Factors affecting the feeding response of larval southern bluefin tuna,Thunnus maccoyii (Castelnau, 1872)

Southern bluefin tuna, Thunnus maccoyii, are cultured in Australia following collection of wild juveniles. Hatchery culture from egg is in the experimental stage. High early mortality has hindered the production of quality juveniles in the hatchery. This study investigated the visual capacity of T. maccoyii during early larval ontogeny in order to describe the best larval rearing conditions to produce high‐quality seed stock. Functional visual ability, determined through behavioural experimentation, identified the effect of light intensity, prey density, turbidity, tank colour and turbulence on the feeding response. Larvae were visually challenged to feed under a range of conditions in short‐duration (4 h) feeding experiments. Feeding performance was measured as the proportion of larvae feeding and the intensity of feeding. First‐feeding performance was positively affected by increasing prey density and lower turbidities and unaffected by light intensity, tank colour, turbulence, prey size and larval density. The key findings from feeding experiments on 6 and 9 dph larvae was that as T. maccoyii aged, lower light intensities and higher prey densities significantly increased feeding performance. In addition, the study has identified that high light intensity and high air‐driven turbulence induced significant mortality. The proficient first‐feeding response indicated that early mortality common in culture is unlikely to be associated with a failure to initiate feeding. Our findings show the use of low light intensity has the potential to significantly improve survival and feeding response during the first two critical weeks of culture, when the major bottleneck in hatchery production is currently experienced.     

Decapsulated Artemia cysts of different quality (high or low hatch‐rate) as direct food for tench (Tinca tinca L.) larvae

Three 30‐day experiments were conducted to evaluate decapsulated Artemia cysts with different quality (high or low hatch‐rate) as food for tench (Tinca tinca L.) larvae from the onset of exogenous feeding. In experiment 1, three diets were tested: Artemia nauplii‐only or cysts‐only for 30 days, and nauplii for the first 7 days and cysts thereafter. The cysts used had 86% hatching rate (high hatch‐rate cysts). The same feeding treatments were replicated in experiment 2 but with low hatch‐rate cysts (10% hatching rate). In experiment 3, five diets were tested: high hatch‐rate cysts only or low hatch‐rate cysts only for 30 days, and nauplii for the first 7, 4 or 2 days and low hatch‐rate cysts thereafter. In overall, survival was high, except with the low hatch‐rate cysts only diet. Feeding tench larvae with cysts resulted in higher growth and lower FCR compared to feeding with live nauplii only. High hatch‐rate Artemia cysts are a suitable food from the onset of exogenous feeding and low hatch‐rate cysts can be successfully used after 2–7 days feeding on nauplii.     

Use of Ox‐Aquaculture© for disinfection of live prey and meagre larvae,Argyrosomus regius (Asso, 1801)

Live prey used for marine larval fish (rotifers and Artemia) as well as intensive larval rearing conditions are susceptible to the proliferation of bacteria that are the cause for reduced growth and larval mortality. Hydrogen peroxide has been recently proved a good disinfectant in aquaculture, either for eggs, larvae or live prey. In this study the effects of a hydrogen peroxide‐based product, Ox‐Aquaculture^©, on live prey (rotifers and Artemia) and meagre larvae bacterial load, composition and final status have been tested. A 34.6% reduction of total heterotrophic bacteria and 59.7% of Vibrionaceae were obtained when rotifers were exposed for 15 min to 40 mg L^?1 of the product. A 34.3% reduction of total heterotrophic bacteria and 37.7% of Vibrionaceae were obtained when Artemia were exposed for 5 min to 8000 mg L^?1 of the product. More than 95% reduction of total heterotrophic bacteria and 75% of Vibrionaceae were obtained when meagre larvae were exposed for 1 h to 20 mg L^?1 of the product. Furthermore, disinfection of enriched live prey with the product did not change the fatty acid composition and survival of the live prey and improved final larval survival.     

The first‐feeding response of larval southern bluefin tuna,Thunnus maccoyii (Castelnau, 1872), and yellowtail kingfish,Seriola lalandi (Valenciennes, 1833), to prey density,prey size and larval density

We investigated the first‐feeding success of two species: southern bluefin tuna (Thunnus maccoyii) and yellowtail kingfish (Seriola lalandi) to determine if similar culture parameters can be used for both, especially when S. lalandi are held in the same tanks as prey for T. maccoyii. The feeding performance (proportion and intensity) was examined in three short‐duration (4 h) experiments: prey density, prey size and larval density. Increasing prey density from 0.5 to 25 rotifers mL^?1 increased the proportion of T. maccoyii and S. lalandi larvae feeding. Prey size alone did not affect feeding in either species. Seriola lalandi had a decreased proportion of larvae feeding when larval density reached 50 larvae L^?1 concurrent with a gradual increase in feeding intensity between 2 and 50 larvae L^?1. In T. maccoyii, there was no pattern to the effect of larval density on the proportion of larvae feeding. The overall feeding performance of larvae was higher in T. maccoyii than S. lalandi. Increased prey density improved the first‐feeding ability of T. maccoyii and S. lalandi larvae. The effect of larval density on S. lalandi feeding requires further investigation, to ensure that they remain feeding when provided as prey in T. maccoyii culture. The identification of factors in this study, which increase first‐feeding success, will improve the culture of both species.     

