Skip to main content
Log in

Effects of production intensity and production strategies in commercial Atlantic salmon smolt (Salmo salar L.) production on subsequent performance in the early sea stage

  • Published:
Fish Physiology and Biochemistry Aims and scope Submit manuscript

Abstract

A data set from commercial Atlantic salmon (Salmo salar L.) producers on production intensity and production strategies in smolt tanks (N = 63–94) was obtained during 1999–2006. The effects of production intensity on subsequent fish mortality and growth during the early sea phase (90 days) were examined by principal component analysis and subsequent generalized linear model analysis. Levels of accumulated metabolites (CO2, total ammonia nitrogen and NH3), and information provided by producers (production density (kg fish m3−1), specific water use (l kg fish−1 min−1) and oxygen drop (mg l−1) from tank inlet to tank outlet), were used as predictor variables. In addition, several other welfare relevant variables such as disease history, temperature during freshwater and sea stage; season (S1) or off-season (S0) smolt production; and the use of seawater addition during the freshwater stage were analyzed. No strong intensity effects on mortality or growth were found. CO2 levels alone (P < 0.001, R 2 = 0.16), and in combination with specific water use (R 2 = 0.20), had the strongest effect on mortality. In both cases, mortality decreased with increasing density. For growth, the intensity model with the most support (R 2 = 0.17) was O2 drop, density and their interaction effects, resulting in the best growth at low and high intensity, and poorer growth at intermediate levels. Documented viral disease outbreaks (infectious pancreatic necrosis and two cases of pancreas disease) in the sea phase resulted in significantly higher mortalities at 90 days compared with undiagnosed smolt groups, although mortalities were highly variable in both categories. The temperature difference between the freshwater stage and seawater had a small, but significant, effect on growth with the best growth in groups stocked to warmer seawater (P = 0.04, R 2 = 0.06). S0 and S1 smolt groups did not differ significantly in growth, but the mortality was significantly (P = 0.02) higher in S1 groups. Seawater addition as a categorical variable had no significant effects, but when analyzed within the seawater addition group, intermediate salinities (15–25 ppt) gave the best results on growth (p = 0.04, R 2 = 0.15). Production intensity had small explanatory power on subsequent seawater performance in the analyzed smolt groups. If anything, the analysis shows a beneficial effect of intensive production strategies on subsequent performance. Analysis of the various production strategies indicates better survival of S0 compared with S1 smolt groups, improved growth when stocked in seawater warmer than freshwater, and a negative effect of viral disease outbreaks on survival. The results clearly demonstrate the difficulty of extrapolating results from experimental work on fish welfare and production intensity variables to commercial production. On the other hand, the presented results may simply demonstrate that the traditional fish welfare criteria growth and mortality may not suffice to evaluate welfare consequences of suboptimal water quality or production strategies in the aquaculture industry.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Banks J (1992) Effects of density and loading on coho salmon during hatchery rearing and after release. Prog Fish-Cult 54:137–147

    Article  Google Scholar 

  • Banks J (1994) Raceway density and water flow as factors affecting spring Chinook salmon (Oncorhynchus tshawytscha) during rearing and after release. Aquaculture 119:201–217

    Article  Google Scholar 

  • Bergheim A, Drengstig A, Ulgenes Y, Fivelstad S (2009) Production of Atlantic salmon smolts in Europe-Current characteristics and future trends. Aquacultural Eng 41:46–52

    Article  Google Scholar 

  • Boef G, Payan P (2001) How should salinity influence fish growth? Comp Biocem Physiol C 130:411–423

    Google Scholar 

  • Brauner CJ, Seidelin M, Madsen SS, Jensen FB (2000) Effects of fresh water hyperoxia and hypercapnia exposures and their influences on subsequent seawater transfer in Atlantic salmon (Salmo salar) smolts. Can J Fish Aquat Sci 57:2054–2064

    Article  Google Scholar 

  • Burnham KP, Anderson DR (1998) Model selection and inferences. Springer Verlag, New York

    Google Scholar 

  • Espmark Å, Baeverfjord G (2009) Effects of hyperoxia on behavioural and physiological variables in farmed Atlantic salmon (Salmo salar) parr. Aquac Int 17:341–353

