Invasion History
First Galapagos Record: 2015General Invasion History:
The colonial tunicate Botrylloides giganteus was first described from Senegal in 1949. In the 1980s, it was found in Brazil, over a limited range from Sao Paulo to Vittorio (Aron and Sole-Cava 1991, Rodrigues and da Rocha 1993, Da Rocha and Costa 2005). In 1997, a colonial tunicate, first identified as B. perspicuum, was found on the coast of southern California (Lambert and Lambert 2003). Recent morphological and genetic studies (in preparation) indicate that the Southern California form was conspecific with B. giganteus and with a colonial tunicate described from the Gulf of Taranto, Italy, B. pizoni (Brunetti and Mastrotaro 2012). It has also been identified in New Zealand (Riding et al. 2014, Ministry of Primary Studies 2015, Rocha et al. 2019). The native and introduced ranges of this tunicate are unresolved.
Invasion History in the Galapagos:
Botrylloides giganteus was collected on settling plates in 2015 and 2016 in Tortuga Bay, Santa Cruz Island, and on Baltra Island. Two color morphs, purple and red, were found. These were the first records from the Galapagos (Lambert 2019).
Invasion history elsewhere in the world:
The native range of Botrylloides giganteus is unknown. The type locality was Senegal (Peres 1949, cited by (Aron and Sole-Cava 1991), but it was subsequently found on the Indian Ocean coast of South Africa and Mozambique (Millar 1955, Millar 1961, Millar 1963, cited by Monniot et al. 2001; Rocha et al. 2019). In Brazil, it was first found in 1986, and is known largely from artificial substrates, and is especially abundant in mussel cultures. It was not seen in previous surveys and is considered introduced and established in Brazil (da Rocha et al. 2009; Rocha et al. 2019; Oricchio et al. 2019). In 2014, B. giganteus was found in Whangarei Harbor, New Zealand (Riding et al. 2014; Rocha et al. 2019), and on Santa Cruz and Baltra Islands, in the Galapagos Archipelago, in 2015 (Lambert 2009; Rocha et al 2019).
Description
Botrylloides giganteus is a colonial tunicate. Colonial tunicates are communities of individuals, called zooids, which share a protective cellulose layer called a tunic. Each zooid is an individual, but they are such an intricate part of the colony that they cannot be separated from it. In fact, the zooids are connected to one another by a network of blood vessels and work together to make the colony function like a single animal.
The colonies of B. giganteus are 2-5 mm thick, translucent, and variable in size and shape, ranging from 30 to 150 mm in diameter. They can grow on algae or other debris. Botrylloides giganteus has linear systems of zooids, which are visible through the tunic. The colonies are red to orange or violet in color. The body walls of its zooids are very delicate and transparent and lack longitudinal or circular musculature. The oral siphon is round, with a smooth margin. There are 24 branchial tentacles in mature zooids. On the branchial sac there are 11-17 pairs (usually 14) of stigmata. The atrial siphon develops a languet, a tongue-like structure, which varies in shape and length. The esophagus is short and curved, and the stomach has 9-10 longitudinal folds. A mature zooid can have a single developing embryo. Description based on: Rodrigues and da Rocha 1993, and da Rocha and Costa 2005.
This tunicate, discovered in Southern California, was initially identified as B. perspicuum (1997, Lambert and Lambert 2003). Recent observations indicate that it is actually B. giganteus (Gretchen Lambert and Rosana da Rocha, personal communications). We are in the process of revising the morphological description and biogeographical history of this species (Rodriques and da Rocha 1993; da Rocha and Costa 2005; Rocha et al. 2019).
Taxonomy
Taxonomic Tree
Kingdom: | Animalia | |
Phylum: | Chordata | |
Subphylum: | Tunicata | |
Class: | Ascidiacea | |
Order: | Stolidobranchia | |
Family: | Styelidae | |
Genus: | Botrylloides | |
Species: | giganteus |
Synonyms
Botrylloides niger var. giganteum (Pérès, 1949)
Botrylloides giganteum (Ryland, 2015)
Botrylloides pizoni (Brunetti and Mastrotaro, 2012)
Potentially Misidentified Species
Rocha et al. 2919, new species, described from Queesland, Australia
Botrylloides leachii
Kott 1972, cited by Kott 1985
Botrylloides nigrum
Michaelson 1919, cited by Kott 1985
Botrylloides perspicuus
This tunicate was initially identified as Botrylloides perspicuum (1997, Lambert and Lambert 2003). Recent observations suggested that it is actually B. giganteum (Gretchen Lambert, Rosana da Rocha, personal communications, 2013–2015).
