The effect of low temperatures and photoperiods on growth and vertebra morphometry in Atlantic salmon

The aim of this study was to reveal possible interactive effects of temperature and photoperiod on somatic and skeletal growth, feed conversion, organ indexes and blood chemistry in Atlantic salmon postsmolts. A total of 1140 (initial mean weight 96.0 g ± 3.1 SEM) juvenile Atlantic salmon reared in seawater were in duplicates exposed to six different combinations of temperatures (4.3, 6.5 or 9.3 °C) and photoperiods (continuous light, LL or simulated natural photoperiod (69ºN), LDN) for 124 days. An interactive effect of photoperiod and temperature on somatic growth was found as the fish exposed to low temperature and continuous light regime (4LL) had a significantly higher growth (30 % gain in overall SGR) than the 4LDN group, corresponding to the effect of approx. 1.2 °C temperature increase. Fish in the 6 and 9 °C groups did not show any significant growth benefit of continuous light. Compared to the 4LDN group, the 4LL group showed higher total feed conversion efficiency, lower levels of blood Na⁺ and lower hepato-somatic and cardio-somatic indexes. In the skeleton, cervical vertebra were largest in the 4LL group, while the length of the head was largest in the 4LDN group, continuous light promotes growth at lower temperatures while supporting a normal development. It is suggested that a considerable growth benefit may be achieved by exposing juvenile Atlantic salmon to continuous light when reared at low (in this trial 4.3 °C) water temperature during winter.     

Physiology during smoltification in Atlantic salmon: effect of melatonin implants

Melatonin implants were used to override natural melatonin rhythm in groups of juvenile Atlantic salmon, Salmo salar, raised at simulated natural photoperiod (SNP) and constant light (LL) from mid-March until end of August. The experiment contained also both sham control (with non-melatonin implants) and control (no implants). No differences were found in the experimental variables between these two control groups. Growth and food intake were negatively affected by melatonin implantation. Overall, higher GH levels were observed in the SNP melatonin-implanted group, whereas no differences in GH levels were seen between the SNP control, LL control, or the LL melatonin-implanted groups. Highest food intake was seen in the LL control group. No differences in food intake were recorded between the LL melatonin-implanted and SNP control groups. Gill Na⁺, K⁺, ATPase (NKA) activity was influenced by time as well as the interaction between photoperiod and time. No differences in gill NKA activity or plasma chloride levels following transfer to seawater were seen between the groups with melatonin implants and their controls. Based on the present results, it seems apparent that melatonin does play a role in regulating food intake and growth in Atlantic salmon smolts.     

Feed intake of Atlantic salmon parr Salmo salar L. in relation to temperature and feed composition

The design and testing of a feed intake monitoring system based on feed waste collection is described. The system was used in a study of feed intake and growth of Atlantic salmon Salmo salar L. parr in relation to temperature (2 °C or 8 °C) and feed composition (21% fat, 50% protein and 22.5 MJ kg^?1 or 34% fat, 40% protein and 24.8 MJ kg^?1). Fish had lower feed intake and slower growth at the lower temperature, but temperature‐corrected growth (TGC) was better in fish held at the lower temperature. There was an increase in TGC over time at low temperature, probably as a result of long‐term thermal acclimation. Feed conversion for an increase in body size from 19 to 38 g was better for the fish held at low temperature. Feed consumption of low‐fat feed was higher than that of high‐fat feed, and growth of the fish fed the low‐fat feed was better at the higher temperature. These data are consistent with the ideas that the fish compensated for differences in feed energy densities to maintain energy and nutrient intakes, and that lipostatic factors may be operating to regulate feed intake and growth.     

Seasonally changing metabolism in Atlantic salmon (Salmo salar L.) I – Growth and feed conversion ratio

To determine seasonal variation in growth and feed conversion ratio (FCR), Atlantic salmon postsmolts (Salmo salar L.) were exposed to either simulated natural photoperiod (SNP) for 12 months or continuous light (LL) from January to June followed by SNP until December. Feed was given to excess and uneaten feed pellets were collected after every meal for estimation of feed intake and calculation of FCR. Body weight increased from 1086 ± 9 g (mean ± SEM) in January to 4970 ± 7 g (SNP) and 5190 ± 23 g (LL) in December. Specific growth rate (SGR), condition factor and feed intake displayed strong seasonal variation in both groups. Measurements of the thermal growth coefficient correlated highly with SGR (r = 0.98, P < 0.05), indicating that the seasonal variation in SGR was independent of temperature and fish size. Continuous light treatment resulted in increased growth from spring, while the fish exposed to simulated natural light had increased growth rate in late summer. Furthermore, LL improved FCR. Periods of high SGR were concurrent with periods of low FCR in both groups.     

