Invasion History
First Non-native North American Tidal Record: 1852First Non-native West Coast Tidal Record: 1972
First Non-native East/Gulf Coast Tidal Record: 1852
General Invasion History:
Styela canopus (Rough Sea Squirt) is now widely distributed in temperate and tropical coastal waters of the world. It was described from the Red Sea in 1816 and was later reported from both sides of the North Atlantic, Ascension Island in the South Atlantic, the Northwest Pacific, the tropical Indo-Pacific, and temperate waters of Australia. (Kott 1998). In the Atlantic, it was first reported (as Cynthia partita) from Boston Harbor in 1852 (Stimpson 1852) and then from the English Channel (as Styela variabilis) in 1868. It was reported from the Mediterranean (as S. canopoides) in 1877 (Kott 1998). By the late 19th century, it was abundant and widespread on both sides of the Atlantic and was generally regarded as a native species. In the Northeast Pacific, where it is a recent introduction, S. canopus was first reported from San Diego Bay, California, in 1972. It has been collected north to Alamitos Bay but is rare outside San Diego Bay (Lambert and Lambert 1998). James Carlton considers S. canopus to be a native of the Indo-West Pacific (Carlton 2000 personal communication), introduced to the Atlantic (possibly a century or more before its description), a judgment which we have adopted here. Kott (1985) considers S. canopus to be the only species of Styela native to the Indo-West Pacific region.
North American Invasion History:
Invasion History on the West Coast:
On the west coast of North America, Styela canopus was first collected in San Diego, California in 1972. To the south, this tunicate was discovered in Mexico, near Mazatlan, in the Urias Estuary, in 1995 (Salgado-Barragan et al. 2004). In 1996-2000, it was collected in Mission Bay, Oceanside Harbor, Newport Bay, Alamitos Bay, Los Angeles-Long Beach Harbors, and Marina del Rey, off Santa Monica Bay (Lambert and Lambert 1998; Fairey et al. 2002; Lambert and Lambert 2003; Ruiz et al., unpublished data). At most sites, it was present at low to moderate levels of abundance (Lambert and Lambert 2003). In 2015, one specimen of S. canopus was identified from fouling plates at the Oakland Yacht Club, San Francisco Bay, while several nearby immature specimens were probably this species. This is the northernmost record of this species on the West Coast, but the establishment of this tunicate in the Bay is still unconfirmed (Tracy et al. 2017).
Invasion History on the East Coast:
In the northeast Atlantic, S. canopus ranges from the south coast of England and Normandy (Hayward and Ryland 1990; Breton et al. 1996) to the Cape Verde Islands, Sierra Leone and Senegal (Monniot and Monniot 1994) to Egypt and Lebanon (Bitar and Kouli-Bitar 2001). It was reported from the Channel Islands, off France, in 1868, as Cynthia variabilis (Hancock 1868, cited by Kott 1998), and from the Adriatic Sea in 1877 as Styela canopoides (Heller 1877, as cited by Kott 1998). On biogeographic grounds, based on its likely origin in the Indo-Pacific, S. canopus appears to be a very early introduction to European waters (Carlton, personal communication 2000).
In the southwest Atlantic, S. canopus was first collected from an abandoned fishnet in Rio de Janeiro Bay, Brazil (Monniot 1969, cited by da Rocha and Kremer 2005). In Brazil, it appears to be most abundant in port areas (da Rocha and Kremer 2005).
Invasion History on the Gulf Coast:
In the northeast Atlantic, S. canopus ranges from the south coast of England and Normandy (Hayward and Ryland 1990; Breton et al. 1996) to the Cape Verde Islands, Sierra Leone and Senegal (Monniot and Monniot 1994) to Egypt and Lebanon (Bitar and Kouli-Bitar 2001). It was reported from the Channel Islands, off France, in 1868, as Cynthia variabilis (Hancock 1868, cited by Kott 1998), and from the Adriatic Sea in 1877 as Styela canopoides (Heller 1877, as cited by Kott 1998). On biogeographic grounds, based on its likely origin in the Indo-Pacific, S. canopus appears to be a very early introduction to European waters (Carlton, personal communication 2000).
In the southwest Atlantic, S. canopus was first collected from an abandoned fishnet in Rio de Janeiro Bay, Brazil (Monniot 1969, cited by da Rocha and Kremer 2005). In Brazil, it appears to be most abundant in port areas (da Rocha and Kremer 2005).
Invasion History in Hawaii:
It was first collected in the Hawaiian Islands on Oahu in 1929 and has also been found in Maui (Coles et al. 2004; Carlton and Eldredge 2009). Styela canopus?has a broad range in the west Pacific and Indian Oceans, from Japan to the Red Sea, South Africa, and Australia, and presumed to be native over most of that range (Nishikawa 1991; Kott 1985; Kott 1998; Monniot and Monniot 2001; Monniot 2002). However, it is introduced on some of the islands of the Central Pacific, including the Hawaiian Islands (Coles et al. 2002; Coles et al. 2004), American Samoa (Coles et al. 2003) and Guam (Lambert 2002; Lambert 2003).
