• ChesReport (current)
  • Marine Invasions Lab
  • Partner Portals
    Nemesis California Panama Galapagos Cocos Island NP JTMD
    Archived Projects
    Chesapeake
  • Browse Species
    Taxonomic Groups All Species
  • News
  • login
You are viewing an archived site. The Chesapeake Bay Introduced Species Database project ended in 2020 and the database is no longer receiving updates. Learn more…
Image of Botrylloides violaceus

Botrylloides violaceus

Tunicates

colonial tunicate

Pond Water-Starwort is an aquatic plant of shallow streams and ponds, native to Eurasia and Africa and possibly Australia. The earliest North American record is from New York in 1861. By 1900, it had been collected in two New Jersey Counties, and strangely, Montana and Oregon. On the East Coast its range now extends from Quebec to Virginia. On the West Coast its found from British Columbia, Canada to Northern California. There are also several scatted inland records, probably from the nurseries or the aquarium trade, but shipping was also a likely vector for the East and West Coasts. There is no reported economic impacts related to this plant in the Chesapeake Bay or elsewhere.

Image Credit: Melissa Frey of the Royal Museum BC

Description Taxonomy Invasion History Ecology Impacts References

Description

Potentially MisidentifIed Species- Records of the Pacific Coast species Botrylloides diegensis on the Atlantic coast of North America appear to refer to B. violaceus. No specimens of B. diegensis have been identified in recent surveys of Narragansett Bay and the Gulf of Maine (Lambert and Lambert, personal communication). Similarly, records of the Northeast Atlantic species B. leachii on the Atlantic coast of North America (Myers 1990) refer to B. violaceus (Lambert and Lambert, personal communication).


Taxonomy

Kingdom Phylum Class Order Family Genus
Animalia Chordata Ascidiacea Stolidobranchia Styelidae Botrylloides

Synonyms

Botryllus aurantius; Botrylloides aurantium; Botrylloides carnosum; Botrylloides violaceum

Invasion History

Chesapeake Bay Status

First Record Population Range Introduction Residency Source Region Native Region Vectors
2000 Established Expanding Introduced Regular Resident Unknown-Marine Western Pacific Shipping(Fouling Community)

History of Spread

Botrylloides violaceus was described from Japan in 1927. It is found in Northwest Pacific from Japan to southern China. Reports from Queensland, Australia (Kott 1985; Kott 1998) may be a misidentification (Gretchen Lambert, pers. comm. 2000). It is now widely introduced, to the Northeast Pacific, the Northwest Atlantic, and parts of the Northeast Atlantic. It was first recorded on the West coast in San Francisco Bay in 1973 (Cohen and Carlton 1995). Subsequently, it was found in Bahia San Quintin, Mexico (2005, Rodriguez et al. 2008) Ensenada, Mexico (2000), (Lambert and Sanamyan 2001) , San Diego Bay (2000) (Lambert, personal communication) , Coos Bay OR (Lambert, personal communication) , Willapa Bay WA (1980) (Cohen and Carlton 1995), Puget Sound WA (1998) (Cohen et al. 1998), and Prince William Sound AK (Hines et al. 2000; Lambert and Sanamyan 2001). In the Northeast Atlantic, B. violaceus was first collected in 1993, in the Lagoon of Venice, in the Mediterranean Sea (Zaniolo et al. 1998). It has also been found in the Western Scheldt estuary, in the Netherlands, in 2000 (Gittenberger 2007), Zeebrugge, Belgium (Kerkhof et al. 2007), many sites on the southern coast of England (Arenas et al. 2006),and on the eastern coast of Ireland (Minchin et al. 2007).

Botrylloides diegensis, native to the NE Pacific, was introduced to Eel Pond, adjacent to Woods Hole Harbor MA, by a scientist, who wanted a supply of experimental animals. He reported successful overwintering and reproduction of these animals (Carlton 1989). Consequently, later occurrences of Botrylloides sp. in the NW Atlantic have been attributed to this species (Berman et al. 1992). However, later examination of Botrylloides sp. along the Northeast Coast of North America indicates that all the specimens found were B. violaceus (Gretchen Lambert, personal communication 2000).

Since B. violaceus was a very recent and local invader to the Pacific Coast of North America in the 1970s, it is unlikely that this species was introduced to Eel Pond. A separate invasion, in the late 1970s is likely for B. violaceus. The fate of the tranplanted B. diegensis is unknown. They may have died out on their own, or been replaced by B. violaceus. Any later reports of 'B. diegensis' on the East Coast, outside of Eel Pond (Berman et al. 1992; Whitlach and Osman 2000), probably refer to B. violaceus (Gretchen Lambert, pers. comm. 2000).