Effects of lipid sources and lipid peroxidation on feed intake, growth, and tissue fatty acid compositions of largemouth bass (Micropterus salmoides)

A 12-week growth trial was conducted to study the effects of replacement of fish oil (FO) with four alternative lipid sources (soybean oil, SO; beef tallow, BT; poultry fat, PF and; palm oil, PO, respectively) on the growth performance, feed intake (FI), and fatty acid (FA) composition in muscle and liver of largemouth bass (Micropterus salmoides) with initial body weight of 6.6 ± 0.01 g. Five isonitrogenous and isoenergetic diets were formulated and added with 5.5 % of each lipid sources, and FO was used as a control group. Until week 8 of the experiment, fish were fed on diets that were conserved at ?20 °C, and fish were fed diets that oxidized at 28–30 °C with natural illumination for 4 weeks during 8–12 week. After 8 weeks of growth trial, specific growth rate and feed conversion of largemouth bass fed BT diet were significantly lower and higher, respectively, than that other dietary treatment (P < 0.05). The fish of PF group had the highest growth performance (P < 0.05). The lipid sources did not affected FI of largemouth bass (P > 0.05). However, growth performance precisely reversed during 8–12 week, and finally, no significant difference was found on growth during 1–12 week. The FA compositions of fish muscle and liver of each treatment reflected the corresponding dietary FA compositions. These results suggested that largemouth bass was sensitive to both of lipid sources and lipid oxidation. Fresh FO, SO, and PF could be optimal lipid sources. Likewise, slightly oxidation of these oils would negatively affected fish growth performance.     

Growth, feed conversion efficiency and growth heterogeneity in Atlantic halibut (Hippoglossus hippoglossus) reared at three different photoperiods

Juvenile Atlantic halibut, Hippoglossus hippoglossus (initial weight (SD) 191.3 (±44.7)) g, were reared for 99 days at a constant temperature of 11°C and subjected to three different light regimes from 13 September to 21 December: continuous light (LD24:0), simulated natural photoperiod of Bergen (60°25′N, LDN) and constant 20 h light:4 h dark (LD20:4). The fish reared on the different photoperiod regimes differed in their growth patterns as juveniles exposed to long days, i.e. LD20:4 and LD24:0, exhibited faster growth than those experiencing a natural photoperiod. The LD20:4 group showed the highest average specific growth rate (0.72% body weight day^?1), whereas fish on LDN displayed the lowest average specific growth rate (0.60% body weight day^?1). The final mean weights of the LD20:4 and the LD24:0 groups were 15% and 12% higher than those of the LDN group. Dividing the duration of the experiment into three time periods shows that the LD20:4 and LD24:0 had a higher feed conversion efficiency (FCE) as compared with the LDN group during the first and the last period, while a reversed situation was observed in the second period. Our data indicate a larger variation in growth rates among individuals in the best‐performing groups (here LD20:4 and LD24:0). This may indicate that formation of size hierarchies is more pronounced in groups with more homogenous growth (here LDN). Overall, our findings indicate that extended light regimes result in faster growth and better feed conversion in juvenile Atlantic halibut. In line with findings on other flatfish species, this supports the concept that constant long day:short night or continuous light regimes should be used by the farmer in order to maximize growth and improve feed conversion in Atlantic halibut.     

Effects of water temperature on feeding and growth of juvenile marbled flounder <Emphasis Type="Italic">Pseudopleuronectes yokohamae</Emphasis> under laboratory conditions: evaluation by group- and individual-based methods

To determine the optimal temperature for juvenile (0 year old) marbled flounder Pseudopleuronectes yokohamae, juveniles of 40–54 mm standard length were reared at six temperature conditions in the range of 8–26 °C, using group- and individual-based methods. Growth of juveniles increased from 8 to 20 °C but decreased from 20 to 26 °C, irrespective of the rearing method used. Food intake was greatest at 20 and 24 °C compared with other temperatures, while feed conversion efficiency was greater at 20 °C than 24 °C in individual rearing. Individual rearing provided more information such as individual variations in growth and food consumption, suggesting the importance of individual-based experiments for exploring the optimal temperature for fish.     