Invasion History Elsewhere in the World:
In the northeast Atlantic, S. canopus ranges from the south coast of England and Normandy (Hayward and Ryland 1990; Breton et al. 1996) to the Cape Verde Islands, Sierra Leone and Senegal (Monniot and Monniot 1994) to Egypt and Lebanon (Bitar and Kouli-Bitar 2001). It was reported from the Channel Islands, off France, in 1868, as Cynthia variabilis (Hancock 1868, cited by Kott 1998), and from the Adriatic Sea in 1877 as Styela canopoides (Heller 1877, as cited by Kott 1998). On biogeographic grounds, based on its likely origin in the Indo-Pacific, S. canopus appears to be a very early introduction to European waters (Carlton, personal communication 2000).
In the southwest Atlantic, S. canopus was first collected from an abandoned fishnet in Rio de Janeiro Bay, Brazil (Monniot 1969, cited by da Rocha and Kremer 2005). In Brazil, it appears to be most abundant in port areas (da Rocha and Kremer 2005).
Description
Styela canopus is a solitary tunicate. Its body shape varies from globular, to elongate, depending on whether it's growing as a single individual or in a dense cluster. When growing singly, it is attached by much of its ventral surface, with the oral siphon slightly below the anterior tip. When crowded, the body is attached by only a small part of the ventral surface, with the oral siphon at the anterior tip, and the atrial siphon slightly below. Both siphons are low and warty. The test is variable in thickness, tough and leathery with rough bumps and wrinkles. Worm tubes, bryozoans and algae frequently grow on the test. The color is usually grayish or yellowish posteriorly, becoming brown, purplish, or red anteriorly, with four dark stripes on the siphons. Internally, the pharynx has four narrow folds on each side, and there are two gonads on the left side and 2-5 on the right. The animal is up to 25-30 mm in length (Van Name 1945; Kott 1985; Lambert and Lambert 1998).
Taxonomy
Taxonomic Tree
Kingdom: | Animalia | |
Phylum: | Chordata | |
Subphylum: | Tunicata | |
Class: | Ascidiacea | |
Order: | Stolidobranchia | |
Family: | Styelidae | |
Genus: | Styela | |
Species: | canopus |
Synonyms
Cynthia stellifera (Verrill, 1871)
Halocynthia partita (Verrill, 1879)
Styela aggregata var. americana (Metcalf, 1888)
Styela barbaris (Kott, 1952)
Styela canopoides (Heller, 1877)
Styela marquesana (Michaelsen, 1918)
Styela orbicularis (Sluiter, 1904)
Styela partita (Verrill, 1901)
Styela rectangularis (Kott, 1952)
Styela variabilis (Hancock, 1868)
Tethyum canopus (Hartmeyer, 1915)
Tethyum partitum (Hartmeyer, 1912)
Cynthia canopus (Savigny, 1816)
Styela bicolor (Sluiter, 1887)
Styela pupa (Heller, 1878)
Styela stephensoni (Michaelsen, 1934)
Tethyum orbiculare (Sluiter, 1904)
Tethyum pupa (Heller, 1878)
Potentially Misidentified Species
Native to NW Pacific, widespread in higher latitude harbors
Styela panamensis
Native to Caribbean Panama (De Barros and da Rocha (2021). Records of S.canopus in Boca del Toros, Panama, and in Venezuela, may refer to this newly described native species (de Barros and da Rocha 2021).
Styela plicata
Possibly native to NW Pacific, widespread in warm-temperate and tropical waters.
Ecology
General:
Life History- A solitary tunicate is ovoid, elongate or vase-like in shape, with two openings or siphons. Most solitary tunicates attach to substrates by their side or base, but some attach with a conspicuous stalk. They are sessile filter feeders with two siphons, an oral and an atrial siphon. Water is pumped in through the oral siphon, where phytoplankton and detritus is filtered by the gills, and passed on mucus strings to the stomach and intestines. Waste is then expelled in the outgoing atrial water.
Solitary ascidians are hermaphroditic, meaning that both eggs and sperm are released to the atrial chamber. Eggs may be self-fertilized or fertilized by sperm from nearby animals, but many species have a partial block to self-fertilization. In internal fertilizers, including S. canopus, eggs are brooded and fertilized within the atrial chamber and then released into the water column upon hatching. Fertilized eggs hatch into a tadpole larva with a muscular tail, notochord, eyespots, and a set of adhesive papillae. The lecithotrophic (non-feeding, yolk-dependent) larva swims briefly before settlement. In S. canopus, the larvae settled after ~2 hours at 25 ?C (Ying et al 2003). Once settled, the tail is absorbed, the gill basket expands, and the tunicate begins to feed by filtering (Barnes 1983).