Owing to the confusion with B. diegensis, the date of first introduction, and the pattern of early spread in the northwest Atlantic is obscure. However, Whitlach and Osman (1995) indicated that B. violaceus was first observed in the late 1970s in Long Island Sound. By 1981, B. violaceus had spread to Great Bay NH, in the Gulf of Maine , and by the mid 1990s, it had reached Penobscot Bay (Whitlach and Osman 2001). In 2004, it was found fouling cultured mussels on Prince Edward Island in the Gulf of St. Lawrence (Locke et al. 2007). We are unsure of its range in estuaries south of Long Island Sound. However, in 2002, Gretchen Lambert confirmed our preliminary identifications of B. violaceus from lower Chesapeake Bay, collected in 2000 and 2001. Specimens were found on settling plates on both the Eastern (Kiptopeke/VA/Chesapeake Bay) and Western shores (Norfolk/VA/Little Creek (Hampton Roads); Poquoson/VA/Hampton Roads; Belle Isle Marina/VA/Rappahannock River; Amoco Refinery, Yorktown/VA/York River) (Ruiz et al., unpublished data).

References: Arenas et al. 2006; Berman et al. 1992; Carlton 1989; Cohen and Carlton 1995; Hines et al. 2000; Gittenberger 2007;Kerkhof et al. 2007; Kott 1985; Kott 1998; Gretchen Lambert, pers. comm. 2000; Gretchen Lambert, pers. comm. 2001; Lambert and Sanamyan 2001; Minchin et al. 2007; Rodriguez et al. 2008; Ruiz et al., unpublished data; Whitlach and Osman 1995; Zaniolo et al. 1998

Invasion Comments

Ecology

Environmental Tolerances

For SurvivalFor Reproduction
Minimum Maximum Minimum Maximum
Temperature (ºC)
Salinity (‰) 20.0 38.0
Oxygen
pH
Salinity Range poly-eu

Age and Growth

Male Female
Minimum Adult Size (mm)
Typical Adult Size (mm)
Maximum Adult Size (mm) 100.0 100.0
Maximum Longevity (yrs)
Typical Longevity (yrs

Reproduction

Start Peak End
Reproductive Season
Typical Number of Young
Per Reproductive Event
Sexuality Mode(s)
Mode(s) of Asexual
Reproduction
Fertilization Type(s)
More than One Reproduction
Event per Year
Reproductive Startegy
Egg/Seed Form

Impacts

Economic Impacts in Chesapeake Bay

The colonial tunicate Botrylloides violaceus appears to be a rare component of the fouling community in Chesapeake Bay, at present (Ruiz et al., unpublished data). It does not appear to have any economic impacts, but if its abundance increases, it could be a nuisance in boat fouling and fouling of oystering gear, similar to its relative Botryllus schlosseri (Golden Star Tunicate).


Economic Impacts Outside of Chesapeake Bay

The colonial tunicate Botrylloides violaceus is a rapidly spreading organism in fouling communities in many parts of the world. Its relative importance in ship fouling is not known, in part because it has been overlooked or misidentified in the past (Gretchen Lambert, personal communication 2001). It has become a pest in mussel culture operations on Prince Edward Island, Canada, overgrowing mussel lines and smoithering mussels (Gittenberger 2009)


Ecological Impacts on Chesapeake Native Species

The colonial tunicate Botrylloides violaceus appears capable of displacing native fouling organisms, through competition for space and food, in experiments on fouling plates in New England waters (Osman and Whitlach 2000; Stachowicz et al. 1999). However, the extent of its impacts in Chesapeake Bay is unknown. At present, this tunicate appears to be much less abundant than Botryllus schlosseri (Golden Star Tunicate) (Ruiz et al., unpublished data).

References- Osman and Whitlach 2001; Stachowicz et al. 1999


Ecological Impacts on Other Chesapeake Non-Native Species

The colonial tunicate Botrylloides violaceus appears capable of displacing other exotic and cryptogenic fouling organisms (e.g. Botryllus schlosseri) through competition for space and food, in experiments on fouling plates in New England waters (Osman and Whitlach 2000; Stachowicz et al. 1999). However, the extent of its impacts in Chesapeake Bay is unknown.

References- Osman and Whitlach 2000; Stachowicz et al. 1999


References

Arenas, F. and 13 authors. (2006) Alien species and other notable records from a rapid assessment survey of marinas on the south coast of England., Journal of the Marine Biological Association of the United Kingdom 86: 329-1337

Barnes, Robert D. (1983) Invertebrate Zoology., , Philadelphia. Pp. 883

Berman, Jody; Harris, Larry; Lambert, Walter; Buttrick, Melanie; Dufresne, Michael (1992) Recent invasions of the Gulf of Maine: Three contrasting ecological histories., Conservation Biology 6: 435-441

Blezard, David J. (1999) Salinity as a refuge from predation in a nudibranch-hydroid relationship within the Great Bay estuary. system., , Durham, New Hampshire. Pp.

