Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-27T19:16:13.418Z Has data issue: false hasContentIssue false

A new lessepsian species in the western Mediterranean (Brachidontes pharaonis Bivalvia: Mytilidae): density, resource allocation and biomass

Published online by Cambridge University Press:  28 January 2009

G. Sará*
Affiliation:
Dipartimento di Biologia Animale, Università di Palermo, Via Archirafi, 18, 90123 Palermo, Italy
C. Romano
Affiliation:
Dipartimento di Biologia Animale, Università di Palermo, Via Archirafi, 18, 90123 Palermo, Italy
A. Mazzola
Affiliation:
Dipartimento di Biologia Animale, Università di Palermo, Via Archirafi, 18, 90123 Palermo, Italy
*
Correspondence should be addressed to: G. Sarà, Dipartimento di Biologio Animale, Università di Palermo, Via Archirafi 18, 90123 Palermo, Italy email: [email protected]
Get access

Abstract

The present study reports on population dynamics and growth performance relative to a lesser known exotic invasive species (Brachidontes pharaonis) inhabiting the southern Mediterranean. The study was carried out in western Sicily, where B. pharaonis is present on both the submerged and emerged surfaces of a hyperhaline saltpan. Individuals were scraped, counted and measured for shell length, total weight, somatic, gonadic and shell biomass. Brachidontes pharaonis intensively colonized all hard substrates of the saltpan with annual average densities of 375 ± 293 ind. 400 cm−2 with density peaks in autumn as a function of habitat. The occurrence of juveniles was different for mediolittoral and infralittoral populations as was mean size, spawning periods and annual organic matter biomass. Organic matter allocated to the shells represented 56.4% (of the total), gonad allocation was 7.3%, while somatic allocation averaged 36.3% for both populations. Brachidontes pharaonis reached high individual density, rare among temperate members of the genus Mytilus in Mediterranean and European waters, but common in tropical dense mussel beds. Considering its invasive potential and the recent warming trend of the Mediterranean, in the future B. pharaonis may actively invade more habitats, threatening indigenous bivalve species which may be unable to compete with B. pharaonis in terms of reproductive effort and density.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2006

