Artificial spawning of European catfish Silurus glanis L.: differences between propagation results after stimulation of ovulation with carp pituitary and Ovopel

The effect of spawning on European catfish females with an average body weight of 5.6 kg and 11.2 kg was investigated, with carp pituitary and Ovopel being used as ovulation stimulators. Ovopel induced ovulation in a higher percentage of females of both smaller and larger body weight. The applied ovulation stimulators did not significantly affect the weight of the obtained eggs. On the other hand, the effect of the stimulators was highly significant (P≤ 0.01) with respect to the percentage of live embryos after 24‐, 48‐ and 56‐h incubation. The fish of greater body weight yielded eggs of a significantly (P≤ 0.05) greater weight, although of poorer quality. The interaction between the ovulation stimulator and female body weight was statistically significant (P≤ 0.05) for the weight of the obtained eggs and highly significant (P≤ 0.01) for the percentage of live embryos after 48‐h incubation. For the percentage of live embryos after 24‐ and 56‐h incubation, the statistical significance (P≤ 0.05) of this interaction was determined. In the case of females of smaller body weight, a statistically significant (P≤ 0.05) phenotypic correlation was found between the percentage of live embryos after 24‐h incubation and that after 48‐h incubation, and also between the percentage of live embryos after 24‐ and 56‐h incubation.     

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%).     

Differences in the effectiveness of reproduction among ten breeding strains of the common carp Cyprinus carpio L. after stimulation of ovulation with carp pituitary homogenate or [(D‐Ala6, Pro9NEt) mGnRH‐a + metoclopramide] (Ovopel)

This study focused on the reproduction effectiveness of 10 breeding strains of common carp (Polish strains 2, 3, 6; Hungarian strains 0, W, 7; Lithuanian strain B; French strain F; Israeli strain D and Yugoslavian strain J) after stimulation of ovulation with carp pituitary homogenate or Ovopel. The percentage of females with recorded ovulation became higher after Ovopel treatment in as many as eight breeding strains (2, 3, 6, 0, W, B, F, D). The interaction between the spawning agent and the breeding strain was statistically significant (P ≤ 0.05) for the mass of spawn and non‐significant for traits determining the quality of eggs. Among the 10 breeding strains, in 4 (3, 7, B, J) the least‐squares means (LSM) for the weight of egg (g) were higher for fish stimulated with Ovopel. Among the strains tested, in seven (3, W, F, J, 2, 7, B), the LSM for the percentage of living embryos after 36 h incubation were higher for fish treated with Ovopel. The evaluation of reproduction effects based on the values of such parameters as the percentage of ovulating females, weight of eggs (g) and the percentage of live embryos (36 h) showed that after Ovopel treatment the poorer effects were obtained only for strains 6, 0 and D.     

Artificial Spawning of African Catfish,Clarias gariepinus

Abstract

The effects of controlled reproduction of African catfish, Clarias gariepinuswere investigated in an experiment with carp pituitary (at the dose 4 mg/kg body weight) or Ovopel (1 pellet/kg body weight) used as ovulation stimulators. The application of the synthetic stimulator led to the significantly (P≤0.01) greater weight of eggs (expressed in grams and as percentage of female body weight) and to the significantly (P≤0.05) higher quality of eggs after 24-hour incubation as compared with the hypophysation effects. Two categories of females were used in the experiment, i.e., light (mean body weight of 3.75 kg) and heavy (mean body weight of 8.86 kg) fish. The results show that a significantly (P≤0.01) greater weight of eggs (expressed in grams) was obtained from heavier females. The quality of eggs expressed as the percentage of live embryos after 12- and 24-hour incubation was significantly (P≤0.01 and P≤0.05, respectively) higher for lighter females. The higher weight of obtained eggs and their better quality after Ovopel stimulation compared to the weight and quality of eggs obtained after hypophysation allow for the recommendation of this ovulation stimulator for the fish species investigated.     

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 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.     

