Composition of ovarian fluid in endangered Caspian brown trout, <Emphasis Type="Italic">Salmo trutta caspius</Emphasis>, and its effects on spermatozoa motility and fertilizing ability compared to freshwater and a saline medium

In this study, ovarian fluid composition and its effects on the motility and fertilizing ability of sperm were studied in endangered Caspian brown trout, Salmo trutta caspius, and were compared with a saline activation medium (125 mM NaCl, 30 mM Glycine, 20 mM Tris–HCl, pH = 9.0) and freshwater as the control. The ovarian fluid was composed of sodium 164.4 ± 4.4 mM l⁻¹, potassium 1.8 ± 0.1 mM l⁻¹, calcium 0.6 ± 0.1 mM l⁻¹, magnesium 0.4 ± 0.02 mM l⁻¹, chloride 127.4 ± 5.9 mM l⁻¹, total protein 389.5 ± 89.6 mg 100 ml⁻¹, cholesterol 9.3 ± 1.2 mg dl⁻¹, and glucose 3.3 ± 0.2 mM l⁻¹. The percentage of motile spermatozoa and the duration of sperm motility were significantly higher in ovarian fluid (62 ± 3%, 74.6 ± 0.8 s) than freshwater (35 ± 4%, 44 ± 1 s), but they did not differ significantly from saline medium (56 ± 3%, 74.3 ± 0.7 s) (P > 0.05). Higher eyeing rates were observed after the activation of sperm in ovarian fluid and saline solution than freshwater when 35,000 or 350,000 spermatozoa per egg were added into the activation media. However, no significant differences were observed at higher concentrations of spermatozoa per egg (730,000) (P > 0.05). Also, this study showed that the ovarian fluid composition can be considered as a species-specific character among salmonid fishes. As a conclusion, the results of this study recommend the use of ovarian fluid or the saline solution as an activation medium in the artificial reproduction of Caspian brown trout.     

Influence of cell volume changes on protein synthesis in isolated hepatocytes of air-breathing walking catfish (<Emphasis Type="Italic">Clarias batrachus</Emphasis>)

The present study aimed at determining the effect of cell volume changes on protein synthesis, measured as the incorporation of [³H]leucine into acid-precipitable protein, in isolated hepatocytes of air-breathing walking catfish (Clarias batrachus). The rate of protein synthesis, which was recorded to be 10.02 ± 0.10 (n = 25) nmoles mg⁻¹ cell protein h⁻¹ in isotonic incubation conditions, increased/decreased significantly by 18 and 48%, respectively, following hypo- (−80 mOsmol l⁻¹)/hypertonic (+80 mOsmol l⁻¹) incubation conditions (adjusted with NaCl), with an accompanying increase/decrease of hepatic cell volume by 12 and 20%, respectively. Similar cell volume-sensitive changes of protein synthesis were also observed when the anisotonicity of incubation medium was adjusted with mannitol. Increase of hepatic cell volume by 9%, due to addition of glutamine plus glycine (5 mM each) to the isotonic control incubation medium, led to a significant increase of protein synthesis by 14%. Decrease of hepatic cell volume by 15 and 18%, due to addition of dibutyl-cAMP and adenosine in isotonic control incubation medium, led to a significant decrease of protein synthesis by 30 and 34%, respectively. Thus, it appears that the increase/decrease of hepatic cell volume, caused either by changing the extracellular osmolarity or by the presence of amino acids or certain other metabolites, leads to increase/decrease of protein synthesis, respectively, and shows a direct correction (r = 0.99) between the hepatic cell volume and protein synthesis in walking catfish. These cell volume-sensitive changes of protein synthesis probably help this walking catfish in fine tuning the different metabolic pathways for better adaptation during cell volume changes and also to avoid the adverse affects of osmotic stress. This is the first report of cell volume-sensitive changes of protein synthesis in hepatic cells of any teleosts.     

