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Neanthes rubicunda (Polychaeta: Nereididae) in the current-swept slope of the Strait of Messina (Mediterranean Sea)

Published online by Cambridge University Press:  17 October 2014

Andrea Cosentino ,
Grazia Cantone  and
Salvatore Giacobbe
Andrea Cosentino*
Affiliation:
Department of Biological and Environmental Sciences, University of Messina, Viale Stagno d'Alcontres, 32–98166Sant'Agata, Messina, Italy
Grazia Cantone
Affiliation:
Department of Biological, Geological and Environmental Sciences, University of Catania, Via Androne, 81–95124Catania, Italy
Salvatore Giacobbe
Affiliation:
Department of Biological and Environmental Sciences, University of Messina, Viale Stagno d'Alcontres, 32–98166Sant'Agata, Messina, Italy
*
Correspondence should be addressed to: A. Cosentino, Department of Biological and Environmental Sciences, University of Messina, Viale Stagno d'Alcontres, 32–98166Sant'Agata, Messina, Italy email: [email protected]
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Abstract

Neanthes rubicunda is a little-known nereidid species, with an east Atlantic, Mediterranean and north-west Indian Ocean distribution. The species was investigated in the Strait of Messina (Italy) from 1993 to 2008 during two ship grab and dredge sampling surveys, and ad hoc SCUBA diving, which provided data on its mesoscale and microscale distribution patterns. Depth distribution was shallower (from 4 to 60 m) and average individual size was more than 50% greater with respect to other Mediterranean populations. The species had average density of 4.1 ± 2.7 ind m−2, from a minimum of 0.15 ind m−2 within 20 m depth to a maximum of 16 ind m−2 up to 60 m. The distribution was asymmetrical on the opposite coastal sides of the Strait of Messina, in accordance with local hydrology and sea floor morphology. Coarse, current-swept sediments represent the elective habitat of N. rubicunda, whose settlement beneath and in the upper side of boulders might represent a strategy to contrast sea floor instability. Gut content, mainly constituted by algal thalli (90%) proved Halopteris filicina, Halopteris scoparia and Jania rubens the most frequently ingested seaweeds. Such algae were also found attached to the worm tube-opening, testifying for an algal-gardening behaviour with a prevalent trophic function. Fertile individuals were observed in May, June and July (sea temperature from 17 to 21°C).

Keywords

Neanthes rubicundaautoecologydistribution patternsfeedinggardening behaviourcoralligenous habitat
Type
Research Article
Information
Marine Biodiversity Records , Volume 7 , 2014 , e117
Copyright
Copyright © Marine Biological Association of the United Kingdom 2014 