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 carp Cyprinus carpio L.: differences between the effects on reproduction in females of Israeli strain Dor-70 and its cross-breed treated with carp pituitary and Ovopel

The effects on carp reproduction were investigated in females of the Dor-70 strain and a cross-breed of this line with a Hungarian one of carp pituitary and Ovopel as ovulation stimulators. It was clear that, in the case of the Ovopel treatment, a higher percentage of females spawned, although the weight of eggs obtained was less than that yielded by hypophysed fish, the differences being highly significant (P ≤ 0.01) with respect to the weight in grams and to percentage of female body weight. No statistically significant differences were determined in the quality of eggs, measured by both the fertilization percentage and the percentage of living embryos, obtained after the two stimulators were used. Neither the provenance of females nor the interaction of female provenance and the stimulator has any effect on the traits investigated. The correlation between the percentage of fertilization and the percentage of live embryos was 0.54 for strain Dor-70 and 0.95 for the cross-breed. The multiple regression equations were calculated for strain Dor-70 and for cross-breed 5 separately, where the percentage of living embryos constituted a dependent variable and the mass of a female, mass of eggs in grams and the percentage of fertilization were independent variables. We appraised the regressions as significant for Dor-70 (P ≤ 0.04) and highly significant for the cross-breed (P ≤ 0.0001).     

Artificial spawning of carp (Cyprinus carpio L.): the use of Aquaspawn and carp pituitary to induce ovulation in females of Lithuanian line B

Ovulation stimulation was carried out in carp (Cyprinus carpio L.) females of Lithuanian line B, using carp pituitary (0.3 + 2.7 mg kg^?1), Aquaspawn (0.5 mL kg^?1) and Aquaspawn + carp pituitary (0.3 mL kg^?1 + 2.7 mg kg^?1). The poorest results of reproduction (the lowest percentage of ovulating females, the lowest weight of eggs and their poorest quality) were obtained after double hypophysation. The best results were induced by the application of Aquaspawn alone. The effect of the applied stimulators was statistically non‐significant with respect to the weight of eggs, being highly significant (P ≤ 0.01) with respect to the percentage of fertilized eggs and that of living embryos after 24‐ and 36‐h incubation. The multiple‐regression equations were calculated for the three groups separately. The percentage of living embryos after 36‐h incubation constituted a dependent variable while the mass of females, the mass of eggs, the fertilization percentage and the percentage of living embryos after 24‐h incubation were independent variables. The regression was only significant (P ≤ 0.01) for the group of fish treated with Aquaspawn.     

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.     

Characteristics of the reproduction effectiveness of four Hungarian breeding lines of carp Cyprinus carpio (L.)

The effectiveness of reproduction of four Hungarian breeding lines 7, 8, W, and 0 of carp Cyprinus carpio was investigated. The highest percentage of ovulating females after Ovopel stimulation of ovulation (1/5 + 1 pellet kg^?1 BW of females) was found in line 8 (100 %), in line 0, it was 86.21 %, and in lines 7 and W, the respective values were 73.68 and 76.47 %. It was noted that the breeding line significantly (P ≤ 0.05) determined the weight of the eggs (expressed in grams and percentage of female BW), the fertilization percentage, the percentage of living embryos after 24- and 36-h incubation, the total number of eggs, and the number of live embryos after 36-h incubation. The highest weight of eggs was obtained from females of line 7 (1,083.41 g) and line 8 (981.54 g), while the lowest weight was noted in the case of females of line W (804.94 g). The highest number of eggs was found in line 7 (722,300) and in line 8 (654,400). For these lines, the highest number of live embryos (36 h) was also found (624,400 and 622,200, respectively). Within each line investigated, the regression equations were derived in order to predict the weight of eggs (g), percentage of live embryos, and the number of live embryos after 36-h incubation.     