Acute toxicity of nitrite on tilapia (Oreochromis niloticus) at different external chloride concentrations

Tilapias (Oreochromis niloticus) juveniles (total length 4.9 ± 0.2 cm and weight 1.8 ± 0.2 g) were exposed to several nitrite concentrations (0, 10, 18, 32, 56 and 100 mg l⁻¹) for 96 h, using a semi-static renewal method at chloride levels of 35.0 and 70.0 mg l⁻¹. At the end of the 96-h period, the median lethal concentration (LC₅₀) of nitrite was 28.18 mg l⁻¹ in water with low chloride content (35.0 mg l⁻¹) and 44.67 mg l⁻¹ with high chloride content (70.0 mg l⁻¹, respectively). It indicated that high concentrations of chloride ions could reduce the toxicity of nitrite. During the toxicity experiments, the behaviour and clinical signs of tilapias were also observed. Furthermore, the test of toxic mechanism was designed taking five test concentrations, viz., 5, 10, 15 and 20 mg l⁻¹ and a nitrite-free control. Nitrite exposure produced high levels of methaemoglobin (MHb) but did not seem to cause mortality, as surviving tilapias showed high levels (85.37 ± 2.23 and 53.82 ± 3.44 at 35.0 and 70.0 mg l⁻¹ chloride, respectively). The percentage of MHb exposed to nitrite was significantly higher (P<0.05) than the control (0 mg l⁻¹ nitrite) and increased with the increasing nitrite concentration. However, the percentage of MHb decreased with the increasing chloride concentration.     

Effect of prebiotic xylooligosaccharides on growth performances and digestive enzyme activities of allogynogenetic crucian carp (<Emphasis Type="Italic">Carassius auratus gibelio</Emphasis>)

The effect of prebiotic xylooligosaccharides (XOS) on the growth performance and digestive enzyme activities of the allogynogenetic crucian carp, Carassius auratus gibelio, was investigated. XOS was added to fish basal semi-purified diets at three concentrations by dry feed weight: diet 1, 50 mg kg⁻¹; diet 2, 100 mg kg⁻¹; diet 3, 200 mg kg⁻¹, respectively. Twelve aquaria (n = 20) with three replicates for each treatment group (diets 1–3) and control treated without XOS were used. Weights of all collected carp from each aquarium were determined at the initial phase and at the end of the experiment, and the carp survival was also determined by counting the individuals in each aquarium. After 45 days, there were significant differences (P < 0.05) in the relative gain rate (RGR), and daily weight gain (DWG) of diets 1–3 were compared with the control. However, the survival rate was not affected (P > 0.05) by the dietary treatments. For enzymatic analysis, dissection produced a crude mixture of intestine and hepatopancreas of each segment to measure. The protease activity in the intestine and hepatopancreas content of fish in diet 2 (487.37 ± 20.58 U g⁻¹ and 20.52 ± 1.93 U g⁻¹) were significantly different (P < 0.05) from that in the control (428.13 ± 23.26 U g⁻¹ and 12.81 ± 1.52 U g⁻¹) and diet 3 (428.00 ± 23.78 U g⁻¹ and 14.04 ± 1.59 U g⁻¹). Amylase activity in the intestine was significantly higher for diet 2 compared to diet 1 and the control. As for amylase in the hepatopancreas, assays showed higher activity in diet 2 (P < 0.05) compared to the rest.     

Acute toxicity of ammonia on juvenile cobia (Rachycentron canadum, Linnaeus, 1766) according to the salinity

