Evaluation of silver perch (Bidyanus bidyanus, Mitchell) nutritional requirements during grow-out with high and low protein diets at two feeding levels

Silver perch (Bidyanus bidyanus, Mitchell) of 65 g average weight were reared at high density under controlled conditions on diets containing 24.8% and 40.6% protein. Diets were fed at 2% or 4% of the fish biomass day^?1. Both protein concentrations and feeding level of the diet influenced growth and proximate composition of the fish at the end of the 50‐day growth trial. Energy requirement for maintenance for these fish was found to be 77 cal BW^?0.8 and for each unit of energy retained 3.78 cal BW^?0.8 needed to be supplied, and for each gram of protein retained per metabolic body weight 5.04 g were required. The results indicate that it is possible to obtain the same weight increment when feeding a 24.8% protein diet at a level of 4% body weight day^?1 as compared with only 2% body weight day^?1 of a 40.6% protein diet. This study indicates that the nutritional requirements for early grow‐out are similar to those found in a previous study with juvenile silver perch and adds information concerning the required relationships between dietary amino acids. The results provide information required for further refinement of nutrition for this species.     

Glucose tolerance in turbot, Scophthalmus maximus (L.)

Eighty turbot, Scophthalmus maximus (L.), (average weight 61 g) were injected intraperitoneally with exactly 1 g glucose per kg body weight. There was a peak in plasma glucose 3 h post injection. Thereafter a gradual decrease to basal levels was seen within 24 h. Plasma triacylglycerol concentrations showed a rapid decline during the first 24 h, and thereafter stable values. Blood haematocrit values decreased from 20% before injection to 16% 72 h after injection. Liver glycogen concentrations showed an initial decrease from 8 to 5 g 100 g^?1 (w.w) during the first 12 h, and thereafter stable values, while muscle glycogen concentrations increased during the first 12 h, and thereafter showed a gradual decline until 72 h. This response was most probably caused by secondary changes upon handling in combination with the direct response to a glucose load. Thus turbot was able to restore alterations in carbohydrate metabolism efficiently within 24 h.     

Utilization of digestible nitrogen and energy from four agricultural ingredients by juvenile silver perch Bidyanus bidyanus

A comparative slaughter, growth assay was carried out using juvenile silver perch to evaluate different inclusion contents of peanut meal, canola meal, meat meal and dehulled field peas. Each ingredient was combined with a nutritionally balanced basal diet composed mainly of fishmeal (27%), soya bean meal (21%), wheat (28%) and sorghum (11%) such that between 15% and 75% of the basal diet was wholly replaced by the test ingredient. In addition, the basal diet was replaced with 15%, 30% or 45% of an inert filler (diatomaceous earth) in order to compare diets containing test ingredients and the inert filler. Fish were fed respective test diets twice a day for 56 days under a slightly restricted feeding regime (90% of apparent satiation) to negate any palatability problems. Weight gain of silver perch decreased steadily as the basal diet was systematically replaced with diatomaceous earth, confirming the limiting contribution to weight gain from the basal diet under a restricted feeding regime. Silver perch fed diets containing a mixture of the basal diet and either peanut meal, meat meal, canola meal or up to 60% field peas gained more weight than fish fed diets containing similar contents of the inert filler, indicating silver perch were able to utilize these ingredients to support growth. Regression analysis was applied to investigate protein and energy retention and models were fitted with 95% confidence and prediction intervals. Inspection of these relationships indicated various outliers which greatly affected the fitted models. We postulate that these outliers represent test diets which contain ingredients that are poorly utilized, or poorly utilized at particular inclusion contents. Removal of these outliers greatly improved the fit of each model. Using this approach, the predicted digestible protein (DP) content that gave maximum protein deposition in silver perch was 41.1%. The DP requirement for maintenance was 0.61 g DP kg BW^?0.6 day^?1 and the efficiency of DP for growth above maintenance was constant (0.45) after diets containing 45% or more of peanut meal and 75% of field peas were removed from the fitted model. The digestible energy (DE) requirement for maintenance was 36.79 kJ kg BW^?0.6 day^?1 and the efficiency of digestible energy for growth above maintenance was constant (0.68) after diets containing 75% of field peas and 75% of canola were removed from the fitted model. Adherence of other diets containing test ingredients to the slope of each regression suggests that silver perch are capable of utilizing any of the protein sources tested at all but the inclusion contents described above. Confirmation of this approach under different feeding regimes is required.     

