Invasion History
First Non-native North American Tidal Record: 2002First Non-native West Coast Tidal Record:
First Non-native East/Gulf Coast Tidal Record: 2002
General Invasion History:
Ophiactis savignyi is considered the world's most common and widely distributed brittle star. It was first described from the Red Sea in 1842, and later found to be widely distributed in the tropical and sub-tropical Indian, Pacific, and Atlantic Oceans. It inhabits marine fouling communities, especially sponges, and has been frequently found on ship hulls, buoys, and marine structures. It has a long-lived planktonic larva, with the potential for ballast water transport (Roy and Sponer 2002). In addition to sexual reproduction, it also reproduces asexually by fission, which is an advantage in colonizing new locations where the possibility of fertilization is low (McGovern 2003). Roy and Sponer (2002) found that most of the Atlantic specimens that they examined, including many from the Indo-Pacific and Atlantic, could be divided into two lineages, A and B. Atlantic specimens of lineage B (from Florida, Bermuda, and the Caribbean coast of Panama) were identical to their Indo-Pacific counterparts (from Philippines, Sri Lanka, Rarotonga, and Samoa), and strongly distinct from lineage A. They considered the possibility of natural invasion around Africa, from the Indian Ocean, but concluded that dispersal by currents was not likely, because this species would not survive the cold waters of the Benguela current. The degree of genetic similarity over a very wide range supported a recent, anthropogenic invasion for lineage B. Lineage A, found from Bermuda and Florida to Brazil, was not found in the Indo-Pacific samples tested, but its occurrence there could not be excluded (Roy and Sponer 2002) so it should be regarded as cryptogenic in the Atlantic. Clark (1919), cited by Roy and Sponer (2002), suggested that O. savignyi was introduced to the Atlantic before the mid-19th century.
We have treated O. savignyi as native to the Indo-Pacific, where it ranges from Japan to the Red Sea, South Africa, and French Polynesia. Further west in the Pacific, where we consider it cryptogenic, O. savignyi ranges from California to Peru, and also occurs in Hawaii, the Galapagos, and Easter Island. It was first collected in the Eastern Pacific in 1854 at Cabo San Lucas, Mexico (United States National Museum of Natural History 2008).
North American Invasion History:
Invasion History on the East Coast:
Ophiactis savignyi was collected in the Western Atlantic at least as early as 1875 in Brazil, 1882 in Bermuda, and 1884 on the East and Gulf Coasts of North America. In RV 'Albatross' cruises in 1884-1885, it was collected from off Cape Lookout, North Carolina; and the Dry Tortugas, Goodland Point, and Sarasota, Florida (US National Museum of Natural History 2011). Roy and Sponer (2002) found two lineages in the Western Atlantic, one (Lineage A) unique to the region and one (Lineage B) found in Florida, Bermuda, and the Caribbean coast of Panama which apparently represents a cryptic introduction from the Indo-Pacific. Roy and Sponer (2002) did not give specific locations for samples, so we have considered all locations with US National Museum specimens on the Florida Peninsula from Cape Canaveral on the Atlantic Coast and Cedar Key on the Gulf Coast, southward to the Florida Keys to contain the introduced lineage B, and other Atlantic sites with O. savignyi collections, to be cryptogenic.
Invasion History Elsewhere in the World:
Ophiactis savignyi is considered a recent invader in the Mediterranean, which it apparently colonized through the Suez Canal, reaching Israel by 1948 (Galil 2007). In the Mediterranean, it is known from the Aegean Sea (in 1994, Pancucci-Papadopoulou et al. 2005), and the Gulf of Gabes, Tunisia (in 1973, United States Museum of Natural History 2008). One specimen was found in Banyuls-sur-Mer, France (in 1968, Guile 1968). It also occurs in the East Atlantic on Madeira (Jesus and Domingos 1998) and Senegal (United States National Museum of Natural History 2011).
