The toxicokinetics of benzo[a]pyrene in juvenile coho salmon, Oncorhynchus kisutch, during smoltification

The activities of Phase I and Phase II biotransformation enzymes in the livers of yearling coho salmon (Oncorhynchus kisutch), were measured biweekly from February until the release date from the hatchery in mid-June, in order to observe any alterations in baseline levels during smoltification. Peak enzyme activities occurred in February and March and then declined through to June. Total cytochrome P450 levels ranged from 0.024±0.009 to 0.095±0.010 nmol mg^-1 microsomal protein, ethoxyresorufin O-deethylase activity ranged from 2.74±0.75 to 9.94±0.85 pmol min^-1 mg^-1 microsomal protein, and glutathione S-transferase activity ranged from 0.07±0.01 to 0.33±0.01 μmol min^-1 mg^-1 cytosolic protein during this period. Following an intraperitoneal injection of [3H]benzo[a]pyrene (B[a]P), elimination occurred rapidly (>71% excreted into the bile within 24h) from February to June. Although the distribution of B[a]P in tissues changed through the sampling period, the highest leels of B[a]P-derived radioactivity were found in the liver, bile and fat. Analysis of the bile revealed that 55 to 63% of the radioactivity was Phase I metabolites, 16 to 24% glucuronide conjugates, 8% sulfate conjugates, 7% other conjugates and 6% aqueous-soluble metabolites. These findings suggest that the transformation from freshwater adapted coho ‘parr’ to ‘smolts’, can significantly alter biotransformation enzyme activities and the distribution and elimination of xenobiotics such as benzo[a]pyrene in these fish. This revised version was published online in July 2006 with corrections to the Cover Date.     

Modulation of calcium uptake in cadmium-pretreated tilapia (Oreochromis mossambicus) larvae

Tilapia larvae were exposed to 0 (control), 50 (50-Cd) or 100 (100-Cd) μg l^-1 cadmium for 4 days and then transferred to cadmium-free fresh water for 3 days of detoxification. Total length and weight, calcium influx and total body calcium and cadmium content were examined at various times during detoxification. All the groups grew normally with regards to total length and body weight. Within the first 12h of detoxification the 50- and 100-Cd exposed groups released cadmium at the similar rate of about 24 ng mg^-1 h^-1 (or 140 ng larva^-1 h^-1). Later, however, this rate declined to only 4–16% of the initial level. Calcium influx in the control group showed a 10–26% increase during the detoxification period. Calcium influx in the 50-Cd group increased by about 280% and reached it peak at 12h. Calcium influx in the 100-Cd group increased by 440% and did not peak until 24h after transfer. After peaking, the influxes in both 50- and 100-Cd groups declined to the level of control at the end of the experiment. Calcium contents in 50- and 100-Cd groups increased more rapidly than that in control group within first 24h of the detoxification period. However the rate of increase in calcium content in three groups was the same after 24h. The changes in calcium influx appeared to be correlated with those in calcium content, and these suggested that tilapia larvae regulate the mechanism of calcium balance to compensate for the reduced calcium level in the body. This revised version was published online in July 2006 with corrections to the Cover Date.     

Investigation into the possible role of androgens in the induction of hepatic vitellogenesis in the European eel:in vivo andin vitro studies