New production strategy for silver perch (Bidyanus bidyanus); over‐wintering fingerlings in a tank‐based recirculating aquaculture system

Slow growth and losses to bird predation and infectious diseases in winter can compromise the profitability of silver perch farming. To evaluate over‐wintering silver perch (Bidyanus bidyanus) in a recirculating aquaculture system (RAS), fingerlings (38 g) were stocked in either cages in a pond at ambient temperatures (10–21 °C) or tanks in the RAS at elevated temperatures (19–25 °C) and cultured for 125 days. Mean survival (96%), final weight (146 g), specific growth rate (1.07% day^?1) and production rate (28.1 kg m^?3) of fish in the RAS were significantly higher than for fish over‐wintered in cages (77%, 73 g, 0.53% day^?1, 11.1 kg m^?3). Fish from both treatments were then reared in cages for a further 129 days. Final mean weight of fish originally over‐wintered in the RAS was 426 g, while fish over‐wintered in cages were only 273 g. To determine optimal stocking densities, fingerlings (11.8 g) were stocked at 500, 1000 or 1500 fish m^?3 in tanks in the RAS and cultured for 124 days. Survival was not affected, but growth was significantly slower and feed conversion ratio higher at 1500 fish m^?3 compared with 500 or 1000 fish m^?3. Results demonstrate that over‐wintering silver perch in an RAS can produce large fingerlings for grow‐out in early spring. This strategy could eliminate bird predation, reduce losses to diseases and shorten the overall culture period.     

Investigation of the nutritional requirements of Australian snapper Pagrus auratus (Bloch & Schneider 1801): digestibility of gelatinized wheat starch and clearance of an intra-peritoneal injection of d-glucose

Two experiments were performed to investigate the digestibility and utilization of carbohydrate sources by Australian snapper Pagrus auratus. In the first experiment, snapper of two different size classes (110 and 375 g) were fed a reference diet containing no starch (REF) or diets containing 150 (PN15), 250 (PN25), 350 (PN35) or 450 g kg^?1 (PN45) of 100% gelatinized wheat starch to investigate the interactive effects of fish size and starch inclusion level on apparent organic matter (OM) or gross energy (GE) digestibility (ADC), post‐prandial plasma glucose concentration, hepatosomatic index (HSI) and liver or tissue glycogen content. A second experiment used a 72 h time course study to investigate the ability of larger snapper (300–481 g) to clear an intra‐peritoneal injection of 1 g d ‐glucose kg^?1 body weight (BW). Organic matter and GE ADCs declined significantly in both fish sizes as the level of starch increased (PN45energy small fishenergy large fish). There was no interaction between fish size and inclusion level with respect to GE or OM ADCs. Gross energy ADC for both sized fish was described by the linear function GE ADC=104.97 (±3.39)–0.109 (±0.010) × inclusion level (R²=0.86). Hepatosomatic index, liver and muscle glycogen concentrations were significantly elevated in both small and large snapper‐fed diets containing gelatinized starch compared with snapper fed the REF diet. Three‐hour post‐prandial plasma glucose concentrations were not significantly affected by fish size, inclusion level or the interaction of these factors (REF=PN15=PN25=PN35=PN45), and ranged between 1.60 and 2.5 mM. The mean±SD resting level of plasma glucose (0 h) was 2.4±1.1 mM. Circulating levels of plasma glucose in snapper peaked at 18.9 mM approximately 3 h after intra‐peritoneal injection and fish exhibited hyperglycaemia for at least 12–18 h. There were no significant differences between the plasma glucose concentrations of snapper sampled 0, 18, 24, 48 or 72 h after injection (0=18=24=48=72<12< 1<3=6 h), indicating snapper required almost 18 h to regulate their circulating levels of glucose to near‐basal concentrations. Australian snapper are capable of digesting moderate levels of gelatinized wheat starch; however, increasing the dietary content of starch resulted in a reduction in OM and GE digestibility. Smaller snapper appear to be less capable of digesting gelatinized starch than larger fish, and levels above 250 and 350 g kg^?1 of diet are not recommended for small and large fish respectively. Snapper subjected to an intra‐peritoneal injection of d ‐glucose have prolonged hyperglycaemia; however, the post‐prandial response to the uptake of glucose from normally digested gelatinized starch appears to be more regulated.     

