Invasion History
First Non-native North American Tidal Record: 1946First Non-native West Coast Tidal Record: 1946
First Non-native East/Gulf Coast Tidal Record:
General Invasion History:
Nematostella vectensis is a small estuarine mud-dwelling sea anemone with a somewhat enigmatic distribution. Its known range includes the south and east coasts of Britain in the Northeast Atlantic (Sheader et al. 1997; Stephenson 1935), the Northwest Atlantic from Nova Scotia to Louisiana, and the Northeast Pacific from Washington to California (Hand and Uhlinger 1994). It was first described from the Isle of Wight, England (Stephenson 1935). The limited and localized distribution of N. vectensis on the European coast (southeast England only, Norfolk to the Fleet), suggests that the English population may have been an introduction from North America, possibly brought with oysters (Crassostrea virginica, Eastern Oyster) (Sheader et al. 1997). Successful crosses of females from six locations (England, Maryland, Georgia, California, Oregon, and Washington) and males from four locations (Nova Scotia, Maryland, Georgia, and Oregon) suggest that populations from both sides of the Atlantic, and the Northeast Pacific constitute a single species. All 24 combinations tested produced viable larvae (Hand and Uhlinger 1994). Recent genetic studies indicate that populations from the southeastern United States have the highest genetic diversity, and that this anemone is native to the East Coast of North America and was introduced to the West coast and to England (Reitzel et al. 2008; Darling et al. 2009).
The potentially long-lived larvae (Hand and Uhlinger 1992) provide one obvious device for spreading populations of N. vectensis in ships’ ballast water. Another possibility is that this species has been spread with oyster transfers. Oysters have been transported widely between estuaries and oceans, and those movements could have carried the anemone between the Atlantic and the Pacific oceans, and in and out of the Gulf of Mexico (Hand and Uhlinger 1994).
North American Invasion History:
Invasion History on the West Coast:
On the Pacific coast, the first verified collection of N. vectensis was in Alameda County, California in 1946, although it may have been seen before this date in San Francisco and Tomales Bays (Hand 1957). It is now found in at least 11 separate estuaries, from San Francisco Bay north to Puget Sound and the San Juan Islands, Washington (by 1973, Hand and Uhlinger 1994). In San Francisco Bay, it was regarded as a cryptogenic species (Cohen and Carlton 1995), but genetic studies indicate that West Coast populations are introduced (Reitzell et al. 2008; Darling et al. 2009). West Coast populations have a higher incidence of asexual reproduction compared to East Coast populations, and two clones occur at multiple locations from Tomales Bay to the San Juan Islands (Darling et al. 2009).
Invasion History on the East Coast:
In the Northwest Atlantic, the wide latitudinal distribution and genetic diversity of N. vectensis suggests native status (Reitzel et al. 2008), but the relatively recent discovery of this species in well-studied areas is puzzling. It was first found on this coast in 1939, at Woods Hole, Massachusetts by Crowell (1946). No anemone of this type was mentioned in extensive early surveys of that area (Smith and Verrill 1873; Sumner et al. 1913). Its typical habitat, in shallow marshy lagoons, is unusual for an anemone, but the site in which it was found (Mill Pond) was surveyed by Sumner et al. (1913), and probably examined occasionally by many other Woods Hole scientists. Extension of this species' range northward along the coast by oyster transplants or shipping is possible. While genetic diversity suggests a southeastern origin, records from North Carolina to Mississippi are relatively recent (1980s) (Hand and Uhlinger 1994). After N. vectensis was reported from Woods Hole in 1939 (Crowell 1946), the next published report was from the Minas Basin, in the Bay of Fundy, Nova Scotia (in 1965, Bailey and Bleakney 1966). Subsequently, it was found in many estuaries, from the Spurwink River, near Portland, Maine to Chesapeake Bay (Calder 1972; Posey and Hines 1991; Hand and Uhlinger 1994). The high genetic diversity in New England suggests limited dispersal and sporadic introductions (Darling et al. 2004).
