Dynamics of yolk sac and oil droplet utilization and behavioural aspects of swim bladder inflation in burbot, Lota lota L., larvae during the first days of life, under laboratory conditions

The study concerns investigation of early larval development of burbot, Lota lota. As part of a two-year study, the first 15 days (until the end of yolk sac resorption) of burbot larvae development under controlled conditions were examined. The aim of the study was to observe the moment of swim bladder inflation and the behavioural aspects of this process, as well as the analysis of yolk and oil droplet resorption and the beginning of exogenous nutrition. It was observed that larvae began to inflate their swim bladder on the 3rd day post-hatch. On 5 DPH, none of the larvae without an inflated bladder was able to swim up the distance separating it (10 cm) from the water surface. Since 9 DPH, 50 % of larvae started exogenous feeding, and the absence of yolk was observed on 13 DPH and oil droplet on 14 DPH, while on 15 DPH, 100 % of feeding larvae were observed. The presented results indicate that the analyzed period is critical for burbot, and it is characterized by a high mortality rate (over 60 %). Additionally, the results suggest that, under controlled conditions, the latest moment when burbot larvae should be given exogenous food is 9–10 DPH and until the moment of the swim bladder inflation, larvae should be kept in tanks with a low water depth (up to 10 cm). The data presented in this study could have a significant influence on the efficiency of larvae rearing, both for aquaculture and for restocking purposes.     

Diel and ontogenetic body density change in Pacific bluefin tuna, Thunnus orientalis (Temminck and Schlegel), larvae

Diel and ontogenetic changes in larval body density related to swim bladder volume were investigated in Pacific bluefin tuna, Thunnus orientalis, to determine the causality of larval mortality – adhesion to the water surface and contact with the tank bottom during seedling production. The density of larvae with deflated swim bladders increased with total length and days post hatch. Diel density change was observed after day 2 post hatch; owing to daytime deflation and night‐time inflation of the swim bladder, the density was relatively higher during the daytime. Increased swim bladder volumes clearly reduced larval density during the night‐time after day 9 post hatch. However, the density of larvae with inflated swim bladders was greater than rearing water density (Δρ>0.0099). The small density difference between larvae and rearing water (Δρ=0.0022?0.0100) until day 4 post hatch may have caused larval mortality by adhesion to the water surface because larvae can be easily transported to the water surface by aeration‐driven upwelling in rearing tanks. Density increased noticeably from day 5 to day 9 post hatch. The increased density difference (Δρ=0.0065?0.0209) in larvae and rearing water possibly induced mortality by contact with the tank bottom because larvae sink particularly during the night‐time on ceasing swimming.     

Analysis of sinking death using video images of the swimming performance of Pacific Bluefin tuna (Thunnus orientalis) larvae

In this study, we aimed to clarify the mechanism of sinking death during the larval stage of Pacific Bluefin tuna Thunnus orientalis by investigating the effects of swimming performance on sinking death, using a behavioral approach. Swimming performance was examined 3–9 days after hatching (DAH) under day and night light conditions in cuboid experimental tanks. Swimming behavior variables such as swimming speed and swimming angle were measured under both light conditions. Larvae in the daytime experiment and larvae with inflated swim bladders at night were distributed on the surface layer of the water column. In contrast, larvae with uninflated swim bladders at night were frequently observed swimming vertically or sinking to the bottom of the tank. Larvae with inflated swim bladders at night were always distributed beneath the surface until the next morning (survival rates were 100 %). However, larvae with uninflated swim bladders at night swam upward repeatedly and later sank to the bottom of the tank (survival rates were 60 % and 38 % at 5 and 9 DAH, respectively). Larvae with uninflated swim bladders were not always able to maintain their swimming depth by swimming until the next morning. Additionally, their swimming speed and vertical swimming frequency (ratio) depended on the illumination and swim bladder conditions. Our findings show that larvae with uninflated swim bladders at night were associated with a higher risk of sinking death. The swimming energy capacity of Pacific Bluefin tuna larvae, which indicates the total amount of the energy that enables individuals to swim throughout the night without feeding, was found to be linked to sinking death.     