Effect of the dusk photoperiod change from light to dark on the incubation period of eggs of the spotted rose snapper, Lutjanus guttatus (Steindachner)

Spotted rose snapper, Lutjanus guttatus (Steindachner), eggs were incubated under different photoperiods to examine the effect of photoperiod on incubation. The eggs from two fish were incubated under five artificial photoperiods: constant dark (D), constant light (L) from 06:00 hours and 6, 10 and 14 h of light from 06:00 hours. The eggs from seven other fish were incubated under a natural photoperiod. Different spawning times (21:00 – 01:00 hours) and different photoperiods combined to give the start of the dusk photoperiod change after 11–23 h of incubation. Constant light or applying the dusk photoperiod change after ≥20 h of incubation appeared to extend the hatching period. The mean hatching period for groups of eggs incubated in darkness or that received the dusk photoperiod change after ≤19 h of incubation (n=8 different groups) was 2 h 15±10 min, which was significantly lower (P<0.05) than the mean hatching period of 4 h±37 min for groups that did not receive the dusk photoperiod change or that received the dusk photoperiod change after ≥20 h of incubation (n=9 groups). However, despite these differences, the majority of the eggs hatched during a 2–3 h period from 17 to 20 h of incubation, and a sigmoid regression (r²=0.9) explained the relationship between percentage hatch and hours of incubation for all photoperiod groups.     

Suspending Mammalian LHRHa‐injected Channel Catfish,Ictalurus punctatus,in Individual Soft Mesh Bags Reduces Stress and Improves Reproductive Performance

Hormone‐induced spawning of channel catfish held communally in tanks is a reliable method to produce channel catfish, Ictalurus punctatus ♀ × blue catfish, Ictalurus furcatus ♂, F₁ hybrid catfish fry. However, mature catfish are crowded, and repeatedly handled during the process of induced ovulation. Repeated handling of gravid females is stressful and may impair ovulation, egg quality, and reproductive performance. Three trials were conducted to evaluate the effects of two methods of confining post‐hormone‐injected female channel catfish on stress response (cortisol concentrations) and reproductive performance: fish were either held individually while suspended in soft, nylon‐mesh bags or communally in a concrete tank. Percent of females ovulated to hormone treatment, relative fecundity, percent egg viability, and latency of channel catfish did not differ for fish in the two treatments. However, percent hatch and fry/kg of females was higher (P < 0.05) for fish held in bags that for fish held communally in tanks. Mean plasma cortisol response immediately prior to the first hormone injection (0 h) did not differ among fish groups in the two treatments. However, mean plasma cortisol concentrations were significantly lower (P < 0.05) for fish in the bag treatment at 16 and 36 h compared to fish held communally in tanks. Plasma estradiol levels (measure of oocyte maturation) were assessed at 0, 16, and 36 h after hormone injection; concentrations were (P < 0.05) higher at 16 h compared to 0 and 36 h; however, estradiol concentrations did not differ for fish held in the two treatments (P > 0.05). Suspending hormone‐injected broodfish individually in soft bags reduced stress response, improved egg hatching rate, and increased hybrid fry produced per kg weight of female broodfish. Using this simple technology, farmers can improve the efficiency of hatcheries producing hybrid catfish fry.     

Application of controlled-release,GnRHa-delivery systems in commercial production of white bass X striped bass hybrids (sunshine bass), using captive broodstocks

Hatchery-produced white bass (Morone chrysops) and striped bass (M. saxatilis) reared to maturity in a commercial aquaculture facility, were successfully spawned using controlled-release delivery systems containing the gonadotropin-releasing hormone analog DAla⁶, Pro⁹[NEt]-GnRH (GnRHa). Two-year-old white bass females (mean weight, 0.81 kg) were implanted with different polymer-based, GnRHa delivery systems at doses ranging from 40 to 89 μg GnRHa kg⁻¹ body weight. GnRHa treatment on 20 February 1994, when females contained oocytes up to 720 μm in diameter, induced ovulation of all fish between 35 to 82 h after treatment. The white bass eggs produced were fertilized with sperm from striped bass for the production of sunshine bass. An average of 294500 eggs kg⁻¹ were produced, with a mean fertility of 81.2%, 24 h survival of 46.5%, and overall hatching success of 45%. Survival from hatch to 30 days post-hatch was 78% and the fry weighed between 0.07 and 0.1 g. Overripening of eggs began within 1 h from ovulation and maximum fertilization (60%) was observed when eggs were stripped 0.5 h after ovulation. Fertilization success decreased thereafter to 31% and 10% by 1 h and 3 h after ovulation, respectively. Control fish not treated with GnRHa did not show any signs of final oocyte maturation during the period of the study. GnRHa administration via controlled-release delivery systems appears to be a very effective method for inducing high fecundity ovulation of captive white bass broodstocks, and producing eggs of high fertility and hatching success.     

