Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-27T07:51:04.707Z Has data issue: false hasContentIssue false
  • English
  • Français

Sabellaria nanella (Sabellariidae): from solitary subtidal to intertidal reef-building worm at Monte Hermoso, Argentina (39°S, south-west Atlantic)

Published online by Cambridge University Press:  04 September 2012

Claudia Bremec ,
Cecilia Carcedo ,
M. Cintia Piccolo ,
Eder dos Santos  and
Sandra Fiori
Claudia Bremec
Affiliation:
Instituto Nacional de Investigación y Desarrollo Pesquero (INIDEP)–Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)–Instituto de Investigaciones Marinas y Costeras (IIMC, UNMP–CONICET)
Cecilia Carcedo
Affiliation:
Instituto Argentino de Oceanografía (IADO)–Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Avenida Rivadavia, 1917 C1033AAJ CABA, Argentina
M. Cintia Piccolo
Affiliation:
Instituto Argentino de Oceanografía (IADO)–Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Avenida Rivadavia, 1917 C1033AAJ CABA, Argentina Universidad Nacional del Sur (UNS)
Eder dos Santos
Affiliation:
Instituto Argentino de Oceanografía (IADO)–Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Avenida Rivadavia, 1917 C1033AAJ CABA, Argentina
Sandra Fiori*
Affiliation:
Instituto Argentino de Oceanografía (IADO)–Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Avenida Rivadavia, 1917 C1033AAJ CABA, Argentina Universidad Nacional del Sur (UNS)
*
Correspondence should be addressed to: S. Fiori, Instituto Argentino de Oceanografía (IADO)–Consejo, Nacional de Investigaciones Científicas y Técnicas (CONICET), Avenida Rivadavia, 1917 C1033AAJ CABA, Argentina email: sfiori@criba.edu.ar
Get access Rights & Permissions [Opens in a new window]

Abstract

This contribution reports the first record of intertidal reefs built by the sabellariid worm Sabellaria nanella in the lower intertidal at Monte Hermoso beach, Argentina (39°S). All previous records of S. nanella in the study area correspond to solitary individuals from shallow subtidal depths in coastal environments, while the present findings refer to well established reefs on stony rocks. Worms sort medium size sand grains to build the reefs, which contain higher amount of organic matter than the surrounding sediments. Size structure of worms shows multiple size cohorts that include recent recruits and mature adults. Many invertebrates, i.e. various annelids, arthropods, molluscs, nemerteans and nematodes, are the frequent organisms living within the reef, some of them already recorded in the area. The presence of intertidal reefs of S. nanella indicates that the species has plasticity to adapt to environments with different physical conditions (subtidal–intertidal areas).

Keywords

Sabellaria nanellareefsintertidalArgentinasouth-west Atlantic
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 93 , Issue 1 , February 2013 , pp. 81 - 86
Copyright
Copyright © Marine Biological Association of the United Kingdom 2012