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References

REFERENCES

Arvanitidis, C. (2000) Polychaete fauna of the Aegean Sea: inventory and new information. Bulletin of Marine Science 66, 73–96.Google Scholar
Azzaro, F., Decembrini, F., Raffa, F. and Crisafi, E. (2007) Seasonal variability of phytoplankton fluorescence in relation to the Straits of Messina (Sicily) tidal upwelling. Ocean Science 3, 451–460.CrossRefGoogle Scholar
Bakken, T., Glasby, C.J. and Wilson, R.S. (2009) A review of paragnath morphology in Nereididae (Polychaeta). Zoosymposia 2, 305–316.CrossRefGoogle Scholar
Ballesteros, E. (2006) Mediterranean coralligenous assemblages: a synthesis of present knowledge Oceanography and Marine Biology: an Annual Review 44, 123–195.Google Scholar
Berke, S.K. and Woodin, S.A. (2008) Tube decoration may not be cryptic for Diopatra cuprea (Polychaeta: Onuphidae). Biological Bulletin. Marine Biological Laboratory, Woods Hole 214, 50–56.CrossRefGoogle Scholar
Branch, G.M., Harris, J.M., Parkins, C., Bustamante, R.H. and Eekhout, S. (1992) Algal ‘gardening’ by grazers: a comparison of the ecological effects of territorial fish and limpets. In John, D.M., Hawkins, S.J. and Price, J.H. (eds) Plant–animal interactions in the marine benthos. Systematics Association Special Volume 46. Clarendon Press, Oxford, pp. 405–423.CrossRefGoogle Scholar
Cammen, L.M. (1980) The significance of the microbial carbon in the nutrition of the deposit feeding polychaete Nereis succinea . Marine Biology 61, 9–20.CrossRefGoogle Scholar
Cantone, G. (2003) Distribution of benthic polychaetous annelids in the Adriatic Sea with zoogeographic considerations. Biogeographia 24, 169–193.Google Scholar
Carlier, A., Riera, P., Amouroux, J.-M., Bodiou, J.-Y. and Grémare, A. (2007) Benthic trophic network in the Bay of Banyuls-sur-Mer (northwest Mediterranean, France): an assessment based on stable carbon and nitrogen isotopes analysis. Estuarine, Coastal and Shelf Science 72, 1–15.CrossRefGoogle Scholar
Caron, A., Desrosiers, G., Olive, P.J.W., Retière, C. and Nozais, C. (2004) Comparison of diet and feeding activity of two polychaetes, Nephtys caeca (Fabricius) and Nereis virens (Sars), in an estuarine intertidal environment in Québec, Canada. Journal of Experimental Marine Biology and Ecology 304, 225–242.CrossRefGoogle Scholar
Castelli, A., Bianchi, C.N., Cantone, G., Çinar, M.E., Gambi, M.C., Giangrande, A., Lanera, P., Licciano, M., Musco, L., Sanfilippo, R. and Simonini, R. (2008) Annelida Polychaeta. In Checklist della Flora e della Fauna dei Mari Italiani. Biologia Marina Mediterranea 15, 323–373.Google Scholar
Çinar, M.E. (2005) Polychaetes from the coast of northern Cyprus (eastern Mediterranean Sea), with two new records for the Mediterranean Sea. Cahiers de Biologie Marine 46, 143–161.Google Scholar
Cosentino, A. and Giacobbe, S. (2006) A case study of mollusc and polychaete soft-bottom assemblages submitted to sedimentary instability in the Mediterranean Sea. Marine Ecology 27, 170–183.CrossRefGoogle Scholar
Dales, R.P. (1962) The polychaete stomatodeum and the interrelationship of the families of the Polychaeta. Proceedings of the Zoological Society of London 139, 389–428.CrossRefGoogle Scholar
Dauer, D.M. (1980) Population dynamics of the polychaetous annelids of an intertidal habitat in upper old Tampa Bay, Florida. Internationale Revue der gesamten Hydrobiologie und Hydrographie 65, 461–487.CrossRefGoogle Scholar
Dauer, D.M., Mahon, H.K. and Sardá, R. (2003) Functional morphology and feeding behavior of Streblospio benedicti and S. shrubsolii (Polychaeta: Spionidae). Hydrobiologia 496, 207–213.CrossRefGoogle Scholar
De Paiva, P.C. (1993) Trophic structure of a shelf polychaete taxocoenosis in southern Brazil. Cahiers de Biologie Marine 35, 39–55.Google Scholar
Di Geronimo, I. and Giacobbe, S. (1987) Cartes des biocénoses de Détroit de Messine. In Barrier, P., Di Geronimo, I. and Montenat, C. (eds) Bionomie des peuplements benthiques des substrats meubles et rocheux plio-quaternaires du Détroit de Messine. Document et Travaux, IGAL Institut Géologique Albert de Lapparent 11, Paris, pp. 153–169.Google Scholar