Juvenile cobia (Rachycentron canadum) (total length 15.16 ± 0.92 cm and weight 19.26 ± 4.5 g) were exposed to different concentrations of ammonia–N (unionized plus ionized ammonia as nitrogen), using the static renewal method at different salinity levels of 5, 20, and 35‰ at pH 8.1 and 25°C. The 24, 48, 72, 96 h LC₅₀ values of ammonia–N for R. canadum juveniles were 60.28, 48.57, 37.42, 22.73 mg l⁻¹ at 35‰; 51.25, 43.63, 28.17, 19.05 mg l⁻¹ at 20‰; and 39.48, 25.31, 19.50, 8.13 mg l⁻¹ at 5‰, respectively. The 24, 48, 72, 96 h LC₅₀ values of NH₃–N (unionized ammonia as nitrogen) were 1.81, 1.46, 1.12, and 0.68 mg l⁻¹ at 35‰; 1.75, 1.49, 0.96, and 0.65 mg l⁻¹ at 20‰; and 1.52, 0.97, 0.71, and 0.31 mg l⁻¹ at 5‰, respectively. As the salinity decreased from 35 to 5‰, susceptibility of ammonia–N increased by 34.5, 47.88, 50.56, and 64.23% after 24, 48, 72, and 96 h exposure, respectively. Furthermore, we found that exposure of fish to ammonia–N caused an increase in oxygen consumption of 129.1, 157.5, and 192% and a decrease in the ammonia excretion level of 53.4, 38.2, and 23.3% with respect to the control.     

Comparative growth of Pacific oyster (Crassostrea gigas) postlarvae with microfeed and microalgal diets

Two trials were carried out in the laboratory in order to assess the effect of microparticulated feed (F) and live (Thalassiosira pseudonana, M) diets on the growth of recently set (396 ± 13 μm shell height) and 2 mm Crassostrea gigas postlarvae. Different proportions of M and F (100:0, 75:25, 50:50; 25:75, 0:100) were delivered in a single dose of 3 h d⁻¹ in trial 1. Dietary M:F proportions of 100:0, 50:50, and 0:100 were delivered as a single pulse of 8 h d⁻¹ (P1) or two pulses of 4 h⁻¹ (P2) in trial 2. Maximal daily M ration was 296 cells μl⁻¹ d⁻¹ (trial 1), 150 M cells μl⁻¹ d⁻¹ (trial 2), or their equivalent F dry weight. Shell height (SH), dry (DW), and organic weight (AFDW) were evaluated weekly. Oysters from trial 1 significantly increased their size after 28 days, and exhibited no significant dietary differences in terms of DW (1.21 ± 0.15 to 2.01 ± 0.28 mg) or AFDW (0.091 ± 0.022 to 0.166 ± 0.029 mg). Newly set postlarvae (trial 2) also exhibited significant growth after 25 days. No dietary differences were observed in trial 2, yet P2 oysters attained significantly higher shell heights (825–912 μm) than P1 oysters (730–766 μm) after 25 d. Pulse effects were marginally not significant in terms of AFDW and growth rate. Together, these findings showed that balanced microfeeds have a practical potential for the culture of early C. gigas postlarvae, when they are delivered in pulse-feeding schemes     

Sensitivity of striped trumpeter, Latris lineata, embryos to mechanical shock and simulated transport

The sensitivity of striped trumpeter, Latris lineata, embryos to transport was assessed through mechanical shock at four stages of embryonic development, and simulated transport at different densities and durations. Fertilised egg mortality due to mechanical shock was greatest for embryos shocked 3 and 27 h post-fertilisation (48.6% ± 4.1 and 36.0% ± 3.2, respectively; mean ± SE), and prior to blastopore closure. Mortality of embryos shocked 51 and 75 h post-fertilisation, and following blastopore closure, did not differ from un-shocked controls (9.5% ± 0.7). Density and duration of incubation affected the survival of embryos in a simulated transport trial. Embryonic mortality remained below 3% for all density treatments up to 24 h post-fertilisation. Significant mortality of fertilised eggs occurred when incubated at 5,000 embryos l⁻¹ (17.2% ± 6.9) for 48 h and was correlated with a drop in dissolved oxygen (DO) levels. Final DO concentrations decreased with increasing embryonic density and incubation duration. DO of embryos incubated at 5,000 embryos l⁻¹ was significantly lower than those incubated at 500, 1,000 and 2,500 embryos l⁻¹, at all incubation durations. Mortality was prevalent in treatments that had a final DO level less than 72% saturation at 14°C. Transportation of fertilised striped trumpeter eggs in seawater is recommended from 51 h post-fertilisation at 14°C, after blastopore closure and neural keel development and at densities of no more than 2,500 embryos l⁻¹ for 24 h transportation duration.     