Changes in the levels of plasma vitellogenin (Vg), estradiol (E₂) and testosterone (T) were examined following gonadal development induced by carp gonadotropin treatment (cGTH) of freshwater female yellow and silver eels (Anguilla anguilla L.). The animals received injections of cGTH (250 μg kg⁻¹ body weight) or saline vehicle three times a week, for 6 to 8 weeks. No effect of vehicle was observed. Steroidogenic activity of the ovary was stimulated by cGTH treatment as shown by the increase in circulating steroid levels in both stages. However, the responses of T, E₂ and Vg differed according to the stage of development of eels. At the yellow stage, the initial steroid plasma levels were undetectable (< 0.01 ng ml⁻¹) before treatment and ovarian steroidogenic activity was slightly stimulated following cGTH treatment; steroid levels reached their highest values after 3 weeks and 6 weeks of treatment for E₂ (0.62 ± 0.13 ng ml⁻¹ and T (0.33 ± 0.30 ng ml⁻¹), respectively. The cGTH treatment slightly increased plasma Vg levels (0.2–0.7 μg ml⁻¹ during the experiment compared with the initial values of the group. At the silver stage, the initial steroid levels were detectable (0.7 ng ml⁻¹ for E₂ and 0.1 ng ml⁻¹ for T); cGTH treatment did not significantly increase plasma E₂ level which remained at initial levels. Nevertheless, plasma T levels dramatically increased from 0.1 to 3 ng ml⁻¹ and peaked after 1 or 2 weeks of cGTH treatment; a rapid increase in plasma Vg levels occurred, reaching its highest value at 5 mg ml⁻¹ after 3 weeks of treatment. Thus, the steroid kinetic profiles in relation to the appearance of Vg in the plasma following cGTH treatment was closely related to androgen levels and there was a strong vitellogenic response induced by chronic cGTH treatment. In order to test if androgens could be implicated in the vitellogenic response, we evaluated the potencies of various androgens (testosterone and 5α-androstane-3β,17β-diol)in vivo andin vitro, associated with E₂ to induce the production of Vg.In vitro experiments showed that Vg synthesis was induced by high doses (10⁻⁶ to 10⁻⁵ M) of androgen in the eel. Tamoxifen totally inhibited the action of androgens suggesting that androgens were acting through binding to the E₂ receptor.In vivo, androgens given alone at 50 μg kg⁻¹ 3 times a week for 1 months had no significant effect on plasma Vg levels. In addition, E₂-androgen cotreatment showed that the presence of androgen did not modify the vitellogenic response induced by E₂.     

Differences in Major Ions Composition of Artificial Seawater from Aquarium Tanks at the New Jersey State Aquarium

Concentrations of major seawater ions were monitored in six aquarium tanks at the New Jersey State Aquarium over a three-year period. The ratios of these ions to chlorinity were compared to those in freshly prepared artificial seawater. The largest aquarium tank (Ocean Tank) exhibits statistically significant (p<0.01) relative enrichment of potassium, calcium and strontium, and relative depletion of magnesium and sulphate. The likely source of excess potassium is from potassium iodide added to prevent goiter in sharks. Based on the excess potassium, a total amount of 650 μmol/kg iodide added over the years was calculated for the Ocean Tank. The excess calcium observed in several tanks correlates with the presence of concrete or arbonaceous shells in these tanks. In Ocean Tank, a calcium leaching rate of 6.7 kg/month was calculated. Continuous formation of white carbonaceous precipitates serves as a sink for magnesium in Ocean Tank, and a magnesium removal rate of 5.1 kg/month was calculated. These and other results show that concentrations of major ions in artificial seawater aquaria are affected by leaching, precipitation and addition of food supplements, and these factors should be taken into account when preparing artificial seawater for aquarium tanks with long water residence time. This revised version was published online in August 2006 with corrections to the Cover Date.     