Description
Ophiactis savignyi has a disk diameter of 2.5 - 5 mm, usually with six arms 13-20 mm in length. This brittle star reproduces by fission, and can regenerate lost arms, so numbers of arms can vary from 1-7. Small spines are scattered over the disk surface. On the ventral side of the disk, three scale-like oral papillae are present around the mouth, and the oral shields are large. On the dorsal side of the disk, the radial shields are large. The aboral arm plates are elliptical with rounded lateral margins, and a convex distal edge with a median lobe made prominent by a dark spot on either side. There are 5-6 arm spines on each arm segment. Body color ranges from brown to brown-green and cream. The radial shields are darker than the rest of the disk and generally have a patch of white along the outer tip. The arms are banded due to the dark markings on distal portions of the arm plates (Smithsonian Marine Station 2011; Stöhr 2011).
Taxonomy
Taxonomic Tree
Kingdom: | Animalia | |
Phylum: | Echinodermata | |
Class: | Stelleroidea | |
Subclass: | Ophiuroidea | |
Order: | Ophiurida | |
Suborder: | Gnathophiurina | |
Family: | Ophiactidae | |
Genus: | Ophiactis | |
Species: | savignyi Lineage B |
Synonyms
Ophiactis incisa (Von Martens, 1870)
Ophiactis krebsi (Luetken, 1856)
Ophiactis rheinhardtii (Luetken, 1859)
Ophiactis sexradia (Grube, 1857)
Ophiactis virescens (Luetken, 1856)
Ophiolepis savignyi (Müller and Troschel, 1842)
Potentially Misidentified Species
Ecology
General:
Ophiactis savignyi is a brittle star which reproduces sexually, broadcasting eggs and sperm, but it can also reproduce asexually by fission. Animals inhabiting sponges tend to be of one sex, dominated by immature animals, and appear to be dependent on asexual reproduction. There appears to be a trade-off between sexual and asexual reproduction, with asexual reproduction being more likely in populations with a lower probability of fertilization. Males are more likely to divide than females, which are more likely to lose their gonads after fission, resulting in a skewed sex ratio (McGovern 2002; McGovern 2003). Ophiactis savignyi can be found in a variety of habitats including rocky shores and seaweed beds, the interior of sponges, mangroves, corals, docks, and boat hulls (Roy and Sponer 2002; McGovern 2003).
Food:
detritus, foraminfera, benthic invertebrates
Trophic Status:
Deposit Feeder
DepFedHabitats
General Habitat | Coral reef | None |
General Habitat | Grass Bed | None |
General Habitat | Marinas & Docks | None |
General Habitat | Vessel Hull | None |
General Habitat | Rocky | None |
General Habitat | Unstructured Bottom | None |
Salinity Range | Polyhaline | 18-30 PSU |
Salinity Range | Euhaline | 30-40 PSU |
Tidal Range | Subtidal | None |
Vertical Habitat | Epibenthic | None |
Tolerances and Life History Parameters
Maximum Duration | 30 | Larval duration, approximate, Roy and Sponer 2002 |
Minimum Length (mm) | 28.5 | Adult radius (disk + arms) |
Maximum Length (mm) | 45 | Adult radius (disk + arms) |
Broad Temperature Range | None | Warm temperate-Tropical |
Broad Salinity Range | None | Polyhaline-Euhaline |
General Impacts
No direct impacts have been reported for this species, but they could be substantial, given the high abundance of this brittle star in some locations.Regional Distribution Map
Bioregion | Region Name | Year | Invasion Status | Population Status |
---|---|---|---|---|
SP-XXI | None | 1902 | Crypogenic | Established |
CIO-II | None | 0 | Native | Established |
SP-IX | None | 0 | Native | Established |
SP-VIII | None | 0 | Native | Established |
CAR-III | None | 2002 | Non-native | Established |
CAR-IV | None | 2002 | Non-native | Established |
