Invasion History

First Galapagos Record: 1987

General Invasion History:

Watersipora subtorquata is an encrusting bryozoan widely distributed around the globe. Its native range is poorly understood because of taxonomic confusion with related species, particularly W. subovoidea, which it has been lumped with in older literature as 'W. cucullata' (Gordon 1989; Gordon and Mawatari 1992), or by treating W. subovoidea as a synonym of W. subtorquata (Seo 1999). This species was described from Rio de Janeiro, Brazil (Gordon 1989). We regard it as cryptogenic in the western Atlantic, where early records (e.g., Osburn 1914, Dry Tortugas; Osburn 1940, Puerto Rico) refer to W. cucullata, and where it has also been recorded as W. subovoidea (Winston 1982). In recent collections, it has been identified in Jamaica (Creary 2003), Puerto Rico (in 2007, Ruiz et al. unpublished data), and in Florida: Biscayne Bay (in 2004, Ruiz et al. unpublished data), Indian River Lagoon (in 2007, Ruiz et al. unpublished data), and Jacksonville (in 2002, Ruiz et al. unpublished data). This bryozoan also occurs in the Southwest Atlantic, on the west coast of South Africa (Florence et al. 2007, cited by Mead et al. 2011b). We also consider it cryptogenic in the Northwest Pacific, where it has been reported from the Sea of Japan and East China Sea coasts of South Korea, the Yellow Sea coast of Korea and China, and the Pacific coast of Japan (Tokyo Bay and southward) south to the Paracel Islands in the South China Sea (Seo 1999; Huang 2001).

In California, molecular surveys identified two clades of Watersipora subtorquata (Clades A and B), and an additional species (Watersipora n. sp.). Clade A is widely distributed globally, including Australia, New Zealand, and South Korea. Clade B is known from China and California (Mackie et al. 2012). In California, Clade A occurred from San Diego to Humboldt Bay, but was most abundant in southern and central-region harbors. Clade B occurred over the same range, but was usually less dominant, and was very spotty in the northern part of the range (Mackie et al. 2012).

Watersipora subtorquata has been introduced to the Northeast Pacific (1st record 1888, Gulf of California, and Cabo San Lucas to Puget Sound, Cohen and Carlton 1995; Cohen 2005; Ruiz et al. unpublished data), much of the coast of Australia (1st record 1950, Sydney Harbor, Winston 1977), New Zealand (1st Record 1983, Gordon and Mawatari 1992), and the Atlantic coast of France (1st Record 1973, d'Hondt 1984, cited by Ryland et al. 2009). This organism has a short planktonic stage (Gordon and Mawatari 1992; Cohen and Carlton 1995) suggesting that ship fouling is its likeliest mode of transport to most locations. However, its appearances in France appear related to culture of the Pacific Oyster (Crassostrea gigas) (Ryland et al. 2009).

Invasion History in the Galapagos:

In 1987, Watersipora subtorquata was collected from a fishing boat in Academy Harbor, Santa Cruz Islands (Carlton, et al. 2019). In 2015 and 2016, W. subtorquata was found on fouling plates on Baltra and Santa Cruz Islands (McCann et al. 2019). Earlier in the 1930s, deep-water collections, identified as W. cucullata, refer to a different species (McCann et al. 2019).

Invasion history elsewhere in the world:

Since Watersipora subtorquata is a member of a complex of cryptic species, its native and introduced ranges are uncertain. Possible native regions include the tropical southwest Atlantic (type locality in Brazil), and the Indo-West Pacific (Vieira et al. 2014). It is found in many parts of the of the Mediterranean, from France to Egypt but the dates are unknown due to confusion with the native W. cucullata (Harmelin 2014; Vieira et al. 2014). In the eastern Atlantic, W. subtorquata was found in the Azores in 1888 (Chainho et al. 201), Madeira in 2006 (Canning-Clode et al. 2016), and South Africa (Florence et al. 2007; Mead et al. 2011). So far, specimens of Watersipora on the Atlantic coast of Europe (d'Hondt 1984; Ryland et al. 2009) have been identified or re-identified as W. subatra (Vieira et al. 2014). 

Watersipora subtorquata's occurrence in Europe was obscured by its confusion with W. subovoidea, but it was collected in the Bay of Arcachon, France on the Bay of Biscay in 1973 (d'Hondt 1984, cited by Ryland et al. 2009). It was collected again in the Bay of Arcachon in 2003, and in 1999–2007, found in many sites in Brittany and the Channel Islands (Ryland et al. 2009). Most of the collection sites were located near oyster-culture operations, and this species was most likely introduced to Europe with the Pacific Oyster (Crassostrea gigas) (Ryland et al. 2009). This bryozoan is also introduced on the west coast of South Africa (Florence et al. 2007, cited by Mead et al. 2011b).