Invasion History Elsewhere in the World:
Although N. vectensis was first described from the Isle of Wight, England (Stephenson 1935), its localized distribution (southeast England only, Norfolk to the Fleet), suggests that the English population may have been an introduction from North America, possibly brought with oysters (Crassostrea virginica, Eastern Oyster) (Sheader et al. 1997). This is supported by its low genetic diversity and the sharing of haplotypes with New England populations (Reitzel et al. 2008). In 2004, seven specimens were collected in the port of Recife, Brazil, the first collections in the Southern Hemisphere. It is not known if a population is established there (Silva et al. 2010).
Description
Nematostella vectensis is a small burrowing anemone, found in mud and silt. It has an elongate, wormlike body, which is usually buried with only the oral disk and mouth protruding. Other burrowing anemones have a posterior section modified for digging, called a physa, and a collar below the oral region, but these are lacking in N. vectensis. It typically has 16 tentacles, but may vary from 12 to 18. The body is translucent and nematosomes (small ciliated spheres) may be seen circulating in the gut. These are unique to this genus. The eight mesenteries are also visible, as lines running the length of the body. The typical size is 10-19 mm, but it may grow larger in culture. The crown of tentacles may reach 8 mm in diameter when extended (description from: Stephenson 1935; Crowell 1946; Hand 1957; Gosner 1978; Fautin, in Carlton 2007).
Taxonomy
Taxonomic Tree
Kingdom: | Animalia | |
Phylum: | Cnidaria | |
Class: | Anthozoa | |
Subclass: | Hexacorallia | |
Order: | Actiniaria | |
Suborder: | Athenaria | |
Family: | Edwardsiidae | |
Genus: | Nematostella | |
Species: | vectensis |
Synonyms
Potentially Misidentified Species
None
Ecology
General:
Nematostella vectensis is a wormlike, burrowing animal, which commonly lives buried in the sediment, with its oral disk and tentacles protruding. Unlike most other anemones, it does not attach to its substrate. It reproduces both sexually, and asexually, by transverse fission (Hand and Uhlinger 1994; Hand and Uhlinger 1995). Sexes are separate. Females lay gelatinous egg masses and males release sperm into the water column. Fertilized eggs divide and develop into planula larvae. After four days they develop tentacle buds, and settle after about seven days (Hand and Uhlinger 1992). Nematostella vectensis is one of only five anemones known to reproduce asexually by transverse fission- most anemones reproduce asexually by longitudinal fission. This mode of reproduction means that the aboral fragment must develop a new mouth and tentacles (Hand and Uhlinger 1995). In small individuals (less than 20 mm), which are the most numerous, 5-10 eggs are typical, but larger individuals may produce up to 2,000 eggs (Hand and Uhlinger 1992; Hand and Uhlinger 1994). A number of known populations appear to consist of one sex only. Only females are known from England (Sheader et al. 1997), and San Francisco and Tomales Bay California, while recent collections from Kingsport, Nova Scotia are all males. This species appears able to sustain populations through asexual reproduction (Hand and Uhlinger 1994; Sheader et al. 1997).
Nematostella vectensis is tolerant of an extremely wide range of salinities and temperatures, from 2-52 PSU and -1.5-32.5ºC (Hand and Uhlinger 1995; Sheader 1997). Sexual reproduction in the laboratory occurred at 12-34 PSU (Hand and Uhlinger 1992). Reproductive temperatures are not known, but sexual reproduction is probably confined to the warmer parts of the year, July-August in Nova Scotia (Frank and Bleakney 1976) and February-October in England (Sheader et al. 1997). Typical habitats for N. vectensis include salt marshes, lagoons, and mudflats (Crowell 1946; Frank and Bleakney 1976; Hand and Uhlinger 1994; Sheader 1997). This anemone feeds on a wide range of small invertebrates, including hydrobiid snails, copepods, ostracods, polychaets, insect larvae, and bivalve larvae (Posey and Hines 1991; Hand and Uhlinger 1994).
