Ficopomatus miamiensis ( Treadwell, 1934 )
publication ID |
https://doi.org/ 10.5852/ejt.2017.344 |
publication LSID |
lsid:zoobank.org:pub:27AA4538-407D-470A-8141-365124193D85 |
DOI |
https://doi.org/10.5281/zenodo.3851353 |
persistent identifier |
https://treatment.plazi.org/id/794587B2-FFD3-FFA8-FDD8-F98FFBE1FD6A |
treatment provided by |
Carolina |
scientific name |
Ficopomatus miamiensis ( Treadwell, 1934 ) |
status |
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Ficopomatus miamiensis ( Treadwell, 1934) View in CoL
Figs 2 View Fig I–K, 3
Sphaeropomatus miamiensis Treadwell, 1934: 339–341 View in CoL ; figs 1–5 (type locality: Miami River, Florida, United States).
Mercierellopsis prietoi Rioja, 1945: 413–417 View in CoL , pl. I, figs 1–20, pl. II, figs 21–23 (type locality: Larios Estuary, Tecolutla and Carmen Lagoon, Veracruz, eastern Mexico; also from Barra de Nautla, Veracruz; in brackish water, on mangrove roots, Ostrea View in CoL and other bivalves).
Ficopomatus miamiensis View in CoL – ten Hove & Weerdenburg 1978: 106 –109, figs 1f–i, 3c, 4h–i, q, v–w, eeii, xx, 5a–b (revision of the genus and specimens from Florida, Louisiana, Jamaica, Barbados, Cura ҫao, Belize, and Canal Zone of Pacific Panama; in brackish water, 2.5–31‰, intertidal to 1 m, on the carapace of Macrobrachium jamaicensis Gundlach, 1887 , now M. carcinus (Linnaeus, 1758) View in CoL , shell of Isognomon alatus (Gmelin, 1791) , pebbles, limestone boulders on sandy mud and Caulerpa View in CoL ). — Perkins 1998: 95 (checklist of shallow-water polychaetes from Florida). — Bastida-Zavala & Salazar-Vallejo 2000a: 813, fig. 4i–s (eastern Mexico: Tecolutla, Veracruz and Chetumal Bay, Mexican Caribbean; on oysters and docks). — Bastida-Zavala & ten Hove 2003: 92 (probably from Costa Rica; on mangrove oysters, Ostrea iridiscens , now Striostrea prismatica (Gray, 1825) View in CoL and Crassostrea columbiensis (Hanley, 1846) View in CoL , with Hydroides humilis ( Bush, 1905) View in CoL and Spirobranchus minutus ( Rioja, 1941b)) View in CoL . — Bastida-Zavala 2008: 19 –21, fig. 5B–D (Sinaloa, Mexican Pacific and Canal Zone of Pacific Panama). — Tovar-Hernández et al. 2009: 327 – 328, figs 3g–i, 6a, 7a–c (as an invasive species in Mazatlán, Sinaloa, Mexican Pacific). — Tovar-Hernández et al. 2012: 12, figs a–e (Gulf of California: La Paz, Baja California Sur).
Material examined
224 specimens: JX (4) Aug. 2001, IR (92) Aug. 2005, BB (65) Aug. 2004, TB (10) Jul. 2002, PB (24) Aug. 2002, GB (27) Sep. 2002, CC (2) Sep. 2002.
Additional material
More than 160 specimens: ECOSUR s.n., 129+ specimens (Chetumal Bay, pier, 1990–1996, coll. S.I. Salazar-Vallejo et al.); UMAR-Poly 51, 10+ specimens (23°09' N, 106°19' W, Urias estuary, Mazatlán, Mexico, 1999, coll. N. Méndez); USNM 58659, 20+ specimens (approx. 8°59'40" N, 79°35'20" W, Miraflores Spillway, Canal Zone, Panama City, Panama, sta. 130–5, “on bottom, standing water”, 2 Apr. 1973, coll. M.L. Jones et al.).