Salinity effects on osmoregulation and gill morphology in juvenile Persian sturgeon (<Emphasis Type="Italic">Acipenser persicus</Emphasis>)

The effect of abrupt and 5-day gradual salinity transfers from freshwater (FW) to 11 ‰ Caspian Sea brackish water (BW) was investigated in juvenile Persian sturgeon Acipenser persicus with three different weight groups: 1–2 g (1.62 ± 0.27 g), 2–3 g (2.55 ± 0.41 g) and 3–5 g (4.28 ± 0.76 g). Mortality rates, blood osmotic pressure, gill morphology and branchial Na⁺, K⁺-ATPase (NKA) activity were measured 4 and 10 days after abrupt transfer and 9 and 15 days after the initial gradual transfer (i.e. 4 and 10 days after reaching Caspian Sea salinity). Fish under 3 g could not survive increased salinity, and the blood osmotic pressure of the remaining surviving fish increased and remained elevated. However, heavier fish were able to survive and successfully acclimate, even to rapid salinity change with osmotic pressure reduced to Caspian Sea osmolality levels. At the gill level, the developmental increase in chloride cell volume and a higher NKA content most probably allow juveniles weighing more than 2 g to sharply increase NKA activity if the fish are transferred to BW. The rapid chloride cell proliferation occurring with increased salinity should strengthen this acclimation response. Therefore, a drastic physiological change occurs when fish weigh more than 2 g that allows migration to higher salinities. The triggering signal on chloride cells must be further investigated in order to optimize this functional step.     

Feed intake, growth and feed conversion efficiency of Atlantic halibut, Hippoglossus hippoglossus (L.)

The individual food intake of each fish in each of four groups of Atlantic halibut, Hippoglossus hippoglossus (L.) (mean weight: 422 g) was monitored by direct observation over a period of 21 days. Gross feed conversion efficiency (= growth·feed intake^?1), net feed conversion efficiency and maintenance ration were estimated by regression analysis. Specific growth rates were found to be linearly related to weight-specific consumption at a temperature of 8–9°C: growth = 1.922· feed intake ? 0.242. Maintenance ration was 0.126% of body weight day^?1. The gross feed conversion efficiency increased asymptotically with increasing feed intakes and growth rates, and was found to approach 1.9 at high growth rates (0.5 on a dry weight basis). One feeding per day seemed to be sufficient for maximum food intake and growth rate.     

Pattern of feed intake in four species of fish under commercial farming conditions: implications for feeding management

Meal duration and feed ingestion rate were measured in sea cage-reared Atlantic salmon Salmo salar, rainbow trout Oncorhynchus mykiss, yellowtail Seriola quinqueradiata and red sea bream Pagrus major fed dry extruded feed in discrete meals. At the population level, satiation times in yellowtail, salmon and trout were typically about 15–25 min, but time to satiation was longer (60–90 min) in red sea bream. In all species, feed ingestion rate declined progressively during the course of the meal as the fish became satiated. Initial feed ingestion rates in salmon were ≈ 0.3–0.5 kg feed tonne fish^–1 min^–1 and in trout 0.5–0.9 kg feed tonne fish^–1 min^–1, although the capacity to deliver feed may have restricted ingestion. Water temperature had little effect on ingestion rates, possibly because the number of meals per day (1–3) was varied with water temperature, and this may have standardized hunger level at the start of meals. Yellowtail ingested feed at ≈ 3.5 kg feed tonne fish^–1 min^–1 at water temperatures of 18 °C and 28 °C, whereas red sea bream ingested feed at initial rates of 0.6 and 1.4 kg feed tonne fish^–1 min^–1at 26.5 °C and 18 °C respectively. The findings are discussed in relation to feeding strategies to minimize interfish competition for feed and to improve the ability of fish farmers to detect the point at which fish are satiated.     