Description

Watersipora subtorquata is an encrusting bryozoan, growing in single layers of flat substrates, but becomes multilamellar on rough substrates, and sometimes erect and leaf-like (foliaceous). Zooids are roughly elongate-rectangular, about twice as long as wide, being740–1,500 µm X 290–680 µm in size. The frontal shield is flat to slightly convex, perforated by numerous round pseudopores. Lateral-oral septulae (connecting the zooids) are absent. The orifice is slightly wider than the long, proximal edge, with a V-shaped or rounded sinus and approximately 130 x 260 (mean ~230) µm in size. It occupies less than 10% of the total zooid area with a well-defined proximal sinus demarcated by triangular condyles, ~55 × 115 µm (Ryland et al. 2009). The rim of the orifice has projecting proximo-lateral, and triangular condyles. The operculum has a dark central band and two lucida (transparent spots) adjacent to the condyles (Vieira et al. 2014). There are no oral spines or avicularia, and no ovicells. However, the zooids brood bright orange-red embryos internally. Colonies are orange to brownish-purple or black with dried or dead colonies becoming dark-orange or gray. (Description from Gordon and Mawatari 1992; Seo 1999; Ryland et al. 2009; Vieira et al. 2014). Colonies can become erect and leaf-like, with extensively overlapping calcareous crusts and curled edges. The crusts are often grayish black or dull orange, with bright orange (New Zealand) or purplish red (Korea) growing edges. The operculum is strongly pigmented with a dark, broad, biconcave band proximally, gradually spreading around paired clear areas. The polypides have orange lophophores 740 x 850 µm long, and 24 tentacles (Gordon 1989).  
 
NOTE: A recent revision of Watersipora taxonomy presented a drastic change in the nomenclature and worldwide biogeography of the genus. Vieira et al.'s (2014), map shows W. subtorquata as absent from the West Coast of North America and shows three species on the West Coast: W. subatraW. atrofusca, and W. arcuata, with W. subatra identified only from California and Pacific Mexico. Watersipora subtorquata is widely distributed in the tropical-subtropical Atlantic and Mediterranean, Red Sea, and Indo-West Pacific. Another previously identified species, W. subovoidea, has been abandoned and partially synonymized with an earlier name W. cucullata, a name until recently regarded as obsolete (Vieira et al. 2015). This worldwide revision of the genus is at odds with current molecular studies (Mackie et al. 2006; Mackie et al. 2012). Vieira et al.'s (2014) map includes only a small number of West Coast samples. A larger regional sample will be required to reconcile morphological and molecular taxonomy of Watersipora on the West Coast of North America. Until this is available, we will use the names W. subtorquata and Watersipora n. sp. in NEMESIS. 


Taxonomy

Taxonomic Tree

Kingdom:   Animalia
Phylum:   Bryozoa
Class:   Gymnolaemata
Order:   Cheilostomata
Suborder:   Ascophora
Family:   Watersiporidae
Genus:   Watersipora
Species:   subtorquata

Synonyms

Escharina torquata (d'Orbigny, 1542)
Watersipora cucullata (Marcus, 1937)
Watersipora subovoidea (d'Orbigny, 1852)

Potentially Misidentified Species

Watersipora subovoidea
Busk 1854. Now considered synonymous with W. cucullata. Described from the Mediterranean Sea, and largely distributed there (Vieira et al. 2014).

Watersipora arcuata
Banta 1969 Described from San Diego, where it was a recent introduction. Possibly native to tropical-subtropical East Pacific, introduced to Hawaii, Australia, and New Zealand (Banta 1969; Mackie et al. 2006; Mackie et al. 2012).

Watersipora atrofusca

Busk 1856. Reported only from Mazatlan, Mexico, and Califonria, little information available (Vieira et al. 2014).



Watersipora cucullata

Busk 1854, described from the Mediterranean Sea



Watersipora n. sp.
This newly identified, undescribed species is morphologically nearly identical to W. subtorquata but distinct at the molecular level (Mackie 2006; Mackie et al. 2012). So far, it is known only from California and South Korea.

Watersipora nigra

Described by Canu and Bassler 1930 as Pachycleithonia nigra from the Galapagos Islands, and moved into the genus Watersipora, by Vieira et al. (2014). It was not found in recent surveys (Carlton et al. 2019; Vieira et al. 2019).



Watersipora subatra

(d'Orbigny 1852) Described from the Aegean Sea. Re-described and redefined by Ryland et al. (2009). Watersipora subatra occurs in the Western Pacific from Japan to New Zealand as well as the West Coast.



Ecology

General:

Watersipora subtorquata is an encrusting, calcified bryozoan, composed of many individual zooids. The zooids feed by extending the ciliated tentacles of the lophophore as a funnel, creating a current and driving food particles into their mouths. The food is guided along the tentacles and through the pharynx by the cilia. Larger food particles can be moved or captured by flicking or contracting the tentacles (Barnes 1983). Watersipora subtorquata is known from pilings, rocks, shells, floats, oil platforms, ships' hulls, and fouling plates (Mackie et al. 2006; Page et al. 2006; Cohen and Zabin 2009; Ryland et al. 2009). 