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Adami, M.L., Tablado, A. and López-Gappa, J. (2004) Spatial and temporal variability in intertidal assemblages dominated by the mussel Brachidontes rodriguezzii (d'Orbigny, 1846). Hydrobiologia 520, 49–59.CrossRefGoogle Scholar
Botello, G and Krug, P.K. (2006) ‘Desperate larvae’ revisited: age, energy and experience affect sensitivity to settlement cues in larvae of the gastropod Alderia sp. Marine Ecology Progress Series 312, 149–159.CrossRefGoogle Scholar
Bremec, C. and Giberto, D. (2004) New records of two species of Sabellaria (Polychaeta, Sabellariidae) from the Argentinean Biogegraphic Province. Revista de Biología Marina y Oceanografia 39, 101–105.Google Scholar
Bremec, C. and Giberto, D. (2006) Polychaetes assemblages in the Argentinean Biogeographical Province (34°–38°S). Scientia Marina 70, 249–257.CrossRefGoogle Scholar
Bremec, C. and Lana, P. (1994) New records of Sabellariidae (Annelida, Polychaeta) from Argentina. Neritica 8, 47–53.Google Scholar
Caline, B., Gruet, I., Legendre, C., Le Rhun, J., L'Homer, A., Mathieu, R and Zbinden, R. (1992) The Sabellariid reefs in the Bay of Mont Saint-Michel, France. Ecology, geomorphology, sedimentology and geologic implications. Contributions to Marine Science 1, 1–156.Google Scholar
Caló, J., Fernández, E., Marcos, A., Aldacour, H. and Varela, P. (2000) Comparación del efecto de dos tormentas en la ciudad de Monte Hermoso. Argentina. Geoacta 25, 40–48.Google Scholar
Caló, J., Fernández, E., Marcos, A. and Aldacour, H. (2005) Observaciones litorales ambientales de olas, corrientes y vientos de la playa de Monte Hermosos entre 1996 y 1999. Geoacta 30, 27–38.Google Scholar
Chiaradia, N., Marchesi, C., Azzone, D., San Martin, A., Giberto, D., Bremec, C. and Elías, R. (2007) An unexpected reef-building worm in Mar del Plata, Argentina (SW Atlantic). Abstract in 9th International Polychaete Conference, 12–17 August, Maine, USA.Google Scholar
Culloty, S., Favier, E., Riada, M., Ramsay, N. and O'Riordan, R. (2010) Reproduction of the biogenic reef-forming honeycomb worm Sabellaria alveolata in Ireland. Journal of the Marine Biological Association of the United Kingdom 90, 503–507.CrossRefGoogle Scholar
Eckelbarger, K. (1977) Larval development of Sabellaria floridenis from Florida and Phragmatopoma californica from Southern California (Polychaeta: Sabellariidae), with a key to the sabellariid larvae of Florida and a review of development in the family. Bulletin of Marine Science 27, 241–255.Google Scholar
Elías, R. and Bremec, C. (2004) Poliquetos. In Boschi, E.E. and Cousseau, M.B. (eds) La vida entre mareas: vegetales y animales de las costas de Mar del Plata, Argentina. Mar del Plata: Publicaciones especiales INIDEP, pp. 123–130.Google Scholar
Elkin, E. and Marshall, D.J. (2007) Desperate larvae: influence of deferred costs and habitat requirements on habitat selection Marine Ecology Progress Series 335, 143–153.CrossRefGoogle Scholar
Fiori, S.M. (2002) Ecalogía poblacional de la almeja amarilla (Mesodesma mactroides) en el extremo austral de su distribución. PhD thesis. Universidad Nacional del Sur, Bahia Blanca, Argentina, 138 pp.Google Scholar
Folk, R.L. and Ward, W. (1957) Brazos River Bar: a study in the significance of grain size parameters. Journal of Sedimentary Petrology 27, 3–26.CrossRefGoogle Scholar
Giangrande, A. (1997) Polychaete reproductive patterns, life cycles and life histories: an overview. Oceanography and Marine Biology: an Annual Review 35, 323–386.Google Scholar
Gilmore, R. (1977) Fishes of the Indian River lagoon and adjacent waters, Florida. Bulletin of the Florida State Museum, Biological Science 22, 101–147.Google Scholar
Gore, R., Scotto, L. and Becker, L. (1978) Community composition, stability, and trophic partitioning in decapod crustaceans inhabiting some subtropical sabellariid worm reefs: studies on decapod Crustacea from the Indian River region of Florida. IV. Bulletin of Marine Science 28, 221–248.Google Scholar
Gruet, Y. (1986) Spatio-temporal changes of sabellarian reefs built by the sedentary polychaete Sabellaria alveolata (Linné). Marine Ecology (P.S.Z.N.) 7, 303–319.CrossRefGoogle Scholar
Hutchings, P. (2000) Family Sabellariidae. In Beesley, P., Ross, G. and Glasby, C.J. (eds) Polychaetes and allies: the southern synthesis. Fauna of Australia, volume 4. Polychaeta, Myzostomida, Pogonophora, Echiura, Sipuncula. Melbourne: CSIRO Publishing, pp. 215–218.Google Scholar
Jaubet, M.L., Sánchez, M.A., Rivero, M.S., Garaffo, G.V., Vallarino, E.A. and Elías, R. (2011) Intertidal biogenic reefs built by the polychaete Boccardia proboscidea in sewage-impacted areas of Argentina, SW Atlantic. Marine Ecology: an Evolutionary Perspective 32, 188–197. doi: 10.1111/j.1439-0485.2010.00415.x.CrossRefGoogle Scholar