Effects of temperature on the growth of pollack (Pollachius pollachius) juveniles

Growth of juvenile pollack was assessed at five constant temperatures (9, 12, 15, 18 and 21 °C) in an 84-day trial. Duplicate groups of 75 fish (initial weight 143 ± 2 g) were held in O₂ saturated water (102–103% saturation) and fed to apparent satiation. Growth increased as temperature increased from 9 °C up to a plateau at 12–15 °C (NS differences between 12 and 15 °C) followed by a decrease from 18 °C. No growth occurred at 21 °C. For the overall period, specific growth rates were 0.52% and 0.53% day^− 1 at 12 and 15 °C compared to 0.40% day^− 1 at 18 °C. Feed intake was maximum at 15–18 °C (0.68–0.69% day^− 1) and it was significantly lower at 21 °C (0.45% day^− 1). Apparent feed conversion ratio was significantly higher at 18 °C than at 12–15 °C (1.8 compared to 1.2–1.4). There was no significant change in fish whole body composition related to temperature.At the end of the experiment, fish growth recovery following a transfer from 18 and 21 °C to 15 °C was assessed using a 50-day challenge test. Growth rate of the previous 21 °C group was the same as in the 15 °C group (NS differences) and in the previous 18 °C group it was significantly lower. The study showed that pollack have a high capacity to recover from a prolonged period of low or no growth induced by high temperatures.     

Adiposity and growth of post-smolt Atlantic salmon Salmo salar L.

The long‐term adipose homeostasis seen in mammals gives rise to a ‘lipostatic’ model in which signals produced in proportion to fat stores serve to regulate energy intake. An extension of this predicts an impact of these signals on growth; downregulation of feeding in animals with increased adiposity should result in reduced growth. This was tested by monitoring fat deposition and growth in Atlantic salmon Salmo salar L. provided with feeds that differed in fat content. Salmon parr (mass c. 20 g) were fed either high‐ (H: 34%) or low‐fat (L: 22%) feeds, based on either fish (F) or vegetable (V) oils for 6 months to create groups of fish that differed in adiposity (10–12% and 5–7% body fat) at parr–smolt transformation (mass c. 130 g). Fish fed the high‐fat feeds deposited more body fat, and this was confirmed by measurement of fat concentrations in the fillet, viscera and remaining carcass. The fish were then grown‐on in sea water (c. 35 g L^?1, 8 °C, 24L:0D) for 14 weeks while being fed either high‐ or low‐fat feed formulated with fish oil to give the following treatments: HF→ H, HF→ L, LF→ L, LF→ H, HV→ H, HV→ L, LV→ L, LV→ H. Although fish exposed to the various feed treatments did not differ markedly in growth rate (SGR range 1–1.14% day^?1) over the 14 weeks of rearing in sea water, the results were in general agreement with predictions from the ‘lipostatic’ model, i.e. fish with the greatest fat reserves after the parr–smolt transformation grew more slowly than fish that were ‘leaner’ at this time. This suggests that adiposity, or ‘fatness’, may exert a negative feedback on feeding in salmon, thereby having an influence upon growth.     

Effect of stocking density,oxygen level,light regime and swimming velocity on the incidence of sexual maturation in adult Atlantic salmon (Salmo salar)

The effects of various environmental parameters on sexual maturation of two sea-winter Atlantic salmon (Salmo salar) were tested in two separate experiments. In the first experiment Atlantic salmon with initial mean individual weight 1.5 kg (smolt 13 months before) were reared for 8 months from June to February at different oxygen levels and stocking densities using continuous light. Oxygen levels of 5–7, 7.5–9.5 and 10–12 mg O₂ l⁻¹ and stocking densities starting at about 20, 30 and 40 kg m⁻³ and increasing as the fish grew to 80–90 kg m⁻³ for the highest densities were tested in a factorial design. Only male fish matured, and incidence of maturation among males varied from 4.1% to 25% between tanks. The highest percentage of mature males was found in the tanks with low stocking density. No clear effect on oxygen level was found.The second experiment lasted 20 months from seawater transfer in May until the fish weighed 3.3–3.5 kg. Two water current speeds (14–16 and 20–24 cm s⁻¹) and two photoperiod regimes (LD 20:4) and continuous light (LL) were tested in a factorial design. Neither swimming velocity nor photoperiod affected growth rate. Continuous light reduced the incidence of sexual maturation. The average proportion of maturation among males was 8% and 25% under the LL and LD 20:4 regimes respectively. The fish reared under the LD 20:4 light regime had a significant lower condition factor and significant larger hearts than the fish reared under continuous light. Swimming velocity had no significant effect on the incidence of maturation. The results indicate that the swimming velocity must be higher than 0.5 BL s⁻¹ in order to influence the energy stores. An important finding in this study is that light cues are not required for gonadal growth. The results also indicate that environmental factors can affect maturation even after the first sea-winter.     