Food:
Small benthic invertebrates; invertebrate larvae
Consumers:
Shrimps
Trophic Status:
Carnivore
CarnHabitats
General Habitat | Grass Bed | None |
General Habitat | Salt-brackish marsh | None |
General Habitat | Unstructured Bottom | None |
General Habitat | Oyster Reef | None |
Salinity Range | Mesohaline | 5-18 PSU |
Salinity Range | Polyhaline | 18-30 PSU |
Salinity Range | Euhaline | 30-40 PSU |
Salinity Range | Hyperhaline | 40+ PSU |
Tidal Range | Subtidal | None |
Tidal Range | Low Intertidal | None |
Vertical Habitat | Endobenthic | None |
Tolerances and Life History Parameters
Minimum Temperature (ºC) | -1.5 | Field data- Bleakney and Meyer 1979 |
Maximum Temperature (ºC) | 32.5 | Field data- Kneib 1988 |
Minimum Salinity (‰) | 7 | Experimental data- Hand and Uhlinger 1992 |
Maximum Salinity (‰) | 52 | Field data-Hand and Uhlinger 1994 |
Broad Temperature Range | None | Cold temperate-Warm temperate |
Broad Salinity Range | None | Mesohaline-Euhaline |
General Impacts
Few economic and ecological impacts have been reported for this species. Hand and Uhlinger (1994) suggested that Nematostella vectensis could be a significant predator of oyster larvae in estuaries, such as Chesapeake Bay, because of its dense populations in marshes and mudflats. However, its apparent scarcity and sporadic appearance (Posey and Hines 1991) argues against a role in recruitment of oysters and other commercially important shellfish in the upper Chesapeake Bay. The importance of N. vectensis as a predator has not yet been studied in other estuaries.Regional Distribution Map
Bioregion | Region Name | Year | Invasion Status | Population Status |
---|---|---|---|---|
NEA-II | None | 1935 | Non-native | Established |
NA-ET2 | Bay of Fundy to Cape Cod | 1965 | Crypogenic | Established |
NA-ET3 | Cape Cod to Cape Hatteras | 1939 | Crypogenic | Established |
CAR-VII | Cape Hatteras to Mid-East Florida | 1980 | Native | Established |
CAR-I | Northern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern Florida | 1982 | Native | Established |
NEP-V | Northern California to Mid Channel Islands | 1946 | Non-native | Established |
NEP-IV | Puget Sound to Northern California | 1973 | Non-native | Established |
NEP-III | Alaskan panhandle to N. of Puget Sound | 1973 | Non-native | Established |
M080 | New Jersey Inland Bays | 1979 | Crypogenic | Established |
M040 | Long Island Sound | 1978 | Crypogenic | Established |
M130 | Chesapeake Bay | 1963 | Crypogenic | Established |
M020 | Narragansett Bay | 1973 | Crypogenic | Established |
M010 | Buzzards Bay | 1964 | Crypogenic | Established |
P090 | San Francisco Bay | 1946 | Non-native | Established |
P110 | Tomales Bay | 1994 | Non-native | Established |
P130 | Humboldt Bay | 1992 | Non-native | Established |
P260 | Columbia River | 1994 | Non-native | Established |
P290 | Puget Sound | 1993 | Non-native | Established |
P292 | _CDA_P292 (San Juan Islands) | 1973 | Non-native | Established |
P170 | Coos Bay | 1973 | Non-native | Established |
P210 | Yaquina Bay | 2009 | Non-native | Established |
P270 | Willapa Bay | 2009 | Non-native | Established |
N135 | _CDA_N135 (Piscataqua-Salmon Falls) | 1975 | Crypogenic | Established |
N106 | _CDA_N106 (Presumpscot) | 1982 | Crypogenic | Established |
M100 | Delaware Inland Bays | 1974 | Crypogenic | Established |