鳗源嗜水气单胞菌主要外膜蛋白基因克隆及其表达

A pair of primers were designed according to the published nucleotide sequence of a putative outer membrane protein gene (omp) of Aeromonas hydrophila . With the specific primers, a target fragment about 1.1 kb was amplified from Aeromonas hydrophila ML316 via PCR .The target fragment was inserted into the linearized pGEM-T easy vector. After enzyme restriction and sequencing analysis,the nucleotide data had been further analyzed by DNAman and ClutalW software. The analysis results showed that the cloned DNA fragment had a longest open reading frame (ORF) of 1035 nt,it predicted to be encoded a 344 aa protein with the molecular weight of 36 kD. Hydrophobicity analysis suggested that the protein was highly hydrophilic, especialy at the first 24 aminoacid, this region could function as signal peptide. The homologious comparison proved the cloned gene had 96% homology to the sequence of the omp gene, and the alignment of the amino acid sequence was 98% . The recombinant plasmid was constructed with the target gene and the expressing vector pGEX-4T-1 and then was transformed into E. coli BL21（DE3）by BamH and Sal I .The fusion protein was expressed under the IPTG inducing condition,and exhibited about 62 kD in size,very close to the predicted molecular weight of GSTMOMP, furthermore,the fusion protein was specifically recognized by antiserum which raised against the major outer membrane protein of AHML316. Considering all these together, it proved that the cloned gene represented the major outer membrane protein gene of AHML316, and the expressed gene products shared identical antigenicity with the natural main outer membrane protein,and also provided technical support for developing an advanced gene engineering vaccine against Aeromonas hydrophila.     

Insulin-like growth factor I of Japanese eel, Anguilla japonica: cDNA cloning, tissue distribution, and expression after treatment with growth hormone and seawater acclimation

In an attempt to understand growth regulation in the Japanese eel, Anguilla japonica, we cloned insulin-like growth factor-I (IGF-I) cDNAs and examined their mRNA expression in several tissues. Two eel IGF-I (eIGF-I) cDNAs encoding preprohormones, eIGF-I-Ea1and eIGF-I-Ea2, were cloned from the liver by polymerase chain reaction (PCR). The preproIGF-Is were identical in signal peptide and mature IGF-I, but different in the E domain—eIGF-I-Ea2 mRNA was 36 bp longer than eIGF-I-Ea1 mRNA. Eel IGF-I was 83–94% identical with that of teleosts, 71% identical with that of dogfish, 87% identical with that of bullfrog and chicken, and 83% identical with that of humans. In both males and females the highest eIGF-I-Ea1 mRNA levels were observed in the liver, with detectable levels also found in the gills, heart, stomach, spleen, kidney, intestine, swim-bladder, muscle, and gonads. eIGF-I-Ea1 mRNA levels in the liver were higher in females than in males whereas in the intestine they were lower than in males. eIGF-I-Ea2 mRNA was detected in all the tissues examined and at similar levels in males and females. In this experiment higher eIGF-I-Ea1 mRNA levels were observed in the liver of larger glass eels than in those of smaller fish. eIGF-I-Ea2 mRNA levels were also higher in larger eels, although they were lower than IGF-I-Ea1 mRNA levels. Both eIGF-I mRNA levels in liver were positively correlated with the body size of the␣glass eels. Intraperitoneal injection of recombinant eel GH (reGH), 0.25 μg g⁻¹ body weight, into glass eels resulted in a significant increase in both eIGF-I mRNAs in the liver 1 day after injection compared with control fish, but no elevation was observed 2 days after injection. Incubation of liver slices with reGH at concentrations of 10, 100, and 1,000 ng mL⁻¹ for 24 h resulted in a significant concentration-dependent increase in the levels of both eIGF-I mRNAs. Higher levels of eIGF-I-Ea1 and Ea2 mRNA were observed in the gills ofseawater-reared eels than in those of freshwater-reared fish, but no differenceswere observed in the whole kidney. These results suggest that IGF-I is involved in the regulation of somatic growth and also in adaptation of the Japanese eel to seawater.     

一种生物净水剂对河蟹养殖水体水质净化效果研究

The biological cleaning agent Pondplus was dowsed each ten days at different dosage into breeding ponds for Chinese mitten crab with stocking rate at 12 000 ind./ha, to evaluate its purification effects on water environment in breeding ponds and its effects on Chinese mitten crab growth. The results showed that dousing treatment improved the water quality significantly as evaluated according to the parameters of DO, CODMn, NH4 ＋ - N and NO2 - -N. Particularly, when the air temperature was higher than 35℃, the diurnal observation on DO values at the bottom of ponds showed that dousing at 450 g/（ ha•m） gave a DO value higher than 4 mg/L all day long, which was 2 mg/L higher than that of control. The observed increase of Chinese mitten crab were 14. 9% , 27.8% , 27.8% by average weight, when dousing at 150, 300, 450 g/（ha • m） , respectively. Accordingly, the production increased by 8.5%, 11.9%, 18.6% through its promotion of Chinese mitten crab growth, and the economic efficiency were enhanced by 96.2% , 159.8% , 180.9%.     