Effects of stocking density on survival and growth of juvenile tench (<Emphasis Type="Italic">Tinca tinca</Emphasis> L.)

In two 120-day experiments, performed in the laboratory at 22°C, the effects of stocking density on the survival and growth of juvenile tench (Tinca tinca L.) were evaluated. Fish were kept in fibreglass tanks, supplied throughout with flow of artesian water, and fed a dry diet for salmonids, in excess, supplemented with restricted amounts of Artemia nauplii. In the first experiment four-month-old juveniles (0.31 ± 0.04 g and 32.00 ± 1.17 mm TL) were stocked at four densities—0.18, 0.88, 1.05, and 2.10 g l⁻¹. Survival was high (>89%) for all treatments. Final densities ranged between 1.10 g l⁻¹ (significantly lowest) and 10.46 g l⁻¹ (significantly highest). The density increase was significantly higher (611%) for fish stocked at the lowest initial density (0.18 g l⁻¹) than for fish stocked at 0.88, 1.05, and 2.10 g l⁻¹, for which the density increase averaged 457%. In the second experiment, 4.5-month-old juveniles (0.58 ± 0.17 g and 39.54 ± 0.83 mm TL) were stocked at three densities—1.05, 3.00, and 4.00 g l⁻¹. Survival was high (>96%) for all treatments. Final densities ranged between 4.08 and 16.53 g l⁻¹ and were significantly higher for greater initial densities. The density increase was greatest (413%) for fish stocked at the highest density (4 g l⁻¹) and was not significantly different for fish stocked at 1.05 and 3 g l⁻¹. Considering all the densities in the two experiments, for stocking at 4 g l⁻¹ the final density was 15 times higher than that reached after stocking at 0.18 g l⁻¹, without harmful effects on survival and growth. This final density (equivalent to 16.53 kg m⁻³) is in the range recommended for other fish species in this period under intensive conditions.     

Acute effects of benzo[a]pyrene on liver phase I and II enzymes,and DNA damage on sea bream <Emphasis Type="Italic">Sparus aurata</Emphasis>

In the present study biotransformation and detoxification responses to acute exposure to the polycyclic aromatic hydrocarbons benzo[a]pyrene (B[a]P) were investigated in the liver of Sparus aurata (sea bream). Sexually immature gilthead sea bream were treated by intraperitoneal injection of B[a]P (20 mg kg⁻¹) for 6, 12, 24, and 48 h. B[a]P accumulation was quantified in sea bream liver by mean of gas phase chromatography (GPC-MS) after the various exposure periods. The following biological responses were measured: (1) ethoxyresorufin-O-deethylase (EROD) activity, as a phase I biotransformation parameter; (2) liver glutathione S-transferase (GST) activity as a phase II conjugation enzyme. DNA damage was assessed over time using the single-cell gel electrophoresis comet assay. B[a]P bioaccumulation in the liver resulted in a biphasic curve with an increasing uptake up to 5.55 ± 0.67 μg g⁻¹ dry weight after only 6 h exposure and 4.67 ± 0.68 μg g⁻¹ dry weight after 48 h exposure. EROD activity showed a nonsymmetrical bell-shaped kinetic with a maximum at 24 h and lower but significant activities at 12 and 48 h with respect to control animals. Hepatic GST activities were only significant after 48 h exposure. Comet assay showed an increase in liver cells DNA damage with a maximum after 48 h exposure reaching up to 12.17 %DNA in the tail.     

Growth,diet, and reproduction of Eurasian perch <Emphasis Type="Italic">Perca fluviatilis</Emphasis> L. in Lake Varese,northwestern Italy