Food:
Phytoplankton, detritus
Trophic Status:
Suspension Feeder
SusFedHabitats
General Habitat | Coarse Woody Debris | None |
General Habitat | Marinas & Docks | None |
General Habitat | Rocky | None |
General Habitat | Vessel Hull | None |
General Habitat | Mangroves | None |
General Habitat | Unstructured Bottom | None |
General Habitat | Coral reef | None |
Salinity Range | Polyhaline | 18-30 PSU |
Salinity Range | Euhaline | 30-40 PSU |
Tidal Range | Subtidal | None |
Vertical Habitat | Epibenthic | None |
Life History
Tolerances and Life History Parameters
Maximum Temperature (ºC) | 30 | Mazatlan/Mexico/Urias estuary, Gulf of California (Salgado Barragan et al. 2004) |
Minimum Salinity (‰) | 23 | Mazatlan//Mexico/Urias estuary, Gulf of California (Salgado Barragan et al. 2004) |
Maximum Salinity (‰) | 43 | Mazatlan/Mexico/Urias estuary, Gulf of California (Salgado Barragan et al. 2004) |
Maximum Length (mm) | 30 | Van Name 1945; Kott 1985; Lambert and Lambert 1998 |
Broad Temperature Range | None | Cold temperate-Tropical |
Broad Salinity Range | None | Polyhaline-Euhaline |
General Impacts
Styela canopus, commonly known as the Rough Sea Squirt, is a widespread member of the fouling community in the world's coastal waters, and has been reported from ships, buoys, piers, and docks (Woods Hole Oceanographic Institution 1952; Lambert and Lambert, 1998). However, its impacts are unknown.
Regional Distribution Map
Bioregion | Region Name | Year | Invasion Status | Population Status |
---|---|---|---|---|
NA-ET2 | Bay of Fundy to Cape Cod | 1852 | Non-native | Established |
NA-ET3 | Cape Cod to Cape Hatteras | 1871 | Non-native | Established |
CAR-VII | Cape Hatteras to Mid-East Florida | 1872 | Non-native | Established |
NA-ET4 | Bermuda | 1901 | Non-native | Established |
SP-XXI | None | 1928 | Non-native | Established |
CAR-I | Northern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern Florida | 1879 | Non-native | Established |
NWP-3a | None | 0 | Native | Established |
AUS-III | None | 1952 | Crypogenic | Established |
AUS-IV | None | 1952 | Crypogenic | Established |
AUS-XIII | None | 0 | Crypogenic | Established |
AUS-XII | None | 0 | Crypogenic | Established |
AUS-XIX | None | 0 | Crypogenic | Established |
SP-IV | None | 0 | Crypogenic | Established |
NWP-4a | None | 0 | Native | Established |
EAS-III | None | 0 | Native | Established |
EAS-IV | None | 0 | Native | Established |
EAS-I | None | 0 | Native | Established |
EAS-II | None | 0 | Native | Established |
AG-1 | None | 0 | Native | Established |
AG-5 | None | 0 | Native | Established |
AG-3 | None | 0 | Native | Established |
AG-4 | None | 0 | Native | Established |
NEP-VI | Pt. Conception to Southern Baja California | 1972 | Non-native | Established |
NEA-II | None | 1868 | Non-native | Established |
MED-VII | None | 1877 | Non-native | Established |
NWP-2 | None | 0 | Native | Established |
MED-V | None | 0 | Non-native | Established |
CAR-II | None | 1984 | Non-native | Established |
CAR-III | None | 2002 | Non-native | Established |
CAR-IV | None | 1921 | Non-native | Established |
RS-1 | None | 1816 | Native | Established |
RS-2 | None | 1816 | Native | Established |
RS-3 | None | 0 | Native | Established |
EA-IV | None | 1918 | Crypogenic | Established |
AUS-II | None | 0 | Crypogenic | Established |
AUS-XIV | None | 0 | Crypogenic | Established |
AUS-XI | None | 0 | Crypogenic | Established |
AUS-I | None | 0 | Crypogenic | Established |
MED-III | None | 0 | Non-native | Established |
MED-IV | None | 0 | Non-native | Established |
SP-XII | None | 2001 | Non-native | Established |
MED-I | None | 0 | Non-native | Established |
SP-XIII | None | 1955 | Crypogenic | Established |
WA-V | None | 0 | Crypogenic | Established |
WA-IV | None | 0 | Crypogenic | Established |
SP-IX | None | 2002 | Non-native | Established |
P020 | San Diego Bay | 1972 | Non-native | Established |
G070 | Tampa Bay | 2002 | Non-native | Established |
G130 | Pensacola Bay | 1963 | Non-native | Established |
