Induction of Out-of-Season Spawning of Pikeperch, Sander Lucioperca (L.)

Pikeperch were induced to spawn 3 months prior to the natural spawning period through photothermal and hormonal stimulation. Females (five specimens in each group) were stimulated with injection of human chorionic gonadotropin (hCG) once (200 IU kg^–1), twice (200 IU kg^–1, second dose after 48 h–400 IU kg^–1) or three times (200 IU kg^–1, after 24 h–200 IU kg^–1 and after another 24 h–200 IU kg^–1). The control group was injected once with 0.9% NaCl. The males were stimulated with a single hormone dose of 200 IU kg^–1. Eggs were obtained from all the hormonally treated fish. None of the control group females, which were only stimulated photothermally, ovulated any eggs. The time of ovulation was 66–71 h following the first injection, and the eggs viability until the eyed stage (from 71.5 to 77.5%) did not depend on the number of hormone doses (P > 0.05). The out-of-season spawning method described in this paper could be used to provide pikeperch larvae for intensive culture systems (recirculating water systems) before natural spawning season and to produce larger-sized pikeperch fingerlings for stocking.     

The First Attempt to Artificially Reproduce the Endangered Cyprinid Lake Minnow Eupallasella Perenurus (Pallas)

The standard artificial reproduction technique with the use of Ovopel (GnRH analogue) was evaluated for the critically endangered cyprinid species in Poland, the lake minnow Eupallasella perenurus. Wild spawners were angled at the beginning of the spawning season. Only females with a condition coefficient value higher than the mean were included in the experiment and then stimulated with Ovopel. Group A (n = 20) was given standard treatment (0.2 pellet kg^–1 and 1.0 pellet kg^–1 after 12 h), whereas group B (n = 8) was treated with a single dose of 2.0 pellets kg^–1. After fertilisation with the dry method, the glutinous eggs attached to the bottom of flow-through aquaria were incubated at 17.1–18.4°C. Throughout incubation (85D°), dead eggs were removed and counted. The same was done with dead larvae, those with deformed bodies or those with empty alimentary tracts after 2 days of external feeding. Two injections of Ovopel resulted in a significantly (P 0.05) higher ovulation rate in comparison with the single dose (70 and 25% in groups A and B, respectively). The individual hatching rates were very high (98.4–100%), as was the share of good quality larvae (91.1 and 96.5% of stripped eggs in groups A and B, respectively). These results indicate that the standard propagation method used with commercially important cyprinid species can also be used to successfully breed E. perenurus.     

In vivo activity of salmon gonadotropin releasing hormone (GnRH), its agonists with structural modifications at positions 6 and 9, mammalian GnRH agonists and native cGnRH-II on the spawning of an Indian catfish

Effects of the native GnRHs and various agonists have been evaluated on the spawning of an Indian catfish, Heteropneustes fossilis. This study tested salmon (s) GnRH agonists and mammalian (m) GnRH agonists where a D-amino acid residue was substituted alone at position 6 or the C-terminal was modified with ethylamide. GnRH agonists with a combination of these structural modifications were also evaluated separately for their effect on the spawning of the catfish. Native sGnRH, [Pro⁹ NEt]-sGnRH agonist and chicken (c) GnRH-II exhibited similar activity and induced spawning within 14–18 h at a dose of 100 g kg^–1 body weight (BW). [D-Lys⁶]-sGnRH agonist and [D-Lys⁶ Pro⁹ NEt]-sGnRH agonist, induced spawning at a dose of 100 g kg^–1 BW and 1 g kg^–1 BW, respectively. The most notable observation in this study was the ineffectiveness of [D-Ala⁶]-mGnRH agonist and [Des Gly¹⁰ D-Ala⁶ Pro⁹ NEt]-mGnRH agonist. The results obtained suggest that substitution at position 6 alone, and in conjunction with an ethylamide-based modification at the C-terminal in the native sGnRH structure, increases the potency of the tested agonists to induce spawning in the catfish. This study also discusses the potential use and incorporation of cGnRH-II for the development of more generic spawning induction therapies.     