CAR-I | Northern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern Florida | 2002 | Non-native | Established |
NA-ET4 | Bermuda | 2002 | Non-native | Established |
MED-VI | None | 1994 | Non-native | Established |
G040 | Rookery Bay | 2002 | Non-native | Established |
S206 | _CDA_S206 (Vero Beach) | 2002 | Non-native | Established |
G060 | Sarasota Bay | 2002 | Non-native | Established |
G080 | Suwannee River | 2002 | Non-native | Established |
S190 | Indian River | 2002 | Non-native | Established |
G010 | Florida Bay | 2002 | Non-native | Established |
S200 | Biscayne Bay | 2002 | Non-native | Established |
S196 | _CDA_S196 (Cape Canaveral) | 2002 | Non-native | Established |
G050 | Charlotte Harbor | 2002 | Non-native | Established |
EAS-VI | None | 0 | Native | Established |
SP-XIII | None | 0 | Native | Established |
WA-V | None | 1952 | Crypogenic | Established |
EAS-III | None | 0 | Native | Established |
SP-XII | None | 0 | Native | Established |
SEP-H | None | 1904 | Crypogenic | Established |
SA-III | None | 1875 | Crypogenic | Established |
MED-V | None | 1937 | Non-native | Established |
SP-XI | None | 0 | Native | Established |
SP-XIV | None | 0 | Native | Established |
NEP-VIII | None | 1854 | Crypogenic | Established |
SP-XVI | None | 1850 | Native | Established |
SEP-Z | None | 1938 | Crypogenic | Established |
NEP-VII | None | 1889 | Crypogenic | Established |
AG-5 | None | 0 | Native | Established |
CAR-V | None | 1903 | Crypogenic | Established |
CAR-II | None | 1914 | Crypogenic | Established |
CAR-VII | Cape Hatteras to Mid-East Florida | 1885 | Crypogenic | Established |
G210 | Terrebonne/Timbalier Bays | 1987 | Crypogenic | Established |
SA-II | None | 1965 | Crypogenic | Established |
SA-IV | None | 1975 | Crypogenic | Established |
G330 | Lower Laguna Madre | 1960 | Crypogenic | Established |
G070 | Tampa Bay | 2002 | Non-native | Established |
AUS-XII | None | 0 | Native | Established |
SP-IV | None | 0 | Native | Established |
SP-I | None | 0 | Native | Established |
MED-IV | None | 1973 | Non-native | Established |
SEP-C | None | 1935 | Crypogenic | Established |
CAR-VI | None | 1957 | Crypogenic | Established |
AG-3 | None | 0 | Native | Established |
EA-V | None | 0 | Native | Established |
WA-I | None | 1971 | Crypogenic | Established |
NWP-3a | None | 0 | Native | Established |
SP-XX | None | 0 | Crypogenic | Established |
NEP-VI | Pt. Conception to Southern Baja California | 1888 | Crypogenic | Established |
CIO-IV | None | 0 | Native | Established |
CIO-V | None | 0 | Native | Established |
EA-IV | None | 0 | Native | Established |
CIO-I | None | 0 | Native | Established |
EA-III | None | 0 | Native | Established |
OM | None | 0 | Native | Established |
SP-III | None | 0 | Native | Established |
NWP-2 | None | 0 | Native | Established |
SP-VII | None | 0 | Native | Established |
SEP-I | None | 0 | Crypogenic | Established |
EAS-I | None | 0 | Native | Established |
NWP-4a | None | 0 | Native | Established |
MED-II | None | 1968 | Non-native | Unknown |
AUS-II | None | 0 | Native | Established |
P058 | _CDA_P058 (San Pedro Channel Islands) | 0 | Crypogenic | Established |
RS-3 | None | 1842 | Native | Established |
S020 | Pamlico Sound | 1885 | Crypogenic | Established |
G100 | Apalachicola Bay | 0 | Crypogenic | Established |
WA-II | None | 1914 | Crypogenic | Established |
PAN_PAC | Panama Pacific Coast | 1904 | Crypogenic | Established |
PAN_CAR | Panama Caribbean Coast | 2002 | Non-native | Established |
MED-IV | None | 1993 | Non-native | Established |
Occurrence Map
OCC_ID | Author | Year | Date | Locality | Status | Latitude | Longitude |
---|---|---|---|---|---|---|---|
6032 | USNM 33896 | 1886 | 1885-02-07 | None | Crypogenic | 29.1917 | -85.4833 |