Drew, E.A., Ireland, J.F., Muir, C., Robertson, W.A.A. and Robinson, J.D. (1982) Photosynthesis, respiration and other factors influencing the growth of Laminaria ochroleuca Pyl. below 50 metres in the Strait of Messina. Marine Ecology 3, 335–355.CrossRefGoogle Scholar
Ehlers, E. (1864–1868) Die borstenwürmer (Annelida Chaetopoda) nach systematischen und anatomischen untersuchungen dargestellt. Leipzig: Engelmann, W. (ed.), pp. 529–533.CrossRefGoogle Scholar
Ergen, Z., Çinar, M.E. and Ergen, G. (2000) On the Nereididae (Polychaeta: Annelida) fauna of the Bay of Izmir. Zoology in the Middle East 21, 139–158.CrossRefGoogle Scholar
Esselink, P. and Zwarts, L. (1989) Seasonal trends in burrow depth and tidal variation in feeding activity of Nereis diversicolor . Marine Ecology Progress Series 56, 243–254.CrossRefGoogle Scholar
Fauchald, K. and Jumars, P.A. (1979) The diet of worms: a study of polychaete feeding guilds. Oceanography and Marine Biology: an Annual Review 17, 193–284.Google Scholar
Fauvel, P. (1914) Annélides polychètes non-pélagiques provenant des campagnes de l'Hirondelle et de la Princesse-Alice (1885–1910). Résultats des Campagnes Scientifiques du Prince de Monaco XLVI, 170–173.Google Scholar
Fauvel, P. (1923) Faune de France, 5: Polychètes errants. Paris: Office Central de Faunistique. Lechevalier, P. (ed.), pp. 340–342.Google Scholar
Fauvel, P. (1937) Les fonds de pèche prés d'Alexandrie. XI.—Annélides Polychètes. Direction des Recherches des Pêcheries. Notes and Mémoires 19, 1–60.Google Scholar
Fidalgo e Costa, P., Oliveira, R.F. and Da Fonseca, L.C. (2006) Feeding ecology of Nereis diversicolor (O.F. Müller) (Annelida, Polychaeta) on estuarine and lagoon environments in the southwest coast of Portugal. Pan-American Journal of Aquatic Sciences 1, 114–126.Google Scholar
Gambi, M.C., Zupo, V., Buia, M.C. and Mazzella, L. (2000) Feeding ecology of Platynereis dumerilii (Audouin & Milne-Edwards) in the seagrass Posidonia oceanica system: the role of the epiphytic flora (Polychaeta, Nereididae). Ophelia 53, 189–202.CrossRefGoogle Scholar
Giaccone, G. (1987) Les algues rouges calcaires du seuil du Détroit de Messine. In Barrier, P., Di Geronimo, I. and Montenat, C. (eds) Bionomie des peuplements benthiques des substrats meubles et rocheux plio-quaternaires du Détroit de Messine. Document et Travaux, IGAL Institut Géologique Albert de Lapparent 11, Paris, pp. 239–141.Google Scholar
Goerke, H. (1971) Die Ernährungsweise der Nereis-Arten (Polychaeta, Nereidae) der deutschen Küsten. Veröffentlichungen des Instituts für Meeresforschung in Bremerhaven 13, 1–50.Google Scholar
Grémare, A. (1988) Feeding, tube-building and particle-size selection in the terebellid polychaete Eupolymnia nebulosa . Marine Biology 97, 243–252.CrossRefGoogle Scholar
Jordana, E., Duchene, J.-C., Charles, F., Grémare, A. and Amouroux, J.-M. (2000) Experimental study of suspension-feeding activity in the serpulid polychaete Ditrupa arietina (O.F. Muller). Journal of Experimental Marine Biology and Ecology 252, 57–74.CrossRefGoogle Scholar
Jordana, E., Charles, F., Grémare, A., Amouroux, J.-M. and Chrétiennot-Dinet, M.-J. (2001) Food sources, ingestion and absorption in the suspension-feeding polychaete, Ditrupa arietina (O.F. Muller). Journal of Experimental Marine Biology and Ecology 266, 219–236.CrossRefGoogle Scholar
Licciano, M., Stabili, L. and Giangrande, A. (2005) Clearance rates of Sabella spallanzanii and Branchiomma luctuosum (Annelida: Polychaeta) on a pure culture of Vibrio alginolyticus . Water Research 39, 4375–4384.CrossRefGoogle ScholarPubMed
Mangum, C.P. and Cox, C.D. (1971) Analysis of the feeding response in the onuphid polychaete Diopatra cuprea (Bosc). Biological Bulletin. Marine Biological Laboratory, Woods Hole 140, 215–229.CrossRefGoogle Scholar
Mangum, C.P., Santos, S.L. and Rhodes, W.R. Jr (1968) Distribution and feeding in the onuphid polychaete, Diopatra cuprea (Bosc). Marine Biology 2, 33–40.CrossRefGoogle Scholar