Artificial spawning of European catfish, Silurus glanis L.: stimulation of ovulation using LHRH-a,Ovaprim and carp pituitary extract

Ovulation was stimulated in four groups of European catfish, Silurus glanis L., using injections of des-Gly¹⁰, [D-Ala⁶]-LHRH Ethylamide (20 μg kg^–1) and pimozide (10 mg kg^–1), Ovaprim (0.33 mL kg^–1), and carp pituitary extract (4 mg kg^–1, in one or two doses). A higher percentage of ovulating females (producing eggs of sufficient quality) was found after the LHRH-a and Ovaprim treatments (100% and 80%) in relation to fish treated with the pituitary extract (60% and 66.67%). The greatest weight of eggs was obtained in the case of repeated hypophysation and LHRH-a (1299.69 and 1298.57 g, respectively), and the smallest after single hypophysation (1144.08 g). After 60 h of incubation, the best quality of eggs was found in the group treated with Ovaprim (62.9% of live embryos) and the poorest in the two groups which underwent hypophysation (50.41% and 50.75%). No statistically significant effect by the ovulation stimulators on the characteristic qualitative and quantitative traits of obtained eggs was ascertained.     

Rates of oxygen consumption and ammonia excretion of juvenile Eurasian perch Perca fluviatilis L.

The impact of feeding, fish size (body weight from 18.5 to 56.5 g) and water temperature (20 and 23 °C) on oxygen consumption (OC, mg O₂ kg^–1 h^–1) and ammonia excretion (AE, mg TAN kg^–1 h^–1) was studied in Eurasian perch held in recirculation systems. OC for both fed and feed-deprived (3 days) fish was higher at 23 °C (278.5 and 150.1 mg O₂ kg^–1 h^–1) than at 20 °C (249.3 and 135.0 mg O₂ kg^–1 h^–1; P < 0.01). AEs for both fed and feed-deprived fish were also significantly higher at 23 °C than at 20 °C (P < 0.001). Water temperature and fish size had a significant impact on the oxygen:feed ratio (OFR, kg O₂ kg^–1 feed fed day^–1) and ammonia:feed ratio (AFR, kg TAN kg^–1 feed fed day^–1; P < 0.001). Their average values at temperatures of 20 and 23 °C were 0.17 and 0.19 kg O₂ kg^–1 feed fed day^–1 and 0.009 and 0.011 kg TAN kg^–1 feed fed day^–1, respectively.     

The effect of dietary vitamin E on the pleopodal egg number of Astacus leptodactylus (Eschscholtz, 1823)

The effect of vitamin E on the pleopodal egg number of Astacus leptodactylus (Eschscholtz, 1823) was studied. Crayfish were fed 2% of their total wet weight daily with vitamin E supplemented diets and a control for 70 days. The vitamin E content of the control diet, diet 1, diet 2 and diet 3 were 20 mg kg^–1, 40 mg kg^–1, 80 mg kg^–1 and 160 mg kg^–1 respectively on a dry weight basis. Vitamin E levels of the control and experimental diets were analysed by High Performance Liquid Chromatography. Results showed that diets containing supplemental vitamin E were associated with an increase in the number of pleopodal eggs. The best result was obtained with diet 2 containing 80 mg kg^–1 supplemental vitamin E.     

Induced ovulation of yellow catfish (Pelteobagrus fulvidraco) using a combination of a gonadotrop‐releasing hormone analogue and domperidone

The effects of an intraperitoneal hormone injection of gonadotropin‐releasing hormone agonist (D‐Ala⁶, Pro⁹‐NEt GnRHa) alone or in combination with a dopamine antagonist, domperidone (DOM), on ovulation induction in yellow catfish Pelteobagrus fulvidraco were tested. The hormone treatments were as follows: 6 mg kg⁻¹ body weight (BW) of carp pituitary extract as a positive control, GnRHa 10, 20, 40 and 80 μg kg⁻¹ BW and a combination of GnRHa and DOM as follows: 10 μg+5 mg, 20 μg+10 mg, 40 μg+20 mg and 80 μg+40 mg kg⁻¹ BW. Physiological saline (0.7% NaCl) was used as a negative control. Significant differences in the ovulation ratio, latency period and ovulation index (OI) were observed among treatments (P<0.05). The combination of GnRHa and DOM at doses of 40 μg+20 mg kg⁻¹ BW had higher values of the ovulation ratio and OI, and a shorter latency period compared with other treatments. The highest OI in GnRHa treatments was only 56.67%, suggesting a dopaminergic tone on gonadotropin secretion in this fish at the pre‐ovulatory stage. Therefore, ovulation can be successfully induced in yellow catfish with 40 μg kg⁻¹ GnRHa+20 mg kg⁻¹ DOM without affecting the egg quality.     