Growth and age at first maturity in turbot and halibut reared under different photoperiods

The effect of extended photoperiods on growth and age at first maturity was investigated in 166 (79 females and 87 males) individually tagged Atlantic halibut Hippoglossus hippoglossus and in 114 (50 females and 64 males) individually tagged turbot Scophthalmus maximus. The halibut were reared at 11 °C on four different light regimes from 10 February to 6 July 1996: simulated natural photoperiod, (LDN), continuous light (LD24:0), constant 8 h light and 16 h darkness (LD8:16) and LD8:16 switched to continuous light 4 May 1996 (LD8:16–24:0). From 6 July 1996 to 9 February 1998 the LD24:0 and LD8:16–24:0 were reared together under continuous light and the LDN and LD8:16 together under natural photoperiod. The turbot were reared at 16 °C on three different light regimes: constant light (LD24:0), 16 h light:8 h darkness (LD16:8), or simulated natural photoperiod (LDN). After 6 months on the different photoperiods, the turbot was reared together on LDN for approximately 12 months until first maturation. Juveniles subjected to continuous light (halibut) or extended photoperiods (halibut and turbot) exhibited faster growth than those experiencing a natural photoperiod or a constant short day. Moreover, when the photoperiod increased naturally with day-length or when fish were abruptly switched from being reared on short-day conditions to continuous light, a subsequent increase in growth rate was observed. This growth enhancing effect of extended photoperiods was more apparent on a short time scale in Atlantic halibut than in turbot, but both species show significant long-term effects of extended photoperiods in the form of enhanced growth. In both species lower maturation of males was seen in groups exposed to extended or continuous light compared to LDN and this could be used to reduce precocious maturation in males leading to overall increase in somatic growth. This revised version was published online in August 2006 with corrections to the Cover Date.     

Rearing temperature affects Senegalese sole (Solea senegalensis) larvae protein metabolic capacity

The present work examined the short- and long-term effects of three rearing temperatures on protein metabolism and growth trajectories of Senegalese sole larvae using ¹⁴C-labelled Artemia protein as feed. A first feeding trial was performed on larvae reared at 15, 18 and 21 °C (at 26, 17 and 14 days post-hatching (dph), respectively) and a second trial conducted on post-larvae after transfer to the same rearing temperature (~20 °C) (49, 35 and 27 dph, in larvae initially reared at 15, 18 and 21 °C, respectively). Temperature greatly influenced larvae relative growth rate (RGR) and survival, since growth at 15 °C was severely depressed. Protein digestibility and retention was highest at 18 °C during the first trial (85.35 ± 1.16 and 86.34 ± 2.33 %, respectively). However, during the second trial, post-larvae from 15 °C had the highest feed intake and protein digestibility (3.58 ± 1.54 and 75.50 ± 1.35 %, respectively), although retention was similar between treatments. Furthermore, after transfer to 20 °C larvae from 15 °C experienced compensatory growth, which was observed until 121 dph, and confirmed by RGR values, which were significantly higher at 15 ºC than at 21 ºC or 18 ºC. Results from the present study show that Solea senegalensis larval development, survival and protein digestion and retention are highly affected by thermal history.     

Daily temperature shifts during the embryonic period do not alter the phenotypic sex ratio of spring-run chinook salmon

The purpose of this study was to determine whether daily-elevated water temperature shifts during the embryonic period in spring-run chinook salmon (Oncorhynchus tshawytscha) could influence the phenotypic sex ratio. Three families of salmon embryos were divided into two groups; one was moved between 7.5 °C and 12 °C each day (6–8 hours) for 105 days while the other (control) remained at a constant 7.5 °C. Sex ratios varied between the three families, but no significant sex ratio differences were observed between the control and temperature shifted groups.     

