (23 July 2012). "Exploiting the Nephrotoxic Effects of Venom from the Sea Anemone, Phyllodiscus semoni, to Create a Hemolytic Uremic Syndrome Model in the Rat". Marine Drugs. 10 (7): 1582–1604. doi:10.3390/md10071582.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  8. 8.0 8.1 "Sea anemone". Columbia Encyclopedia (6th ed.). 2008.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  9. Smith, Nathan III; Lenhoff, Howard M. (1976). "Regulation of Frequency of Pedal Laceration in a Sea Anemone". Coelenterate Ecology and Behavior: 117–125. doi:10.1007/978-1-4757-9724-4_13.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  10. Schlesinger A, Kramarsky-Winter E, Rosenfeld H, Armoza-Zvoloni R, Loya Y (2010). "Sexual plasticity and self-fertilization in the sea anemone Aiptasia diaphana". PLoS ONE. 5 (7): e11874. doi:10.1371/journal.pone.0011874. PMC 2912375. PMID 20686700.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  11. Lieske, E.; and R. Myers (1999). Coral Reef Fishes. ISBN 0-691-00481-1
  12. Debelius, H. (1997). Mediterranean and Atlantic Fish Guide. ISBN 978-3925919541
  13. Fretwell, K.; and B. Starzomski (2014). Painted greenling. Biodiversity of the Central Coast. Retrieved 29 January 2015.
  14. 14.0 14.1 14.2 Debelius, H. (2001). Crustacea Guide of the World. ISBN 978-3931702748
  15. Wittmann, K.J. (2008). Two new species of Heteromysini (Mysida, Mysidae) from the island of Madeira (N.E. Atlantic), with notes on sea anemone and hermit crab commensalisms in the genus Heteromysis S. I. Smith, 1873. Crustaceana, 81(3): 351–374.
  16. 16.0 16.1 Mercier, A.; and J. Hamel (2008). Nature and role of newly described symbiotic associations between a sea anemone and gastropods at bathyal depths in the NW Atlantic. Journal of Experimental Marine Biology and Ecology 358(1): 57-69.
  17. 17.0 17.1 Goodwill, R.H.; D.G. Fautin; J. Furey; and M. Daly (2009). A sea anemone symbiotic with gastropods of eight species in the Mariana Islands. Micronesica 41(1): 117–130.
  18. 18.0 18.1 Ates, R.M.L. (1997). Gastropod carrying actinians. In: J. C. den Hartog, eds, Proceedings of the 6th International Conference on Coelenterate Biology, 1995, pp. 11-20. National Naturhistorisch Museum, Leiden, The Netherlands.
  19. Karplus, I; G.C. Fiedler; and P. Ramcharan (1998). The intraspecific fighting behavior of the Hawaiian Boxing Crab, Lybia edmondsoni - Fighting with dangerous weapons? Symbiosis 24: 287-302.
  20. Eliabeth M. Wood (1985). Exploitation of Coral Reef Fishes for the Aquarium Trade. Report to the Marine Conservation Society.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  21. Frank A. Chapman, Sharon A. Fitz-Coy, Eric M. Thunberg, Charles M. Adams (1997). "United States of America trade in ornamental fish" (PDF). Journal of the World Aquaculture Society. 28 (1): 1–10. doi:10.1111/j.1749-7345.1997.tb00955.x.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  22. Sherry L. Larkin & Robert L. Degner (2001). "The U.S. wholesale market for marine ornamentals". Aquarium Sciences and Conservation. 3 (1–3): 13–24. doi:10.1023/A:1011329300967.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  23. 23.0 23.1 Craig S. Shuman, Gregor Hodgson & Richard F. Ambrose (2005). "Population impacts of collecting sea anemones and anemonefish for the marine aquarium trade in the Philippines" (PDF). Coral Reefs. 24 (4): 564–573. doi:10.1007/s00338-005-0027-z.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  24. Daphne Gail Fautin (1991). "The anemonefish symbiosis: what is known and what is not" (PDF). Symbiosis. 10: 23–46.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  25. Ronald L. Shimek (2004). Marine Invertebrates. Neptune City, NJ: T.F.H. Publications. p. 83. ISBN 978-1-890087-66-1.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  26. Schwabe, Calvin W. (1979). Unmentionable cuisine. Charlottesville: University Press of Virginia. p. 362. ISBN 0-8139-0811-6.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  27. Rodríguez, E., Barbeitos, M. S., Brugler, M.R., Crowley, L. M., Grajales, A., Gusmão, L., Häussermann, V., Reft, A. & Daly, M. (2104). Hidden among sea anemones: The first comprehensive phylogenetic reconstruction of the order Actiniaria (Cnidaria, Anthozoa, Hexacorallia) reveals a novel group of hexacorals. PLoS ONE 9(5): e96998. doi:10.1371/journal.pone.0096998
  28. Carlgren O. (1949). A survey of the Ptychodactiaria, Corallimorpharia and Actiniaria. K Svenska VetenskapsAkad Handl 1: 1–121.

External links