Controlled reproduction of an important indigenous fish species, Spinibarbus denticulatus (Oshima, 1926), in Southeast Asia

Aquaculture of Spinibarbus denticulatus (Oshima, 1926), a fish species indigenous to North Vietnam and Eastern China, is constrained by lack of fingerlings for stocking ponds and cages. As these fish do not naturally breed in captivity, carp pituitary extract (CPE), luteinizing hormone-releasing hormone analogue (LHRHa) with domperidone (DOM) and human chorionic gonadotropin (HCG) were administered at various doses to induce ovulation. A first set of experiments evaluated the response to LHRHa (30, 40 and 50 μg kg⁻¹) with or without DOM (10 mg kg⁻¹), CPE (20, 30 and 40 mg kg⁻¹) and HCG (3000, 4000 and 5000 IU kg⁻¹). A second set of experiments evaluated the dose response to LHRHa (30, 35, 40 and 50 μg kg⁻¹) primed with 6 mg kg⁻¹ of CPE, and HCG (3000, 3500, 4000, 5000 IU kg⁻¹) primed with 6 mg kg⁻¹ of CPE. The treatment groups were compared with each other and the control (injected with 0.9% saline solution). Only 25% and 50% ovulation resulted when treated with LHRHa at 40 and 50 μg kg⁻¹, whereas 100% ovulation was achieved with an addition of DOM to LHRHa. Both 30 and 40 mg kg⁻¹ CPE induced 100% ovulation. However, HCG (4000 and 5000 IU kg⁻¹) induced ovulation in only 33% of females. When primed with CPE, the minimum dose of LHRHa required was 35 μg kg⁻¹ to achieve 70% ovulation. Priming HCG with CPE also resulted in 100% ovulation, and the minimum effective dose of HCG to induce ovulation was 3500 IU kg⁻¹ with 60% ovulation. Fertilization and hatch rates observed in this study with different hormonal stimulation were high (80–93%). The results indicate that while the use of combined hormone strategy has no apparent advantage over a single hormone strategy, LHRHa+DOM (40 μg kg⁻¹+10.0 mg kg⁻¹) and CPE (30 mg kg⁻¹) are most effective in consistently inducing ovulation and thus can be used for commercial hatchery production of S. denticulatus larvae.     

Quantifying the dietary biotin requirement of the catfish,Clarias batrachus

Asian catfish, Clarias batrachus, were fed semi-purified basaldiets containing 0, 0.1, 0.5, 1, 3 and 5 mg biotin kg^–1diet for 60 days. Fish fed the control diet (no biotin) showed(P < 0.05) higher mortality, lower weight gain, specificgrowth rate (SGR), feed efficiency ratio (FER) and protein efficiencyratio (PER) than in fish fed diets supplemented with biotin. The highestweight gain, SGR, FER and PER were noticed in fish fed 1 mg biotinkg^–1, followed by 0.5, 5, 3 and 0.1 mg biotinkg^–1, except for PER (followed by 0.5, 5, 0.1 and 3 mgbiotin kg^–1). Quadratic analysis showed that the optimumdietary biotin requirements for maximal weight gain, PER and PER were2.49, 2.54 and 2.52 mg kg^–1, respectively. Liver biotinconcentrations were influenced by levels of biotin in the diet.Concentration of liver biotin increased as level of dietarysupplementation increased and no biotin was detected in the liver of thecontrol fish. Liver pyruvate carboxylase and acetyl CoA carboxylaseactivities were higher in fish fed biotin-supplemented diets than incontrols. Biotin concentrations, pyruvate carboxylase and acetyl CoAcarboxylase activities in liver associated with normal growth rangedfrom 10.59 to 10.66 g g^–1, 147.97 to 148.18 units mgprotein^–1 and 12.76 to 12.78 units mg protein^–1, respectively. Biotin deficiency symptoms such as anorexia, darkskin colour and convulsions were observed in fish fed the control diet.The optimum dietary biotin requirement for maximal growth of C.batrachus is about 2.49 mg kg^–1 diet.     