Particle size distribution of wastes from freshwater fish farms

Waste water treatment on freshwater fish farms is problematic as waste material and water flows can vary greatly on a daily basis, and, in terms of effluent standards, fish farm effluent represents a dilute waste water output. A study was undertaken to investigate in detail the nature of the waste outputs under field conditions. Waste water samples were split by meshes into the following size ranges: >200μm, 200-100μm, 100-60μm, 60-30μm and <30μm. Waste water quality parameters, suspended solids (SS), biochemical oxygen demand (BOD₅) and total phosphorus (TP) were examined for each size range at two freshwater fish farm sites in Scotland, as part of a wider investigation into waste water quality of aquaculture operations. Results indicated that during periods of peak waste output i.e. tank cleaning, approximately 80% of BOD₅ and SS was present in a particle size range of 100-60μm, but only 66% of TP transport occurred in this size range. At other times, low levels (≤40%) of entrapment of wastes by the chosen meshes was observed, suggesting a reversion to predominantly dissolved material transport. Compared against a larger data set of outflow concentrations obtained from another section of the study, maximum removal rates of 46%, 48% and 30% for BOD₅, SS and TP respectively were determined. The implications for waste water treatment at fish farms are discussed.     

The bioactivity of gonadotropin releasing hormones and its regulation in the gilthead seabream,Sparus aurata: in vivo andin vitro studies

Thein vivo andin vitro potency of native and modified forms of gonadotropin releasing hormone (GnRH) to release gonadotropin (GtH) was studied inSparus aurata and correlated with their relative susceptibility to degradation by cytosolic-bound enzymes of the pituitary, kidney, and liver. Salmon (s) GnRH and luteinizing hormone-releasing hormone (LHRH) are equipotent whereas analogs of these peptides ((D-Arg⁶-Pro⁹NET)-sGnRH, (D-Ala⁶-Pro⁹NET)-LHRH, (D-Trp⁶)-LHRH) are superactive in inducingin vivo GtH release (at 10 μg/kg body weight). In anin vitro superfusion system of pituitary fragments all analogs are equipotent to the native peptides (at 10⁻¹⁰ to 2.5 × 10⁻⁷M). sGnRH and LHRH are rapidly degraded by cytosolic peptidases of the pituitary, liver, and kidney. The preferred site of cleavage is the Tyr⁵-Gly⁶ bond. Substitution of the position 6 glycine by D-amino acids renders the 5–6 bond resistant to degradation and shifts the main site of cleavage to the Pro⁹-Gly¹⁰NH₂ bond. Substitution at position 6 (as above) and at position 10 with Pro⁹NET results in analogs that are resistant to degradation. We propose that enzymatic cleavage terminates GnRH bioactivityin vivo and thus increased resistance to degradation is a major determinant of GnRH analog superactivity.     