Influence of lipid level and supplemental lecithin in diet on growth,feed utilization and body composition of juvenile flounder (Paralichthys olivaceus) in suboptimal water temperatures

This study was conducted to investigate the influence of dietary lipid level and supplemental soy lecithin on growth, feed utilization and body composition of juvenile flounder reared at two suboptimal water temperatures, 12 and 17 °C. Three isonitrogenous (CP 50%) diets containing 1% squid liver oil (S7), 7% squid liver oil (S14), and a mixture of 2% soy lecithin and 5% squid liver oil (SL14) were formulated to obtain 7% and 14% of crude lipid. Triplicate groups of fish (6.3 ± 0.2 g) were fed to apparent satiation twice a day for 60 days. Weight gain, daily feed intake, feed efficiency and protein efficiency ratio were significantly higher for fish reared at 17 °C than at 12 °C. Daily feed intake was significantly decreased with the increase of dietary lipid level at the same water temperature, but weight gain was not affected by dietary lipid composition. At 12 °C, feed efficiency and protein efficiency ratio were significantly higher for fish fed the S14 and SL14 diets than those of fish fed the S7 diet, while at 17 °C feed efficiency and protein efficiency ratio of fish fed the S14 diet, which were not significantly different from those of fish fed the SL14 diet, were significantly higher than those of fish fed the S7 diet. There were no significant effects of dietary lipid composition or temperature range on the whole body contents of moisture, crude protein, lipid or ash. Dietary lipid composition and temperature affected the fatty acid content of the polar lipid from the liver; and the n-3HUFA contents such as 20:5n-3 and 20:6n-3 were higher at 12 °C than at 17 °C. The results of this study indicate that an increase of dietary lipid level from 7% to 14% has beneficial effects on feed utilization of flounder when reared in suboptimal water temperatures. The increase of water temperature from 12 to 17 °C improved growth and feed utilization, but 2% soy lecithin had no substantial effect on growth and feed efficiency of juvenile flounder.     

Influence of dietary concentrations of protein,lipid and carbohydrate on growth,protein and energy utilization,body composition,and plasma titres of growth hormone and insulin-like growth factor-1 in non-transgenic and growth hormone transgenic coho salmon,Oncorhynchus kisutch (Walbaum)

This study compared the ability of juvenile non-transgenic (NT) and transgenic growth hormone (T; gene construct OnMTGH1) coho salmon (Oncorhynchus kisutch) to metabolically utilize energy from lipid and carbohydrate for growth at two dietary protein concentrations. Triplicate groups of size-matched (initial weight, 28.2–29.1 g) NT and T salmon held in 10.5–10.8 °C well water on a natural phototocycle (12.25 h → 8.25 h) were each fed one of four isoenergetic (~ 17.5 MJ of digestible energy (DE)/kg) dry diets twice daily to satiation for 83 days. These diets contained 340 g (LP) or 430 g (HP) of estimated digestible protein (DP)/kg and either 123 g (LL) or 164 g (HL) of estimated digestible lipid (DL)/kg at each DP level (dry weight basis). Estimated digestible carbohydrate (DCHO) concentrations ranged from 45 to 269 g/kg to equalize dietary DE. Under the preceding conditions 46–66% of NT and 18.7–27.5% of T coho, depending upon diet treatment, exhibited no growth or lost weight during the study. NT coho are known to grow slowly or lose weight between the fall equinox and winter solstice but this was unexpected for T coho. Considering all fish T coho, regardless of diet treatment, exhibited significantly higher specific growth rates (SGR) than NT fish due to enhanced feed intake, feed and protein (gross and available deposited) utilization and generally improved available energy utilization. Diet treatment did not affect the growth performance of T fish. Within NT fish, the HP diets supported best gross and available protein and energy utilization. SGR values for growing fish (F_G) only followed identical trends to those for all fish in relation to diet treatment. Regardless of fish genotype, terminal hepatosomatic indices for F_G were directly related to dietary DCHO content and maximum values were noted in NT fish fed LP–LL (significantly higher than observed in NT or T fish fed HP–HL). Final whole body protein concentrations adjusted for dissimilar fish size were higher in T fish fed HP–HL than in T fish fed LP diets and NT fish fed LP–LL. This was also true for T fish fed HP–LL versus T fish fed the LP diets. Within HP groups, whole body lipid and energy contents were generally higher in NT versus T fish whereas within the LP groups energy content was significantly higher in T versus NT fish and was highest in T fish fed LP–LL. Terminal plasma titres for GH and IGF–1 (all fish) were significantly higher in T than in NT fish and were generally uninfluenced by diet treatment. Non-growing NT and T fish had elevated GH relative to NT and T fish that grew. Also, GH was higher in growing T fish relative to growing NT fish whereas the opposite was true in non-growing fish. Plasma IGF-1 levels were higher in growing NT and T fish than in their respective non-growing counterparts. Within F_G only, IGF-1 levels were higher in T versus NT fish.It is concluded that T coho have enhanced ability to effectively utilize DE from DCHO relative to NT fish especially when DP is near the bottom of the optimal range and DL is concurrently suboptimal for NT fish. This is likely due to the elevated titres of GH, IGF-1 and 3,5,3′-triiodo-l-thyronine (measured in another study) in T fish. Also, the enhanced ability of T fish to store energy under these dietary conditions suggests enzymatic improvements in their anaerobic and aerobic metabolism of glucose.     