M020 | Narragansett Bay | 1880 | Non-native | Established |
M010 | Buzzards Bay | 1873 | Non-native | Established |
M040 | Long Island Sound | 1871 | Non-native | Established |
M130 | Chesapeake Bay | 2000 | Non-native | Established |
S190 | Indian River | 2005 | Non-native | Established |
S180 | St. Johns River | 2000 | Non-native | Established |
G310 | Corpus Christi Bay | 2002 | Non-native | Established |
G260 | Galveston Bay | 2000 | Non-native | Established |
P050 | San Pedro Bay | 1998 | Non-native | Established |
SA-III | None | 2005 | Non-native | Established |
SA-II | None | 1925 | Non-native | Established |
EA-III | None | 0 | Crypogenic | Established |
GAden | Gulf of Aden | 0 | Native | Established |
CIO-I | None | 0 | Native | Established |
P030 | Mission Bay | 1996 | Non-native | Established |
P023 | _CDA_P023 (San Louis Rey-Escondido) | 1996 | Non-native | Established |
P040 | Newport Bay | 1997 | Non-native | Established |
NEA-IV | None | 1868 | Non-native | Established |
N195 | _CDA_N195 (Cape Cod) | 1871 | Non-native | Established |
NWP-3b | None | 0 | Native | Established |
NEA-III | None | 1868 | Non-native | Established |
MED-VI | None | 0 | Non-native | Established |
S030 | Bogue Sound | 1872 | Non-native | Established |
NA-ET1 | Gulf of St. Lawrence to Bay of Fundy | 1885 | Non-native | Unknown |
S050 | Cape Fear River | 1885 | Non-native | Established |
G080 | Suwannee River | 1887 | Non-native | Established |
N100 | Casco Bay | 1873 | Non-native | Established |
S056 | _CDA_S056 (Northeast Cape Fear) | 1980 | Non-native | Established |
M030 | Gardiners Bay | 1983 | Non-native | Established |
S010 | Albemarle Sound | 1980 | Non-native | Established |
G074 | _CDA_G074 (Crystal-Pithlachascotee) | 1983 | Non-native | Established |
G020 | South Ten Thousand Islands | 1990 | Non-native | Established |
S200 | Biscayne Bay | 1946 | Non-native | Established |
S080 | Charleston Harbor | 2004 | Non-native | Established |
MED-II | None | 0 | Non-native | Established |
G330 | Lower Laguna Madre | 2003 | Non-native | Established |
N170 | Massachusetts Bay | 1852 | Non-native | Established |
N010 | Passamaquoddy Bay | 2004 | Non-native | Established |
P060 | Santa Monica Bay | 2001 | Non-native | Established |
NEP-VIII | None | 1995 | Non-native | Established |
N140 | Hampton Harbor | 2007 | Non-native | Established |
SEP-H | None | 2008 | Non-native | Established |
G030 | North Ten Thousand Islands | 1982 | Non-native | Established |
G045 | _CDA_G045 (Big Cypress Swamp) | 1982 | Non-native | Established |
N180 | Cape Cod Bay | 1879 | Non-native | Established |
WA-VI | None | 1906 | Non-native | Established |
SP-XVI | None | 1905 | Non-native | Established |
G100 | Apalachicola Bay | 1986 | Non-native | Established |
SA-IV | None | 2009 | Non-native | Established |
S206 | _CDA_S206 (Vero Beach) | 1887 | Non-native | Established |
N185 | _CDA_N185 (Cape Cod) | 1884 | Non-native | Established |
CIO-II | None | 2008 | Native | Established |
NEP-VII | None | 2012 | Non-native | Established |
WA-I | None | 1994 | Non-native | Established |
NEA-V | None | 0 | Non-native | Established |
PAN_PAC | Panama Pacific Coast | 2008 | Non-native | Established |
PAN_CAR | Panama Caribbean Coast | 2003 | Non-native | Established |
P090 | San Francisco Bay | 2015 | Non-native | Unknown |
NEP-V | Northern California to Mid Channel Islands | 2015 | Non-native | Unknown |
SEP-Z | None | 2016 | Non-native | Established |
S045 | _CDA_S045 (New) | 2018 | Non-native | Established |
Occurrence Map
OCC_ID | Author | Year | Date | Locality | Status | Latitude | Longitude |
---|---|---|---|---|---|---|---|
7591 | US National Museum of Natural History 2007 | 1885 | 1885-01-01 | Sable Island, NW Of/ | Non-native | 43.9500 | -59.9158 |
7592 | Trott 2004 | 2004 | 2004-01-01 | Cobscook Bay | Non-native | 44.9095 | -67.0555 |
7593 | US National Museum of Natural History 2007 | 1873 | 2007-01-01 | Casco Bay | Non-native | 43.8023 | -70.0564 |
7594 | Stimpson 1852 | 1852 | 1852-01-01 | Boston Harbor | Non-native | 42.3418 | -70.9662 |