Use of formalin and copper to control ichthyophthiriosis in the Australian freshwater fish silver perch (Bidyanus bidyanus Mitchell)

Infestations of the protozoan parasite, Ichthyophthirius multifiliis, cause the serious disease ichthyophthiriosis in freshwater fish throughout the world. Formalin is a recommended treatment for ichthyophthiriosis in the Australian fish silver perch (Bidyanus bidyanus Mitchell), but the disease is difficult to control in ponds, particularly at low water temperatures. Experiments were carried out to develop an improved treatment regime for formalin and to evaluate copper as a therapeutant. Silver perch fingerlings infested with I. multifiliis were stocked into 55 L aquaria at temperatures of 14.8–17.6 °C and alkalinities of 70–110 mg L^?1. Formalin (34–38% formaldehyde) or copper (24.5% copper sulphate) were added to the aquaria and then monitored and readjusted to nominal concentrations daily. A concentration of 30 mg L^?1 formalin controlled ichthyophthiriosis, but fish treated with 20 mg L^?1 remained infested with theronts and trophonts on day 17; survival at both concentrations was 100%. A concentration of 10 mg L^?1 formalin did not control ichthyophthiriosis and all fish were dead from the infestation by day 17. Fish treated with 0.1 or 0.2 mg L^?1 copper were free of theronts and trophonts by days 17 and 14, respectively, and survival was 100%. Survival at 0.05 mg L^?1 copper was 100%, but fish remained infested. At 0.25 mg L^?1 copper, survival was 82.5% and there were no theronts or trophonts on gill and skin tissues of fingerlings by day 14. There was total mortality of fish treated with 0.5 or 1.0 mg L^?1 copper suggesting these concentrations are toxic to silver perch. All fish in infested‐control treatments died. In earthen ponds containing silver perch, 0.2 mg L^?1 copper was depleted to below 0.1 mg L^?1 within 24 h, and concentrations of 25–38 mg L^?1 formalin were depleted to below 15 mg L^?1 within 48 h. Treatment regimes involving daily applications of formalin or copper controlled ichthyophthiriosis in silver perch in earthen ponds at costs of $US466.37 and $US65.58 hectare^?1 day^?1 respectively. This study has developed a new formalin‐treatment regime for the control of ichthyophthiriosis, and demonstrated that copper sulphate is a potential therapeutant for this serious disease of silver perch.     

Renal threshold for urinary glucose excretion by tilapia in response to orally administered carbohydrates and injected glucose

Two experiments, oral carbohydrate administration (Experiment 1) and vein glucose injection (Experiment 2), were conducted to gain more insight into the ability of hybrid tilapia, Oreochromis niloticus × O. aureus, to utilize different carbohydrates and to establish the kidney threshold for urinary glucose excretion. In Experiment 1, both glucose and starch were administered orally after the tilapia were fasted for 24 h. Plasma and urine were sampled from the fish at selected time intervals from 1 to 24 h thereafter. Higher (p<0.05) plasma and urine glucose concentrations were found in fish fed on glucose than in fish fed on starch. The concentration of plasma glucose of tilapia peaked at 3 h (25.45 mM for glucose; 8.24 mM for starch) after the oral ingestion of both carbohydrates. Maximum urinary glucose concentrations (48 mM for glucose; 10 mM for starch) in fish fed glucose and starch were at 3 and 4 h post administration. In Experiment 2, five concentrations (0, 0.08, 0.12, 0.16 and 0.24 g glucose ml^–1) of glucose solution were injected into the caudal vein of the tilapia. Urine were sampled from the fish at 30-min time intervals from 0 to 6 h after the injection. Blood was sampled at 1 h after the injection. Higher urinary glucose concentrations were observed in fish injected with 0.12 g glucose ml^–1. When the urinary glucose concentrations in fish injected with the various glucose concentrations were plotted against the plasma glucose concentrations of the fish 1 h after injection, the kidney threshold for urinary glucose excretion in tilapia appeared to be about 6 mM.     