Kirtley, D. (1968) The reef builders. Natural history. Journal of the American Museum of Natural History 77, 40–55.Google Scholar
Kirtley, D. (1994) A review and taxonomic revision of the Family Sabellariidae Johnston, 1865 (Annelida; Polychaeta). Vero Beach, FL: Sabecon Press Science Series, 223 pp.Google Scholar
La Porta, B. and Nicoletti, L. (2009) Sabellaria alveolata (Linnaeus) reefs in the central Tyrrhenian Sea (Italy) and associated polychaete fauna. Zoosymposia 2, 527–536.CrossRefGoogle Scholar
Lana, P. and Bremec, C. (1994) Sabellariidae (Annelida, Polychaeta) from South America. In Dauvin, J.C., Laubier, L. and Reish, D.J. (eds) Actes de la 4ème Conférence Internationale des Polychètes. Memoires du Muséum National d'Histoire Naturelle 162, 211–222.Google Scholar
Lindeman, K.C. and Snyder, D.B. (1999) Nearshore hardbottom fishes of southeast Florida and effects of habitat burial caused by dredging. Fisheries Bulletin 97, 508–525.Google Scholar
Morgado, E. and Tanaka, M. (2001) The macrofauna associated with the bryozoan Schizoporella serrata (Walters) in southern Brazil. Scientia Marina 65, 173–181.CrossRefGoogle Scholar
Nelson, W. and Demetriades, L. (1992) Peracarids associated with sabellariid worm rock (Phragmatopoma lapidosa Kinberg) at Sebastian Inlet, Florida, U.S.A. Journal of Crustacean Biology 12, 647–654.CrossRefGoogle Scholar
Obenat, S. (2002) Estudios ecológicos de Ficopomatus enigmaticus (Polychaeta: Serpulidae) en la laguna Mar Chiquita, Buenos Aires, Argentina. PhD thesis. University of Mar del Plata, Mar del Plata, Argentina.Google Scholar
Olivier, S., Escofet, A., Orensanz, J.M., Pezzani, S., Turró, A.M. and Turró, M. (1966) Contribución al conocimiento de las comunidades bentónicas de Mar del Plata. I. El litoral rocoso entre Playa Grande y Playa Chica. Anales de la Comisión de Investigaciones Científicas de la Provincia de Buenos Aires 7, 185–206.Google Scholar
Pawlik, J.R. (1988) Larval settlement and metamorphosis of sabellariid polychaetes with special reference to Phragmatopoma lapidosa, a reef building species, and Sabellaria floridens, a non-gregarious species. Bulletin of Marine Science 43, 41–60.Google Scholar
Pawlik, J.R., Butman, C.A. and Starczak, V.R. (1991) Hydrodynamic facilitation of gregarious settlement of a reef-building tube worm. Science 251, 421–424.CrossRefGoogle ScholarPubMed
Pérez, C.D., Vila-Nova, D. and Santos, A.M. (2005) Associated community with the zoanthid Palythoa caribaeorum (Duchassaing and Michelotti, 1860) (Cnidaria, Anthozoa) from littoral of Pernambuco, Brazil. Hydrobiologia 548, 207–215.CrossRefGoogle Scholar
Posey, M., Pregnall, A. and Graham, R. (1984) A brief description of a subtidal sabellariid (Polychaeta) reef on the southern Oregon coast. Pacific Science 38, 28–33.Google Scholar
Rouse, G. and Fauchald, K. (1997) Cladistics and polychaetes. Zoologica Scripta 26, 139–204.CrossRefGoogle Scholar
Santos, A.S., Riul, P., Brasil, A. and Christofferesen, M. (2010) Encrusting Sabellariidae (Annelida: Polychaeta) in rhodolith beds, with description of a new species of Sabellaria from Brazilian coast. Journal of the Marine Biological Association of the United Kingdom 91, 425–438.CrossRefGoogle Scholar
Toonen, R.J. and Pawlik, J.R. (1994) Foundations of gregariousness. Nature (London) 370, 511–512.CrossRefGoogle Scholar
Toonen, R.J. and Tyre, A.J. (2007) If larvae were smart: a simple model for optimal settlement behavior of competent larvae. Marine Ecology Progress Series 349, 43–61.CrossRefGoogle Scholar
Uebelacker, J.M. (1984) Family Sabellariidae. In Uebelacker, J.M and Johnson, P.G. (eds) Taxonomic guide to the polychaetes of the northern Gulf of Mexico. Barry Matarie, LA: A. Vittor & Associates, Inc., 7:49.1–49.10Google Scholar
Vallarino, E.A. (2002) La comunidad bentónica intermareal de Brachidontes rodriguezii (D'orb.) y su relación con el efluente cloacal de la ciudad de Mar del Plata (38°S). PhD thesis. University of Mar del Plata, Mar del Plata, Argentina.Google Scholar
Vaquero, M.C., Pascale, J.C. and Ercolani, P. (2004) Comunidad–Municipio–Universidad. Propuesta de desarrollo turístico. Estudio de caso: Municipio de Monte Hermoso. Aportes y Transferencias 8, 75–88.Google Scholar
Walkley, A. and Black, C.A. (1965) Organic carbon. In Black, C.A. (ed.) Methods of soil analysis. Madison, WI: American Society of Agronomy, pp. 1372–1375.Google Scholar
Wilson, D.P. (1971) Sabellaria colonies at Duckpool, North Cornwall, 1961–1970. Journal of the Marine Biological Association of the United Kingdom 51, 509–580.CrossRefGoogle Scholar
Zale, A. and Merrifield, S. (1989) Species profiles: life histories and environmental requirements of coastal fishes and invertebrates (South Florida). Reef building tube worm. Biological Report of the Army Corps of Engineers 82, 1–12.Google Scholar