No data have previously been reported on Eurasian perch Perca fluviatilis L. in Lake Varese. In this study, the growth, diet, and reproductive biology of the Eurasian perch population were investigated with the aim of providing information that may serve as a basis for efficient resource management. A total of 240 specimens were caught during the monthly sampling campaign from November 2006 through October 2008. The length-to-weight relationships were W _t = 8.4 × 10⁻³ L _t^3.10 (males) and W _t = 4.1 × 10⁻³ L _t^3.36 (females). The parameters for the von Bertalanffy growth function for pooled sexes were L _∞  = 33.17 cm, k = 0.20 year⁻¹, and t ₀ = −1.34 year. Perch in Lake Varese spawn from April through May. Sexual maturity is reached when males are 2 years old, in females mostly when they are 3 years old. Relative fecundity (F _rel) and absolute fecundity (F _abs) were assessed for females. Fecundity values were similar to data reported for other European populations: females of age 2+ F _rel = 102,457 ± 12,275, age 3+ F _rel = 131,767 ± 5,891, and age 4+ F _rel = 131,252 ± 15,555. Perch diet spectrum was wide and somewhat characterized by season. Perch in Lake Varese feed on macroinvertebrates, mainly Chironomidae and Chaoborus, zooplankton, and juvenile rudd Scardinius erythrophthalmus.     

Tolerance of striped trumpeter Latris lineata embryos to ozonated seawater

The tolerance of striped trumpeter, Latris lineata (Bloch and Schneider 1801) embryos to ozonated seawater was examined as a possible means of disinfection. The effect of a range of ozone doses and exposures (CT = concentration × exposure time) was tested at different stages of embryonic development. Three-day-old embryos two-thirds developed around the yolk were exposed for 0.5, 1 or 5 min to ozone concentrations of 0.5, 1, 2 and 5 mg O₃ l⁻¹ in a fully orthogonal factorial design. For each treatment there were four replicate 250 ml containers that each received 100 ± 15 embryos. There was no significant difference in hatching success between control-treated embryos or embryos ozonated at 0.5 or 1 mg O₃ l⁻¹ for 0.5, 1 or 5 min (P < 0.05). However, hatching success was significantly reduced when embryos were treated with 2 or 5 mg O₃ l⁻¹ for 5 min or 5 mg l⁻¹ O₃ for 1 min (P < 0.05). The tolerance of embryos to 0, 0.5 or 2 mg O₃ l⁻¹ for 1 min at different stages of development (Day 0, 1, 2, 3 or 4), was then examined. An ozone concentration of 0.5 mg l⁻¹ had no effect on hatching success at any stage of development, but a concentration of 2 mg l⁻¹ significantly reduced hatching success on all days except Day 3. A safe and tested hatchery practise is to disinfect striped trumpeter embryos with 1 mg O₃ l⁻¹ for 1 min on Day 3 post-fertilisation when the embryo is two-thirds developed around the yolk.     

Relationship between concentrations of odorous compounds and biomass of phytoplankton and actinomycetes in freshwater ponds of Beijing,China

The odorous compounds including geosmin and 2-methylisoborneol (MIB) were detected in intensively cultivated freshwater ponds in Beijing, China, by coupling head space solid-phase microextraction with gas chromatography mass spectrometry (GC-MS). Moreover, the biomass of phytoplankton and actinomycetes in the fishponds were determined simultaneously, and the relationship between the concentrations of these odorous compounds and the biomass of phytoplankton and actinomycetes was assessed. The results showed that among the odorous compounds detected, geosmin was the main one, and concentrations of 1.22–35.58 ng l⁻¹ were found in all fishponds. Besides, MIB with 1.39–6.00 ng l⁻¹ was found in parts of fishponds. Six phyla and 22 genera of algae were observed in the fishponds with a biomass of 17.33–178.34 mg l⁻¹, among which dominant phyla were Bacillariophyta and Euglenophyta. Four genera of actinomycetes with a gross biomass of 0–76 × 10⁴ ind l⁻¹ were found in the fishponds, of which Streptomyces spp. was the dominant genera. This indicated that geosmin concentration in fishponds was related with the total biomass of the dominant algae. The results showed that Melosira spp. and Cyclotella spp. were the main microalgae to cause off-flavor in Beijing’s intensively cultivated freshwater ponds in summer and autumn, while Euglenophyta and other algaes played a small role in causing off-flavor.     