Development of a feeding strategy for silver perch, Bidyanus bidyanus (Mitchell), based on restricted rations

To develop a feeding strategy for the Australian freshwater fish silver perch (Bidyanus bidyanus Mitchell), a series of eight experiments was done in 1 m³ cages in an aerated, earthen pond to determine the effects of feeding rate (% body weight) and feeding frequency (no. of feeds day^?1) on the growth and feed conversion ratio (FCR) of fingerlings and larger fish under ambient water temperatures over the range 13.8–30.6°C. Fish were fed extruded pellets of a silver perch diet containing 34% digestible protein and 14 MJ kg^?1 digestible energy. Commercial silver perch farmers were consulted about feeding practices for large fish (>500 g) and at water temperatures below 12°C, and winter feeding practices for other warmwater species were used to complete the strategy. In the feeding experiments, growth and FCR increased with increasing feeding rates to a level above which only FCR increased. Optimal feeding rates and frequencies were those which resulted in maximal growth, while minimizing effort (feeding frequency) and FCR. The highest feeding frequency required for maximal growth, including that of small fingerlings was twice (2 ×) daily, and the optimal feeding rates varied with water temperature and size of fish. The optimal daily regimes were: small fingerlings (initial mean weight, 2.0 g) 7.5% 2 × at a mean temperature of 23.3°C; fingerlings (14.9–27.7 g) 7.5% 2 × at 27.1°C, 5.0% 2 × at 23.7°C and 2.0% 1 × at 16.8°C; and large silver perch (162.5–510.6 g) 0.5% 1 × daily or 1.0% on alternate days at 15.6°C, 1.0% 1 × at 17.3°C, 3.0% 2 × at 24.1°C and 2.0% 2 × at 27.9°C. It is suggested that regimes of 0.5% 1 × daily for fingerlings (<50 g) and 0.5% 1 × on alternate days for larger fish are used at temperatures of 9–12°C, and 0.5% 3 days week^?1 and 0.5% 1 day week^?1 for fingerlings and larger fish, respectively, at 6–9°C. Feed inputs should not exceed 150 kg ha^?1 day^?1 in ponds less than 0.3 ha and 100 kg ha^?1 day^?1 in larger ponds. Our research has established a feeding strategy for silver perch based on restricted rations.     

Evaluation of juvenile silver perch Bidyanus bidyanus (Mitchell) nutritional needs using high- and low-protein diets at two feeding levels

Juvenile silver perch Bidyanus bidyanus (Mitchell) of 3.2 g average weight were reared under controlled conditions on diets containing 23.4% and 40.6% protein. Diets were administered at 3% or 6% of the fish biomass per day. Both the protein concentrations and the feeding level of the diet influenced growth and proximate composition of the fish at the end of the 100-day growth trial. The energy requirement for these fish for maintenance was found to be 81.9 kcal × BW^–0.8 and, for each unit of energy retained per metabolic body weight, 7.05 needed to be supplied, whereas for each gram of protein retained per metabolic body weight, 5.79 g were required. The results indicate that it is possible to obtain the same weight increment when feeding a 23.4% protein diet at a level of 6% body mass day^–1 compared with only 3% body mass day^–1 of a 40.6% protein diet. This study provides the first estimation of nutrient requirements for juvenile silver perch, and these estimations require further refinement.     

Carbohydrate utilization by juvenile silver perch, Bidyanus bidyanus (Mitchell). II. Digestibility and utilization of starch and its breakdown products

Abstract The ability of silver perch ( Bidyanus bidyanus ) to digest and utilize dietary starch or starch breakdown products was investigated. For experiment 1 the ability of silver perch (2.7 ± 0.01 g) to digest wheat starch at two dietary inclusion levels (30% or 60%), each at four levels of gelatinization (0%, 25%, 50% or 80%), was investigated over a 31-day period. For experiment 2, the ability of silver perch (15.9± 0.25 g) to digest wheat starch, dextrin (at three levels of dextrinization), maltose, glucose and pea starch, all at the 30% inclusion level, was investigated over a 41-day period. Water temperature for both experiments was 25 ± 1 °C. Apparent digestibility coefficients (ADCs) for starch, dry matter (DM) and energy were affected by both degree of gelatinization (80% > 50% > 25% = 0%) and inclusion level (30% > 60%). Specific growth rate (SGR) was unaffected by the inclusion of 30% starch; however, it was reduced at the 60% starch content level. Degree of gelatinization had no effect on SGR. For experiment 2, there were significant differences between carbohydrate and DM ADCs for the test ingredients. The carbohydrate, DM and energy ADCs were ranked as follows: dextrin (Fieldose 9) = dextrin (Fieldose 17) = dextrin (Fieldose 30) = gelatinized wheat starch = maltose = glucose > raw wheat starch > raw pea starch. The protein ADC of the diets, postprandial plasma glucose concentration and SGR were all unaffected by ingredient type. For both experiments, HSI tended to increase with carbohydrate inclusion. Liver glycogen concentrations were also elevated, but muscle glycogen and liver and muscle triacylglycerol concentrations were unaffected. Digestibility of starch by silver perch is clearly affected by inclusion content and processing.     