Effect of water surface condition on survival,growth and swim bladder inflation of yellowfin tuna,Thunnus albacares (Temminck and Schlegel), larvae

Early‐stage mortality due to surface water tension‐related death and due to sinking to the tank bottom was investigated for yellowfin tuna, Thunnus albacares (YFT), larvae. Different aeration rates and rearing water surface conditions were examined to evaluate the effect on larval survival, swim bladder inflation and growth. The percentage survival of yolk sac larvae was significantly higher when the rearing water surface was covered with fish oil at aeration rates of 0 and 50 mL min^?1. The highest mortality occurred at the highest aeration rate of 250 mL min^?1 regardless of surface water condition. A second experiment was conducted twice under different water surface conditions: the water surface was covered by fish oil (FO), skimmed of fish oil (SS), and was not treated (NC). The percentage survival was not significantly different between treatments after 7 days of feeding. In contrast to the survival, the proportion of larvae with inflated swim bladders was significantly higher for the NC and SS groups than that of the FO group. Results of these experiments indicate that the addition of oil to the rearing water surface without its removal interferes with the initial swim bladder inflation in YFT larvae. These results also indicate that YFT larvae need to obtain (gulp) air at the water surface for initial swim bladder inflation, and success of initial swim bladder inflation may be crucial for their survival.     

The effects of cadmium and copper on embryonic and larval development of ide Leuciscus idus L.

The effects of Cd and Cu on embryos and larvae of the ide Leuciscus idus were evaluated. The ide is an European cyprinid fish, natural populations of which tend to decrease. The ide is also used as a bioindicator organism to evaluate water quality. However, sensitivity of ide early developmental stages to heavy metal intoxication is not known. Fish were exposed to Cd or Cu (100 μg/L) during embryonic, larval or both developmental periods. Survival of the embryos, time of hatching, size and quality of newly hatched larvae were evaluated at the end of embryonic period. Correctly developed larvae from the control and Cd or Cu-exposed groups were transferred to clean water, Cd or Cu solutions (100 μg/L) immediately after hatching. Larval development was observed, and the larvae were photographed. Time of yolk sac resorption, onset of active feeding and swim bladder inflation were evaluated, and the measurements were done on body and swim bladder size. The results showed that exposure of embryos to Cd and Cu significantly reduced embryonic survival and increased frequency of body malformations and death in newly hatched larvae and delayed hatching. Exposure to Cd and Cu during larval period reduced larval survival, growth and delayed development (yolk utilization, beginning of active feeding and swim bladder inflation). Cadmium was more toxic to the ide embryos and larvae than copper. Exposures to metals during embryonic period alone caused adverse impact on larval performance even when larval development took place in clean water. However, exposure of embryos to Cu reduced toxic impact of metal on larvae in continuous Cu exposure compared to the non-preexposed fish, but no such an effect occurred in case of Cd exposure. The results show that even a short-term exposure to Cd or Cu during early development of ide may adversely affect recruitment of this species. Among the measured endpoints, quality of newly hatched larvae (frequency of body malformations and larvae dead immediately after hatching) and swim bladder size were the most sensitive to intoxication with both metals. Embryos were more sensitive to Cu intoxication than larvae, while in case of Cd, sensitivity of both stages was similar.     

Effect of different algae used for enrichment of rotifers on growth, survival, and swim bladder inflation of larval amberjack Seriola dumerili