The effect of stocking density on yield,growth, and survival of Asian river catfish (<Emphasis Type="Italic">Pangasius</Emphasis><Emphasis Type="Italic">bocourti</Emphasis> Sauvage, 1880) cultured in cages

Asian river catfish (Pangasius bocourti Sauvage, 1880) were cultured at five different stocking densities in cages (submerged volume 1 m³) suspended in a dugout pond from August to November 2009. Pangasius bocourti fingerlings (mean weight 27.09 ± 0.54 g) were stocked at densities of 12, 25, 50, 100, and 200 fish m⁻³. At the end of 3 months, the harvest weights (gross yields) were, respectively, 2.05 ± 0.30, 5.20 ± 0.31, 10.60 ± 0.42, 19.98 ± 0.78, and 42.37 ± 0.41 kg m⁻³. The mean fish weights among the stocking densities of 25, 50, 100, and 200 fish m⁻³ were not significantly different, but were significantly higher than that of the 12 fish m⁻³ density. The specific growth rates among high stocking densities of 50, 100, and 200 fish m⁻³ were not significantly different; however, they were significantly higher than those of the low stocking densities of 12 and 25 fish m⁻³. Asian river catfish performed poorly at the lowest density. The results indicate an initial lower stocking threshold for Asian river catfish of above 5.20 kg m⁻³. The Asian river catfish cultured in small cages placed in a pond reached the desirable market size (>200 g) within a 90-day grow-out period. The results show that the maximum yield for Asian river catfish during a 3-month production cycle was not reached.     

The effects of continuous photoperiod (24L:0D) on growth of juvenile barramundi (<Emphasis Type="Italic">Lates calcarifer</Emphasis>)

The efficacy of photoperiod manipulation to influence growth and developmental processes is well documented in a range of temperate aquaculture species. However, the application of such techniques with tropical species requires further investigation. This preliminary 20-day study investigated the influence of continuous photoperiod on growth of barramundi (Lates calcarifer). In addition, diel plasma melatonin profiles provided a physiological measure of how the endocrine system of barramundi responded to continuous photoperiod. Juvenile barramundi (1.33 ± 0.02 g) were held in recirculation systems under 12-h light: 12-h dark (12L:12D) or 24-h light (24L:0D) with a light intensity of 1,000 lux throughout the water column. Fish from both treatments grew to more than 14 times their original weight, with final weight (24L:0D = 21.59 ± 0.85 g; 12L:12D = 19.12 ± 0.55 g), total length (24L:0D = 12.67 ± 0.14 cm; 12L:12D = 11.96 ± 0.13 cm) and specific growth rate (24L:0D = 9.60 ± 0.05% bw day⁻¹; 12L:12D = 9.14 ± 0.06% bw day⁻¹) being significantly higher for fish grown on 24L:0D compared with 12L:12D. There were no significant differences in feed intake (24L:0D = 226.46 ± 6.27 g; 12L:12D = 219.02 ± 5.73 g) or feed conversion ratio (24L:0D = 0.71 ± 0.06; 12L:12D = 0.80 ± 0.07) between light treatments. Barramundi held under 12L:12D exhibited diel melatonin secretion, which peaked mid-dark phase (171.83 ± 4.81 pg ml⁻¹) followed by a gradual decrease in base levels at the onset of illumination (68.61 ± 8.77 pg ml⁻¹). When juvenile barramundi were subjected to 24L:0D, the amplitude of peak melatonin secretion was significantly suppressed during the subjective mid-dark phase (129.71 ± 2.36 pg ml⁻¹). This preliminary study confirmed that barramundi respond to photoperiod manipulation in a similar manner to many temperate fish species, thus demonstrating the future potential use of artificial lighting to improve growth in this species commercially.     