Effect of rearing temperatures on the growth and maturation of Arctic charr (Salvelinus alpinus) during juvenile and on‐growing periods

The effect of rearing temperature on the growth and maturation of Arctic charr (Salvelinus alpinus) was investigated. Arctic charr juveniles were reared for 6 months (phase I, October–April, size range 20–500 g) at constant temperatures of 9, 12 and 15 °C and according to two temperature‐step groups (T_step) i.e. fish transferred from 15 to 12 °C or from 12 to 9 °C. All the previous treatments were then reared either at 7 °C or at 12 °C for an additional 4 months (phase II, size range 300–1000 g) and then slaughtered in August 2008. The overall growth rate was the highest at a constant temperature of 15 °C for the first 6 months of the trial, with the fish in this group being 44% and 78% heavier than the fish reared at a constant temperature of 12 or 9 °C respectively. Arctic charr showed a negative response in terms of the growth rate when transferred from higher to lower temperatures, especially for groups previously reared at 15 °C. There was a trend for higher gonadosomatic index values at the end of the experiment for groups of fish that were exposed to higher rearing temperatures during the juvenile phase i.e. 4.18% (±0.79) and 7.29% (±0.89), for the temperature groups of 12 and 15 °C, respectively, compared with 2.49% (±0.74) for the 9 °C group. Our results suggest that for the production of fish >1000 g, moderate or low temperatures (here 9 °C) should be applied during the juvenile phase in order to reduce the negative effects arising from maturation. Farmers with access to heat sources should accordingly choose more moderate rearing temperatures during the juvenile stage, especially if the fish is to be moved down in the temperature regime during the on‐growing period.     

Production of market-size European strain Atlantic salmon (Salmo salar) in land-based freshwater closed containment aquaculture systems

Interest in land-based farms using recirculating aquaculture systems (RAS) for market-size Atlantic salmon (Salmo salar) continues to grow, and several commercial facilities are already rearing fish. Performance data for commercially available mixed-sex, all-female, and triploid all-female Atlantic salmon reared to market-size in freshwater land-based facilities, however, are limited, particularly for European strain fish. Accordingly, eight groups of European-sourced Atlantic salmon (five groups of diploid mixed-sex, two groups of diploid all-female, and one group of triploid all-female fish) were reared from eyed egg to market-size in a semi-commercial scale land-based aquaculture systems over five separate production cycles to quantify performance metrics. Fish reached market-size (4−5 kg) in 24.7–26.3 months post-hatch. Fish were reared at a mean water temperature of 12.3–13.7 °C from first feeding to a mean size of 466–1265 g, then 13.3–15.1 °C during growout. On average, all-female groups grew faster than mixed-sex groups; however, environmental conditions and performance of individual cohorts varied. In a comingled production cycle, diploid all-female salmon grew faster than triploid counterparts. Early maturation rates ranged from 0 % to 67 %, with a mean maturation rate of 34 % for diploid mixed-sex fish and 67 % and 13 % for two diploid all-female groups, respectively. Triploid all-female Atlantic salmon did not mature. This research confirms biological and technological feasibility of growing Atlantic salmon to market-size in land-based systems but controlling early maturation of diploid salmon remained a challenge under the conditions utilized in these trials. This research provides important data inputs to optimize operational and financial projections for existing and potential land-based Atlantic salmon farms.