Effects of dietary carnitine and lipid on growth and body composition of hybrid striped bass (Morone chrysops ♀× M. saxatilis ♂)

A study was undertaken to investigate the effects of graded dietary levels and different types of carnitine on hybrid striped bass (Morone chrysops × M. saxatilis %) fed different levels of lipid. An incomplete factorial design was utilized in which diets containing lipid at either 5 or 10% were supplemented with l-carnitine at 0, 500, or 1000 mg kg^–1 diet, dl-carnitine at 1000 mg kg^–1 diet, or carnitine chloride to provide 1000 mg carnitine kg^–1 diet. Juvenile hybrid striped bass (3.3 g fish^–1) were stocked into individual 38-l aquaria connected as a brackish water (6), recirculating system and fed each diet in triplicate for 9 weeks.Supplementation of the diet with 1000 mg carnitine kg^–1 increased muscle carnitine from 35.5 to 47.7 g g^–1 tissue. Carnitine supplementation did not result in increased weight gain regardless of carnitine level or type; however, weight gain showed a significant (p<0.05) response to dietary lipid with fish fed diets containing 10% lipid growing 34% more than fish fed diets with 5% lipid. The hepatosomatic index also was unaffected by diet, but the intraperitoneal fat (IPF) ratio was significantly elevated (5.1 vs 3.2%) in fish fed diets with 10% lipid compared to those fed diets with 5% lipid. Fish fed diets containing 1000 mg carnitine kg^–1 had increased IPF ratio values at 4.7% compared to 3.9% for fish fed the basal diet. Liver lipid also was responsive to dietary treatment, increasing from 6.7 to 8.8% of wet weight as dietary lipid increased from 5 to 10%. The relative quantities of triglycerides, free fatty acids and phospholipids in muscle and liver were not influenced by carnitine level, carnitine type or dietary lipid level. Supplementation of carnitine does not appear to be beneficial to hybrid striped bass based on either growth performance or body composition.     

Effects of emulsified versus saline administration of GnRHa on induction of ovulation in rainbow trout, Oncorhynchus mykiss

The effects of saline-dissolved or Freund's incomplete adjuvant (FIA)-emulsified GnRHa treatment on the induction of ovulation in rainbow trout, Oncorhynchus mykiss, were examined. The FIA-emulsified GnRHa was first diluted in 0.25 ml physiological saline and then mixed with an equal volume of FIA. Fish were selected in the beginning of the spawning season and were allocated into four groups and were treated intraperitoneally with (a) 0.5 ml of emulsified GnRHa (GnRHa–FIA), (b) 0.5 ml saline-dissolved GnRHa in a single injection (GnRHa-1), (c) 0.5 ml saline-dissolved GnRHa in two injections spaced 1 d apart (GnRHa-2) and (d) 0.5 ml of saline (Control). The GnRHa dose in all hormone treatments was 25 µg kg^− 1. All fish in the FIA–GnRHa and GnRHa-2 groups ovulated within 10 and 11 d after treatment, respectively. In contrast, only 75% in the Control fish and 60% of the fish in the GnRHa-1 group ovulated within 36 d after treatment. None of the treatments caused any pre- or post-spawning mortality in the broodstock. Fertilization, eyeing and hatching percentages of the produced progeny were normal in all the treatment groups and did not differ significantly among them. In conclusion, FIA-emulsified GnRHa can be effective in advancing the onset of and synchronizing the ovulation of rainbow trout within a two-week period, thus shortening the egg collection period, without affecting broodstock survival and egg quality.     

Tilapia wild spawning control through predator fishes: Israelitrial with red-drum and hybrid bass

Tilapia wild spawning is a nuisance in warm freshwater aquaculture growout ponds. To cope with this problem two experiments were carried out with predatory fish that do not reproduce in fresh water. One experiment tested the capacity of hybrid bass (Morone saxatilis × M. chrysops) and red-drum (Sciaenops ocellatus) as predators of wild spawning of hybrid tilapia (Oreochromis niloticus × O.aureus), and the other compared predation effectiveness of red-drum of different sizes and stocking densities.Both hybrid bass and red-drum effectively reduced tilapia wild spawning and improved by 15–20% tilapia performance and food conversion ratio. These effects were obtained stocking small red-drum (20 g) or large red-drum (60–80 g) or bass (135 g) at stocking densities of 500–1000 predators/ha, together with 15000 tilapia/ha of 65–75 g. Hybrid bass stocked at 750/ha and large red-drum stocked at 500/ha presented over 90% survival. Red-drum at higher stocking density and/or lower stocking weight presented reduced survival (40–60%). Red-drum of all examined stocking weights presented better growth rates when stocked at 500/ha than at higher densities.     