鱼类白细胞介素1β基因的研究概况

Interleukin-1β(IL-1β) is one of the most pleiotropic cytokines and a central regulator of the immune and inflammatory responses. Interleukin-1β was initially discovered within mice and humans and over the last 10 years has been characterized within a wide variety of animals. The IL-1β plays a key role in the inflammatory process, enhancing cell-mediated immunity by inducing the growth and proliferation of lymphocytes, connective tissue cells, and by stimulating immune and inflammatory response effector cells.As an immunoregulatory cytokine, IL-1β has the potential to enhance the immune response induced by a vaccine and/or to modulate the immune response leading to different effector mechanisms. It is produced by many cell types, including monocytes, macrophages,T and B lymphocytes, fibroblasts, and endothelial and epithelial cells. Expression is induced by a diverse range of stimuli, including mitogens, cytokines, and microbial products. There have been considerable evidences provided by biological cross reaction that fish produce IL-1β during immune responses, and the bioactivity of IL-1 in fish has been known for over a decade. But only. since 1999,IL-1β gene has been cloned from the rainbow trout. And from then on, IL-1β gene has been cloned and expressed in many fish confirming that fish produces IL-1β gene during immune responses. In mammals it is produced as an inactive precursor that is processed by interleukin converting enzyme (ICE) to give a biologically active ‘mature‘ peptide. There is no signal peptide in IL-1β and its mechanism is unknown. This is the special part of the gene structure of the IL-1β. And through the program analyzing, we found this special structure in fish IL-1β gene. This paper reviews the functions and structure of gene IL-1β and the studies of the gene IL-1β in fish recently.     

Growth and Feed Conversion of Juvenile Heterobranchus longifilis Fed Live Oreochromis niloticus with or without Artificial Feed

Growth and feed conversion were monitored in triplicate groups of the African catfish Heterobranchus longifilis (mean weight 11 ± 1.8 g) fed small (2.5–5.54 cm) tilapia (Oreochromis niloticus) and artificial feeds at various rates (treatments 1, 2, and 3), and tilapia or artificial feed (treatments 4 and 5, respectively). Artificial feed was a 42% crude protein commercial pellet. Live O. niloticus were fed at a rate of 4 g live tilapia/catfish/day. Pelleted feeding rate was 2%, 1%, 0.5%, and 1% of body weight thrice daily in treatments 1, 2, 3, and 5, respectively. After 70 days, mean weight was 180 ± 9.5 g, 157 ± 15.7 g, 147 ± 2.6 g, 77 ± 10.9 g, and 74 ± 10 g, in treatments 1, 2, 3, 4, and 5, respectively. Treatment significantly affected SGR (% day^?1) (P < 0.03) and pelleted feed conversion ratio (P < 0.0003). FCR was 1.09 ± 0.01, 0.63 ± 0.08, 0.42 ± 0.11, and 1.12 ± 0.13 in treatments 1, 2, 3, and 5, respectively. Profit was highest (P < 0.01) in treatment 2. Tilapia consumption seems to improve utilization of artificial feed and may be a way for some catfish farmers to save money.     

Growth,water quality and oxidative stress of Nile tilapia Oreochromis niloticus (L.) in biofloc technology system at different pH

The objective of this study was to demonstrate the pH effects on growth, survival, water quality, proximal composition of bioflocs and oxidative stress of Nile tilapia in biofloc technology (BFT) system. Twenty‐five fish (3.68 ± 0.93 g) were distributed in each tank (useful vol. 37.5 L), utilizing treatments with pH 8.3, 7.5 and 6.5 at 60 days. During the experiment, the oxidation of total ammonia was similar among the treatments. However, the NO₂^?‐ N oxidation was slower at pH 6.5 (10.1 ± 1.0 mg/L) compared to pH 7.5 (7.0 ± 0.6 mg/L) and 8.3 (7.1 ± 1.5 mg/L). The final weight was higher for pH 7.5 treatment (44.1 ± 0.9 g) compared to pH 8.3 (37.1 ± 3.9 g), while the pH 6.5 (40.4 ± 4.1 g) was like to the other treatments. Moreover, the survival, daily growth rate and the food conversion rate were not affected by treatments. When evaluating physiological and biochemical parameters, no alterations were detected, therefore, indicating that fish have a good health status. Thus, the present study demonstrates that BFT for a Nile tilapia nursery, utilizing pH 6.5–7.5, promotes the best results in terms of growth, net yield and efficiency.     