The effect of algae with different DHA contents used for the enrichment of rotifers on the growth performance, survival, and swim bladder inflation of larval amberjack Seriola dumerili was investigated. Rotifers were enriched with freshwater Chlorella vulgaris containing three levels of DHA (rotifer containing DHA 0.04, 0.60, 1.32?g DHA 100?g^?1 DM) and Nannochloropsis (0.04?g DHA 100?g^?1 DM; 2.54?g EPA 100?g^?1DM). The larvae were fed the enriched rotifers in triplicate from 3?days post-hatch for 7?days in static condition. The same algae used for rotifer enrichment were supplied to the larval tanks. Growth and survival rate of fish fed the rotifers enriched with Nannochloropsis were higher than those of fish fed the rotifers enriched with all three Chlorella treatments. Swim bladder inflation was lowest in fish fed the rotifers enriched with Nannochloropsis. The proportion of EPA was higher in fish fed the rotifers enriched with Nannochloropsis, while that of DHA increased proportionally with the DHA levels in the rotifers enriched with Chlorella. These results suggest that rotifers enriched with Nannochloropsis (EPA-rich rotifers) are effective to enhance growth and survival, but DHA instead of EPA is essential to improve the swim bladder inflation in amberjack larvae.     

Initial swim bladder inflation in the larvae of Tilapia mossambica (Peters) and Morone saxatilis (Walbaum)

Tilapia and striped bass larvae inflate their swim bladders on the 7th–9th and 5th–7th days after hatching, respectively. The primordial bladder of Tilapia has no pneumatic duct and larvae do not gulp atmospheric gas for the initial swim bladder inflation. Prominent columnar epithelium is characteristics of the bladder of Tilapia prior to inflation. Hypoxic conditions inhibit inflation and result in degeneration of the columnar epithelium and the irreversible malfunction of the swim bladder. The swim bladder of the striped bass has a glandular epithelium and a pneumatic duct prior to inflation. The mode of the initial inflation and functional role of the pneumatic duct remain unclear, although strong aeration and turbulent water in the rearing containers were observed to be main factors enhancing normal inflation of the larval swim bladder.     

Ontogeny of swim bladder inflation and caudal fin aspect ratio with reference to vertical distribution in Pacific bluefin tuna Thunnus orientalis larvae

It is necessary to understand the processes involved in sinking death in Pacific bluefin tuna Thunnus orientalis aquaculture in order to develop methods to prevent or minimize this problem. We observed the nighttime vertical distribution of Pacific bluefin tuna in the water column on 2–9 DAH and the morphological characteristics of the larvae, in order to clarify the processes involved in sinking death. A cuboid tank (height 300 cm) was used to measure vertical distribution. The number of larvae was counted in each of 4 regions in the observation tank: upper layer (water depth 0–100 cm), middle layer (100–200 cm), lower layer (200–300 cm), and bottom area. The distribution of larvae in these regions at 4 days after hatching was polarized to the upper layer and bottom area. Individuals with inflated swim bladders were observed in the upper layer 3 days after hatching. No larvae with inflated swim bladders were observed in the bottom area on any day after hatching. Total body length and caudal fin aspect ratio of larvae with both inflated and un-inflated swim bladders were greater in the upper layer than those of larvae in the bottom area. Larvae with un-inflated swim bladders that failed to develop sufficiently for swimming sank to the tank bottom and died. Swim bladder development and caudal fin swimming ability are strongly related to sinking death.     

Cost comparisons of rearing larvae of freshwater shrimp,Macrobrachium acanthurus and M. rosenbergii,to juveniles

Costs were determined for rearing larval Macrobrachium rosenbergii (De Man) and M. acanthurus (Wiegmann). Rearing was conducted in two phases. First-phase rearing (first 10 days) was conducted in conical fiberglass tanks with recirculated, filtered, brackish water; second-phase rearing (final 30 days) was done in aerated 1 000-l concrete tanks. To minimize water quality problems and debris accumulation in second-phase rearing, larvae were transferred every 4 to 5 days to a new tank of clean water. Larval food consisted of newly hatched Artemia and either freshly ground fish or freeze-fried fish.Mean survival in five M. rosenbergii rearing trials was 43% in 40 days at a final density of 12 juveniles per liter. Mean survival of four M. acanthurus trials was 25% in 44 days at a final density of 3 juveniles per liter. Average total cost of labor, operation (electricity), food and water per thousand juveniles produced was $3.56 for M. rosenbergii and $13.42 for M. acanthurus.Extrapolation of results to larger (3 000-l) second-phase rearing tanks showed M. rosenbergii rearing cost could be reduced to $\text{\$1.87}\text{1 000}$.     