Spawning induction in Kutum Rutilus frisii kutum (Kamenskii, 1901) using carp pituitary extract or GnRH analogue combined with metoclopramide

Kutum Rutilus frisii kutum (Kamenskii, 1901), Cyprinidae is an endemic fish of the Caspian Sea. Iranian Fisheries Organization (Shilat) produce up to 200 million fry (1–2 g body weight (b.w.)) to restock the Caspian Sea population annually. Some of these fry are produced by spawning induction in broodfish by carp pituitary extract (CPE). The objective of this study was to assay the effectiveness of the gonadotropin releasing hormone analogue (d ‐Ala⁶, Pro⁹‐Net GnRH) alone or in combination with metoclopramide (MET), a dopamine antagonist, on the percentage of ovulated females, latency period, ovulation index and fertilization success. The following hormone treatments were tested: single injection of 2 mg kg^?1 b.w. of CPE as a positive control, GnRHa alone 20 and 40 μg kg^?1 b.w. and combination of GnRHa and MET as follows: 5 μg+2.5 mg, 10 μg+ 5 mg and 20 μg+10 mg kg^?1 b.w. Negative control group was injected with 0.7% saline. The percentage of ovulated females, ovulation index and fertilization success were 90%, 71.3±1.24%, 68.4±2.3%, respectively, in the group treated with GnRHa+MET at a dose of 20 μg+10 mg kg^?1 b.w. and were significantly higher than those in the positive control (60%, 64.5±0.23%, 69.1±4.5%) (P<0.05). However, the latency period in this group was longer than that in the positive control (P<0.05). Only 20% and 40% fish ovulated in groups that received 20 or 40 μg kg^?1 b.w. GnRHa. No fish ovulated in the negative control.     

Induction of ovulation in ornamental common carp (Koi, Cyprinus carpio L.) using LHRHa ([d-Ser(tBu)6, Pro9-NEt]-LHRH) combined with haloperidol and carp pituitary extract

The effects of a single injection of mammalian superactive analogue [d ‐Ser(tBu)⁶,Pro⁹‐NEt]‐LHRHa (20 μg/ kg^?1) combined with the dopamine antagonist, haloperidol (HAL, 0.5 mg kg^?1), for induction of ovulation in the koi carp broodstocks were determined under routine hatchery conditions. The results were compared with classic carp pituitary extract (CPE, double injection) application (water temperature 22 °C). Physiological saline (0.7% NaCl)‐injected fish were used as a control group and no ovulation occurred in this group. The spawning ratio was high in the LHRHa+HAL treatment group and in the CPE treatment group (6/7 and 5/7 respectively). The latency period was 14–16 h in the LHRHa+HAL treatment group and 12–14 h in the CPE treatment group (after the second injection). There was no difference between the two ovulating groups with respect to the spawning index (the weight of eggs as a percentage of female body weight) and fertilization rate of eggs (P>0.05). As a result, ovulation can be induced successfully in koi carp broodstocks with 20 μg kg^?1 [d ‐Ser(tBu)⁶,Pro⁹‐NEt]‐LHRHa+0.5 mg kg^?1 HAL treatment in a single injection without decreasing the egg quality. Application of this combination can be useful for hatchery and broodstock management in koi carp culture.     

Utilization of carotenoids from various sources by rainbow trout: muscle colour,carotenoid digestibility and retention

Rainbow trout (Oncorhynchus mykiss) with a mean (sd) weight of 120 (2) g were fed diets supplemented with astaxanthin extracted from the yeast Phaffia rhodozyma (OY1 = 50 mg carotenoids kg^–1 feed, OY2 = 100 mg carotenoids kg^–1 feed), astaxanthin (AX = 100 mg astaxanthin kg^–1 feed) and canthaxanthin (CX = 100 mg canthaxanthin kg^–1 feed) for 4 weeks. Muscle analyses at the end of the experiment indicated a significantly higher carotenoid concentration in the AX group, while CX and OY1 groups were similar in spite of the differences in dietary concentration. The measure of total muscle colour difference (E^* _ab) between initial samples and 4 week ones was higher for the AX fish group but showed no significant difference between OY1, OY2, and CX. The hue and the reflectance ratio (R₆₅₀:R₅₁₀) of fish muscle increased in proportion to carotenoid intake. Digestibility (ADC) of yeast astaxanthin in OY1 and OY2 groups was significantly higher than that in the AX group. Canthaxanthin ADC was about one sixth of that of astaxanthin (AX group). Carotenoid retention in the muscle, expressed as a percentage of carotenoid intake, was higher for the AX group than that recorded for OY1 and OY2. According to ADC, carotenoid retention showed a marked lower value for the CX group. Muscle retentions were similar for astaxanthins from both sources.     