7595 | Yale Peabody Museum 2009 | 1879 | 1879-01-01 | Provincetown Harbor | Non-native | 42.0418 | -70.1661 |
7596 | US National Museum of Natural History 2007 | 1884 | 1884-01-01 | Nantucket Shoals, South Of | Non-native | 39.9417 | -69.7222 |
7597 | Verrill and Smith 1873 | 1873 | 1873-01-01 | Buzzards Bay | Non-native | 41.5667 | -70.6000 |
7598 | US National Museum of Natural History 2007 | 1881 | 1881-01-01 | Nyes Neck, North Falmouth | Non-native | 41.6376 | -70.6536 |
7599 | Verrill and Smith 1873 | 1873 | 1873-01-01 | Woods Hole | Non-native | 41.5168 | -70.6828 |
7600 | Verrill and Smith 1873 | 1873 | 1873-01-01 | Edgartown | Non-native | 41.4001 | -70.4870 |
7601 | MIT Sea Grant 2003 | None | 9999-01-01 | Tripps Marina, Westport | Non-native | 41.5126 | -71.0889 |
7603 | US National Museum of Natural History 2002 | 1880 | 1880-01-01 | Newport Harbor | Non-native | 41.4826 | -71.3256 |
7604 | MIT Sea Grant 2003 | 2000 | 2000-01-01 | Warwick Cove Marina | Non-native | 41.6840 | -71.3912 |
7605 | Ruiz et al., unpublished data | None | 9999-01-01 | Barrington Yacht Club | Non-native | 41.7340 | -71.2934 |
7606 | Ruiz et al. unpublished data | 2003 | 2003-01-01 | Sakonnet River Railroad Bridge | Non-native | 41.5673 | -71.2239 |
7607 | Verrill 1871, cited by Kott 1998 | 1871 | 1871-01-01 | New Haven Harbor | Non-native | 41.2734 | -72.9176 |
7608 | US National Museum of Natural History 2007 | 1874 | 1874-01-01 | Noank | Non-native | 41.3279 | -71.9906 |
7609 | MIT Sea Grant 2003 | 2003 | 2003-01-01 | Brewer Yacht Haven Marine Center, Stamford | Non-native | 41.0232 | -73.5368 |
7610 | National Museum of Natural History 2007 | 1983 | 1983-01-01 | Great Peconic Bay | Non-native | 40.9407 | -72.4831 |
7611 | MIT Sea Grant 2003 | 2003 | 2003-01-01 | East Creek Marina, Jamesport | Non-native | 40.9382 | -72.5709 |
7612 | Ruiz et al., unpublished data | 2000 | 9999-01-01 | Kiptopeke | Non-native | 37.1379 | -75.9666 |
7613 | Ruiz et al., unpublished data) | 2000 | 2000-01-01 | Silver Beach | Non-native | 37.4854 | -75.9605 |
7614 | Ruiz et al., unpublished data | 2000 | 2000-01-01 | Norfolk Naval Station | Non-native | 32.3000 | -64.7833 |
7615 | Van Name 1902 | 1901 | 1901-01-01 | Bermuda | Non-native | 32.3000 | -64.7833 |
7616 | S National Museum of Natural History 2007 | 1980 | 1980-01-01 | Off North Carolina | Non-native | 35.3417 | -75.3600 |
7617 | Coues and Yarrow 1878 | 1878 | 1878-01-01 | Fort Macon | Non-native | 34.6957 | -76.6885 |
7618 | US National Museum of Natural History 2007 | 1885 | 1885-01-01 | Cape Fear, SE Of | Non-native | 33.6333 | -77.6000 |
7619 | US National Museum of Natural History 2007 | 1980 | 1980-01-01 | Off North Carolina | Non-native | 33.5433 | -77.4233 |
7620 | Ruiz et al. unpublished data | 2004 | 2004-01-01 | Charleston Harbor | Non-native | 32.7638 | -79.8973 |
7621 | uiz et al., unpublished data | 2000 | 2000-01-01 | Mayport Naval Station | Non-native | 30.3796 | -81.4286 |
7622 | Ruiz et al., unpublished data | 2000 | 2000-01-01 | Browns Creek Bridge, Jacksonville | Non-native | 30.4214 | -81.5209 |
7623 | da Rocha pers. comm. | 2005 | 2005-01-01 | Sebastian | Non-native | 27.8164 | -80.4706 |
7624 | da Rocha pers. comm. | 2005 | 2005-01-01 | Cape Marina, Cape Canaveral/ | Non-native | 28.4058 | -80.6048 |
7625 | da Rocha pers. comm. | 2005 | 2005-01-01 | Pelican Marina, Fort Pierce | Non-native | 27.4467 | -80.3256 |
7626 | Ruiz et al., unpublished data | 2004 | 2004-01-01 | Port of Miami | Non-native | 25.7745 | -80.1709 |
7627 | Ruiz et al., unpublished data | 2004 | 2004-01-01 | Matheson Hammock Marina | Non-native | 25.6786 | -80.2606 |
7628 | US National Museum of Natural History 2007 | 1990 | 1990-01-01 | Cape Sable, West Of | Non-native | 25.2271 | -81.1437 |
7629 | US National Museum of Natural History 2007 | 1887 | 1887-01-01 | Dry Tortugas | Non-native | 24.6652 | -82.8554 |
7630 | US National Museum of Natural History 2007 | None | 9999-01-01 | Naples, SW of | Non-native | 26.0531 | -82.1408 |