Protein: energy ratio in practical diets for Nile tilapia Oreochromis niloticus

The present study was conducted to evaluate the interaction of protein and energy ratio in low protein (20, 25 and 30 %) diets for juvenile Nile tilapia (Oreochromis niloticus) (initial weight 7.44 ± 0.03 g). Dietary protein to energy (P/E) ratio of nine practical diets ranged from 66.84 to 115.14 mg protein/kcal energy. Each diet was randomly assigned to four replicate groups of fifteen fish. After 10 weeks, Fish fed the lowest dietary protein (20 %) and lowest energy (2,600 kcal/kg) diets were significantly smaller than fish maintained on D5 (25/2800) and D6 (30/2800), However, there were no significant differences among all the treatments except D1. The whole body moisture and protein levels were significantly influenced by dietary protein and energy content. Whole body energy content and digestible energy retention were significantly influenced by energy content of the diet. Conversely, dietary protein level significantly influenced protein retention but it did not influence digestible energy retention. Under the reported conditions, the response of tilapia to dietary energy or protein was seen only at the lower levels of inclusion and tilapia demonstrated limited protein sparing as dietary energy was increased. However, this did modify the carcass composition through higher dietary energy.     

Comparative digestion efficiencies in conventional, genetically improved and genetically male Nile tilapia, Oreochromis niloticus (L.)

Apparent digestibility of dry matter, protein, lipid and energy of a fishmeal‐based feed (41% crude protein, 9% crude lipid and 19 kJ g⁻¹ gross energy) was compared in genetically improved farmed tilapia (GIFT), genetically male Nile tilapia (GMNT) and conventional Nile tilapia (CNT) (Oreochromis niloticus). The experimental fish were reared individually under standardized conditions in a recirculation system at 27±0.1°C for 10 weeks. Titanium dioxide (TiO₂) was used as a marker. Faeces of individual fish were collected daily by siphoning and stored at −18°C before analysis. No significant differences (P<0.05) were observed in the digestibility coefficients of feed dry matter (78.2±3.4%, 77.7±4.4% and 76.4±3.7%), protein (87.9±3.0%, 88.4±2.8% and 88.0±3.3%), lipid (90.0±2.5%, 91.0±2.1% and 89.4±3.0%) and energy (90.4±1.9%, 90.7±2.0% and 89.4±2.3%) in GIFT, GMNT and CNT respectively. At the end of the experiment, there were no significant differences (P<0.05) in average percentage growth (82.2±7.2, 87.3±7.7 and 74.7±4.1 respectively for GIFT, GMNT and CNT), growth rates or feed utilization efficiencies between the three tilapia groups. We conclude that the higher growth claimed for improved GIFT and GMNT as compared with CNT, if ever existing, cannot be attributed to higher nutrients or energy digestibility.     

Comparison of NADH-dependent cytochrome b5 reductase activity and in vitro methemoglobin induction by sodium nitrite in Oncorhynchus mykiss, Salmo salar, and Salvelinus fontinalis

Methemoglobin is hemoglobin containing ferric iron. Methemoglobin cannot bind to oxygen and at high concentrations causes tissue hypoxia. Brook trout (Salvelinus fontinalis) develop significantly greater methemoglobinemia than Atlantic salmon (Salmo salar) or rainbow trout (Oncorhynchus mykiss) following general anesthesia with benzocaine or tricaine methanesulfonate. The objective of this study was to compare the activity of the major methemoglobin reducing enzyme, NADH-dependent cytochrome b5 reductase (CB5R), in brook trout erythrocytes to the activity of CB5R in Atlantic salmon and rainbow trout erythrocytes. Methemoglobin levels were compared using co-oximetry following in vitro incubation of erythrocytes with sodium nitrite (NaNO₂). The CB5R activity was measured using a ferricyanide assay. There was significantly greater methemoglobin at time 0 in brook trout erythrocytes than in rainbow trout or Atlantic salmon erythrocytes (2.79 ± 0.29 %, 2.19 ± 0.23 %, 2.08 ± 0.14 %), (P < 0.001). There was significantly greater methemoglobin induction by NaNO₂ in brook trout erythrocytes (33.14 ± 3.32 %) than in rainbow trout or Atlantic salmon erythrocytes (28.73 ± 2.92 % and 24.85 ± 1.40 %, respectively), (P < 0.001). The CB5R activity was significantly less in brook trout erythrocytes (median of 3.05 μmol/min/μl) than in rainbow trout erythrocytes (median of 6.73 μmol/min/μl). The CB5R activity in Atlantic salmon erythrocytes (median 4.09 μmol/min/μl) was not significantly different than in brook or rainbow trout erythrocytes. Total methemoglobin at any one time is a balance between induction by oxidants and reduction by antioxidants. Lower CB5R activity in brook trout erythrocytes may contribute to a species-specific sensitivity to methemoglobin induction; however, there are likely additional factors.     