Comparison of Two Environmental Regimes for Culture of Australian Snapper, Pagrus auratus, Larvae in Commercial-scale Tanks

The performance of Australian snapper, Pagrus auratus, larvae from 4 to 33 days posthatch (dph) under two environmental rearing regimes was evaluated in 2000‐L commercial‐scale larval rearing tanks (N = 3 tanks/treatment). The treatments were the following: (1) a varying regime of salinity (20–35 ppt), temperature (24 C), and photoperiod (12 light [L] : 12 dark [D] to swim bladder inflation and then 18L : 06D) and (2) a constant regime of salinity (35 ppt), temperature (21 C), and photoperiod (14L : 10D). The final total length (TL) and wet and dry weights (mean ± SEM) of larvae grown in the varying regime were greater (15.6 ± 0.5 mm; 42.4 ± 3.4 mg wet weight; and 7.3 ± 0.6 mg dry weight) than those of larvae grown in the constant regime (11.1 ± 0.2 mm; 12.9 ± 0.8 mg wet weight; and 2.1 ± 0.2 mg dry weight). By 33 dph, larvae in the varying regime were fully weaned from live feeds to a formulated pellet diet and were suitable for transfer from the hatchery to a nursery facility. In contrast, larvae in the constant regime were not weaned onto a pellet diet and still required live feeds. Neither survival (Treatment 1, 14.2 ± 3.0% and Treatment 2, 13.3 ± 1.9%) nor swim bladder inflation (Treatment 1, 70.0 ± 17.3% and Treatment 2, 70.0 ± 11.5%, by 13 dph) was affected by rearing regime. The incidence of urinary calculi at 7 dph was greatest initially in the varying regime; however, by 19 dph, when larvae were 8.0 ± 0.28 mm TL, very few larvae in this treatment had urinary calculi. In contrast, many larvae in the constant regime had developed urinary calculi and this continued until the end of the experiment. The incidence of urinary calculi was not associated with larval mortality. Extrapolation of the snapper larval growth curves for the constant larval rearing regime predicts that a further 15–18 d, or approximately 1.5 times longer, will be required until these larvae attain the same size and development of larvae reared in the varying regime.     

Combined Effects of Diet and Salinity on European Sea Bass Larvae Dicentrarchus labrax

Effects of diet, salinity, and consumption of endogenous reserves on the growth, survival and swim bladder inflation of European sea-bass larvae were studied. Primary inflation of the swim bladder occurs in 7-day-old larvae. Inflation is synchronized with the absorption of endogenous reserves. The kinetics of the consumption of these reserves varies with the diets tested, and is the slowest at higher salinity (28.7 and 37.7‰). Best results were obtained with larvae fed on Artemia nauplii. Larvae raised at lower salinity (19.7 and 10.7‰) had the highest proportion of inflated swim bladders. Larvae raised at 28.7‰ salinity had the best survival rate, while those raised at 38.7‰ had the best growth rate. Larval mortality was associated with inappropriate functioning of the swim bladder. Larvae exposed to decreasing salinity during rearing showed very high survival rates and normal swim bladder inflation.     

Ceramic clay reduces the load of organic matter and bacteria in marine fish larval culture tanks

