Artificial spawning of female Polish line 3 carp (Cyprinus carpio L.) after treatment with pituitary homogenate and/or Ovopel

Stimulation of ovulation was carried out in female carp (Cyprinus carpio L.) of Polish line 3, with carp pituitary homogenate, Ovopel (the preparation contains d ‐Ala⁶, Pro⁹NEt‐mGnRH and metoclopramide), and Ovopel and carp pituitary homogenate. The effect of the ovulation stimulators on the weight of eggs expressed in grams and as a percentage of female body weight was determined. The effect of the treatments on the quality of eggs expressed as the percentage of living embryos after 24‐ and 36‐h incubation was also determined. The best results were obtained after stimulation with Ovopel (the priming dose) and pituitary homogenate (the resolving dose). In this case all the females spawned, and the highest yield and quality of eggs were recorded. The poorest results were noted if the ovulation was stimulated with repeated injection of carp pituitary homogenate. The females treated with carp pituitary homogenate gave eggs of poorer quality than those stimulated with two doses of Ovopel or with Ovopel and pituitary homogenate. The percentage of living embryos after 24‐ and 36‐h incubation of eggs was significantly higher for the group stimulated with Ovopel and pituitary homogenate than for the other treatments.     

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.     

Artificial spawning of African catfish Heterobranchus longifilis: differences between the effects on reproduction in females treated with carp pituitary homogenate or Ovopel

The effects of the controlled reproduction of African catfish Heterobranchus longifilis after ovulation stimulation with carp pituitary homogenate (CPH; 4 mg kg^?1; group I) or Ovopel (1/5+1 pellet kg^?1; group II) were investigated. After the application of Ovopel, eggs were obtained from a higher percentage of females than after a CPH treatment (87.5% and 75.0% respectively). The statistically significant (P≤0.05) effect of ovulation stimulator was specified only in the case of the weight of eggs (expressed in grams and in percentage of female body weight), being higher in fish treated with Ovopel compared with CPH‐treated fish (176.02 g, 8.43% and 109.51 g, 5.48%). The quality of eggs expressed in percentage of live embryos after 24 h incubation was higher by 7.5% in fish treated with Ovopel. Latency period did not significantly affect the weight of eggs, fertilization percentage or percentage of living embryos after 24 h of egg incubation. However, the weight of eggs and percentage of living embryos after 24 h incubation were higher in fish spawning after 12 h latency (159.38 g and 85.30%) compared with the weight and quality of eggs obtained from females spawning after 14 h latency (126.15 g and 76.04%).     

Artificial spawning of carp (Cyprinus carpio L.): differences between females of Polish strain 6 and Hungarian strain W treated with carp pituitary homogenate, Ovopel or Dagin

Investigations of the effects of controlled reproduction were conducted on carp females of Polish strain 6 and Hungarian strain W after ovulation stimulation with carp pituitary homogenate (CPH) (0.3 mg+2.7 mg kg^?1 body weight), Ovopel (1/5+1 pellet kg^?1 body weight) or Dagin (1 dose kg^?1 body weight). In both strains, the highest percentage of spawning females was found after the Ovopel treatment. After treatments with CPH and Dagin this percentage did not differ in strain 6; however, after Dagin, it was higher in fish of strain W. After CPH or Ovopel stimulation the females of line 6 yielded eggs of higher weight compared with line W. After the Dagin treatment the weight of eggs obtained from females, both strains was similar but much lower than after the two remaining agents. The quality of eggs expressed both by the percentage of fertilization and that of living embryos after 24 and 36 h incubation was similar in the two strains only in the group treated with Ovopel. After CPH application eggs of better quality were obtained from strain 6 compared with strain W; however, after the treatment with Ovopel, eggs of much better quality were noted in strain W. In general, the best effects of reproduction were recorded in the case of Ovopel and the poorest in that of Dagin. Females of strain 6 yielded eggs of a higher weight but the percentages of spawning females were higher in strain W after each of the applied spawning agents. A new approach to this problem consisted in investigating the interaction between ovulation stimulators and origin of females of fish treated with Dagin.     

Artificial spawning of carp (Cyprinus carpio L.); differences between the effects of reproduction in females of Hungarian, Polish and French origin treated with carp pituitary homogenate or [D-Tle6, ProNHEt9] GnRH (Lecirelin)

The investigation concerned the reproduction effects in carp females of the Hungarian strain 8, Polish strain 2 and French strain F of ovulation stimulation with carp pituitary homogenate (0.3 mg kg^?1 and after 12 h 2.7 mg kg^?1) or [D‐Tle⁶, ProNHEt⁹]GnRH (Lecirelin) with metoclopramide (15 μg kg^?1 and 10 mg kg^?1 respectively). The ovulation stimulators did not affect the weight of eggs (expressed in g and as the percentage of female body weight). However, in the group treated with pituitary homogenate (I) the least‐square means estimated for these parameters were higher than in the group treated with Lecirelin (II). A statistically significant (P≤0.05) difference in the mean percentage of living embryos after 48‐h incubation was observed between groups I and II, with the eggs obtained from females of group I being of better quality. The origin of females significantly (P≤0.05) affected the weight of eggs. The weight of eggs from females of Hungarian strain 8 was higher (P≤0.05) than the weight of eggs of the other two lines. With respect to parameters for egg quality (percentage of fertilized eggs and percentage of living embryos after 24‐, 36‐ and 48‐h incubation), no effect of the origin of females was observed. The interaction between the spawning agent and the origin of the females was not statistically significant with respect to the two parameters for the weight of the eggs. The least‐square means test for the investigated interaction showed that after the application of pituitary homogenate, the weight of eggs obtained from strains 8 and F was similar (respectively 711.2 g and 665.0 g). However, after the application of Lecirelin the females of strain 8 yielded eggs of a high weight (934.3 g) and those of strain F of a very low weight (373.2 g). A statistically significant (P≤0.05) interaction between ovulation stimulator and origin of females was recorded for the percentage of living embryos after 24‐ and 36‐h incubation. A dependence was found between the latency time and the reproduction effects.