Changes During Chilled Storage of Whole Tilapia and Short-Term Frozen Storage of Tilapia Fillets

This study evaluated the physicochemical changes in Nile tilapia (n = 82, 373.71 ± 61.91 g) refrigerated for up to 92 h and in the frozen fillets. The tilapias were captured with nets, slaughtered by ice and water shock (1:1) in a temperature of approximately 2°C for 30 min, and stored refrigerated at 4°C in polystyrene boxes containing ice. The fish were filleted, and filets were weighed and frozen. The drip loss and protein were determined after 23 days of frozen storage. After 4 h of storage, all fish were in full rigor mortis. The pH of the muscles decreased for up to 45 h of the storage period. The fillets obtained from tilapia stored for more than 72 h lost more weight and protein. Thus, the filleting or processing of tilapia should be done before 72 h of cold storage, since deterioration of the fish starts to occur after this period.     

Effects of Two Densities of Caged Monosex Nile Tilapia, Oreochromis niloticus, on Water Quality, Phytoplankton Populations, and Production When Polycultured with Macrobrachium rosenbergii in Temperate Ponds

The effects of different densities of caged Nile tilapia, Oreochromis niloticus, on water quality, phytoplankton populations, prawn, and total pond production were evaluated in freshwater prawn, Macrobrachium rosenbergii, production ponds. The experiment consisted of three treatments with three 0.04‐ha replicates each. All ponds were stocked with graded, nursed juvenile prawn (0.9 ± 0.6 g) at 69,000/ha. Control (CTL) ponds contained only prawns. Low‐density polyculture (LDP) ponds also contained two cages (1 m³; 100 fish/cage) of monosex male tilapia (115.6 ± 22 g), and high‐density polyculture (HDP) ponds had four cages. Total culture period was 106 d for tilapia and 114 d for prawn. Overall mean afternoon pH level was significantly lower (P ≤ 0.05) in polyculture ponds than in CTL ponds but did not differ (P > 0.05) between LDP and HDP. Phytoplankton biovolume was reduced in polyculture treatments. Tilapia in the LDP treatment had significantly higher (P ≤ 0.05) harvest weights than in the HDP treatment. Prawn weights were higher (P ≤ 0.05) in polyculture than prawn monoculture. These data indicate that a caged tilapia/freshwater prawn polyculture system may provide pH control while maximizing pond resources in temperate areas.     

Use of shrimp protein hydrolysate in Nile tilapia (Oreochromis niloticus, L.) feeds

A 45-day feeding trial was carried out to evaluate the use of shrimp protein hydrolysate (SPH) in diets for Oreochromis niloticus, L. SPH was included in isonitrogenous diets replacing fish meal protein by 0, 5, 10, and 20% and offered to Nile tilapia juveniles (1.7 ± 0.4 g) stocked in 40-L glass aquaria. The inclusion of SPH produced no significant differences (P ≥ 0.05) in final weight, survival, weight gain, average daily gain, specific growth rate, feed conversion ratio, protein efficiency ratio, or apparent net protein utilization. The inclusion of SPH Nile tilapia diets significantly affected (P < 0.05) the final fish body composition. Protein and ash contents decreased and fat content increased slightly with the increase in SPH. This study has demonstrated that SPH is a promising protein feedstuff and could account for as much as 6% of Nile tilapia diets with no adverse effects on growth and nutrient utilization.     

