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Preprint volume - SIBM

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Pre-print Volume – Posters<br />

AQUACULTURE COMMITEE<br />

immediately anaesthetized using 0.1 g/l of tricaine methanesulphonate; careful netting<br />

and handling were implemented to minimize stress.<br />

Biochemical parameters were carried out using commercial kits: cortisol: (ELISA<br />

method); glucose (GOD-POD method); lactate: (LOD-POD method). Haematocrit was<br />

determined by microhaematocrit capillary tube method by centrifugation at 14000 g for<br />

5 min. Haemagglutinating activity against sheep erythrocytes were determined in<br />

serum samples according to Caruso et al. (2005). Lysozyme content was measured, on<br />

samples of mucus, plasma and kidney, according to plate diffusion method (Ossermann<br />

and Lawlor, 1966).<br />

Results and conclusions – No significant differences were shown in specific growth<br />

rate between the two groups, even if fish cultured in submerged cage reached the<br />

largest size.<br />

Main results of this study underline a clear relation between observed changes in<br />

physiological parameters commonly used as stress and immunocompetence indicators<br />

in fish (Weendelar Bonga, 1997; Tort et al., 1996) and the cage type. Submergence<br />

seems to be a favourable condition for sea bass culturing, as evidenced by growth,<br />

haematological, biochemical and immunological parameters. Particularly, in<br />

submerged sea bass, serum cortisol and glucose and haematocrit value appeares<br />

significantly lower than those of surface cages indicating a more welfare. Moreover<br />

fish of submerged cages also show significant higher value in non-specific haemolytic<br />

activity and mucus lysozyme, highlighting a positive effect of submergence some<br />

components of innate immune system.<br />

References<br />

CARUSO G., GENOVESE L., MARICCHIOLO G., MODICA A. (2005) – Haematological,<br />

biochemical and immunological parameters as stress indicators in Dicentarchus labrax and<br />

Sparus aurata farmed in off-shore cages. Aquaculture International, 1-2: 67-73.<br />

DEMPSTER T., JUELL J.E., FOSSEIDENGEN J.E., FREDHEIM A., LADER P. (2008) –<br />

Behaviour and growth of atlantic salmon (Salmo salar L.) subjected to short-term submergence<br />

in commercial scale sea-cages. Aquaculture, 276: 103-111.<br />

DEMPSTER T., KORSØEN O., FOLKEDAL O., JUELL J.E., OPPEDAL F. (2009) – Submergence<br />

of atlantic salmon (Salmo salar I.) in sea-cages; a potential short-term solution to poor surface<br />

conditions. Aquaculture, 288: 254-263.<br />

KORSØEN O.J., DEMPSTER T., FJELLDAL P.G., OPPEDAL F., KRISTIANSEN T.S. (2009) –<br />

Long-term culture of atlantic salmon (Salmo salar L.) in submerged cages during winter affects<br />

behaviour, growth and condition. Aquaculture, 276: 103-111.<br />

LE CREN E.D. (1951) – The length-weight relationship and seasonal cycle in gonad weight and<br />

condition in the perch (Perca fluviatilis). J. Anim. Ecol., 20: 201-219.<br />

OSSERMANN E.F., LAWLOR D.P. (1966) – Serum and urinary lysozyme (muramidase) in<br />

monocytic and monomyelocytic leukaemia. J. Exper. Med., 124: 921-951.<br />

TORT L., SUNYER J.O., GÓMEZ E., MOLINERO A. (1996) – Crowding stress induces changes in<br />

serum haemolytic and agglutinating activity in gilthead seabream Sparus aurata. Vet. Immunol.<br />

Immunopathol., 51: 179-188.<br />

WEENDELAR-BONGA S.E. (1997) – The stress response in fish. Physiol. Rev., 77: 591-625.<br />

41 st S.I.B.M. CONGRESS Rapallo (GE), 7-11 June 2010<br />

250

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