References
Amor, Kounofi-Ben; Rifi, M.; Ghanem, R.; Draief, I.; Zouali, J.; Souissi, J. Ben (2016) Update of alien fauna and new records of Tunisian marine fauna, Mediterranean Marine Science 17(1): 124-143Barboza, Carlos Alberto de Moura; Mattos, Gustavo; Paiva, Paulo Cesar (2015) Brittle stars from the Saint Peter and Saint Paul Archipelago: morphological and molecular data, Marine Biodiversity Records 8: e16
Boffi, E. (1972) Ecological aspects of ophiuroids from the phytal of S. W. Atlantic Ocean warm waters., Marine Biology 15: 316--328
California Academy of Sciences 2005-2015 Invertebrate Zoology Collection Database. <missing URL>
Chung, W. K.; King, Gary M. (1999) Biogeochemical transformations and potential polyaromatic hydrocarbon degradation in macrofaunal burrow sediments, Aquatic Microbial Ecology 19: 285-295
Çinar, Melih Ertan and 7 authors (2021) Current status (as of end of 2020) of marine alien species in Turkey, PLOS ONE 16: Published online
de Jesus, Dora Cunha; Abreu, Antonio Domingos (1998) Contribution to the knowledge of the soft bottom echinoderms of Madeira Island, Boletim do Museu Municipal do Funchal 50: 59-69
Galil, Bella S. (2007) Seeing Red: Alien species along the Mediterranean coast of Israel., Aquatic Invasions 2(4): 281-312
Guille, Alain (1968) Sur la presence de Ophiactis savgnyi Muller and Troschel dans la region de Banyls-sur-Mer., Vie et Milieu Serie A: Biologie Marine 19(2A): 497-500
Hendler, Gordon; Baldwin, Carole C.; Smith, David G.; Thacker, Christine E. (1999) Planktonic dispersal of juvenile brittle stars (Echinodermata: Ophiuroidea) on a Caribbean reef., Bulletin of Marine Science 65(1): 283-288
Hendler, Gordon; Brugneaux, Sophie J. (2013) New records of brittle stars from French Guiana: Ophiactis savignyi and the alien species Ophiothela mirabilis (Echinodermata: Ophiuroidea), Marine Biodiversity Records 6: e113
Katsanevakis, S.; Tsiamis, K.; Ioannou, G.; Michailidis, N.; Zenetos, A. (2009) Inventory of alien marine species of Cyprus, Mediterranean Marine Science 10(2): 109-133
Lima, Maria Lilian F; Correia, Monica D.; Sovierzoski, Hilda H.; Cynthia L. C. Manso (2011) New records of Ophiuroidea (Echinodermata) from shallow waters off Maceio, State of Alagoas, Brazil, Marine Biodiversity Records 4: 1-10
McGovern, Tamara M. (2002) Sex-ratio bias and clonal reproduction in the brittle star Ophiactis savignyi., Evolution 56(3): 511-517
McGovern, Tamara M. (2003) Plastic reproductive strategies in a clonal marine invertebrate., Proceedings of the Royal Society B. Biological Sciences. 270(1532): 2517-2522
Mead, A.; Carlton, J. T.; Griffiths, C. L. Rius, M. (2011b) Introduced and cryptogenic marine and estuarine species of South Africa, Journal of Natural History 39-40: 2463-2524
Pancuci-Papadopoulou., M. A.; Zenetos, A , Corsini-Foka; Politou, Ch. (2005) Update of marine alien species in Hellenic waters., Mediterranean Marine Science 6(2): 1-11
Roy, M. S.; Sponer, R. (2002) Evidence of a human-mediated invasion of the tropical western Atlantic by the world's most common brittlestar., Proceedings of the Royal Society of London. Series B 269: 1017-1023
Smithsonian Marine Station at Fort Pierce 2011 Field Guide to the Indian River Lagoon. <missing URL>
Stöhr, Sabine (Ed.) 2011 World Ophiuroidea Database. <missing URL>
U.S. National Museum of Natural History 2002-2021 Invertebrate Zoology Collections Database. http://collections.nmnh.si.edu/search/iz/
United States National Museum of Natural History 2004 Flora of the Washington-Baltimore Area. <missing URL>
Zibrowius, Helmut (2002) Assessing scale and impact of ship-transported alien fauna in the Mediterranean?, CIESM Workshop Monographs 20: 63-68