 

Food:

Phytoplankton

Trophic Status:

Suspension Feeder

SusFed

Habitats

General HabitatCoarse Woody DebrisNone
General HabitatMarinas & DocksNone
General HabitatRockyNone
General HabitatVessel HullNone
General HabitatCoral reefNone
Salinity RangePolyhaline18-30 PSU
Salinity RangeEuhaline30-40 PSU
Tidal RangeSubtidalNone
Tidal RangeLow IntertidalNone
Vertical HabitatEpibenthicNone

Life History

Ecology- Watersipora arcuata is known from pilings, rocks, floats and ships' hulls (Banta 1969; Gordon and Mawatari 1992).


Tolerances and Life History Parameters

Minimum Temperature (ºC)6.7Field, based on coldest site in geographical range, Port Townsend WA (Zerebecki and Sorte 2011)
Maximum Temperature (ºC)30.6Field, based on warmest site in geographical range, Red Sea (Zerebecki and Sorte 2011)
Minimum Salinity (‰)25Field salinity (California) (Cohen 2005)
Maximum Salinity (‰)40Field salinity (Shark Bay, Western Australia) (Wyatt et al. 2005)
Minimum Duration0Larva- Cohen and Carlton 1995
Maximum Duration1Larva- Cohen and Carlton 1995
Broad Temperature RangeNoneWarm-Temperate-Tropical
Broad Salinity RangeNonePolyhaline-Euhaline

General Impacts

Watersipora subtorquata is an encrusting bryozoan widely distributed around the globe. Its colonies can be erect and leaf-like, with extensive overlapping calcareous crusts and curled edges, which create secondary habitat for the settlement of other marine invertebrates. Its native range is poorly understood because of taxonomic confusion with related species, particularly W. subatra. However, introduced populations have been recorded on the West coast of the United States, Hawaii, Australia, New Zealand, Europe, and South Africa. This species is known from rocks, oyster shells, pilings, floats, oil platforms, ships' hulls, and fouling plates. It is tolerant of copper and mercury antifouling paints and has outcompeted congeneric species in some areas of its introduced range.  

Economic Impacts Shipping and Boating- Watersipora spp. have long been known to be tolerant of copper and mercury in antifouling paint (Allen 1953; Ryland 1971; Piola and Johnston 2006). Their hard encrusting colonies are tolerant of moving water, and their colonies also provide non-toxic points of attachment for other organisms, allowing a diverse fouling community to develop (Floerl et al. 2004), which can adversely affect the speed and efficiency of ships. McKenzie et al. (2011) found that colonies from different sites varied in copper tolerance, and that tolerance was heritable in cultures. Colonies that produced large larvae tended to be more copper-tolerant (McKenzie et al. 2011).  

Ecological Impacts Competition- In New Zealand, W. subtorquata (arriving in 1983) quickly replaced W. arcuata at most locations (Gordon and Mawatari 1992). In Port Phillip Bay, Victoria, Australia W. subtorquata (arriving in 1976) also became the dominant Watersipora species (Keough and Ross 1999). In southern California, W. subtorquata was as of 2000–2003 the dominant or only form at several sites (Oceanside Harbor, Alamitos Bay, King Harbor; Geller et al. 2008 where W. arcuata was previously predominant (Banta 1969). Geller et al. (2008) suggest that W. subtorquata may be more competitive than W. arcuata in warm-temperate climates and may be expected to extend its range northward as the climate warms. Watersipora subtorquata was one of a group of seven non-native species in Bodega Harbor, most of which were rare or absent in 1970–1971 but were among the eight most abundant species in 2006. Spawning periods and abundance of species in this group appeared to be favored by a 1°C increase in average temperatures at this site over a 30-year period (Sorte and Stachowicz 2011).  

Habitat Change- Watersipora subtorquata colonies provide habitat for other organisms. Its colonies often develop elevated leaf-like folds rising above the substrate, creating additional space for colonization by other organisms. In Bodega Harbor, Geller et al. 2008 found where morphologically identical species (either W. subtorquata or Watersipora n. sp.) had more than 10% cover on fouling plates, native diversity was correlated with exotic diversity, as both groups of organisms occupied the expanded area (Sellheim et al. 2010). On the hulls of ships, and other surfaces treated with antifouling paints, W. subtorquata is often the only species able to settle, and its colonies provide surfaces on which more sensitive organisms can settle (Floerl et al. 2004). 


Regional Distribution Map

Bioregion Region Name Year Invasion Status Population Status
SEP-Z 1987 Def Estab

Occurrence Map

OCC_ID Author Year Date Locality Status Latitude Longitude

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