Effects of formalin on water quality and parasitic monogeneans on silver perch (Bidyanus bidyanus Mitchell) in earthen ponds

Infestations of parasitic monogenean trematodes (Lepidotrema bidyana and Gyrodactylus sp.) on freshwater silver perch (Bidyanus bidyanus Mitchell) in earthen ponds were treated with formalin (37% formaldehyde). Concentrations of 30 and 40 mg L^?1 formalin were effective, but fish in ponds treated with 20 or 25 mg L^?1 remained infested. At temperatures of 24.1–26.9°C, concentrations of 30 or 40 mg L^?1 formalin caused dissolved oxygen (DO) to decline from 10.1–11.9 to 3.0–3.3 and 1.2–1.7 mg L^?1, respectively, within 36–42 h of treatment. In addition, pH declined from 7.2–8.4 to 6.3–6.7, within 36 h and turbidity decreased over 48 h. In the ponds where DO was 1.2–1.7 mg L^?1, silver perch showed signs of severe stress, but continuous aeration (10 hp ha^?1) for 3 days and inflow of well‐oxygenated water for 6–8 h prevented mortalities. At temperatures of 13.2–15.7°C, concentrations of 30 or 40 mg L^?1 formalin caused DO to decline from 9.0–10.0 to 6.0–8.1 mg L^?1 and pH from 7.0–7.3 to 5.9–6.6 within 72 h. Total ammonia‐nitrogen increased over 72 h in ponds treated with 30 or 40 mg L^?1 formalin. Fish became re‐infested with L. bidyana in all ponds within 30 days of treatment. A concentration of 30 mg L^?1 formalin is recommended as a treatment for monogeneans on silver perch in ponds, but aeration is necessary to maintain adequate water quality at higher temperatures.     

Effects of chronic confinement on physiological responses of juvenile gilthead sea bream, Sparus aurata L., to acute handling

Understanding how gilthead sea bream, Sparus aurata L., an important Mediterranean Sea species for aquaculture, respond physiologically to stressors commonly encountered in intensive rearing is important for effective production, as managing for stress is a major factor in maintaining healthy fish stocks. Our objective was to determine whether holding juvenile gilthead sea bream at a high density (HD), as a chronic stressor, would affect their physiological responses to a subsequent acute handling stressor. After acclimation at a low density (LD) of 6 kg m^?3 in 200‐L circular tanks containing 33–36 g L^?1 recirculating seawater at 19°C under a normal photoperiod, juvenile 37‐g gilthead sea bream were confined for 14 days at a HD of 26 kg m^?3 and then subjected to 30‐s aerial emersion in a dipnet. Plasma levels of cortisol, glucose, lactate, osmolality and chloride were determined in fish held in separate lots during LD (control) and HD confinement at 0, 1, 2, 7 and 14 days, and then after handling at 0, 1, 2, 4 and 8 h. Although plasma cortisol levels were similar in LD and HD fish groups after 14 d of confinement (15 and 23 ng mL^?1, respectively), the cortisol response in fish from the HD treatment at 1 and 2 h following acute handling (70 and 37 ng mL^?1, respectively) was only about half of that measured in the control group (139 and 102 ng mL^?1); plasma cortisol was similar in both groups by 4 and 8 h. In contrast, plasma glucose elevations in response to handling were higher at 4 and 8 h in the HD‐held fish (94 and 72 mg dL^?1, respectively) than in those from the LD treatment (59 and 51 mg dL^?1); glucose responses were similar in both groups at 1 and 2 h after handling and throughout confinement. Plasma lactate levels were higher in LD fish than in the HD group at the beginning of the experiment but were similar after 14 d confinement and responses to handling were similar (e.g. 33 and 35 mg dL^?1 at 1 h). Plasma osmolality showed increases during the first 2 h after acute handling but no differences were evident between the two density treatments at any time during confinement or posthandling. Plasma chloride levels did not change throughout the experiment. The reduced plasma cortisol response to acute handling likely resulted from negative feedback of mildly but chronically elevated circulating cortisol caused by the confinement stressor on the hypothalamic–pituitary–interrenal axis. While other post‐handling physiological changes also showed differences between treatment groups, the suppressed cortisol response in the HD‐held fish suggests a reduction in the gilthead sea bream's normal capacity to respond to an acute stressor.     