Botyrllus firmus
Monniot and Monniot 2001
Ecology
General:
Life History- A colonial (or compound) tunicate consists of many zooids, bearing most or all of the organs of a solitary tunicate, but modified to varying degrees for colonial life. Colonial tunicates of the genera Botrylloides have small zooids, usually not organized in systems, and fully embedded in a mass of tunic material. Each zooid has an oral siphon and an atrial canal, opening to a shared cloacal chamber. Water is pumped into the oral siphon, through finely meshed ciliated gills on the pharynx, where phytoplankton and detritus is filtered, and passed on mucus strings to the stomach and intestines. Excess waste is expelled in the outgoing atrial water (Van Name 1945; Barnes 1983).
Colonial tunicates reproduce both asexually, by budding, and sexually, from fertilized eggs developing into larvae. Buds can form from the body wall of the zooid. Colonies vary in size and can range from small clusters of zooids to huge spreading masses. The zooids are hermaphroditic, with eggs and sperm being produced by a single individual. Eggs may be self-fertilized or fertilized by sperm from nearby animals, but many species have a partial block to self-fertilization. Eggs are internally fertilized, and embryos are incubated in a brood pouch. Once they are mature, 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. Swimming periods are usually less than a day, and some larvae can settle immediately after release, but the larval period can be longer at lower temperatures. Once settled, the tail is absorbed, the gill basket expands, and the tunicate begins to feed by filtering (Van Name 1945; Barnes 1983).
Food:
Phytoplankton
Consumers:
fishes, crabs
Trophic Status:
Suspension Feeder
SusFedHabitats
General Habitat | Rocky | None |
General Habitat | Coral reef | None |
General Habitat | Marinas & Docks | None |
Salinity Range | Polyhaline | 18-30 PSU |
Salinity Range | Euhaline | 30-40 PSU |
Tidal Range | Subtidal | None |
Tidal Range | Low Intertidal | None |
Vertical Habitat | Epibenthic | None |
Life History
Tolerances and Life History Parameters
Broad Temperature Range | None | Warm temperate-Tropical |
Broad Salinity Range | None | Polyhaline-Euhaline |
General Impacts
Competition: The colonial tunicate Botrylloides giganteus (then identified as B. perspicuum) covered extensive areas crowding out other species. This was seen in San Diego Bay in 1997 (Lambert and Lambert 2003).
Regional Distribution Map
Bioregion | Region Name | Year | Invasion Status | Population Status |
---|---|---|---|---|
SEP-Z | 2015 | Non-native | Established |
Occurrence Map
OCC_ID | Author | Year | Date | Locality | Status | Latitude | Longitude |
---|
References
Aron, Simone; Sole-Cava, Antonio (1991) Genetic evaluation of the taxonomic status of two varieties of the cosmopolitan Botryllus niger (Ascidiaceae: Botryllidae), Biochemical Systematics and Ecology 19(4): 271-276Baker, H. R. (1984) Diversity and zoogeography of marine Tubificidae (Annelida, Oligochaeta), with notes on variation in widespread species, Hydrobiologia 115: 191-196
Barnes, Robert D. (1983) Invertebrate Zoology, Saunders, Philadelphia. Pp. 883
Bastida-Zavala, Rolando; de León-González, Jesús Ángel; Carballo Cenizo, José Luis; Moreno-Dávila, Betzabé (2014) [Aquatic Invasive Species in Mexico], Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, <missing place>. Pp. 317-336
Blanco, Andreu; Beger, Maria; Olabarria, Celia (2021) First confirmed occurrence of Codium fragile (Suringar) Hariot in the Iberian Peninsula coast of Portugal, BioInvasions Records 10: <missing location>
Brunetti. R.; Mastrototaro, F. (2012) Botrylloides pizoni, a new species of Botryllinae (Ascidiacea) from the Mediterranean Sea, Zootaxa 3258: 28-36
California Department of Fish and Wildlife (2014) Introduced Aquatic Species in California Bays and Harbors, 2011 Survey, California Department of Fish and Wildlife, Sacramento CA. Pp. 1-36
da Rocha, Rosana M.; Costa, Luciana (2005) Ascidians (Urochordata: Ascidiacea) from Arriaal do Cabo, Rio de Janeiro, Brazil., Iheringia Series Zoologie 95(1): 57-64