Cod CGRP and tachykinins in coeliac artery innervation of the Atlantic cod, <Emphasis Type="Italic">Gadus morhua</Emphasis>: presence and vasoactivity

The presence and vasoactive effects of native calcitonin gene-related peptide (CGRP), substance P (SP), and neurokinin A (NKA) were studied on isolated small branches of the coeliac artery from Atlantic cod, Gadus morhua, using immunohistochemistry and myograph recordings, respectively. Immunohistochemistry revealed nerve fibers containing CGRP- and SP/NKA-like material running along the wall of the arteries. CGRP induced vasorelaxation of precontracted arteries with a pD₂ value of 8.54 ± 0.17. Relaxation to CGRP (10⁻⁸ M) was unaffected by l-NAME (3 × 10⁻⁴ M) and indomethacin (10⁻⁶ M) suggesting no involvement of nitric oxide or prostaglandins in the CGRP-induced relaxation. SP and NKA (from 10⁻¹⁰ to 3 × 10⁻⁷ M) contracted the unstimulated arteries at concentrations from 10⁻⁸ M and above in 42% and 33%, respectively, of the vessels. It is concluded that the innervation of the cod celiac artery includes nerves expressing CGRP-like and tachykinin-like material, and that a vasodilatory response to CGRP is highly conserved amongst vertebrates while the response to tachykinins is more variable.     

Serum biochemical characteristics of Beluga, Huso huso (L.), in response to blood sampling after clove powder solution exposure

In order to investigate the effect of anesthesia on serum parameters, Beluga, Huso huso (L.) were blood-sampled immediately without anesthesia (control) or subjected to following anesthesia procedure: 40, 120, and 240 s exposure to 3,000, 700, and 500 mg l⁻¹ clove solution, respectively. Blood samples were collected after these periods, when fish were immobile and reached stage 4 anesthesia. Results showed that cortisol and glucose levels were significantly high in 700 and 500 but not 3,000 mg l⁻¹ group compared to control. Serum lactate levels were significantly high in 500 mg l⁻¹ group compared to control group. Lactate levels were not significantly differed between control, 3,000, and 700 mg l⁻¹ groups. There were no significant differences in serum levels of cholesterol, total protein, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase, Na⁺, Cl⁻, K⁺, and Ca²⁺. Results suggest that rapid anesthesia with higher dose is better than slow anesthesia with lower dose for blood sampling in Beluga.     

Difference Between Tetrodotoxin and Saxitoxins in Accumulation in Puffer Fish Takifugu rubripes Liver Tissue Slices

In vitro accumulation of tetrodotoxin (TTX) and paralytic shellfish toxin (PST) in tiger puffer fish Takifugu rubripes was investigated using liver tissue slices. When T. rubripes liver slices were incubated with Leibovitz’s L-15 medium containing 0.13 mM TTX at 20 °C in air with saturated humidity, they accumulated 21.5 ± 7.3 μg TTX g⁻¹ liver after the incubation for 12 h and increased to 55.3 ± 8.2 μg TTX g⁻¹ liver at 48 h. In the incubation of T. rubripes liver slices with 0.13 mM PST-containing medium, PST was detected 6.3 ± 0.9 μg g⁻¹ liver at 12 h and reached a plateau thereafter. These results reveal the difference between TTX and PST in accumulation in T. rubripes liver tissue slices. To examine the variation in PST accumulation among fish species, the liver tissue slices from tiger puffer fish T. rubripes, parrot-bass Oplegnathus fasciatus and green ling Hexagrammos otakii were incubated at a concentration of 0.027 mM PST. The toxin contents of 3.0 μg g⁻¹ liver were observed at 8 h regardless of fish species but were not increased subsequently, showing no variety among these three species as to accumulation patterns of PST. It is noted that the tiger puffer fish T. rubripes liver specifically accumulate TTX in preference to PST.     

Yields of great scallop, Pecten maximus, larvae in a commercial flow-through rearing system in Norway