Spawning induction and hormonal levels during final oocyte maturation in the silver perch (Bidyanus bidyanus)

The silver perch (Bidyanus bidyanus Mitchell) (Teraponidae), is a native Australian freshwater fish that, due to its high potential for aquaculture, was introduced to Israeli fish farming. The objective of this study was to find an optimal method for inducing spawning of silver perch. The agents tested for this purpose were: human chorionic gonadotropin (hCG; 150 or 200 IU/kg BW); salmon gonadotropin releasing hormone analogue (sGnRHa at 10, 20, 30, or 40 μg/kg BW); mammalian GnRH analogue (mGnRHa at 30 μg/kg) and the combination of sGnRHa at 20 μg/kg and domperidone at 5 mg/kg BW. Based on spawning success and relative fecundity, sGnRHa at the dose of 30 μg/kg was found to be more efficient than hCG, mGnRHa or sGnRHa with domperidone. Since domperidone does not improve the GnRHa effect on final oocyte maturation (FOM) and spawning, it is suggested that the dopaminergic inhibition during the stages of FOM in the silver perch is weak. Therefore, the use of GnRHa alone is sufficient to induce spawning in this fish. Immunoreactive gonadotropin (IR-GtH) and estradiol levels increased after a single injection of sGnRHa, and peaked after 24 h. Plasma levels of 17α,20β-dihydroxy-4-pregnen-3-one (17,20-P) also increased significantly 24 h after the injection of mGnRHa, 12 h before spawning, suggesting that 17,20-P is the maturation-inducing steroid in silver perch. In order to reveal whether the heterologous gonadotropin may elicit an immunological reaction, silver perch was subjected to prolonged treatment with hCG. This treatment resulted in no detectable titer of antibodies against the mammalian gonadotropin. In conclusion, although hCG has no deleterious effects in this fish, and is the more commonly used for spawning induction, sGnRHa at 30 μg/kg is the recommended treatment for spawning induction of female silver perch under the conditions prevailing in Israeli aquaculture.     

Plasma cortisol and hypothalamic monoamine responses in yellow perch <Emphasis Type="Italic">Perca flavescens</Emphasis> after intraperitoneal injection of lipopolysaccharide

The concentrations of monoamines in the hypothalamus were determined in yellow perch Perca flavescens before and after injection with lipopolysaccharide (LPS; 3 mg kg⁻¹ fish weight) or saline to test for the presence of neurochemical changes potentially associated with changes in plasma cortisol characteristic of intraperitoneal (ip) challenge with LPS. In the first experiment, yellow perch were injected with saline or LPS and the hypothalamus removed and plasma sampled before and at 0.5, 1.5, 3.0, and 6 h after injection. Plasma cortisol was elevated in both saline- and LPS-injected fish through 1.5 h after injection and returned to levels resembling pre-injection by 3 h after injection. Significantly higher amounts of cortisol in plasma from LPS-injected relative to saline-injected fish were observed 6 h following injection. A significant decrease relative to levels observed 0.5–3 h after handling was observed in serotonin concentrations at 6 h following LPS and saline injection with a concomitant increase in the ratio of 5-hydroxyindoleacetic acid:serotonin. In the second experiment, hypothalamic monoamines were sampled before and at 3, 6, 9, 12, and 24 h after injection with LPS or saline. Significant increases from pre-injection levels were observed in the ratio 5-hydroxyindoleacetic acid:serotonin at 9, 12, and 24 h after injection, but no differences were detected between LPS- and saline-injected fish. These results support a model linking serotonergic system activation following handling stress, but no correlations with the sustained elevations of plasma cortisol associated with inflammatory challenge were observed.     