Influence of the length of time after hormonal stimulation on selected parameters of milt of ide Leuciscus idus L.

Milt of the Leuciscus idus L. was collected from five experimental groups, and selected parameters of its quality were analysed for 36 h (group II), 60 h (group III), 84 h (group IV) and 108 h (group V), respectively, after hormonal stimulation with Ovopel (1 granule kg^?1 of body weight). The control (group I) fish were not subjected to hormonal stimulation. The highest milt volume was obtained from the fish in group IV (0.70 ± 0.55 mL), where the largest volume of milt expressed per kilogram was also obtained (3.03 ± 1.94 mL kg^?1). Significant differences were also found in milt volumes obtained between group I and groups III (P<0.01) and IV (P<0.05). The highest percentage of motile spermatozoa was found in the milt of group IV (59%); significant differences were found between group I and groups II (P<0.01) and III (P<0.001). The value of osmotic pressure of seminal plasma was the highest in group IV (203.19 ± 37.63 mOsm kg^?1), and the lowest in group I (118.31 ± 41.13 mOsm kg^?1). Parameters determining milt quality and quantity indicate that the period of 60–84 h after hormonal stimulation with Ovopel is optimal for obtaining milt from ide.     

LHRHa‐induced ovulation of the endangered‐Caspian brown trout (Salmo trutta caspius) and its effect on egg quality and two sex steroids: testosterone and 17α‐hydroxyprogestrone

To induce synchronized ovulation, migrating wild Caspian brown trout (Salmo trutta caspius) females were treated with two interperitoneal injections of Des‐Gly¹⁰, d ‐Ala⁶ LHRH (LHRHa), given 3 days apart. Two injections of 100 μg kg^?1 body weight of this hormone effectively induced ovulation. Within 27 days from the second injection, all fish injected with 100 μg kg^?1 LHRHa had ovulated compared with 54.5% of the controls. The mean time to ovulation was reduced significantly (P<0.05) from 31.67±4.84 days in control fish and 28.83±7.31 days in sham‐treated fish to 16.36±1.61 days in fish injected with 100 μg kg^?1 LHRHa. The fertilization rate in 50 and 100 μg kg^?1 LHRHa‐injected fish was significantly lower than that in the control fish (P<0.05). In fish injected with 50 and 100 μg kg^?1 LHRHa, significant (P<0.05) changes in testosterone (T) and 17α‐hydroxyprogestrone (OHP) levels were observed. After the second LHRHa injection, the fish injected with 100 μg kg^?1 showed the highest serum levels of testosterone and OHP. These results demonstrate that the use of LHRHa can effectively reduce the mean time to ovulation and induce synchronized ovulation in Caspian brown trout.     

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.     

Out-of-season spawning of cultured pikeperch [Sander lucioperca (L.)]

