The aim of the study was to determine the optimum temperature shock timing to induce androgenetic and gynogenetic growth in common tench (Tinca tinca L.). UV radiation at the dose of 3,456 J m -2 was used to inactivate the genome of oocytes (androgenesis) and sperm (gynogenesis). In each case, the optimum timing was sought (between 20 and 60 min) before the beginning of diploidization of genetic material with a temperature shock (40°C, duration 2 min). Eggs were incubated under laboratory conditions at 21°C. The highest survival rate for androgenotes was observed after the temperature shock was applied for 30 min and for gynogenotes 40 min after the activation. The survival rate for embryos did not exceed 2 % in the best variants, either in andro-or gynogenesis. A negative correlation was found to exist between the quality of spawn and the occurrence of spontaneous andro-and gyno-genotes.
Four broodstocks of European huchen (Hucho hucho) from: Poland, Germany, Slovakia, and Ukraine were investigated using ten microsatellite DNA loci. Microsatellite DNA analysis was successfully applied for the first time in the Polish broodstock of this fish species. The genetic variation and genetic distance between these broodstocks were evaluated. In addition, we examined the potential effects of a genetic bottleneck on the genetic variation of the broodstocks. The European huchen broodstocks exhibited moderate genetic diversity (PIC = 0.405–0.496 and I = 0.831–1.047) with the exception of German broodstock which presented higher genetic diversity (PIC = 0.590 and I = 1.254). Observed (Ho) and expected (He) heterozygosity across the investigated loci in all broodstocks ranged from 0.434 to 0.686 and from 0.452 to 0.650, respectively. Overall, the studied broodstocks were in Hardy-Weinberg equilibrium (HWE); however, from 8 to 42 % of the loci deviated from HWE in each stock. The Garza-Williamson index (M = 0.146–0.279) and values of the heterozygosity excess revealed a reduction of genetic variation in all studied broodstocks because of the founder or bottleneck effect. The analysis of genetic differentiation (Fst) and Nei’s genetic distance between pairs of broodstocks revealed that Polish and Ukrainian broodstocks of European huchen were characterized by the closest genetic distance. In contrast, the highest genetic divergence parameters (Fst and Nei’s distance) were observed among German, Slovak, and Ukrainian broodstocks.
Four broodstocks of European huchen (Hucho hucho) from Poland, Germany, Slovakia, and Ukraine were investigated using five selected fragments of mtDNA. The mitochondrial DNA sequence analysis was successfully applied to the Polish and German broodstocks of European huchen for the first time. A very low haplotype (h = 0.097) and nucleotide (π = 0.00013) diversity across 3573 bases of mtDNA fragments (partial regions of NADH-1, ATPase 6, Cytochrome b, evidenced by three closely related mtDNA haplotypes were found. The analysis of pairwise genetic differentiation (Fst) displayed a statistically significant differentiation between German (clade A) and the rest of examined broodstocks (clade B), clustering them into two separate groups. Moreover, the applied mtDNA markers did not reveal any differences among fish from the clade B, suggesting that other markers should be used to display a deeper genetic background of the studied broodstocks. The two clusters of European huchen distinguished under the current study should be considered as distinct management units by managers, who may be tempted to transport brood fish or yearlings across the range of European huchen distribution. It means that stocking material and spawners of European huchen from the upper parts of the Danube River (Clade A) should not be mixed with those from the lower parts (Clade B). Moreover, for any supplementation of broodstocks in order to increase their genetic variability only the fishes within the described management units should be used.
Summary The feeding rate effects were studied on the growth performance of gynogenetic diploid larvae of sterlet Acipenser ruthenus during the first 4 weeks of exogenous feeding. The experimental rearing was conducted from 7 to 38 days post‐hatch (dph) in a circulation system. This was set up in four groups with three replicates (440 individuals/replicate), viz: AC‐control larvae fed Artemia sp., CFC‐control larvae fed compound feed, AG‐gynogenetic larvae fed Artemia sp., and CFG‐gynogenetic larvae fed compound feed. The larvae were reared in glass tanks (44 L volume, 10 individuals/L) with the temperature maintained at 18 ± 0.5°C, photoperiod of 12L:12D and water flow regime of 1‐L/min and fed 50%, 25%, 25%, and 9% of their total biomass/day during feeding. Highest TL and WBW of gynogenetic diploid larvae (AG) were observed with 50.6 ± 1.2 mm and 607.3 ± 36.1 mg (n = 30) at 38 dph. Highest TL and WBW of control larvae (AC) were recorded with 49.5 ± 3.8 mm and 600.8 ± 88.0 mg (n = 30), respectively, with 73.1% ± 11.4% survival; the lowest survival rate was at 46.4% ± 7.1% (n = 30) for the CFG group. The results indicate that the gynogenetic and normal larvae of sterlet fed with live food (Artemia nauplii) from 7 dph can achieve higher growth and survivability compared to the larvae fed with formulated test feed. Results of this study suggest that the effective rearing of sterlet larvae from 7 to 38 dph strongly depends upon the types of feed rather than the genome manipulation performed.
In Poland the conservation program of Atlantic sturgeon Acipenser oxyrinchus is conducted during over 10 years by Inland Fisheries Institute in Olsztyn, Poland. Material of A. oxyrinchus is annually transported from Canada to Poland and the broodstock of this species is created. Part of imported fish material is breed and released into local rivers e.g. Drweca River, Vistula River. All the imported material is obligatory genetically analyzed. The analysis must include the species verification and the genetic diversity of fish. Such analyses are necessary to issue a permit for restocking the local rivers. This paper presents a genetic characteristics of juvenile Atlantic sturgeon imported from Canada by Fish Farm Komorowo, Poland intended for restocking the river Vistula. Genetic analysis of the 45 juvenile Atlantic sturgeon was conducted using five microsatellite DNA markers (Spl-106, Spl-101, ATR-113, Aox-23A, Aox-23B) and one fragment (240 base pairs) encoding the cytochrome b gene (Cytb). In the present paper the genetic information about optimal genetic diversity and good condition of restocked materials of Atlantic sturgeon were described.
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