The interaction of temperature and salinity on growth and food conversion in juvenile turbot (Scophthalmus maximus)
By A. Imsland, A. Foss, S. Gunnarsson, M. Berntssen, Richard FitzGerald, S. W. Bonga, E. V. Ham, G. Nævdal, S. Stefansson. 2001
293 citations recorded by the source corpus.
Subfields: Aquatic Science, Global and Planetary Change, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/896384a7206ab682d5bf585b47eac93e23e60529
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Aquatic Science
In Global and Planetary Change
In Nature and Landscape Conservation
- K. Miller
- A. Imsland
- Kevin Stierhoff
- T. Targett
- Carsten Schulz
- Joachim Krieter
- A. Baer
- S. Stefansson
Citations in the corpus
- Ecophysiological responses of juvenile summer and winter flounder to hypoxia: experimental and modeling analyses of effects on estuarine nursery quality (2006, background): “…as nurseries is attributed primarily to physicochemical regimes (e.g. temperature and salinity) that are physiologically suitable or optimal, abundant prey resources, and low predation risk, conditions that promote rapid growth and enhance survival of young fishes (Joseph 1973, Miller et al. 1985).”
- Tertiary stress responses in Senegalese sole (Solea senegalensis Kaup,1858) to osmotic challenge: Implications for osmoregulation, energy metabolism and growth (2009, background): “The effects of salinity on growth have been investigated in a wide number of species (reviewed by Boeuf and Payan, 2001) including flatfish (Scophthalmus maximus: Gaumet et al., 1995; Imsland et al., 2001; Paralichthys orbignyanus: Sampaio and Bianchini, 2002; Hippoglossus hippoglossus: Imsland et a”
- Effects of reduced salinities on growth, feed conversion efficiency and blood physiology of juvenile Atlantic halibut (Hippoglossus hippoglossus L.) (2008, unknown): “salinity (34‰ )( Imsland et al., 2001, 2002, 2003 ).”
- The chronic effect of nitrate on production performance and health status of juvenile turbot (Psetta maxima) (2012, result): “exposure, total-Hb does not confirm a respiro-circulatory dysfunction as values are within a comparable range as previously reported by Person-Le Ruyet et al. (2002), Pichavant et al.”
- A review of the culture potential of Solea solea and S. senegalensis (2003, background): “For turbot (Imsland et al., 2001, 2002) rearing juveniles at intermediate salinities improved growth by 10–15% compared to full salinity.”
- Gill Na+, K+-ATPase activity, plasma chloride and osmolality in juvenile turbot (Scophthalmus maximus) reared at different temperatures and salinities (2003, background): “Since it is believed that fish have to spend more energy on osmoregulation as salinity increases (Kinne, 1960; Brett, 1979; Febry and Lutz, 1987), it can be hypothesized that lower energy budget for osmoregulation at 15xmight add to higher growth (Imsland et al., 2001) in these groups.”
- Effects of temperature on growth and metabolism in a Mediterranean population of European sea bass, Dicentrarchus labrax (2004, background): “In turbot, temperature and oxygen and their interactions exhibited long-term effects on growth but there are differences between fish from different geographic areas (Bœuf et al., 1999; Imsland and Jonassen, 2001; Imsland et al., 2001;).”
- Analysing the growth of turbot (Psetta maxima) in a commercial recirculation system with the use of three different growth models (2011, background): “Endogenous and exogenous factors are responsible for the different growth rates within the examined turbot population (Imsland et al. 2001; Regost et al. 2003).”
- The effect of supplementation with polysaccharides, nucleotides, acidifiers and Bacillus strains in fish meal and soy bean based diets on growth performance in juvenile turbot (Scophthalmus maximus) (2015, background): “…have an influence on performances in turbot and have to be considered when comparing results (Blanquet and Oliva-Teles, 2010; Foss et al., 2009; Imsland et al., 2001; Irwin et al., er of initial fish samples and turbot fed the control and experimental diets over 84 days in 1999; vanBussel et…”
- Growth and Lipid Metabolism of the Pacific White Shrimp Litopenaeus vannamei at Different Salinities (2014, background): “in many fish, such as Spams sarba (Woo & Kelly 1995), Salmo salar (Handeland et al. 1998), Anarhichas minor (Foss et al. 2001), Scophthalmus maximus (Imsland et al. 2001), Pagrus auratus (Fielder et al. 2005), and Sparus aurata (Laiz-Carrion et al. 2005).”
- The effect of temperature and fish size on growth, feed intake, food conversion efficiency and stomach evacuation rate of Atlantic salmon post-smolts (2008, unknown): “…pattern for salmonids in freshwater (Brett, 1979; Fleming et al., 2000; Forseth et al., 2001; Jonsson et al., 2001) and is in line with findings on Atlantic halibut (Björnsson and Tryggvadóttir, 1996; Jonassen et al., 1999), Atlantic cod (Björnsson et al., 2001) and turbot (Imsland et al., 2001).”
- Growth and survival of juvenile cobia, Rachycentron canadum, at different salinities in a recirculating aquaculture system (2006, background): “Marine species such as Atlantic cod (Gadus morhua) and turbot (Scophthalmus maximus) have been shown to exhibit increased growth rates (cod), food conversion ratios (cod), and food intake (turbot) when cultured at intermediate salinities of 12–19 ppt (Lambert et al., 1994; Gaumet et al., 1995; Dutil”
- Growth performance of gilthead sea bream Sparus aurata in different osmotic conditions: Implications for osmoregulation and energy metabolism (2005, background): “…and Perera, 1985; O. niloticus : Woo et al., 1997), cod Gadus morhua (Lambert et al., 1994) and turbot Scopththalmus max-imus (Gaumet et al., 1995; Imsland et al., 2001) where the best growth occurred at 10–15 ppt environmental One unit of enzyme activity is defined for HK as that which utilizes…”