    Google Scholar 

  • Fivelstad S, Kallevik H, Iversen HM, Møretrø T, Våge K, Binde M (1993) Sublethal effects of ammonia in soft water on Atlantic salmon smolts at a low temperature. Aquaculture Int 1:157–169

    Article  Google Scholar 

  • Fivelstad S, Olsen AB, Kløften H, Ski H, Stefansson S (1999) Effects of carbon dioxide on Atlantic salmon (Salmo salar L.) smolts at constant pH in bicarbonate rich freshwater. Aquaculture 178:171–187

    Article  Google Scholar 

  • Fivelstad S, Waagbø R, Zeitz SF, Hosfeld ACD, Olsen AB, Steffansson S (2003a) A major water quality problem in smolt farms: combined effects of carbon dioxide, reduced pH and aluminium on Atlantic salmon (Salmo salar L.) smolts: physiology and growth. Aquaculture 215:339–357

    Article  CAS  Google Scholar 

  • Fivelstad S, Olsen AB, Åsgård T, Baeverfjord G, Rasmussen T, Vindheim T, Stefansson S (2003b) Long-term sublethal effects of carbon dioxide on Atlantic salmon smolts (Salmo salar L.): ion regulation, haematology, element composition, nephrocalcinosis and growth parameters. Aquaculture 215:301–319

    Article  CAS  Google Scholar 

  • Fivelstad S, Bergheim A, Hølland PM, Fjermedal AB (2004) Water flow requirements in the intensive production of Atlantic salmon (Salmo salar L.) parr–smolt at two salinity levels. Aquaculture 231:263–277

    Article  Google Scholar 

  • Handeland SO, Stefansson SO (2001) Photoperiod control and influence of body size on off-season parr-smolt transformation and post-smolt growth. Aquaculture 192:291–307

    Article  Google Scholar 

  • Handeland SO, Stefansson SO (2002) Effects of salinity acclimation on pre-smolt growth, smolting and post-smolt performance in off-season Atlantic salmon smolts (Salmo salar L.). Aquaculture 209:125–137

    Article  CAS  Google Scholar 

  • Hosfeld CD, Engevik A, Mollan T, Lunde TM, Waagbø R, Olsen AB, Breck O, Stefansson S, Fivelstad S (2008) Long-term separate and combined effects of environmental hypercapnia and hyperoxia in Atlantic salmon (Salmo salar L.) smolts. Aquac 280:146–153

    Google Scholar 

  • Hosfeld C, Hammer J, Handeland S, Fivelstad S, Stefansson S (2009) Effects of fish density on growth and smoltification in intensive production of Atlantic salmon (Salmo salar L.). Aquac 294:236–241

    Google Scholar 

  • Imsland AK, Våge KA, Handeland S, Stefansson S (2010) Growth and osmoregulation in Atlantic salmon (Salmo salar L.) smolts in response to different feeding frequencies and salinities. Aquaculture Res 42:469–479

    Article  Google Scholar 

  • Jolliffe IT (2002) Principal component analysis, 2nd edn. Springer-Verlag, New York

    Google Scholar 

  • Kristensen T, Åtland Å, Rosten T, Urke HA, Rosseland BO (2009) Important influent-water quality parameters at freshwater production sites in two salmon producing countries. Aquacultural Eng 41:53–59

    Article  Google Scholar 

  • Kroglund F, Finstad B, Steffansson S, Nilsen TO, Kristensen T, Rosseland BO, Teien HC, Salbu B (2007) Exposure to moderate acid water and aluminum reduces Atlantic salmon post-smolt survival. Aquaculture 273:360–373

    Article  CAS  Google Scholar 

  • Lygren B, Hamre K, Waagbø R (2000) Effect of induced hyperoxia on the antioxidant status of Atlantic salmon Salmo salar L. fed three different levels of dietary vitamin E. Aquac Res 31:401–407

    Article  Google Scholar 

  • Lysfjord G, Jobling M, Solberg C (2004) Atlantic salmon smolt startegy affects body composition and early seawater growth. Aquaculture 237:191–205