7631 | US National Museum of Natural History 2009 | 1982 | 1982-01-01 | Sanibel Island, SW Of | Non-native | 26.4404 | -82.1137 |
7632 | Ruiz et al., unpublished data) | 2002 | 2002-01-01 | Lands End, Apollo Beach, Tampa | Non-native | 27.7717 | -82.4062 |
7633 | Ruiz et al., unpublished data) | 2002 | 2002-01-01 | Port Manatee | Non-native | 27.6336 | -82.5615 |
7634 | Ruiz et al., unpublished data | 2002 | 9999-01-01 | St. Petersburg Municipal Marina | Non-native | 27.7609 | -82.6298 |
7635 | US National Museum of Natural History 2007 | 1983 | 1983-01-01 | Crystal Bay | Non-native | 28.9233 | -82.7137 |
7636 | US National Museum of Natural History 2007 | 1887 | 1887-01-01 | Cedar Key, | Non-native | 29.1486 | -83.0185 |
7637 | Dalby and Young 1992 | 1986 | 1986-01-01 | Carrabelle | Non-native | 29.8533 | -84.6643 |
7638 | Cooley 1978 | 1963 | 1963-01-01 | Santa Rosa Sound | Non-native | 30.3724 | -86.9719 |
7639 | Ruiz et al., unpublished data | None | 2002-01-01 | Port of Pensacola | Non-native | 30.4044 | -87.2114 |
7640 | Ruiz et al., unpublished data | 2002 | 2002-01-01 | Port of Texas City | Non-native | 29.3669 | -94.8166 |
7641 | Ruiz et al., unpublished data | None | 9999-01-01 | sland Moorings Marina, Port Aransas | Non-native | 27.8075 | -97.0867 |
7642 | Ruiz et al., unpublished data | 2002 | 2002-01-01 | Corpus Christi Naval Air Station | Non-native | 27.6941 | -97.2840 |
7644 | Lambert et al. 2005 | 2003 | 2003-01-01 | Sea Ranch Marina, Port Isabel | Non-native | 26.0759 | -97.1647 |
7645 | US National Museum of Natural History 2007 | 1914 | 1914-01-01 | Los Arroyos | Non-native | 22.3533 | -84.3825 |
7646 | Goodbody 2003 | 2003 | 2003-01-01 | Kingston Harbor | Non-native | 17.9539 | -76.8037 |
7647 | US National Museum of Natural History 2007 | 1984 | 1984-01-01 | Pelican Cays | Non-native | 16.6500 | -88.2000 |
7648 | Goodbody 2004) | None | 9999-01-01 | Twin Cays | Non-native | 16.8167 | -88.1000 |
7649 | Van Name 1921 | 1921 | 1921-01-01 | Guanica Harbor, Caribbean Sea | Non-native | 17.8605 | -66.9163 |
7650 | da Rocha et al. 2005 | 2005 | 2005-01-01 | St. Thomas | Non-native | 18.3533 | -64.9365 |
7652 | Monniot and Monniot 1985 | 1985 | 1985-01-01 | Guadeloupe | Non-native | 16.2500 | -61.5833 |
7653 | da Rocha et al. 2005 | 2005 | 2005-01-01 | Martinique | Non-native | 14.6667 | -61.0000 |
7654 | Van Name 1945 | 1945 | 1945-01-01 | Curacao | Non-native | 12.1833 | -69.0000 |
7655 | da Rocha et al. 2005 | 2003 | 2003-01-01 | Bocas del Toro | Non-native | 9.3333 | -82.2500 |
7656 | da Rocha et al. 2005 | 2005 | 2005-01-01 | Bonaire | Non-native | 12.1833 | -68.2500 |
7657 | da Rocha et al. 2005 | 2005 | 2005-01-01 | Isla Margarita | Non-native | 10.9869 | -63.9356 |
7658 | Carman et al. 2011 | 2009 | 2009-01-01 | Colon | Non-native | 9.3333 | -79.9000 |
7659 | Ruiz et al. unpublished data | 2008 | 2008-01-01 | Panama City | Non-native | 8.9833 | -79.5167 |
7660 | Tovar-Hernandez et al. 2012 | 2012 | 2012-01-01 | Puerto Ángel, | Non-native | 15.6667 | -96.4906 |
7661 | Tovar-Hernandez et al. 2012 | 2012 | 2012-01-01 | Puerto Vallarta, | Non-native | 20.6667 | -105.2667 |
7662 | Tovar-Hernandez et al. 2012 | 1995 | 1995-01-01 | Mazatlan | Non-native | 23.2200 | -106.4200 |
7663 | Tovar-Hernandez et al. 2012 | 2012 | 2012-01-01 | Isla Talchichitle, Navolato | Non-native | 24.9833 | -108.0667 |
7664 | Lambert and Lambert 1998 | 1972 | 1972-01-01 | South San Diego Bay | Non-native | 32.6098 | -117.1300 |
7666 | Lambert and Lambert 2003 | 1997 | 1997-01-01 | Bahia Point, San Diego | Non-native | 32.7756 | -117.2467 |
7667 | Lambert and Lambert 2003 | 1996 | 1996-01-01 | Oceanside Harbor | Non-native | 33.2078 | -117.3950 |
7669 | Lambert and Lambert 2003 | 1998 | 1998-01-01 | Watchorn Marina, Los Angeles | Non-native | 33.7200 | -118.2770 |
7670 | Lambert and Lambert 2003 | 2000 | 2000-01-01 | Long Beach Marina | Non-native | 33.7528 | -118.1112 |
7672 | Carlton and Eldredge 2009 | 1928 | 1928-01-01 | Pearl Harbor | Non-native | 21.3550 | -157.9722 |