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

Abada-Boudjema, Y. and Dauvin, J. (1995) Recruitment and life span of two natural mussel populations Perna perna (Linneaus) and Mytilus galloprovincialis (Lamarck) from the Algerian Coast. Journal of Molluscan Studies 61, 467481.CrossRefGoogle Scholar
Allen, B.J. and Williams, S.L. (2003) Native eelgrass Zostera marina controls growth and reproduction of an invasive mussel through food limitation. Marine Ecology Progress Series 254, 5767.CrossRefGoogle Scholar
Ardizzone, G.D., Belluscio, A., Gravina, M.F. and Somaschini, A. (1996) Colonization and disappearance of Mytilus galloprovincialis Lam. on an artificial habitat in the Mediterranean Sea. Estuarine, Coastal and Shelf Science 43, 665676.CrossRefGoogle Scholar
Bayne, B.L. (1976) Marine mussels, their ecology and physiology. Cambridge: Cambridge University Press.Google Scholar
Carlton, J.T. (1992) Introduced marine and estuarine mollusks of North America: an end-of-the-20th-century perspective. Journal Shellfish Research 11, 489505.Google Scholar
Carlton, J.T. (1999) Molluscan invasions in marine and estuarine communities. Malacologia 41, 439454.Google Scholar
Ceccherelli, V.U. and Rossi, R. (1984) Settlement, growth and production of the mussel Mytilus galloprovincialis. Marine Ecology Progress Series 16, 173184.CrossRefGoogle Scholar
Dix, T.G. and Ferguson, A. (1984) Cycles of reproduction and condition in Tasmanian blue mussels, Mytilus edulis planulatus. Australian Journal of Marine and Freshwater Research 35, 307313.CrossRefGoogle Scholar
Ehrlich, P.R. (1984) Which animal will invade? In Mooney, H.A. and Drake, J.A. (eds) Ecology of biological invasions of North America and Hawaii, New York: Springer-Verlag.Google Scholar
Erkom Schurink, C. van and Griffiths, C.L. (1991) A comparison of reproductive cycles and reproductive output in four southern African mussel species. Marine Ecology Progress Series 76, 123134.CrossRefGoogle Scholar
Gilboa, A. (1976) Experiments in mytilids recolonization. MS Dissertation, Hebrew University of Jerusalem, Israel.Google Scholar
Gould, S.J. (1966) Allometry and size in ontogeny and phylogeny. Biological Reviews 41, 587640.CrossRefGoogle ScholarPubMed
Griffiths, C.L. and Griffiths, R.J. (1987) Bivalvia. In Pandian, T.J. and Vernberg, F.J. (ed.) Animal energetics, Vol 2. Bivalvia through Reptilia, New York: Academic Press.Google Scholar
Hicks, D.W., Tunnell, J.W. Jr and McMahon, R.F. (2001) Population dynamics of the non-indigenous brown mussel Perna perna in the Gulf of Mexico compared to other world-wide populations. Marine Ecology Progress Series 211, 181192.CrossRefGoogle Scholar
Inoue, T. and Yamamuro, M. (2000) Respiration and ingestion rates of the filter-feeding bivalve Musculista senhousia: implications for water-quality control. Journal of Marine System 26, 183192.CrossRefGoogle Scholar
LaBarbera, M. (1989) Analysing body size as a factor in ecology and evolution. Annual Review of Ecology and Systematics 20, 97117.CrossRefGoogle Scholar
Lewis, D.E. and Cerrato, R.M. (1997) Growth uncoupling and the relationship between shell growth and metabolism in the soft shell clam Mya arenaria. Marine Ecology Progress Series 158, 177189.CrossRefGoogle Scholar
McMahon, R.F. (2002) Evolutionary and physiological adaptations of aquatic invasive animals: r selection versus resistance. Canadian Journal of Fisheries and Aquatic Sciences 59, 12351244.CrossRefGoogle Scholar
McQuaid, C.D. and Lindsay, T.L. (2000a) Effect of wave exposure on growth and mortality rates of the mussel Perna perna: bottom up regulation of intertidal populations. Marine Ecology Progress Series 206, 147154.CrossRefGoogle Scholar
McQuaid, C.D., Lindsay, J.R. and Lindsay, T.L. (2000b) Interactive effects of wave exposure and tidal height on population structure of the mussel Perna perna. Marine Biology 137, 925932.CrossRefGoogle Scholar
Mistri, M. (2003) Foraging behaviour and mutual interference in the Mediterranean shore crab, Carcinus aestuarii, preying upon the immigrant mussel Musculista senhousia. Estuarine, Coastal and Shelf Science 56, 155159.CrossRefGoogle Scholar
Mohammed, S.Z. (1992) The interaction between adults and recruitments in the Brachidontes variabilis L. (Lamellibranchiata) bed in the Bitter Great Lake, Suez Canal. Quaternary University Science Journal 12, 228232.Google Scholar
Mohammed, S.Z. (1997) Influence of age structure of Brachidontes variabilis on the community structure of its associated fauna in the Greater Bitter Lake, Suez Canal. Journal of Egyptian German Zoology 24, 5167.Google Scholar
Morton, B. (1988) The population dynamics and reproductive cycle of Brachidontes variabilis (Bivalvia: Mytilidae) in a Hong Kong mangrove. Malacological Review 21, 109117.Google Scholar
Pusceddu, A., Sarà, G., Armeni, M., Fabiano, M. and Mazzola, A. (1999) Seasonal and spatial changes in sediment organic matter composition of a semi-enclosed marine system (W-Mediterranean Sea). Hydrobiologia 397, 5970.CrossRefGoogle Scholar
Rajagopal, S., Venugopalan, V.P., Van der Velde, G. and Jenner, H.A. (2003) Tolerance of five species of tropical marine mussels to continuous chlorination. Marine Environment Research 55, 277291.CrossRefGoogle ScholarPubMed
Root, T.L., MacMynowski, D.P., Mastrandrea, M.D. and Schneider, S.H. (2005) Human-modified temperatures induce species changes: joint attribution. Proceedings of the National Academy of Sciences 102, 74657469.CrossRefGoogle ScholarPubMed
Safriel, U.N. and Ritte, U. (1985) Suez Canal migration and Mediterranean colonization - their relative importance in Lessepsian migration. Rapports de la Commission International pour l'Exploration Scientifique de la Mer Méditerranée 29, 259263.Google Scholar
Safriel, U.N. and Sasson-Frostig, Z. (1988) Can colonising mussel out-compete indigenous mussel? Journal of Experimental Marine Biology and Ecology 117, 211226.CrossRefGoogle Scholar
Sarà, G., Leonardi, M. and Mazzola, A. (1999) Spatial and temporal changes of suspended matter in relation to wind and vegetation cover in a Mediterranean shallow coastal environment. Chemistry and Ecology 16, 151173.CrossRefGoogle Scholar
Sarà, G., Romano, C., Caruso, M. and Mazzola, A. (2000) The new Lessepsian entry Brachidontes pharaonis (Fischer P., 1870) (Bivalvia, Mytilidae) in the western Mediterranean: a physiological analysis under varying natural conditions. Journal of Shellfish Research 19, 967977.Google Scholar
Sarà, G., Vizzini, S. and Mazzola, A. (2003) Sources of carbon and dietary habits of new Lessepsian entry Brachidontes pharaonis (Bivalvia, Mytilidae) in the western Mediterranean. Marine Biology 143, 713722.CrossRefGoogle Scholar
Sokal, R.R. and Rohlf, F.J. (1981) Biometry. San Francisco: W.H. Freeman.Google Scholar
Thompson, R.J. (1979) Fecundity and reproductive effort in the blue mussel (Mytilus edulis), the sea urchin (Strongylocentrotus droebachiensis) and the snow crab (Chionoecetes opilio) from populations in Nova Scotia and Newfoundland. Journal of Fisheries Research Board Canada 36, 955964.CrossRefGoogle Scholar