Ceramic clay has been increasingly used to improve contrast and prey detection in tanks for rearing of fish larvae. In contrast to live microalgae or algae pastes, clay increases turbidity without contributing to the organic matter load. In addition, clay may aggregate and sediment organic matter and bacteria, facilitating its removal. Marine larvae are sensitive to infections by opportunistic bacteria. Fish, algae, and live feed increase the microbial carrying capacity of the rearing water which allow exponential growth of bacteria and favor fast-growing opportunists. Reducing substrate levels by replacing microalgae with clay may reduce bacteria proliferation and benefit larvae. We compared the effects of three rearing regimes including live Isochrysis galbana, Nannochloropsis oculata paste, and ceramic clay on the bacterial community, concentration of organic matter, and growth and survival of Atlantic cod larvae (Gadus morhua L.). The application of clay resulted in reduced substrate levels for bacteria in the rearing water compared to the addition of live algae or algae paste. To some extent, clay aggregated and transported organic matter to the bottom of the larval fish tanks, where it could be effectively removed. Fish tanks receiving clay showed a lower abundance of bacteria in the water than tanks added algae paste or live algae. Fish tanks with algae paste showed a higher abundance of bacteria and a higher share of cultivable bacteria and TCBS counts than the other two treatments. Tanks with live algae showed low relative abundances of opportunistic bacteria and TCBS counts in both water and rotifers. Cod larvae in tanks with clay or live algae initiated exponential growth earlier than larvae in tanks with algae paste. Larvae in tanks receiving clay had significantly higher dry weight than larvae in tanks receiving algae paste at day 5 and 20 post hatching. The survival of larvae in the tanks added clay was variable. Two of the three tanks with clay had significantly higher larval survival than the tanks with live algae or algae paste. However, one tank with clay underwent 100% mortality. It is not possible to conclude whether this was related to the use of clay or an incidental development of a harmful microbial community in this tank. The effects of clay addition on larval performance should be studied further. Clay addition appears to be an easy way to reduce bacterial load during early first feeding of marine larvae without compromising the beneficial effects of turbidity.     

The pseudo-green water technique for intensive rearing of sea bream (Sparus aurata) larvae

The “pseudo green water” technology for sea bream(Sparus aurata) larval rearing was evaluated by analyzingresults of a 2-year study, performed in a pilot scale system. Thetechnology is characterized by the daily addition of phytoplankton in therearing tanks during the first month of rearing. Effects of egg origin,spawningseason and initial larval density on the larval rearing were investigated. Fishreared in “pseudo green water” systems for 60 days, presented highbiological performance in terms of survival (56 ± 16%), meanweight (62 ± 12 mg), total length (20 ± 1mm), conformity with wild standard (88 ± 9%), andfunctional swim bladder (93 ± 4%). The results present homogenitybetween the categories (origin of eggs, time of spawning, initial egg density)studied, proving the stability of the technology.     

Apparent Problems and Potential Solutions for Production of Fingerling Striped Bass,Morone saxatilis

Data on production of fingerling striped bass, Morone saxatilis, in 103 ponds at 17 hatcheries in 1988 were related to information on management practices and water qualities. Production was highly variable, with a median of 50,000/ha. No survival was evident in 12% of ponds; numbers harvested exceeded 250,000/ ha in 5% of ponds. Best survival resulted when larvae were stocked within 2 days after pond filling was started and at hatcheries with relatively low application rates of fertilizers during the prestocking interval. No survival was evident in ponds with pH >9.0 in the week after stocking. High pH's and probably toxic concentrations of un-ionized ammonia were related to water being in ponds for too long prior to stocking and to high applications of fertilizers. Examination of samples of larvae collected at stocking and the week after stocking documented a problem with swim bladder inflation. When larvae were stocked at D5 or D6 (Dl is day of hatch), inflation success averaged 91%: when stocked at ≥D7. inflation success averaged 60%. Measures proposed to improve production include: (1) Stock larvae prior to the critical period of swim bladder inflation(D4-D5). (2) Start filling ponds as close to stocking as is feasible (filling can be completed after stocking). (3) If the concentration of available nitrogen is low, apply no more than 300 µg/L of nitrogen in the prestocking interval. (4) Add phosphorus as needed, but avoid pH>8.5 until larvae are D14.     