N160 | Plum Island Sound | 0 | Crypogenic | Established |
N170 | Massachusetts Bay | 0 | Crypogenic | Established |
P280 | Grays Harbor | 2009 | Non-native | Established |
P293 | _CDA_P293 (Strait of Georgia) | 2005 | Non-native | Established |
M060 | Hudson River/Raritan Bay | 2008 | Crypogenic | Established |
SA-III | None | 2004 | Non-native | Unknown |
NA-ET1 | Gulf of St. Lawrence to Bay of Fundy | 1985 | Crypogenic | Established |
Occurrence Map
OCC_ID | Author | Year | Date | Locality | Status | Latitude | Longitude |
---|---|---|---|---|---|---|---|
30538 | Hand 1957 | 1953 | 1953-01-01 | Bay Farm Island | Non-native | 37.7388 | -122.2530 |
30544 | Hand 1957 | 1946 | 1946-01-01 | Richardsons Bay | Non-native | 37.8738 | -122.5038 |
References
Bailey, Kanioulano; Bleakney, J. Sherman (1966) First Canadian record of the brackish water anthozoan Nematostella vectensis Stephenson, Canadian Field-Naturalist 80: 251-252Bleakney, J. S.; Meyer, Kaniaulono Bailey (1979) Observations on saltmarsh pools, Minas Basin, Nova Scotia, 1965-1977, Proceedings of the Nova Scotian Institute of Science 29: 351-371
Boyd, Milton J.; Mulligan, Tim J; Shaughnessy, Frank J. (2002) <missing title>, California Department of Fish and Game, Sacramento. Pp. 1-118
Calder, Dale R. (1972) Phylum Cnidaria, Special Scientific Report, Virginia Institute of Marine Science 65: 97-102
Carlton, James T. (Ed.) (2007) The Light and Smith Manual: Intertidal Invertebrates from Central California to Oregon Fourth Edition, Completely Revised and Expanded, University of California Press, Berkeley. Pp. <missing location>
Cohen, Andrew N.; Carlton, James T. (1995) Nonindigenous aquatic species in a United States estuary: a case study of the biological invasions of the San Francisco Bay and Delta, U.S. Fish and Wildlife Service and National Sea Grant College Program (Connecticut Sea Grant), Washington DC, Silver Spring MD.. Pp. <missing location>
Crowell, Sears (1946) A new sea anemone for Woods Hole, Massachusetts, Journal of the Washington Academy of Sciences 36(2): 57-60
Darling, J. A.; Reitzel, A. M.; Finnerty, J. R. (2004) Regional population structure of a widely introduced estuarine invertebrate: Nematostella vectensis Stephenson in New England., Molecular Ecology 13: 2969-2981
Darling, John A.; Bagley, Mark J.; Roman, Joe; Tepolt, Carolyn K; Geller, Jonathan B.. (2008) Genetic patterns across multiple introductions of the globally invasive crab genus Carcinus., Molecular Ecology 17: 4992-5007
Darling, John A.; Kuenzi, Ashley; Reitzel, Adam M. (2009) Human-mediated transport determines the nonnative distribution of the anemone Nematostella vectensis, a dispersal-limited estuarine invertebrate, Marine Ecology Progress Series 380: 137-146
Fautin, Daphne G.; Hand, Cadet (2007) <missing title>, University of California, Berkeley. Pp. 173-184
Frank, Peter G.; Bleakney, J. Sherman (1978) Asexual reproduction, diet, and anomalies of the anemone Nematostella vectensis in Nova Scotia, Canadian Field-Naturalist 92(3): 259-263
Frank, Peter; Bleakney, J. Sherman (1976) Histology and sexual reproduction of the anemone Nematostella vectensis Stephenson 1935, Journal of Natural History 10: 441-449
Gimenez, Lucas H.; Brante, Antonio (2021) Do non-native sea anemones (Cnidaria: Actiniaria) share a common invasion pattern? – A systematic review, Aquatic Invasions 16: 365-390