Size‐related oxygen consumption and ammonia excretion of Eurasian perch (Perca fluviatilis L.) reared in a recirculating system

Oxygen consumption (OC) and ammonia excretion rates (AE) of perch were measured under commercial‐like conditions (temperature 23.3 °C) in both fed (F) and feed‐deprived groups (D). Measurements were taken in triplicate in six sized batches of perch ranging from 44.8 to 336.2 g. The mean daily OC was 288.3–180.6 mg O₂ kg^?1 h^?1 for group F fish ranging in size from 44.8 to 279.4 g body weight. The mean daily AE expressed as total ammonia nitrogen (TAN) was 13.8–5.2 mg TAN kg^?1 h^?1 in the same groups. Daily peaks of OC in group F perch were observed 6 h after the onset of feeding for each size group with relatively stable values up to the end of feeding. Peaks of daily AE in group F perch were observed 10 h after the onset of feeding in each size group, with a rapid decrease up to 16 h after onset. In group D, OC was 181.1–110.5 mg O₂ kg^?1 h^?1 in the weight range 57.9–336.2 g. The daily mean AE was 1.7–0.5 TAN kg^?1 h^?1 in this group. No dramatic peaks of OC and AE were observed in group D perch.     

A wide difference in susceptibility to nitrite between Eurasian perch (Perca fluviatilis L.) and largemouth bass (Micropterus salmoides Lac.)

Influence of nitrite on two fish species, Eurasian perch (Perca fluviatilis L.) and largemouth bass (Micropterus salmoides Lacépède), was assessed in two acute toxicity tests. In the first one, lethal concentrations (48hLC50) of nitrite were estimated at 11 mg l^?1 NO₂ ^? for perch and 882 mg l^?1 NO₂ ^? for bass. In the second test, fishes were exposed for 48 h to concentrations representing ¼ and ½ value of 48hLC50 for each species. This test showed that the higher nitrite concentration in the water the higher methaemoglobin content in the blood, and nitrite levels in the blood plasma were observed in both species. On the other hand, leucocyte count showed opposite trend. Activity of NADH-methaemoglobin reductase was markedly lower in largemouth bass compared to Eurasian perch and was stimulated by nitrite exposure in neither of the species.     

The growth performance of southern catfish fed diets with raw, precooked cornstarch and glucose at two levels

The ability of juvenile carnivorous southern catfish (Silurus meridionalis Chen) to use different levels, kinds and physic state (glucose, raw cornstarch and precooked cornstarch) of dietary carbohydrate was evaluated in term of growth performance. All diets contained 100 g kg^?1 lipid and 16 kJ metabolizable energy. Three isonitrogeneus (400 g kg^?1) diets were formulated to contain 150 g kg^?1 raw cornstarch, precooked cornstarch and glucose. Another three isonitrogeneus (300 g kg^?1) diets were formulated to contain 300 g kg^?1 raw cornstarch, precooked cornstarch and glucose. A control diet was formulated with no carbohydrate containing 500 g kg^?1 protein. Each experimental diet was fed to four tanks of 10 fish (28.3 ± 0.5 g) for 8 weeks at 27.5 °C. Specific growth rate (SGR) of 300 g kg^?1 glucose diet was significantly lower than those of other diets (P < 0.05). Feeding rates (FR) of 300 g kg^?1 glucose and control diets were significantly lower than those of the other diets (P < 0.05). Feed efficiency (FE) was significantly decreased with increased dietary carbohydrate level (P < 0.05). Feed efficiency of the 300 g kg^?1 glucose diet was significantly lower than those of the 300 g kg^?1 raw and precooked cornstarch diets (P < 0.05). The protein efficiency ratio (PER) was significantly increased with dietary carbohydrate level except that of the 300 g kg^?1 glucose diet, which was lowest among all diets (P < 0.05). The results suggested that both dietary starch and glucose were utilized for energy in southern catfish and had a protein‐sparing effect. At 150 g kg^?1 inclusion level, the utilization of raw and precooked cornstarch and glucose did not vary significantly, but a higher dietary glucose level (300 g kg^?1) had a markedly detrimental effect on growth in southern catfish.     

Carbohydrate utilization by juvenile silver perch,Bidyanus bidyanus (Mitchell). IV. Can dietary enzymes increase digestible energy from wheat starch,wheat and dehulled lupin?