Survival, growth and yield of competent great scallop (Pecten maximus) larvae were investigated during a full production season in a commercial hatchery in western Norway. Broodstock were collected from natural scallop beds and 12 groups were induced to spawn during the period December 2002 to July 2003. Larvae were reared on a large scale in 36 flow-through tanks (3500 l) at 17±1 °C and continuously fed a mixture of five algal species produced in an indoor continuous-flow system. Large variations in larval performance between spawning groups and tanks were observed, but the results were as good as earlier results using the batch system and prophylactic addition of chloramphenicol. Growth from days 3–24 averaged 4.8 μm day⁻¹±0.8 (sd) and survival 22.4%±21.8 (sd). Mean yield of day 3 larvae was 7.1%±10.0 (sd) and 26.6%±25.9 (sd) for those surviving to day 24. Yield was significantly correlated to larval survival. Larval success was related to initial larval density, algal concentration and season. It was found that the best production regime had an initial larval density lower than 6 ml⁻¹ and algal concentration of less than 12 μl⁻¹ regardless of season. Seventeen tanks met these criteria and produced a mean yield of 0.5 larvae ml⁻¹ to settlement. Flow-through systems are currently regarded as the only feasible method for viable hatchery production of P. maximus larvae in Norway.     

A preliminary study on the use of mannan oligosaccharides (MOS) in freshwater crayfish, <Emphasis Type="Italic">Astacus leptodactylus</Emphasis> Eschscholtz, 1823 juvenile diets

The effects of dietary mannan oligosaccharides (MOS) on the survival and growth of Astacus leptodactylus juveniles were evaluated. Experimental diets were prepared by using supplementation of 0 (Control), 1.5, 3.0, and 4.5 g MOS kg⁻¹ commercial trout larvae diet containing 43 g kg⁻¹ protein and 15.74 g kg⁻¹ lipid. A. leptodactylus juvenile with an average total length of 3.6 ± 0.46 cm (TL) and average weight of 1.25 ± 0.43 g was stocked in 0.2-m² aquariums at a rate of 50 crayfish/m² and reared for 60 days at 22.8°C. The experiment consisted of four treatments with three replicates each. Each aquarium contained ten crayfish. Crayfish juvenile fed with 0, 1.5, 3.0, and 4.5 MOS attained 6.15 ± 0.49, 5.94 ± 0.29, 7.34 ± 0.39, and 5.94 ± 0.27 cm final total length and 50, 56.67, 46.67, and 50% survival rates, respectively. Moreover, molting frequencies in 0, 1.5, 3.0, and 4.5 g kg⁻¹ MOS groups were detected as 44.44, 61.11, 83.33, and 38.88%, respectively. At the end of the experiment, a general enhanced growth performance (P < 0.05) and feed conversion ratio were observed in crayfish fed on the diet containing 3.0 g kg⁻¹. Crayfish juveniles fed with 3.0 g kg⁻¹ MOS had the highest final length (7.34 ± 0.39 cm), although their survival was the lowest (46.67%) compared to other treatments but not significant. Specific growth rates were significantly different (P < 0.05) among the treatment groups at the end of the 60-day experiment. There were no significant differences (P > 0.05) in percentage moisture, protein, and ash (wet-weight basis) in the tail meat of A. leptodactylus juvenile among treatments (diet) that averaged 82.3, 16.1, and 1.2%, respectively. However, lipid value was significantly different among the diets P < 0.05), with values between 0.13 and 0.32. From the current results, it could be advised to use MOS at the rate of 3.0 g kg⁻¹ in A. leptodactylus juvenile diets.     

Effect of light intensity and photoperiod on biomass and fatty acid composition of the microalgae, Chlorella vulgaris

The effects of irradiance and photoperiod on the biomass and fatty acid (FA) composition of Chlorella vulgaris were examined in the exponential growth phase. Results indicated significant differences in biomass and FA at different intensities and photoperiods. Maximum biomass (2.05 ± 0.1 g l⁻¹) was at 62.5 μmol photons m⁻² s⁻¹ and 16:8 h light/dark photoperiod. FA composition changed considerably in different light regimes; the maximum percentage of total saturated (SFA) (33.38%) was recorded at 100 μmol photons m⁻² s⁻¹ and 16:8 h photoperiod, while monounsaturated (MUFA) and polyunsaturated (PUFA) fatty acids decreased with increasing irradiance and light duration. The maximum percentage of total MUFA (15.93%) and PUFA (27.40%) was recorded at 37.5 μmol photons m⁻² s⁻¹ and 8:16 h photoperiod.