Favites pentagona
| Favites pentagona | |
|---|---|
 | |
| Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Cnidaria |
| Class: | Anthozoa |
| Subclass: | Hexacorallia |
| Order: | Scleractinia |
| Family: | Merulinidae |
| Genus: | Favites |
| Species: | F. pentagona |
| Binomial name | |
| Favites pentagona (Esper, 1795) [2] | |
| Synonyms[2] | |
| |
Favites pentagona is a species of stony coral in the family Merulinidae, sometimes known as larger star coral. It is native to the Indo-Pacific region and its range extends from the Red Sea through the Indian Ocean to the Western Pacific Ocean. This is a common species throughout its wide range and the International Union for Conservation of Nature has rated its conservation status as being of "least concern".
Description
Colonies of Favites pentagona are encrusting or massive, sometimes with lobes forming irregular columns. The colony may spread to about a metre (yard) across. The corallites are less than 6 mm (0.24 in) in diameter. The corallite walls are sharply-angled and thin, and several polyps may share a common wall. The palliform lobes are clearly visible on the oral disc and there are a small number of septa. This coral is often vividly coloured, with contrasting (often green) oral discs and brown, red or purple coenosarc, the living tissue that covers the skeleton between the polyps.[2]
Distribution
Favites pentagona is native to the Indo-Pacific region where it occurs in shallow tropical and subtropical seas. Its range extends from the Red Sea and South Africa to India, Indonesia, Japan and Australia, where it occurs both in Western Australia and the Great Barrier Reef.[3][4] Its depth range is down to 25 metres (82 ft) and it is common on rocky reefs, outer reef channels, reef slopes and lagoons.[1]
Ecology
Favites pentagona is a zooxanthellate species of coral. This means that it harbours symbiotic unicellular dinoflagellates in its tissues, which use the energy from sunlight to synthesize nutrients, from which the host coral benefits. It is an aggressive species of coral. At night it extends its polyps to feed on plankton, and expands its elongated sweeper tentacles armed with stinging cells well beyond the limits of its base, so as to avoid being crowded or overgrown by other organisms.[4] It clears away sand that settles on its surface by inflating its polyps to dislodge the sediment.[5]
F. pentagona is a simultaneous hermaphrodite, the eggs and sperm being released in well-formed bundles. In any one area, spawning tends to occur in synchrony, with all the corals liberating their gamete bundles at the same time. These rise to the sea surface and float, thus maximising the chance of successful fertilisation.[6]
F. pentagona is susceptible to black band disease and white plague, two coral diseases which have become more common since the 1990s.[7]
Status
Favites pentagona has a very wide range and is common over much of that range. There is no precise information on population trends but this coral faces the same threats as other species; global warming, ocean acidification and degradation of its coral reef habitats. The International Union for Conservation of Nature has assessed its conservation status as being of "least concern".[1]
References
- 1 2 3 DeVantier, L.; Hodgson, G.; Huang, D.; Johan, O.; Licuanan, A.; Obura, D.O.; Sheppard, C.; Syahrir, M.; Turak, E. (2014). "Favites pentagona". IUCN Red List of Threatened Species. Version 2014.3. International Union for Conservation of Nature. Retrieved 2015-04-27.
- 1 2 3 Hoeksema, Bert (2015). "Favites pentagona (Esper, 1795)". World Register of Marine Species. Retrieved 2015-04-25.
- ↑ "Favites pentagona". Australian Institute of Marine Science. 2013. Retrieved 2015-04-26.
- 1 2 Sprung, Julian (1999). Corals: A quick reference guide. Ricordea Publishing. pp. 110–111. ISBN 1-883693-09-8.
- ↑ Riegl, B. (1995). "Effects of sand deposition on scleractinian and alcyonacean corals". Marine Biology 121 (3): 517–526. doi:10.1007/BF00349461.
- ↑ Oliver, J.;. Babcock, R. (1992). "Aspects of the Fertilization Ecology of Broadcast Spawning Corals: Sperm Dilution Effects and in situ Measurements of Fertilization". The Biological Bulletin 183 (3): 409–417. doi:10.2307/1542017.
- ↑ Sutherland, K.P.; Porter, J.W.; Torres, C. (2004). "Disease and immunity in Caribbean and Indo-Pacific zooxanthellate corals" (PDF). Marine Ecology Progress Series 266: 273–302. doi:10.3354/meps266273.