The effects of exogenous digestive enzyme supplements on the digestibility of wheat starch or diets containing either wheat or dehulled lupin (Lupinus angustifolius var. gungurra) by silver perch (Bidyanus bidyanus) were investigated. In the first experiment, Natustarch^® (α‐amylase supplement specific to starch) was added at three nominal concentrations (0, 50, 100 or 150 mg kg^?1 diet) to diets containing either raw or 100% gelatinized wheat starch (30% dietary inclusion content) and fed to silver perch. The apparent digestibility coefficients (ADCs) for dry matter, starch and energy were calculated. The action of Natustarch^® on the diet and in the digestive tract was also investigated. The addition of Natustarch^® to diets containing raw and gelatinized wheat starch led to an average increase in reducing sugar content of diets of 67% and 340% respectively, indicating that the α‐amylase was more efficient at hydrolysing wheat starch in the gelatinized form. Gelatinized wheat starch was digested more efficiently than raw wheat starch. However, although the addition of Natustarch^® at ≥ 50 mg kg^?1 led to a significant increase in digestibility of raw wheat starch; the digestibility of gelatinized wheat starch, which was already high, was not further improved. Leaching due to immersion in water caused a minor loss of α‐amylase activity from diet pellets treated with Natustarch^® (～ 13% after 5 min). The α‐amylase activity in the anterior section of the intestinal tract of silver perch fed diets containing Natustarch^® was not affected, indicating that the α‐amylase had been denatured by the acidic conditions in the stomach of silver perch. In the second experiment, diets containing wheat or lupin (at the 30% inclusion content) were treated with Natugrain‐blend^®[an enzyme supplement containing β‐glucanase and β‐xylanase, specific to non‐starch polysaccharides (NSPs)] at three nominal concentrations (0, 75, 150 or 300 μL kg^?1) and fed to silver perch. ADCs for energy and protein were calculated. The addition of Natugrain‐blend^® had no effect on dry matter, energy or protein digestibility of the diets or ingredients.     

Impact of inducing general anesthesia with Propiscin (etomidate) on the physiology and health of European perch (<Emphasis Type="Italic">Perca fluviatilis</Emphasis> L.)

The aim of the study was to describe the course and timing of the different stages of anesthesia induced with Propiscin (etomidate) on juvenile European perch (experiment I) and to describe the effect of immersing specimens of this species had on selected hematological and biochemical parameters (experiment II). The study was conducted on material with body weights (BW) of 162.98 (experiment I) and 171.60 g (experiment II). In experiment I, general anesthesia was induced with two different anesthetic concentrations (1 or 2 ml l^?1; anesthesia time 10 min). In experiment II, blood was drawn for hematological and biochemical analyses from the fish that had been exposed to anesthetic immersion baths with two different concentrations of Propiscin (1 and 2 ml l^?1) and for different exposure times (3 and 10 min). Blood samples were collected immediately following immersion (0 h) and 24 h later (24 h). Specimens that were immersed at the higher concentration of anesthetic achieved subsequent stages of general anesthesia two times faster (P ≤ 0.05). However, during recovery, some statistically significant differences were observed, but these lasted only until stage I was achieved. Among the hematological parameters (0 h), significant differences were observed in hematocrit (HCT) and mean corpuscular volume (MCV), while among the biochemical determinations (0 h), statistically significant differences were noted in the concentrations of glucose, calcium, lactate, and ammonia. After 24 h, the levels of these parameters in all fish groups returned to initial values. The hematological and biochemical tests conducted permit concluding that the anesthetic tested, at the concentrations (1 and 2 ml l^?1) and the exposure times of up to 10 min at which it was tested, is safe and can be used successfully to induce general anesthesia in perch.     

Blood chemistry and organ nutrient composition in Atlantic salmon, Salmo salar L., fed graded amounts of wheat starch

After feeding Atlantic salmon, Salmo salar L., five graded amounts of wheat starch from 0 to 310 g kg^?1, low but increased levels of glycogen in kidney, heart and gills were determined. No variations were found in proximate or glycogen compositions of muscle, whereas the liver composition reflected the diet composition. Whole-body homogenates varied in dry matter and lipid levels; the variation was according to g lipid eaten per fish. Plasma glucose levels ranged above average levels only when the starch level in the feed was higher than 220 g kg^?1. Although feed intake and thereby lipid intake increased as dietary carbohydrate increased in the present experiment, no differences in plasma concentrations of cholesterol and only small changes in triglycerides were determined. The increase in dietary carbohydrate was balanced with protein, and total plasma protein concentrations followed the decrease in feed protein content. Haematocrit, haemoglobin, mean cell volume and mean cell haemoglobin all showed significantly reduced levels as dietary starch increased, indicating a fibre effect from ‘left-over’ starch in the intestine followed by reduced absorption of divalent ions, such as iron.