da Rocha, Rosana M.; Kremer, Laura P.; Baptista, Mariah S.; Metri, Rafael (2009) Bivalve cultures provide habitat for exotic tunicates in southern Brazil., Aquatic Invasions 4(1): 195-205
de Rivera, Catherine, and 27 authors (2005) Broad-scale non-indigenous species monitoring along the West Coast in National Marine Sanctuaries and National Estuarine Research Reserves report to National Fish and Wildlife Foundation, National Fish and Wildlife Foundation, Washington, D.C.. Pp. <missing location>
Fisheries and Oceans Canada 2018b Haplosporidium costale (SSO) of Oysters. https://www.dfo-mpo.gc.ca/science/aah-saa/diseases-maladies/hcoy-eng.html
Florida Museum of Natural History 2009-2013 Invertebrate Zoology Master Database. <missing URL>
Huang, Xuguang, Bingyu;; Guo, Donghu; Zhong;, Yanping; Li, Shunxing; Liu, Xin;; Laws, Edward A.; Huang, Bangqin (2021) Blackfordia virginica blooms shift the trophic structure to smaller size plankton in subtropical shallow waters, Marine Pollution Bulletin 182(111990): Published online
Lambert, Charles C; Lambert, Gretchen (2003) Persistence and differential distribution of nonindigenous ascidians in harbors of the Southern California Bight., Marine Ecology Progress Series 259: 145-161
Lins, Daniel M. ; Rocha, Rosana M. (2023) Marine aquaculture as a source of propagules of invasive fouling species , Polar Biology 11(e5456): Published online
Monniot, Claude; Monniot, Francoise; Griffiths, Charles; Schleyer, Michael (2001) South African Ascidians., Annals of the South African Museum 108(1): 1-141
Monniot, Francoise; Monniot, Claude (2001) Ascidians from the tropical western Pacific., Zoosystema 23(2): 201-383
Montanaro, Renee C.; O’Connor, Nancy J. (2024) Temporal and spatial refugia modify predation risk for non-native crabs in rocky intertidal habitats, PeerJ 22(e16852): Published online
DOI 10.7717/peerj.16852
New Zealand, Ministry of Primary Industries 2015 <em>Botrylloides giganteum</em> (Sea Squirt). <missing URL>
Nydam, Marie L.; Lemmon, Alan R.; Cherry, Jesse R.; Michelle L. Kortyna3, Clancy, Darragh L.; Hernandez, Cecilia;; Cohen, C. Sarah (2021) Phylogenomic and morphological relationships among the botryllid ascidians (Subphylum Tunicata, Class Ascidiacea, Family Styelidae), Scientific Reports 11(8351): Published online
Quintanilla, Elena; Thomas Wilke; Ramırez-Portilla, Catalina; Sarmiento, Adriana; Sanchez, Juan A. () , None <missing volume>: <missing location>
Quintanilla, Elena; Thomas Wilke; Ramırez-Portilla, Catalina; Sarmiento, Adriana; Sanchez, Juan A.2017 (2017) Taking a detour: invasion of an octocoral into the Tropical Eastern Pacific, Biological Invasions <missing volume>(17): 2583–2597
DOI 10.1007/s10530-017-1469-2
Riding, Tim; Morrisey, Don; Wilkens, Serena; Inglis, Graeme (2014) Marine and freshwater: Marine surveillance annual report, Surveillance 41(3): 59-62
Rodrigues, S. A.; da Rocha, R. M. (1993) Littoral compound Ascidians (Tunicata) from Sao Sebastiao, Estado de Sao Paulo, Brazil., Proceedings of the Biological Society of Washington 106: 728-739
Rodriguez, Laura F. (2006) Can invasive species facilitate native species? Evidence of how, when, and why these impacts occur., Biological Invasions 8: 927-939
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(2): 337-343
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>
Ryland, John S. (2015) Gender of the genus Botrylloides Milne Edwards (1841) [Tunicata: Ascidiacea], Zootaxa 3973(2): 398-400
Simkanin, Christina; Fofonoff, Paul W.; Larson, Kriste; Lambert, Gretchen; Dijkstra, Jennifer A.; Ruiz, Gregory M. (2016) Spatial and temporal dynamics of ascidian invasions in the continental United States and Alaska, Marine Biology 163: Published online
U.S. National Museum of Natural History 2002-2021 Invertebrate Zoology Collections Database. http://collections.nmnh.si.edu/search/iz/
Van Name, Willard G. (1945) The North and South American ascidians, Bulletin of the American Museum of Natural History 84: 1-462