    Article  Google Scholar 

  • Martens LG, Witten PE, Fivelstad S, Huysseune A, Sævareid B, Vikeså V, Obach A (2006) Impact of high water carbon dioxide levels on Atlantic salmon smolts (Salmo salar L.): Effects on fish performance, vertebrae composition and structure. Aquaculture 261:80–88

    Article  Google Scholar 

  • McCullagh P, Nelder JA (1989) Generalized linear models, 2nd edn. Chapman and Hall, London

    Google Scholar 

  • Monette MY, Bjornsson BT, McCormick SD (2008) Effects of short-term acid and aluminum exposure on the parr-smolt transformation in Atlantic salmon (Salmo salar): Disruption of seawater tolerance and endocrine status. Gen Compar Endocrinol 158:122–130

    Article  CAS  Google Scholar 

  • Moore A, Scott AP, Lower N, Katsiadaki I, Greenwood N (2003) The effects of 4-nonylphenol and Atrazine on Atlantic Salmon (Salmo salar L) Smolts. Aquaculture 222:253–263

    Article  CAS  Google Scholar 

  • Moore A, Lower N, Mayer I, Greenwood L (2007) The impact of a pesticide on migratory activity and olfactory function in Atlantic salmon (Salmo salar L.) smolts. Aquaculture 273:350–359

    Article  CAS  Google Scholar 

  • North BP, Turnbull JF, Ellis T, Porter MJ, Migaud H, Bron J, Bromage NR (2006) The impact of stocking density on the welfare of rainbow trout (Oncorhynchus mykiss). Aquaculture 255:466–479

    Article  Google Scholar 

  • Olsvik PA, Kristensen T, Waagbø R, Rosseland BO, Tollefsen KE, Bæverfjord G, Berntssen MHG (2005) SOD, CAT and GSH-Px mRNA expression and lipid peroxidative stress in liver of Atlantic salmon Salmo salar exposed to hyperoxic conditions during smoltification. Comp Biochem Physiol C 141:314–323

    Article  CAS  Google Scholar 

  • Person-Le Ruyet J, Labbe L, Le Bayon N, Severe A, Le Roux A, Delliou H, Quemener L (2008) Combined effects of water quality and stocking density on welfare and growth of rainbow trout (Oncorhynchus mykiss). Aquatic Living Resour 21:185–195

    Article  Google Scholar 

  • R Development Core Team (2010) R: a language and environment for statistical computing, version 2.10.1.R foundation for statistical computing. Vienna, Austria

    Google Scholar 

  • Rosten T, Kristensen T, Knight CM, Suciu R (2010) Landbased intensive aquaculture of sturgeons: can we learn something from the salmon experiences? J Appl Ichthyoly (submitted)

  • Thurston RV, Russo RC, Luedtke RE, Smith CE, Meyn EL, Chakoumakos C, Wang K (1984) Chronic toxicity of Ammonia to rainbow trout. Trans Am Fish Soc 113:56–73

    Article  CAS  Google Scholar 

  • Waring CP, Moore A (2004) The effect of atrazine on Atlantic Salmon (Salmo salar) smolts in fresh water and after sea water transfer. Aquat Toxicol 66:93–104

    Article  PubMed  CAS  Google Scholar 

  • Wicks BJ, Joensen R, Tang Q, Randall DJ (2002) Swimming and ammonia toxicity in salmonids: the effect of sub lethal ammonia exposure on the swimming performance of coho salmon and the acute toxicity of ammonia in swimming and resting rainbow trout. Aquatic Toxicol 59:55–69

    Article  CAS  Google Scholar 

Download references

Acknowledgments

The authors would like to thank all participating industry partners for supplying the data. Data compilation and analysis were funded by NIVA and the Research Council of Norway through contract no. 165239/S40.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to T. Kristensen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kristensen, T., Haugen, T.O., Rosten, T. et al. Effects of production intensity and production strategies in commercial Atlantic salmon smolt (Salmo salar L.) production on subsequent performance in the early sea stage. Fish Physiol Biochem 38, 273–282 (2012). https://doi.org/10.1007/s10695-011-9566-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10695-011-9566-0

Keywords

Navigation