7673 | Coles et al. 2002 | 2002 | 2002-01-01 | Kuapa Pond, Kaneohe Bay | Non-native | 21.2897 | -157.7047 |
7674 | Coles et al. 2004 | 2003 | 2003-01-01 | Kahului Harbor | Non-native | 20.8817 | -156.4675 |
7675 | Monniot and Monniot 1985 | 1905 | 905-01-01 | Outer reef, Hao | Non-native | -18.0753 | -140.9453 |
7676 | Monniot and Monniot 1985 | 1984 | 1984-01-01 | Port of Papeete | Non-native | -17.5350 | -149.5697 |
7677 | Coles et al. 2003 | 2002 | 2002-01-01 | Pago Pago Harbor | Non-native | -14.2814 | -170.6742 |
7678 | Monniot and Monniot 2001 | 1995 | 1995-01-01 | Koror, Goby Lake | Crypogenic | 7.3153 | 134.5019 |
7679 | Lambert 2002; Lambert 2003 | 2002 | 2002-01-01 | Apra Harbor | Non-native | 13.4497 | 144.6500 |
7680 | Kott 1985 | None | 9999-01-01 | New Caledonia | Crypogenic | -21.2500 | 165.3000 |
7681 | Kott 1985 | None | 9999-01-01 | Heron Island | Crypogenic | -23.4420 | 151.9140 |
7682 | Kott 1985 | None | 9999-01-01 | Lizard Island | Crypogenic | -14.6689 | 145.4567 |
7683 | Kott 1998 | None | 9999-01-01 | Torres Strait | Crypogenic | -10.0000 | 142.0000 |
7684 | Kott 1985 | None | 9999-01-01 | Broome | Crypogenic | -17.9619 | 122.2361 |
7685 | Kott 1953, cited by Kott 1998 | None | 9999-01-01 | Fremantle | Crypogenic | -32.0569 | 115.7439 |
7686 | Monniot and Monniot 2001 | None | 9999-01-01 | Davao, Mindinao | Non-native | 7.1042 | 125.6632 |
7687 | US National Museum of Natural History 2007 | 1909 | 9999-01-01 | Luzon Island | Native | 17.0000 | 122.5000 |
7688 | Sluiter 1904, cited by Kott 1985 | 1904 | 1904-01-01 | Java Sea | Native | -7.3233 | 116.8250 |
7689 | Millar1975, cited by Kott 1985 | None | 9999-01-01 | Gulf of Thailand | Native | 13.0000 | 101.0000 |
7690 | Kott and Goodbody 1982, cited by Kott 1985 | None | 9999-01-01 | Hong Kong | Native | 22.2783 | 114.1589 |
7691 | Huang 2001 | None | 9999-01-01 | Luoyuan Bay | Native | 26.4169 | 119.7160 |
7692 | Nishikawa 1991 | None | 9999-01-01 | Ariake Sea | Native | 32.9069 | 130.3722 |
7693 | Rho and Lee 1991 | None | 9999-01-01 | Komundo | Native | 34.0264 | 127.3125 |
7694 | Rho et al. 2000 | None | 9999-01-01 | Chindo Islands | Native | 34.4831 | 126.2619 |
7695 | Nishikawa 1992 | None | 9999-01-01 | Tottori | Native | 35.5000 | 134.2333 |
7696 | Huang 2001 | None | 9999-01-01 | Lianyungang, | Native | 34.6000 | 119.1667 |
7697 | Huang 2001) | None | 9999-01-01 | Quindao | Native | 36.0667 | 120.3833 |
7698 | Huang 2001 | None | 9999-01-01 | Yantai | Native | 37.4000 | 121.2667 |
7699 | Huang 2001 | None | 9999-01-01 | Penglai | Native | 37.8167 | 120.7333 |
7700 | Rho and Lee 1991 | None | 9999-01-01 | Anmado | Native | 35.5142 | 126.0186 |
7701 | Rho and Lee 1991 | None | 9999-01-01 | Toksan | Native | 36.7000 | 126.6680 |
7702 | Nishikawa 1991 | None | 9999-01-01 | Kagoshima Bay | Native | 31.4697 | 130.6356 |
7703 | Nishikawa 1991) | None | 9999-01-01 | Seto Inland Sea | Native | 34.1667 | 133.3333 |
7704 | Tokioka 1953, cited by Nishikawa 1991 | None | 9999-01-01 | Osaka Bay | Native | 34.5000 | 135.3000 |
7705 | Tokioka 1953, cited by Nishikawa 1991) | None | 9999-01-01 | Ise Bay | Native | 34.7500 | 136.7500 |
7706 | Tokioka 1953, cited by Nishikawa 1991 | None | 9999-01-01 | Sagami Bay | Native | 35.1167 | 139.3833 |
7707 | Oka 1934, cited by Nishikawa 1991 | None | 9999-01-01 | Tokyo Bay | Native | 35.4167 | 139.7833 |
7708 | Tamilselvi, et al. 2011 | None | 9999-01-01 | Tuticorin | Native | 8.8100 | 78.1400 |
7709 | Ali et al. 2009) | None | 9999-01-01 | Azhikkal | Native | 11.9000 | 75.3500 |
7710 | Abdul and Sivakumar 2007 | None | 9999-01-01 | Vizhinjam | Native | 8.3792 | 76.9914 |
7711 | Millar1975, cited by Kott 1985 | None | 9999-01-01 | Persian Gulf | Native | 26.0000 | 52.0000 |
7712 | Savigny 1816, cited by Kott 1998 | 1816 | 9999-01-01 | Red Sea | Native | 20.0000 | 38.0000 |
7713 | Monniot et al. 2002 | None | 9999-01-01 | Ibo Island | Crypogenic | -12.3500 | 40.6333 |
7714 | Michaelsen 1918, cited by Kott 1998 | 1918 | 1918-01-01 | Laurenco Marques (Maputo) | Crypogenic | -25.6333 | 32.5833 |