Ionic composition and osmolality of paddlefish (Polyodon spathula, Acipenseriformes) seminal fluid

Changes in ionic composition as Na⁺,K⁺, Ca²⁺ and Mg²⁺, osmolality inseminal fluid, percentage of motile spermatozoaand velocity were investigated in response toCPP and different dosage of LHRHa. The lowestvelocity of sperm was observed after use CPPtreatment. The velocity of spermatozoa,significant main effect of the treatment(P < 0.0001) and the time of sperm collection(P < 0.0104) were evaluated. The osmolality ofseminal fluid was different betweenexperimental groups of LHRHa (48.0–62.7mOsmol.kg^–1) and CPP (33.0–46.3mOsmol.kg^–1) treatments. The osmolalitywas significantly higher on the first day andone-half, then declined on day three, rangingfrom 33.0 to 62.7 mOsmol.kg^–1. Analysisof variance showed significant main effects ofthe treatment (P < 0.0001) and the time ofsperm collection (P < 0.0002) on the osmolalityof seminal fluid. The level of Na⁺ andK⁺ ion was different between experimentalgroups of LHRHa and CPP treatment. The highestconcentration of 11.11 mmol.l^–1 wasobserved at Na⁺ ion. Then theconcentrations declined on the level 1.56, 0.52and 0.36 mmol.l^–1 for K⁺, Ca²⁺and Mg²⁺ ions, respectively. There werehighly positive correlations between osmolalityof seminal fluid and dosage of LHRHa treatment(r = 0.84), velocity of spermatozoa andosmolality of seminal fluid (r = 0.57) andosmolality of seminal fluid and Na⁺concentration at seminal fluid (r = 0.70).Injection with LHRHa increased quality of spermas velocity of sperm, level of Na⁺,K⁺ and osmolality at seminal fluidcompared to CPP treatments.     

Performance of the heat of the hagfish,Eptatretus cirrhatus

The maximum power output of isolated perfused ventricles of the hafish (Eptatretus cirrhatus) averaged 0.367±0.031 mW g^–1 (n=9), considerably high than estimates for the heart of the Atlantic hagfish (Myxine glutinosa). Maximal minute volumes averaged 21.55±1.28 ml min^–1kg^–1, with a mean stroke volume of 0.71±0.14 ml kg^–1 body weight, values which are similar to those reported for many teleost and elasmobranch hearts.Ventricular output showed the characteristic dependence upon atrial filling pressure up to an optimum filling pressure ofc. 4 mm Hg. At output pressures exceeding 14 mm Hg the stroke volume and power output fell sharply. At these afterloads, the ventral aorta remained distended following semilunar valve closure and so the volume of fluid ejected on ventricular systole was reduced. There was little change in the frequency of the heart as either input or output pressures were varied.     

Ovulation and spawning induction in Caspian kutum Rutilus frisii kutum by administration of GnRHa and catecholaminergic pharmaceutical compounds with Ovaprim

The acceleration of final oocyte maturation and ovulation is recognized as a principal process in Caspian kutum Rutilus frisii kutum, a commercial and valuable species in Caspian Sea. The aim of this study was to evaluate the effects of catecholaminergic pharmaceutics which include Salbutamol (β₂‐adrenergic receptor agonist), Metoprolol (β₁‐adrenergic receptor antagonist), Clozapine and Olanzapine (the third generation of D₄ and D₂ dopamine receptor antagonists) which can be more efficient than the first and second generations, in combination with Buserelin ([D‐Ser(tBu)⁶,Pro⁹‐NEt]‐GnRHa) and Ovaprim (D‐Ala⁶,Pro⁹‐Net)‐sGnRH+Domperidone on ovulation and spawning induction in Caspian kutum. One hundred eight adult females were injected once with Buserelin Acetate (BUS) 5 μg kg^?1 BW, Ovaprim 0.5 mL kg^?1 BW, Salbutamol Sulphate (SLB) 4 mg kg^?1 BW, Olanzapine (OLZ) 5 mg kg^?1 BW, Clozapine (CZ) 12 mg kg^?1 BW and Metoprolol Tartrate (MTP) 5 mg kg^?1 BW, being divided into 12 groups: group 1, intact (negative control); group 2, Ovaprim (positive control); group 3, OLZ+SLB; group 4, OLZ+MTP; group 5, OLZ+BUS; group 6, CZ+SLB; group 7, CZ+MTP; group 8, CZ+BUS; group 9, OLZ+BUS+SLB; group 10, OLZ+BUS+MTP; group 11, CZ+BUS+SLB and group 12, CZ+BUS+MTP (N = 9). The results showed that the highest mean value in ovulation success, ovulation index, fertilization success, relative fecundity and the number of eggs belonged to Ovaprim treatment. On the other hand, spawning was successful in OLZ+BUS+SLB and CZ+BUS treatments (P < 0.05), whereas it was lower in CZ+MTP, CZ+BUS+MTP and OLZ+BUS than the other treatments. Therefore, it could be concluded that Clozapine and Olanzapine potentiated the effect of Buserelin treatment in ovulation and spawning induction, while Metoprolol blocked the stimulatory effects of GnRHa, Clozapine and Olanzapine. Salbutamol also can amplify stimulatory effect of all mentioned pharmaceutics.     