The role of temperature in the prey capture probability of drift‐feeding juvenile brown trout (Salmo trutta)

Abstract – Cold water temperatures are widely supposed to reduce the food intake of stream salmonids. Although cold temperatures have been documented to reduce swimming ability, digestion and gastric evacuation rates, little is known about how temperature influences the ability of fish to capture prey. We examined the effects of water temperature on the prey capture probability of drift‐feeding juvenile brown trout (Salmo trutta) in a laboratory stream. Temperatures ranged between 5.7 °C and 14 °C. We found significant effects of water temperature on prey capture probability and capture manoeuvre time. The mean capture probability dropped from 96% at 14 °C to 53% at 5.7 °C. At 8 °C and higher temperatures, foraging performances did not differ much among treatments. We suggest that reduced swimming ability could be one of the most important mechanisms for the observed pattern of reduced prey capture probability at cold water temperatures, but prey detection limitations and predator avoidance may play a role. Our results will be of use for bioenergetics‐based drift‐foraging models, which to date have not incorporated a temperature‐dependent prey capture function.     

Year‐round natural spawning,early development,and the effects of temperature,salinity and prey density on captive ornate goby Istigobius ornatus (Rüppell, 1830) larval survival

Natural spawning, early development and larviculture of the ornate goby Istigobius ornatus in captivity were studied for the first time. I. ornatus spawned 46 times from 31 October 2013 to 31 October 2014. Fecundity ranged from 246 to 10,214 eggs per clutch, with an average hatching rate of 77.8% ± 9.9% (M ± SEM). Fertilized eggs (1.31–1.54 × 0.46–0.50 mm in diameter) were adhesive demersal and oval‐shaped. Embryonic development lasted 84 hr at 27.5 ± 0.5°C. Newly hatched larvae [2.12 ± 0.04 mm in total length (TL)] transformed to the juvenile stage completely when TL was 7.79 mm. Effects of different water temperatures (24, 28 and 32°C) and salinities (10, 15, 20, 25, 30, 35 and 40 g/L) on per cent survivals (%) and survival activity indices (SAIs) were tested. Survival was not significantly different under different temperatures; SAIs was significantly higher at 28°C. Larvae showed the significantly higher survival and SAIs at salinities 10–30 g/L than at 35 and 40 g/L. Effect of different prey densities on survival was significantly higher in 7 days post hatch larvae fed 20 and 30 rotifers/ml. These findings could guide future programs in captive breeding technology development and commercial production of other marine ornamental gobies.     

Change in nutrient composition of Artemia grown for 3–4 days and effects of feeding on‐grown Artemia on performance of Atlantic halibut (Hippoglossus hippoglossus,L.) larvae

Major challenges in culture of Atlantic halibut larvae have been slow growth during the late larval stages and inferior juvenile quality due to pigmentation errors and incomplete eye migration during metamorphosis. The hypothesis of this study was that feeding on‐grown Artemia would alleviate these problems. Artemia were grown for 3–4 days on Origreen or Origo. The growth and nutrient composition of Artemia nauplii and on‐grown Artemia were analysed, and both Artemia types were fed to Atlantic halibut larvae, on‐grown Artemia from 15 days post‐first feeding (dpff). The body length of Artemia increased with 20%–70% in response to on‐growing. In all experiments, protein, free amino acids and the ratio of phospholipid to total lipid increased, while lipid and glycogen decreased. The fatty acid composition improved in some cases and not in others. The micronutrient profiles were not negatively affected in on‐grown Artemia. All these changes are thought to be beneficial for marine fish larvae. The final weight of Atlantic halibut postlarvae was similar, and 90% of the juveniles had complete eye migration in both groups. It is concluded that the present version of Artemia nauplii probably covers the nutrient requirements of Atlantic halibut larvae.     

Embryonic development and larval and post‐larval growth of the tropical scallop Nodipecten (= Lyropecten) nodosus (L. 1758) (Mollusca: Pectinidae)

This work describes for the first time the embryonic development of the tropical scallop Nodipecten nodosus. Larval and post‐larval growth parameters and some characteristics of larvae shell morphology were also ascertained. The larvae were obtained from the induced spawning of a group of broodstocks under controlled laboratory conditions. After fertilization, larval cultivation was carried out in conical tanks at a temperature of 26–27 °C. Larval density was controlled as a function of larval growth to give 10, 5 and 3 larvae mL^?1 from days 1, 3 and 8 respectively. The larvae were nourished with a 1:1 mix of Isochrysis galbana (clone T‐ISO) and Chaetoceros gracilis in portions varying between 30 000 and 70 000 cells mL^?1. Expulsion of polar groups was observed 5 and 15 min after fertilization, whereas the first cellular division occurred after 30 min. The first gastrule ciliates and trocophore larvae were noted after 8 and 18 h had elapsed, respectively, whereas prodissoconch I, or D‐larvae, were discerned after 26 h. Subsequently, larvae with prodissoconch II or veliger‐conch appeared at 30 h. Larval development continued for 10–12 days, followed by metamorphosis, at an approximate length of 208–230 µm. The growth of the post‐larvae was evaluated for 9 days. Larval and post‐larval growth corresponded to the linear equations L = 71.85 + 10.85t, r² = 0.99, and L = 44.09 + 17.81t, r² = 0.94 respectively. Accordingly, larval morphology and size disparities are discussed with respect to other tropical pectinids.