Carlton, James T. (1989) Man's role in changing the face of the ocean: biological invasions and implications for conservation of near-shore environments, Conservation Biology 3: 265-273

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, , Washington DC, Silver Spring MD.. Pp.

Cohen, Andrew; and 16 authors. (1998) Puget Sound expedition: a rapid assessment survey of non-indigenous species in the shallow waters of Puget Sound., , Olympia, Washington. Pp. 1-37

Gittenberger, Adriaan (2007) Recent population expansions of non-native ascidians in the Netherlands., Journal of Experimental Marine Biology and Ecology 342: 122-126

Gittenberger, Adriaan (2009) Invasive tunicates on Zeeland and Prince Edward Island mussels, and management practices in The Netherlands., Aquatic Invasions 4: 279-281

Grosholz, Edwin (2001) Small spatial-scale differentiation among populations of an introduced colonial invertebrate, Oecologia 129-: 58-64

Hines, Anson H.; Ruiz, Gregory M.; Godwin, L. Scott (2000) Assessing the risk of nonindigenous species invasion in a high-latitude ecosystem: ballast water treatment facility in Port Valdez, Alaska., In: Pederson, Judith(Eds.) Marine Bioinvasions. , Cambridge. Pp. 81-88

Kerckhof, Francis; Haelters, Jan; Gollasch, Stephan G. (2007) Alien species in the marine and brackish ecosystem: the situation in Belgian waters., Aquatic Invasions 2: 243-257

Kott, P. (1998) Tunicata, Zoological Catalogue of Australia 34: 51-252

Kott, Patricia (1985) The Australian Ascidiacea Part 1, Phlebobranchia and Stolidobranchia., Memoirs of the Queensland Museum 23: 1-440

Lambert, G.; Sanamyan, K. (2001) Distaplia alaskensis sp. nov. (Ascidiacea, Aplousobranchia) and other new ascidian records from South-central Alaska, with a redescription of Ascidia columbiana (Huntsman, 1912)., Canadian Journal of Zoology 79: 1766-1781

Locke, Andrea; Hanson, Mark; Ellis, Karla M.; Thompson, Jason; Rochette, Rémy (2007) Invasion of the southern Gulf of St. Lawrence by the clubbed tunicate (Styela clava Herdman): Potential mechanisms for invasions of Prince Edward Island estuaries., Journal of Experimental Marine Biology and Ecology 342: 69-77

Minchin, Dan (2007) Rapid coastal survey for targeted alien species associated with floating pontoons in Ireland, Aquatic Invasions 2: 63-70

Nishikawa, Teruki (1991) The Ascidians of the Japan Sea., Publication of the Seto Marine Biological Laboratory 35: 25-170

Osman, Richard W.; Whitlatch, Robert B. (2000) Ecological interactions of invading ascidians within epifaunal communities of southern New England., In: Peterson, Judith(Eds.) Marine Bioinvasions. , Cambridge. Pp. 164-174

Rodriguez, Laura F.; Ibarra-Obando, Silvia E. (2008) Cover and colonization of commercial oyster (Crassostrea gigas) shells by fouling organisms in San Quintin Bay, Mexico, Journal of Shellfish Research 27: 337-343

Saito, Y.; Mukai, H.; Watanabe, H. (1981) Studies on Japanese compound styelid ascidians II. A new species of the genus Botrylloides and redescription of B. violaceus Oka., Publications of the Seto Marine Biological Laboratory 26: 357-368

Stachowicz, John J.; Whitlatch, Robert B.; Osman, Richard W. (1999) Species diversity and invasion resistance in a marine ecosystem, Science 286: 1577-1579

Whitlatch, Robert B.; Osman, Richard (2000) Geographical distributions and organism-habitat associations of shallow water introduced marine fauna in New England., In: Pederson, Judith(Eds.) Marine Bioinvasions. , Cambridge MA. Pp. 61-65

Whitlatch, Robert B.; Osman, Richard W.; Frese, Annette, Malatesta, Richard, Mitchell, Patricia, Sedgwick, Lynn (1995) The ecology of two introduced marine ascidians and their effects on epifaunal organisms in Long Island Sound, In: Balcom, N. C.(Eds.) Proceedings of the Northeast Conference on Non-Indigenous Aquatic Nuisance Species. , Groton, CT. Pp. 28-29

Zaniolo, G.; Brunetti, R.; Burighel, P. (1998) Brood pouch differentiation in Botrylloides violaceus, a viviparous ascidian (Tunicata), Invertebrate Reproduction and Development 33: 11-23


Direct questions and comments to chesnemo@si.edu.

©