Sublethal effects of ammonia in soft water on Atlantic salmon smolts at a low temperature

Atlantic salmon (Salmo salar L.) smolts were exposed to ammonia at 4 °C in an open flow system. The concentrations of un-ionized ammonia nitrogen (NH₃-N) and total ammonia nitrogen (TAN) were increased abruptly twice during a period of 28 days. For concentrations in the range 1–15 µgl^–1 un-ionized ammonia nitrogen (4.3–21.1 mgl^–1 TAN), no effects were observed on the smolts. However, plasma glucose was not measured in this range. The observed results for higher concentrations may be divided into two categories of sublethal effects. (1) In smolts exposed to the concentration range 19–37 µgl^–1 NH₃-N (average 26 µgl^–1 NH₃-N; 34.9–50.5 mgl^–1 TAN), the mean plasma glucose concentration was 1.3 times the mean of the control group. No other measured parameters were significantly altered. (2) For smolts exposed to 37–65 µgl^–1 NH₃-N (average 47 µgl^–1 NH₃-N; 57.7–84.5 mgl^–1 TAN), the mean plasma glucose concentration was increased to 2.3 times, the mean plasma chloride level was reduced to 0.9 times, and mean haematocrit was increased to 1.1 times the control values. Histological examination of the gill tissue revealed extensive lamellar hypertrophy. Weight, length, condition factor and ventilation frequency were not significantly affected and no mortality took place during the exposure period (1–65 µgl^–1 NH₃-N; 4.3–84.5 mgl^–1 TAN). Plasma glucose seemed to be the most sensitive parameter in detecting the sublethal stress response, and this investigation may thus demonstrate the importance of measuring plasma glucose in experiments concerning safe levels for ammonia.     

Artificial spawning of female Lithuanian strain B carp (Cyprinus carpio L.) after treatment with carp pituitary homogenate, Ovopel or [d-Tle6, ProNHEt9] GnRH-a (Lecirelin)

The results of reproduction of females from Lithuanian strain B carp after ovulation stimulation with carp pituitary homogenate (CPH; 0.3+2.7 mg kg^?1; group I), Ovopel (1/5+1 pellet kg^?1; group II) or [d ‐Tle⁶, ProNHEt⁹] GnRH‐a (Lecirelin) with metoclopramide (15 μg kg^?1+10 mg kg^?1 respectively; group III) were investigated. The lowest percentage of spawning females (71%) was recorded in the group treated with CPH. In case of Ovopel or Lecirelin induced ovulation, 86% of females spawned. No statistically significant effect of the ovulation stimulator (group) on the weight of eggs was found; however, the highest mean weight of eggs (expressed both in grams and in the percentage of female body weight) was recorded for the group treated with Ovopel (1400 g and 13%). After the treatment with CPH or Lecirelin, the weight of eggs was 1140 g (11%) and 1100 g (10%) respectively. The ovulation stimulator significantly affected the percentage of live embryos after 36 and 48 h incubation of eggs (P≤0.05; P≤0.01). After treatment with [d ‐Tle⁶, ProNHEt⁹] GnRH‐a, eggs of the best quality were obtained and after 36 and 48 h incubation the mean percentages of live embryos were significantly higher than the means calculated for the remaining two groups. No statistically significant differences were found between the percentage of living embryos after 36 and 48 h incubation of groups I and II.