7715 | Monniot et al. 2001; Mead et al. 2011b | None | 9999-01-01 | Port Elizabeth | Crypogenic | -33.9581 | 25.6000 |
7716 | Monniot et al. 2001 | None | 9999-01-01 | Kommetjie | Crypogenic | -34.1403 | 18.3292 |
7717 | da Rocha and Bonnet 2009 | 2009 | 2009-01-01 | Arquipélago de Alcatrazes | Non-native | -24.1000 | -45.7000 |
7718 | da Rocha et al. 2005 | 1998 | 1998-09-28 | Arvoredro | Non-native | -24.2856 | -48.3736 |
7719 | da Rocha et al. 2009 | 1999 | 1999-01-01 | Santa Catarina State | Non-native | -26.7694 | -48.7844 |
7720 | Marins et al. 2010 | None | 9999-01-01 | Angra dos Reis, | Non-native | -23.0067 | -44.3181 |
7721 | US National Museum of Natural History 2007 | 1925 | 1925-01-01 | Rio de Janeiro | Non-native | -22.9083 | -43.1964 |
7722 | Rocha et al. 2012 | 1999 | 1999-07-08 | Salvador | Non-native | -12.8000 | -38.6333 |
7723 | da Rocha and Kremer 2005 | 2005 | 2005-01-01 | Pernambuco | Non-native | -8.0706 | -35.2658 |
7724 | da Rocha and Kremer 2005 | 2005 | 9999-01-01 | Rio Grande de Norte | Non-native | -5.0000 | -36.0000 |
7725 | Oliveira Filho and Lotufo 2010 | 2009 | 2009-01-01 | Pecem and Mucuripe Harbors | Non-native | -3.7183 | -38.5428 |
7726 | Rennie and Wiseman, 1906, cited by Van Name 1921 | 1906 | 1906-01-01 | Cape Verde Islands | Non-native | 15.1111 | -23.6167 |
7727 | Monniot and Monniot 1994 | 1990 | 1990-01-01 | Senegal | Non-native | 14.6928 | -17.4467 |
7728 | Canning-Clode et al., in prep | 2006 | 2006-01-01 | Madeira | Non-native | 32.6511 | -16.9097 |
7729 | Naranjo et al. 1996 | 1996 | 1996-01-01 | Algeciras Bay | Non-native | 36.1275 | -5.4539 |
7730 | Clausade 1969 | 1969 | 1969-01-01 | Mediterranean Sea | Non-native | 43.2964 | 5.3700 |
7731 | Peres 1957 | 1957 | 1957-01-01 | Balearic Islands | Non-native | 39.5000 | 3.0000 |
7732 | Chimenz 1985 | 1985 | 1985-01-01 | Ischia | Non-native | 40.7313 | 13.8957 |
7733 | Ghannudi et al. 1978 | 1978 | 1978-01-01 | Tripoli/ | Non-native | 32.9022 | 12.1858 |
7734 | Heller 1877, cited by Kott 1998 | 1877 | 1877-01-01 | Lesina | Non-native | 41.7667 | 15.4333 |
7735 | Tursi et al. 1979 | 1979 | 1979-01-01 | Bari | Non-native | 41.1253 | 16.8667 |
7736 | Manoudis et al. 2005 | 2005 | 2005-01-01 | Cape Fanari/ | Non-native | 40.9500 | 25.1333 |
7737 | Antoniadou and Chintiroglou 2007 | 2007 | 2007-01-01 | Chalkidiki Peninsula, Thessalonica | Non-native | 40.3333 | 23.5000 |
7738 | Koukouras et al. 1995 | 1995 | 1995-01-01 | Port Said | Non-native | 31.2600 | 32.2900 |
7739 | Bitar and Kouli-Bitar 2001 | 2001 | 2001-01-01 | Lebanon | Non-native | 33.8869 | 35.5131 |
7740 | Hancock 1868, cited by Kott 1998 | 1868 | 1868-01-01 | Guernsey Island | Non-native | 49.4500 | -2.5500 |
7741 | Alder and Hancock 1868, cited by Kott 1985 | 1868 | 1868-01-01 | English Channel | Non-native | 50.8000 | -1.0000 |
7742 | Appeltans et al. 2012 | 1975 | 1975-01-01 | N of Crab Rock, Sherkin Island | Non-native | 51.4570 | -9.4420 |
7743 | Breton et al. 1996 | 1996 | 1996-01-01 | Le Havre | Non-native | 42.4900 | 0.1000 |
7744 | Appletans et al. 2012 | 1983 | 1983-01-01 | Carreg-yr-Afr (Bardsey, Lleyn Peninsula) | Non-native | 52.9272 | 4.6793 |
8104 | Turon 1987 | None | 9999-01-01 | Tossa de Mar | Non-native | 41.7206 | 2.9322 |
767685 | Ruiz et al., 2015 | 2013 | 2013-07-17 | Naval Station San Diego, San Diego Bay, CA, California, USA | Non-native | 32.6867 | -117.1333 |
767735 | Ruiz et al., 2015 | 2013 | 2013-07-22 | Coronado Cays Marina, San Diego Bay, CA, California, USA | Non-native | 32.6257 | -117.1309 |
767752 | Ruiz et al., 2015 | 2013 | 2013-07-18 | NAB Fiddlers Cove, San Diego Bay, CA, California, USA | Non-native | 32.6524 | -117.1486 |
767777 | Ruiz et al., 2015 | 2013 | 2013-07-20 | Chula Vista Marina, San Diego Bay, CA, California, USA | Non-native | 32.6252 | -117.1036 |
767792 | Ruiz et al., 2015 | 2013 | 2013-07-28 | Marriott Marquis and Marina, San Diego Bay, CA, California, USA | Non-native | 32.7059 | -117.1655 |
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