Swim bladder function and buoyancy control in pink snapper (Pagrus auratus) and mulloway (Argyrosomus japonicus)

Physoclist fish are able to regulate their buoyancy by secreting gas into their hydrostatic organ, the swim bladder, as they descend through the water column and by resorbing gas from their swim bladder as they ascend. Physoclists are restricted in their vertical movements due to increases in swim bladder gas volume that occur as a result of a reduction in hydrostatic pressure, causing fish to become positively buoyant and risking swim bladder rupture. Buoyancy control, rates of swim bladder gas exchange and restrictions to vertical movements are little understood in marine teleosts. We used custom-built hyperbaric chambers and laboratory experiments to examine these aspects of physiology for two important fishing target species in southern Australia, pink snapper (Pagrus auratus) and mulloway (Argyrosomus japonicus). The swim bladders of pink snapper and mulloway averaged 4.2 and 4.9 % of their total body volumes, respectively. The density of pink snapper was not significantly different to the density of seawater (1.026 g/ml), whereas mulloway were significantly denser than seawater. Pink snapper secreted gas into their swim bladders at a rate of 0.027 ± 0.005 ml/kg/min (mean ± SE), almost 4 times faster than mulloway (0.007 ± 0.001 ml/kg/min). Rates of swim bladder gas resorption were 11 and 6 times faster than the rates of gas secretion for pink snapper and mulloway, respectively. Pink snapper resorbed swim bladder gas at a rate of 0.309 ± 0.069 ml/kg/min, 7 times faster than mulloway (0.044 ± 0.009 ml/kg/min). Rates of gas exchange were not affected by water pressure or water temperature over the ranges examined in either species. Pink snapper were able to acclimate to changes in hydrostatic pressure reasonably quickly when compared to other marine teleosts, taking approximately 27 h to refill their swim bladders from empty. Mulloway were able to acclimate at a much slower rate, taking approximately 99 h to refill their swim bladders. We estimated that the swim bladders of pink snapper and mulloway ruptured after decreases in ~2.5 and 2.75 times the hydrostatic pressure to which the fish were acclimated, respectively. Differences in buoyancy, gas exchange rates, limitations to vertical movements and acclimation times between the two species are discussed in terms of their differing behaviour and ecology.     

Characterization of swim bladder non-inflation (SBN) in angelfish, Pterophyllum scalare (Schultz), and the effect of exposure to methylene blue

Failure to inflate the swim bladder is regarded a major obstacle in the rearing of many fish species. We present a study of swim bladder non-inflation (SBN) in angelfish, Pterophyllum scalare. A normal developing primordial swim bladder was first discernable at the end of the first day post-hatch (p.h.) as a cluster of epithelial cells with a central lumen, surrounded by presumably mesenchymal cells. Initial inflation occurred on the fourth day p.h. Prior to inflation the swim bladder epithelium consisted of an outer squamous and inner columnar layer. Cells of the inner layer were filled at their basal region with an amorphous material, which disappeared upon inflation. A pneumatic duct was absent, and larvae presented no need to reach the water surface for inflation, suggesting that angelfish are pure physoclists. A model for the role of the amorphous material in normal initial inflation is proposed. Abnormal swim bladders were apparent from the fourth day p.h., and methylene blue (MB) at a concentration of 5 ppm significantly increased the prevalence of SBN. Histologically, abnormal swim bladders in larvae hatched in 5 ppm MB could not be distinguished from those in fish raised under routine conditions (0.5 ppm MB). We suggest that MB may have a teratogenic effect in angelfish.     

Promotion of initial swim bladder inflation and effect of initial inflation failure on skeletal malformation in cultured seven‐band grouper Hyporthodus septemfasciatus (Thunberg)

The effects of the removal of the oily surface film on initial swim bladder inflation and survival in cultured seven‐band grouper Hyporthodus septemfasciatus were investigated during the larval stage. Additionally, the relationship between swim bladder inflation failure and malformations in later stages was examined. To explore promotion conditions for inflation, duplicate experiments were conducted under three different water surface conditions: removal of the oily surface film (ROF group), covering the water surface with an oil film (COF group), and sealing the water surface with liquid paraffin (SLP group). Larval swim bladder inflation was first observed 14 days after hatching (DAH) in the ROF group; thereafter, swim bladder inflation rates increased to 11.1% and 38.7% until the end of the experiments. This indicates that initial swim bladder inflation occurs at the pre‐flexion stage in larval development. Conversely, bladder inflation was rarely observed in the COF or SLP groups, indicating the promotional effect of surface film removal on larval swim bladder inflation and suggesting that gulping atmospheric air is necessary for initial inflation. Although larval water surface death occurred frequently in the ROF group, no significant difference existed in any group between the survival rates at 10 DAH and at the end of the experiment. The incidence rate of spinal curvature and deformation of the centra was significantly higher in individuals without initial swim bladder inflation, and these malformations mainly occurred in the caudal vertebra. Therefore, the removal of the oily surface film promotes initial swim bladder inflation and reduces larval malformations.     