Biochemical Composition of Seminal Plasma and Annual Variations in Semen Characteristics of Jundiá <Emphasis Type="Italic">Rhamdia quelen</Emphasis> (Quoy and Gaimard,Pimelodidae)

This study investigated the composition of milt of the South American silver catfish (Rhamdia quelen) or jundiá. The semen was taken from jundiá in different periods during the four seasons. The biochemical composition of seminal fluid and the characteristics of sperm were analyzed. The semen quantity which can be extracted per fish in one day was 0.95 ± 0.08 ml during spring (maximum) and 0.24 ± 0.03 ml during winter (minimum). Sperm density (spermatocrit) showed higher values in the spring (75.1 ± 1.3%) decreasing slightly afterwards and reaching 63.0 ± 2.4% to 65.0 ± 2.2% in the fall and winter. Immediately after water dilution, 90–100% of the spermatozoa presented vigorous straightforward motility that remained for at least 20 s. The total duration of the motility was 47.9 ± 1.3 s in the spring and 38.6 ± 0.6 s in the other seasons (P < 0.05). This pattern of motility is maintained for more than 2 h after storage of the milt at room temperature. The pH from 5 to 10 of the water dilution does not influence the sperm motility. The mean seminal pH and osmolality values were 8.7 ± 0.07 and 274.8 ± 11.2 (mOsm/kg), respectively. The ion concentration was: Na 153.7 ± 2.4, K 10.7 ± 2.4, Cl 139.4 ± 2.1, Ca 4.2 ± 0.2, Mg 0.9 ± 0.05, P 0.9 ± 0.08 (mEq/l). The total protein was 0.6 ± 0.05 mg/dl and cholesterol concentration was 13.9 ± 0.9 mg/dl.     

Apparent digestibility coefficient of duckweed (Lemna minor), fresh and dry for Nile tilapia (Oreochromis niloticus L.)

Dry matter (DMD), protein (PD), ash (AD), fat (FD), gross energy (ED) and phosphorus (PhD) digestibility coefficients were determined for five different iso‐N fish diets fed to Nile tilapia (Oreochromis niloticus). The control diet contained fishmeal (35%), corn (29%), wheat (20%), wheat bran (10%), fish oil (3%), diamol (2%) and premix (1%). Partial replacement of dry matter of fishmeal, corn grain, wheat grain, wheat bran and fish oil by 20% and 40% of dry matter of duckweed, in a dry and fresh form, was performed. Diets of treatments 1 and 2 included 20% and 40% of duckweed, respectively, in a dry form. In treatments 3 and 4, tilapia received formulated diets 4 and 5 in addition to 20% and 40% fresh duckweed providing the same amount of dry matter and protein as in control. The specific growth rates (SGRs) of tilapia were 1.51±0.07, 1.38±0.03, 1.31±0.06, 1.44±0.02 and 1.33±0.05, in control and treatments 1–4. There was no significant difference between SGR for the control diet and the diet with 20% fresh duckweed, while the other treatment groups had significantly lower SGR. All the treatment diets provide good values for feed conversion ratios (FCRs) and protein efficiency ratio (PER). Dry matter of diets ranged from 61.8% in treatment 4 to 85.2% in control. All the diets have high PD (88.4–93.9%) and high‐energy digestibility (78.1–90.7%). Dry matter of duckweed were 66.8, 63.3, 45.8 and 28.3 in treatments 1 to 4 respectively. Protein values were 78.4, 79.9, 77.6 and 75.9, while ED values were 59.8, 60.9, 64.5 and 58.4 in treatments 1 to 4 respectively. Analysis of body composition shows that tilapia fed diets with duckweed contain significantly (P<0.05) higher phosphorus and protein content and significantly (P<0.05) lower lipid content. In contrast, tilapia fed control diet had a significant higher (P<0.05) dry matter content and lower ash content.