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Vliv chovatelských zásahů na produkční parametry chovu keříčkovce červenolemého (Clarias gariepinus).
Doule, Jan
The aim of the work was to evaluate, based on a feeding test, the influence of commonly performed husbandry interventions on the production results of the breeding of the African catfish (Clarias gariepinus, Burchell 1822). The longterm feeding test was performed on the RAS recirculation system and the fish were reared in aquariums (180 l). The test itself lasted 56 days and was preceded by an 18-day adaptation of the fish to new conditions. Husbandry interventions (control weighing, refishing, mixing and sorting of fish) were applied to the fish at 14-day intervals, and each variant of the husbandry intervention was tested in two repetitions. The results were statistically evaluated by the Kruskal-Wallis test. The Control, Overfishing, Mixing variant achieved the same production results (FCR/SGR 0.25). The Sorting variant showed better production results (FCR/SGR 0.23). In this test, it was proven that the selected breeding interventions do not negatively affect the production results of the breeding of the African catfish. The partial goal of the work was to evaluate how acute stress affects the quality of the internal environment of this species. A 2-day experiment was carried out. In the experiment, the fish were divided into 2 group variants Control and Stress. For the Stress variant, the husbandry intervention of overfishing was applied for 10 minutes (induction of acute stress). Subsequently, blood was collected from 10 fish from both groups in the time interval of 0, 1, 3, 6, 12 and 24 hours of exposure to the stressor. The results of the hematological and biochemical parameters of the stressed fish were compared with the control group. As a result of the stress reaction in the Stress variant, there was first an increase in the values of the Hk, Hb and Ery parameters, then a decrease in them and, after the stressor had subsided, a return to the original range before the stressor (after 24 hours). In the Stress variant fish, there was an increase in glucose content values from 6 to 24 hours compared to the Control variant, which was apparently caused by glycogenolysis in the muscles and liver.
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Vliv teploty na udržení schopnosti oplození a líhnivosti při přechovávání neoplozených jiker u keříčkovce červenolemého
BORŮVKA, Vít
When hormonally induced artificial spawning of african catfish (Clarias gariepinus), was several female injected intraperitoneally in one dose preparation Ovopel at doses of 1.5 pellet × kg-1. Females were kept separately in the tanks at a temperature of 21.5 °C. All females were spawned at the same time latency 19.2 hours. Eggs from three spawned females were mixed and divided into 6 doses. Each batch was placed into thermoboxes at temperature 5 °C, 10 °C, 15 °C, 20 °C, 25 °C and 30 °C. These eggs were stored in thermoboxes and after times of storage 0.5 h, 1 h, 1.5 h, 2 h, 3 h, 4 h, 6 h, 8 h, 10h, part of the eggs (approximately 50 to 100 pieces) were taken out from each thermoboxes in three replications and was placed into individuals cups and fertilized by adding 5 drops of sperm and 20 ml of water. In these samples were subsequently observed fertilization, hatching rate and survival rate. When watching fertilization was in individual temperature the highest values and also statistically non-significant difference ( = 0.05) achieved: at 5 °C in times of fertilization 0.5 2 hrs. (61.6 +- 5.81 % - 47.7 +- 1.48 %), at 10 °C in times 0.5 - 1.5 hrs. (70 +- 6.7 % - 62.1 +- 8.9 %), at 15 °C in times 0.5 - 3 hrs. (59.6 +- 9.4 % - 59.6 +- 2.9 %), at 20 °C in times 0.5 - 3 hrs. (61.4 +- 3.6 % - 56.1 +- 2.5 %), at 25 °C in times 0.5 - 4 hrs. (55.5 +- 7.2 % - 49.7 +- 9.3 %) and at 30 °C in times 0,5 - 3 hrs. (61.6 +- 10.3 % - 51.8 +- 17.8 %). When watching hatching rate was in individual temperature the highest values and also statistically non-significant difference ( = 0.05) achieved: at 5 °C in times of fertilization 0.5 - 1 hrs. (28.4 +- 2.9 % - 21.1 +- 9.5 %), at 10 °C in times 0.5 - 1 hrs. (36.6 +- 17.3 % - 22.1 +- 7 %), at 15 °C in times 0.5 - 2 hrs. (34.1 +- 5.5 % - 26.9 +- 5.1 %), at 20 °C in times 0.5 - 2 hrs. (33 +- 8.2 % - 28.8 +- 1.6 %), at 25 °C in times 0.5 - 4 hrs. (31.4 +- 6.2 % - 15.3 +- 13.5 %) and at 30 °C in times 0.5 - 2 hrs. (33.1 +- 9.2 % - 21.2 +- 8 %). When watching survival rate was in individual temperature the highest values and also statistically non-significant difference ( = 0.05) achieved: at 5 °C in times of fertilization 0.5 - 1 hrs. (20.1 +- 6 % - 13 +- 3.3 %), at 10 °C in times 0.5 - 3 hrs. (19.8 +- 15.31 % - 3.1 +- 3 %), at 15 °C in times 0.5 - 6 hrs. (23.3 +- 9 % - 5 +- 2.8 %), at 20 °C in times 0.5 - 2 hrs. (22.4 +- 1.9 % - 15.1 +- 5.2 %), at 25 °C in times 0.5 - 4 hrs. (18.7 +- 4.4 % - 4.1 +- 1.9 %) and at 30 °C in times 0.5 - 1.5 hrs. (26.2 +- 5.5 % - 21.4 +- 6.8 %). Suitable temperatures for the storage of unfertilized eggs after spawning are two hours before fertilization at temperatures from 15 to 30 °C. Other suitable temperatures which are useful for storage are temperatures 15 to 25 °C, for preservation after 3 hrs. and longer after fertilization.
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Demembranation of fish sperm: Design and verification this procedure for the different species of freshwaterfish and demonstration usage of this technique by study the effect of heavy metals to sperm axoneme
BLAŽKOVÁ, Jaroslava
The object of this study is to design demembranation method on four freshwater species and its application on study of the influence of HgCl2 on the axoneme and motity sperm motility parameters. Demembranation was designed and examined for all investigated species common carp (Cyprinus carpio), sterlet (Acipenser ruthenus), perch (Perca fluviatilis) and african catfish (Clarias gariepinus). One-step and two-step method was designed and tested for common carp. One-step method was designed for sterlet and perch. Two-step method of demembranation was designed for african catfish. Demembranation was designed and examined for all species under examination. Sperm motility was evidently increased above normal physiological value. Other sperm motility parameters (velocity, percent of motile cells) slightly decreased. HgCl2 in concentration 0,01 mM to the demembranation medium didn't show effect on flagellar microtubule aparat and then to the motility parameters, except sterlet; demembranated sterlet sperm was inhibited at all used concentration of HgCl2. Concentration 0,1 mM had inhibition effect on carp and africant catfish spermatozoa. Concentration 1 mM HgCl2 inhibited sperm of all tested species.
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