The aim of this study was to determine the effectiveness of out‐of‐season spawning of cultivated pikeperch (fish that were reared from the larval stage in re‐circulating systems and fed commercial feed exclusively) stimulated hormonally with human chorionic gonadotropin (hCG). The impact of fish age (2+ and 3+) and hormone dosage [200 or 400 IU hCG kg⁻¹ body weight (BW)] on spawning was analysed and expressed as the share of stripped females, commercial fecundity (% BW) and survival of embryos until the eyed‐egg stage (EES index). The possibility of utilizing changes in female pikeperch body weight (CBW index) that are observed following hormone injections as an additional indicator for determining maturity was also investigated. The age and hormone dosage were not noted to have a significant impact on the number of stripped females (≥80% on all groups), the latency period (90–100 h), commercial fecundity (11.3–13.3% BW) or the values of the EES index (61–73%; P>0.05). The mean value of EES from the 3+ age group females was higher than that in the 2+ females, and the interaction between the tested factors (fish age and hormone dosage) wasstatistically significant (P<0.05). In the fish from the control group (injected with a 0.9% NaCl solution), no progress was noted in the maturation of oocytes and no eggs were obtained from any female. It was noted that these females lost BW over the course of the subsequent 24 h of the measurements (P<0.05). In the groups of females that were stimulated hormonally, the opposite phenomenon was observed; in these groups, the CBW index increased significantly between 48 and 96 h following hormone injection. The value of the CBW index was not noted to have been statistically significantly determined by either hormone dose or fish age (P>0.05). The regression equations that described the dependence between CBW and the oocyte maturity stage were highly significant statistically, and the determination coefficient R² assumed a value of 0.76. The most significant increase in BW was related to the oocytes achieving maturity stage III. The BW of pikeperch females with oocytes in this stage was 103% higher than the initial BW. This might be a valuable and useful tool for determining maturity in females of this fish species.     

Hormonally Induced Spawning, Embryonic Development, and Larval Rearing of the Southern Temperate Banded Morwong, Cheilodactylus spectabilis

Banded morwong (Cheilodactylus spectabilis) are of interest for marine finfish aquaculture in temperate southern Australia. To improve their ovulatory response, adult females were implanted during the autumn spawning season with slow‐release pellets containing 0–400 μg luteinizing‐hormone‐releasing hormone analogue (LHRHa)/kg body weight within 24 h of capture from the wild. Compared to the sham control group, animals treated with LHRHa produced significantly more eggs on each day after implantation for the following 7 d (91 ± 39 and 290 ± 38 mL) and a higher proportion ovulated (8/12 and 27/27). Of fish treated with LHRHa, 93% ovulated 2 d after implantation and 79% ovulated three times at 2‐d intervals, whereas control animals showed no cyclicity of ovulation and few ovulated more than once. Egg production was highest at the first ovulation after LHRHa treatment and declined at subsequent ovulations. In a second experiment investigating the range 100–400 μg LHRHa, there was no effect of dose rate on ovulation parameters, which additionally examined implantation either immediately after capture or after a 5‐d delay. Compared to immediate implantation, a delay resulted in a lower proportion of animals that could be stripped after implantation (100 and 50%, respectively) and the volume of eggs was lower (135 ± 15 and 107 ± 10 mL). The egg quality was poor following delayed implantation, resulting in no fertilization after artificial insemination compared with immediate implantation in which fertilization and hatch rates were higher for eggs collected on Day 2 after implantation (79 ± 8% and 58 ± 9%) than on Day 4 (23 ± 7% and 15 ± 6%). Thus, it is important to implant animals as soon as possible after capture to ensure optimum egg quality. Good‐quality eggs were buoyant and spherical and had a diameter of 1050 ± 25 μm with a single pigmented oil droplet of 190 ± 9 μm. When a separate large batch of eggs collected 2 d after implantation with 100 μg LHRHa was inseminated and cultured at 18 C, larvae hatched after 63 ± 2 h at a standard length of 2.6 ± 0.4 mm. Newly hatched larvae were buoyant and transparent with only a few melanophores, eyes were nonpigmented and jaws were nonfunctional. By the fourth day, jaws were functional and eyes were fully pigmented. Utilization of the endogenous yolk and oil was completed by Day 6, and swimming commenced with exogenous feeding. Larvae, initially fed lipid‐enriched rotifers followed by Artemia, reached 8.9 ± 0.7 mm length on Day 55, after which they metamorphosed to the postlarval paperfish stage of development, 22 ± 0.9 mm on Day 100, and 43 ± 1.0 mm at 6 mo of age. The results show that treatment of wild‐caught females with slow‐release pellets containing LHRHa is effective for the production of eggs for hatchery rearing.