Maurer, D. and Leathem, W. (1981) Polychaete feeding guilds from Georges Bank, USA. Marine Biology 62, 161–171.CrossRefGoogle Scholar
Miller, D.C., Bock, M.J. and Turner, E.J. (1992) Deposit and suspension feeding in oscillatory flows and sediment fluxes. Journal of Marine Research 50, 489–520.CrossRefGoogle Scholar
Muir, A.I., Smith, B.D. and García-Alonso, J. (2014) Neanthes nubila (Annelida: Polychaeta)—a review of its biogeography and breeding habits. Cahiers de Biologie Marine 55, 275–280.Google Scholar
Nash, R. and Keegan, F. (2003) Aspects of the feeding biology of the fanworm Bispira volutacornis (Polychaeta: Sabellidae). Journal of the Marine Biological Association of the United Kingdom 83, 453–456.CrossRefGoogle Scholar
Núñez, J. (1995) Aportaciones sobre cinco especies de Nereidos (Polychaeta, Nereidae) y clave para la identificacion de las especies presentes en Canarias. Vieraea 24, 71–85.Google Scholar
Núñez, J. (2004) Familia Nereididae Savigny, 1822. In Ramos, M.A. et al. (eds) Annelida, Polychaeta I. Fauna Iberica, 25. Madrid: Museo Nacional de Ciencias Naturales and CSIC, pp. 293–390.Google Scholar
Núñez, J. and Brito, M.C. (2006) A new species of Rullierinereis and new records of Nereididae from sublittoral sandy bottoms off Lanzarote (Canary Islands). In Sardá, R., San Martín, G., López, E., Martin, D. and George, D. (eds) Scientific advances in polychaete research. Barcelona: Institut de Ciènces del Mar, pp. 145–150.Google Scholar
Olivier, M., Desrosiers, G., Retiere, C. and Brethes, J.-C. (1993) Variations spatio-temporelles de l'alimentation du polychaete Nereis virens en zone intertidale (Estuaire maritime du Saint-Laurent, Québec). Vie et Milieu 43, 1–12.Google Scholar
Olivier, M., Desrosiers, G., Caron, A., Retière, C. and Caillou, A. (1997) Juvenile growth of Nereis diversicolor (O.F. Müller) feeding on a range of marine vascular and macroalgal plant sources under experimental conditions. Journal of Experimental Marine Biology and Ecology 208, 1–12.CrossRefGoogle Scholar
Pardo, E.V. and Dauer, D.M. (2003) Particle size selection in individuals from epifaunal versus infaunal populations of the nereidid polychaete Neanthes succinea (Polychaeta: Nereididae). Hydrobiologia 496, 355–360.CrossRefGoogle Scholar
Pardo, E.V. and Amaral, A.C.Z. (2006) Foraging and mobility in three species of Aciculata (Annelida: Polychaeta). Brazilian Journal of Biology 66, 1065–1072.CrossRefGoogle ScholarPubMed
Riisgård, H.U. (1994) Filter-feeding in the polychaete Nereis diversicolor: a review. Netherlands Journal of Aquatic Ecology 28, 453–458.CrossRefGoogle Scholar
Simboura, N. and Nicolaidou, A. (2001) The polychaetes (Annelida, Polychaeta) of Greece: checklist, distribution and ecological characteristics. Monographs on Marine Sciences 4, 1–115.Google Scholar
Sokal, R.R. and Rohlf, F.J. (1995) Biometry: the principles and practice of statistics in biological research. 3rd edition. New York: W.H. Freeman, 887 pp.Google Scholar
Taghon, G.L. and Greene, R.R. (1992) Utilization of deposited and suspended particulate matter by benthic ‘interface’ feeders. Limnology and Oceanography 37, 1370–1391.CrossRefGoogle Scholar
Taghon, G.L., Nowell, A.R.M. and Jumars, P.A. (1980) Induction of suspension feeding in spionid polychaetes by high particulate fluxes. Science 210, 562–564.CrossRefGoogle ScholarPubMed
Tsuchiya, M. and Kurihara, Y. (1979) The feeding and food sources of the deposit-feeding polychaete Neanthes japonica (Izuka). Journal of Experimental Marine Biology and Ecology 36, 79–89.CrossRefGoogle Scholar
Tzetlin, A. and Purschke, G. (2005) Pharynx and intestine. Hydrobiologia 535/536, 199–225.Google Scholar
Wilson, W.H. Jr and Ruff, R.E. (1988) Species profiles: life histories and environmental requirements of coastal fishes and invertebrates (North Atlantic). Sandworm and bloodworm. US Fish and Wildlife Service Biological Report 82(11.80)—US Army Corps of Engineers TR EL-82-4, 23 pp.Google Scholar
Woodin, S.A. (1977) Algal ‘gardening’ behavior by nereid polychaetes: effects on soft-bottom community structure. Marine Biology 44, 39–42.CrossRefGoogle Scholar