Biology:Brachidontes pharaonis

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Short description: Species of bivalve

Brachidontes pharaonis
Naturalis Biodiversity Center - ZMA.MOLL.412936 - Brachidontes pharaonis (Fischer, 1870) - Mytilidae - Mollusc shell.jpeg
Museum specimens of the shell of Brachidontes pharaonis
Scientific classification edit
Domain: Eukaryota
Kingdom: Animalia
Phylum: Mollusca
Class: Bivalvia
Order: Mytilida
Family: Mytilidae
Genus: Brachidontes
Species:
B. pharaonis
Binomial name
Brachidontes pharaonis
(Fischer P., 1870)[1][2]
Synonyms[1]
  • Brachidontes arabicus Lamy, 1919
  • Brachyodontes karachiensis Melvill & Standen, 1907
  • Modiola compressula Martens & Thiele, 1908
  • Mytilus arabicus Jousseaume in Lamy, 1919
  • Mytilus pharaonis P. Fischer, 1870

Brachidontes pharaonis is a species of mussel from the family Mytilidae. It is native to the Indian Ocean and the Red Sea, and has colonised the Mediterranean Sea where it is regarded as an invasive species.

Description

Brachidontes pharaonis is a small bivalve that grows its shell up to 40mm in length. The external surfaces of the shell are dark brownish black while the interior of the shell is purplish-black. The two halves of the shell are equal in size and similar in shape, being elongated and asymmetrical, with a dysodont hinge between the valves. The sculpture of the valves consists of numerous fine radial bifurcating ribs, which become coarser posteriorly and finely scalloped towards the edge. The outline is mytiliform with a terminal umbo, but the shape is very variable and specimens may be highly expanded posteriorly, occasionally curved; sometimes almost cylindrical with the beaks being sub-terminal.[3] The animal is attached to the substrate by thick byssus.

Habitat

Brachidontes pharaonis is found on rocky substrates and man made structures in the intertidal zone. They appear to be able to tolerate wide temperature variations in their invasive Mediterranean range, but low winter temperatures may inhibit their physiology.[4] In the cooler waters of the western Mediterranean, B. pharaonis is restricted to habitats with higher temperatures and salinities, where it establishes dense mussel beds on hard substrates, especially where it is sheltered from waves.[3]

Distribution

Native

Brachidontes pharaonis is native only to the Red Sea and adjacent Indian Ocean (see Taxonomy).[3]

Invasive

Brachidontes pharaonis was first recorded in the Mediterranean Sea in 1876 off Port Said in Egypt, reaching Lebanon and Palestine by the 1930s; Sicily by 1971; Greece by 1979; Syria and Turkey by 1985, Rhodes by 1989, Cyprus by 1996, and the northern Adriatic coast of Croatia by 1997.[5]

The populations in the Levantine Sea most likely arose from larvae that entered the Mediterranean through the Suez Canal. This is thought to be the earliest example of a Lessepsian migration. The colonisation of the central Mediterranean is probably due to transportation by ships.[4]

Biology

Feeding

Brachidontes pharaonis is a filter feeder, filtering suspended food from the water, mainly phytoplankton or suspended organic detritus.[3]

Reproduction

There are two sexes. The sperm and eggs are released into the water column by the adults. There are two larval stages: a trochophore stage which lasts around 24 hours, and a veliger stage which lasts for some weeks before they achieve competence and settle on the substrate.[3]

Colony form

In warmer, saltier regions it forms dense beds which, exclude other sessile bivalves;[3] but in colder, less saline regions, such as the Aegean Sea, it forms smaller, less densely populated beds.[3]

Predators

A species of whelk, Stramonita haemastoma, was found to preferentially prey on B. pharaonis off the coast of Israel[3] and in the south of Italy.[6][7]

Invasive impact

Economic

Brachidontes pharaonis is regarded as a fouling organism. It has been recorded colonising the hulls of boats in harbours, and may foul intake pipes.[3]

Ecological

Brachidontes pharaonis can displace the native mussel Mytilaster minimus by interfering with the recruitment of M. minimus. The presence of B. pharaonis also has detrimental effects on the survival and growth of the native mussel. By the late 1990s Israeli surveys were showing that there had been a rapid shift in dominance, demonstrating that some populations of B. pharaonis had reached densities of up to 300 specimens per 100 cm², while M. minimus was very infrequently encountered.[4] Even higher densities have been reached in the saltpans of western Sicily, where 10,000 specimens per m² have been counted.[3]

Taxonomy

There is some controversy about the species limits of Brachidontes pharaonis and further genetic studies are required. The current thinking is that the name B. pharaonis is best applied to the Mediterranean and Red Sea. Other species within the complex are Brachidontes exustus, Brachidontes semistriatus and Brachidontes variablis, but more study is needed to determine their distributions.[3]

References

  1. 1.0 1.1 "Brachidontes pharaonis (P. Fischer, 1870)". World Register of Marine Species. http://www.marinespecies.org/aphia.php?p=taxdetails&id=140437. Retrieved 30 December 2016. 
  2. Mohammed-Geba, Khaled; Sheir, Sherin K.; El-Aziz Hamed, Elsayed Abd; Galal-Khallaf, Asmaa (October 2020). "Molecular and morphological signatures for extreme environmental adaptability of the invasive mussel Brachidontes pharaonis (Fischer, 1870)". Molecular and Cellular Probes 53: 101594. doi:10.1016/j.mcp.2020.101594. 
  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 "Brachidontes pharaonis". The Invasive Species Compendium. cabi.org. http://www.cabi.org/isc/datasheet/109127. Retrieved 30 December 2016. 
  4. 4.0 4.1 4.2 "Brachidontes pharaonis". Delivering Alien Species Inventories for Europe. http://www.europe-aliens.org/pdf/Brachidontes_pharaonis.pdf. Retrieved 30 December 2016. 
  5. "Brachidontes pharaonis". ciesm.org. http://www.ciesm.org/atlas/Brachidontespharaonis.html. Retrieved 30 December 2016. 
  6. Giacoletti, A.; Maricchiolo, G.; Mirto, S.; Genovese, L.; Umani, M.; Sarà, G. (2017-04-05). "Functional and energetic consequences of climate change on a predatory whelk". Estuarine, Coastal and Shelf Science 189: 66–73. doi:10.1016/j.ecss.2017.03.007. 
  7. Giacoletti, A.; Rinaldi, A.; Mercurio, M.; Mirto, S.; Sarà, G. (2016-06-01). "Local consumers are the first line to control biological invasions: a case of study with the whelk Stramonita haemastoma (Gastropoda: Muricidae)" (in en). Hydrobiologia 772 (1): 117–129. doi:10.1007/s10750-016-2645-6. ISSN 0018-8158. 

Wikidata ☰ Q13443168 entry