Mortality,growth and swim bladder stress syndrome of sea bass (Dicentrarchus labrax) larvae under varied environmental conditions

Responses to variations in light, temperature and salinity by sea bass larvae are described here. Massive mortality of larvae has been common in Mediterranean culture efforts. This mortality, associated with swim bladder malfunction, has been analysed regarding its association with individual stresses.Optimum temperatures for sea bass growth are clearly unsuited to larval rearing, while brackish sea water (25‰) just as clearly improves growth and survival. Light and nutritional regimes as well as water quality are other sources of environmental stress that may induce the swim bladder stress syndrome (SBSS) and reduce growth and survival. SBSS should not be confused with “gas bubble” disease and its most effective treatment depends on an understanding of larval environmental requirements.Larval growth was enhanced by both decreased salinity and increased temperature, but not by increased light. SBSS and mortality were avoided only when larvae were held at ambient temperature (12.5°C), natural light, and reduced salinity (25‰). Larvae dying with distended swim bladders also had other symptoms of environmental stress—spinal abnormalities, calculi in the urinary bladders, copious mucous and opaque (edemous) tissues. Elevations of temperature and light, as well as ambient sea water (36‰) are environmental stressors and induce SBSS.     

A technical solution to the mass-culturing of larval turbot

A 1000 litre recirculation system of eight cylindrical rearing tanks has been tested in three 40-day periods to determine its capacity for rearing larval turbot (Scophthalmus maximus L.).The larvae were fed on rotifers and Artemia nauplii, as well as mixed marine algae. Continuous artificial light of 1500–2000 lux was applied at the surface. The applied algae served a dual function; keeping rotifers and Artemia at a high nutritional level as well as effectively removing the released ammonia. The combination of upwelling water and light at the surface maximized the contact surface between larvae, food items and algae.With this system, using a stocking density of 16 larvae litre^?1 in the rearing tanks, a survival total of 40% at Day 40 was achieved, giving a production of 6·4 larvae litre^?1 or 3000 larvae metre^?2 of the surface of the rearing tanks.     

Effects of Tank Wall Color and Up-welling Water Flow on Growth and Survival of Eurasian Perch Larvae (Perca fluviatilis)

The influence of tank wall color and up‐welling water flow on growth and survival of Eurasian perch larvae (Perca fluviatilis) was tested in an intensive culture system. Newly hatched larvae were fed Artemia nauplii, later combined with dry feed, and reared for 5 wk in either black tanks with up‐welling water flow or in gray tanks with or without up‐welling water flow. The perch larvae grew significantly faster in black tanks than in gray tanks regardless of water flow. Two weeks after hatching, a significantly higher mean weight was shown in larvae reared in black tanks compared to larvae reared in gray tanks with up‐welling water flow, and after 4 wk, the mean weight was significantly higher than in both of the other treatments. The difference in growth was further enhanced during the last week of the experiment, and the final mean weights were 51.1 ± 1.9 mg in black tanks with up‐welling water flow, 23.8 ± 2.1 mg in gray tanks with up‐welling water flow, and 23.7 ± 2.2 mg in gray tanks without up‐welling water flow. The cumulative mortality at the end of the experiment averaged 75% in all treatment groups. Taken together, the enhanced growth of Eurasian perch larvae in black tanks could be explained by high prey contrast and increased prey consumption. Up‐welling water flow had no impact on growth and survival of the perch larvae in gray tanks, indicating that the availability and consumption of the prey were independent of water movement.