Gimenez, Lucas H.; Rivera, Reinaldo J.; Brante, Antonio (2022) One step ahead of sea anemone invasions with ecological niche modeling: potential distributions and niche dynamics of three successful invasive species, Marine Ecologicy Progress Series 690: 83–95
https://doi.org/10.3354/meps14044
Gosner, Kenneth L. (1978) A field guide to the Atlantic seashore., In: (Eds.) . , Boston. Pp. <missing location>
Hand, Cadet; Uhlinger, Kevin R. (1992) Culture, sexual and asexual reproduction, and growth of the sea anemone Nematostella vectensis, Biological Bulletin 182: 169-176
Hand, Cadet (1957) Another sea anemone from California, Journal of the Washington Academy of Sciences 47(12): 411-414
Hand, Cadet; Uhlinger, Kevin R. (1994) Unique, widely distributed, estuarine sea anemone, Nematostella vectensis Stephenson: A review, new facts, and questions, Estuaries 17(2): 501-508
Hand, Cadet; Uhlinger, Kevin R. (1995) Asexual reproduction by transverse fission and some anomalies in the sea anemone Nematostella vectensis, Invertebrate Biology 114(1): 9-18
Kneib, R. T. (1988) Testing for indirect effects of predation on an intertidal soft-bottom community, Ecology 69(6): 1795-185
Posey, Martin H.; Hines, Anson H. (1991) Complex predator-prey interactions within an estuarine benthic community, Ecology 72: 2155-2169
Reise, K.; Gollasch, S.; Wolff, W.J. (1999) Introduced marine species of the North Sea coasts., Helgoländer Meeresuntersuchungen 52: 219-234
Reitzel, Adam M.; Darling, John A.; Sullivan, James C.; Finnerty, John R. (2008) Global population genetic structure of the starlet anemone Nematostella vectensis: multiple introductions and implications for conservation policy., Biological Invasions 10(8): 1197-1213
Ruiz, Gregory M.; Geller, Jonathan (2018) Spatial and temporal analysis of marine invasions in California, Part II: Humboldt Bay, Marina del Re, Port Hueneme, and San Francisco Bay, Smithsonian Environmental Research Center & Moss Landing Laboratories, Edgewater MD, Moss Landing CA. Pp. <missing location>
Sheader, M.; Suwailem, A.M.; Rowe, G.A. (1997) Anemone, Nematostella vectensis, in Britain: Consideration for conservation management, Aquatic Conservation: Marine and Freshwater Ecosystems 7: 13-25
Silva, Janine F.; Lima, Carlos A. C.; Perez, Carlos D.; Gomes, Paula B. (2010) First record of the sea anemone Nematostella vectensis (Actiniaria: Edwardsiidae) in Southern Hemisphere waters, Zootaxa 2343: 66-68
Smith, Ralph I. (1964) <missing title>, Systematics-Ecology Program, Marine Biological Laboratory, Woods Hole, Massachusetts. Pp. <missing location>
Stephenson, T. A. (1935) <missing title>, Ray Society, London. Pp. <missing location>
Sumner, Francis B., Osburn, Raymond C., Davis, Bradley M. (1913a) A biological survey of the waters of Woods Hole and vicinity. Part I. Section I. Physical and Zoological. Section II. Botanical, Bulletin of the Bureau of Fisheries 31: 1-544
Sytsma, Mark D.; Cordell, Jeffrey R.; Chapman, John W.; Draheim, Robyn, C. (2004) <missing title>, Center for Lakes and Reservoirs, Portland State University, Portland OR. Pp. <missing location>
Verrill, A.E.; Smith, S.I. (1873) <missing title>, 1 Report of the United States Commission of Fish and Fisheries, <missing place>. Pp. 1-757