Diagnosis
This species is gregarious and can form colonies. Tube white, with small peristomes; without transverse ridges, longitudinal ridges or alveoli ( Fig. 2I View Fig ). Opercular peduncle smooth, white. Operculum spherical or with a flat end-plate, never with spines ( Fig. 2 View Fig J–K). Thoracic membranes not fused dorsally. Special collar chaetae coarsely serrated.
Measurements: Total length = 6.2 mm (n = 10, r: 2.6–11.9, SD = 2.9); thorax length = 1.6 mm (n = 13, r: 0.7–3.2, SD = 0.6), thorax width = 0.6 mm (n = 13, r: 0.4–0.9, SD = 0.2); peduncle and operculum length = 1.3 mm (n = 13, r: 0.6–2.8, SD = 0.6); operculum length = 0.6 mm (n = 13, r: 0.3–0.9, SD = 0.2); operculum diameter = 0.4 mm (n = 13, r: 0.2–0.7, SD = 0.2).
Taxonomic remarks
Ficopomatus miamiensis has a spherical ( Fig. 2J View Fig ), slightly convex ( Fig. 2K View Fig ) or flat operculum that lacks spines, while, the other two species of Ficopomatus recorded as NIS in the United States have spines on the operculum ( Fig. 2G View Fig , M–N).
The native distribution of F. miamiensis is assumed to be the Gulf of Mexico and Caribbean Sea. The NIS records from Urías Estuary, Sinaloa, Mexican Pacific ( Salgado-Barragán et al. 2004; Tovar-Hernández et al. 2009), were likely due to the accidental introduction of larvae included in the water with shrimp transported from the Gulf of Mexico for aquaculture, or as adults encrusting bivalves moved from the Gulf of Mexico to Sinaloa, Mexican Pacific, with oysters for oyster culture, while the specimens recorded from Pacific Panama ( Bastida-Zavala 2008) and Costa Rica ( Bastida-Zavala & ten Hove 2003: 92) presumably invaded following transport by ballast water or by oyster translocation. Recently, F. miamiensis was found in La Paz, Baja California Sur, Gulf of California ( Tovar-Hernández et al. 2012).
Ecology
Intertidal to sublittoral (3 m). On mangrove roots, oysters, shrimp carapace, algae, and rocky and artificial substrates ( ten Hove & Weerdenburg 1978).
Distribution
Gulf of Mexico and Caribbean Sea, in tropical brackish water lagoons and the mouth of rivers. Also recorded from the Pacific side of the Canal Zone of Panama ( Bastida-Zavala 2008) and Urías Estuary, Sinaloa, Mexican Pacific, as an invasive species ( Tovar-Hernández et al. 2009). In this work, Ficopomatus miamiensis was found abundantly on fouling plates from the Indian River, Biscayne Bay and Pensacola Bay, Florida, and Galveston Bay, Texas; and occasionally from Jacksonville and Tampa Bay, Florida, and Corpus Christi, Texas ( Fig. 3 View Fig ). This species extends its westward range from Lake Pontchartrain, Louisiana ( ten Hove & Weerdenburg 1978) to Galveston Bay, Texas (500 km).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Genus |
Ficopomatus miamiensis ( Treadwell, 1934 )
Bastida-Zavala, J. Rolando, McCANN, Linda D., Keppel, Erica & Ruiz, Gregory M. 2017 |
Mercierellopsis prietoi
Rioja E. 1945: 417 |
Sphaeropomatus miamiensis
Treadwell A. L. 1934: 341 |
Ficopomatus miamiensis
ten Hove & Weerdenburg 1978: 106 |
Perkins 1998: 95 |
Bastida-Zavala & Salazar-Vallejo 2000a: 813 |
Bastida-Zavala & ten Hove 2003: 92 |
Bastida-Zavala 2008: 19 |
Tovar-Hernández et al. 2009: 327 |
Tovar-Hernández et al. 2012: 12 |