Diet and Light Intensity Effects on Survival, Growth and Pigmentation of Southern Flounder Paralichthys lethostigma

Interest in the culture of flatfishes has increased globally due to high consumer demand and decreased commercial landings. The Southern flounder Paralichthys lethostigma inhabit South Atlantic and Gulf of Mexico waters and support important commercial and recreational fisheries. In spring, 1996, a two-part larval rearing study was performed with Southern flounder to examine the effects of three larval diets and two light intensities on survival, growth, and pigmentation. The first part of the study consisted of feeding 6 d post-hatch (dph) (3.0 ± 0.1 mm TL) larvae three diets: 1) rotifers Brachionus plicatilis at a rate of 10/mL from day 1–9 and Artemia nauplii (3/mL) from day 7 through metamorphosis; 2) rotifers fed day 1 through metamorphosis and Artemia fed day 7 through metamorphosis; or 3) same diet as treatment 1 plus a commercial larval diet added day 13 through metamorphosis. The second part of the study examined the effects of two light levels: low-light (mean 457 lux) and high-light (mean 1362 lux). At 24 C, metamorphosis began on day 23 (mean fish size 8.2 ± 0.6 mm TL) in all treatments and was completed by day 30. Analysis of survival, size, and pigmentation data indicated there were no significant differences among feed treatments or between light treatments. Overall survival was 33.4% (±15.9) and mean length was 11.5 mm TL ± 1.3. Only 35% of the larvae were normally pigmented. Reexamination of the pigmentation on day 37 indicated fish reared at the low light intensity through metamorphosis (day 30) but exposed to high light intensity for 1 wk post-metamorphosis had become significantly more pigmented.     

Early weaning of winter flounder (Pseudopleuronectes americanus Walbaum) larvae on a commercial microencapsulated diet

Like most small marine fish larvae, the stomachs of winter flounder Pseudopleuronectes americanus are undeveloped at first feeding and have relatively reduced digestive capacity. This work was undertaken to test whether larvae at the onset of stomach differentiation (larval size about 5.5 mm) could be early weaned onto a commercial microencapsulated diet. We assessed the effect of early weaning by first comparing growth performance (standard length, total protein content and age at metamorphosis) of larvae fed enriched live prey from first feeding to a size of 5.5 mm and then reared on three different feeding regimes until metamorphosis: (1) live prey (LP) as a control group; (2) mixed feeding of live prey and microencapsulated diet (LP‐ME); (3) exclusively microencapsulated diet (ME) after fast weaning over 4 days (to a larval size of 6.2 mm). No differences were observed between larval development in the two first groups, which began metamorphosis at 40 days old. The larvae of the third group showed significantly slower growth that resulted in a delay of 4 days in the onset of metamorphosis. Differences in live prey availability between the treatments and the short transition period to allow the larvae to adapt to the new diet were identified as possible contributing factors to the slower growth and to the delay in metamorphosis of early weaned larvae. In a second experiment, the transitional weaning period was increased until the larvae were 6.6 mm in length. Weaning at that size resulted in no slowing of growth or delay in metamorphosis, suggesting that the feeding schedule was adequate.     

Effect of diet and rearing conditions on growth and survival throughout developmental stages of larvae and juveniles of dusky grouper <Emphasis Type="Italic">Epinephelus marginatus</Emphasis> (Lowe 1834)

Two rearing conditions, tank light-dimensions and diet, were tested in dusky grouper—larvae and juveniles—in order to improve larval rearing techniques for this species. Larvae reared in high-volume and fluorescent tubes showed the highest survival rate at 18 dph (17.67%, 16%). This might be due to a higher depth and less trapping area during surface death in high-volume tanks than in low volume. Besides, a 500-lx evenly distributed light with fluorescent tubes might improve survival rate at early stages rather than illumination with energy-efficient light bulbs (4.68%, 9.64%). Light bulbs created shaded areas with less illumination inducing low larval activity. First feeding was performed with minimum rotifer lorica width of 102?±?10.2 μm. No mixed diet was supplied. Throughout metamorphosis, stress shock syndrome appeared to be the main cause of mortality. Diet A showed best growth and survival (4.1–7.36%) during this period probably due to its high HUFA content (9.5%). Contrary to what was observed during first stages, groupers showed best performance with lower illumination. Cannibalism was observed during this period in all culture conditions.     

Effects of Light Intensity and Salinity on Growth, Survival, and Whole-Body Osmolality of Larval Southern Flounder Paralichthys lethostigma

The southern flounder Paralichthys lethosligma is a high‐valued flatfish found in estuarine and shelf waters of the south Atlantic and Gulf coasts of the United States. Wide temperature and salinity tolerances exhibited by juveniles and adults make it a versatile new candidate for commercial culture, and studies are underway in the southeastern U.S. to develop hatchery methods for this species. The objectives of this study were to establish illumination and salinity conditions that optimize growth and survival of larval southern flounder reared through the yolk‐sac and first feeding stages to 15‐d post‐hatching (15 dph). Early embryos were stocked into black 15‐L tanks under light intensities of 5, 50, 100, and 1,000 Ix and at salinities of 24 and 34 ppt in a 4 ± 2 factorial design. Significant (P 0.05) effects of both light intensity and salinity on growth and survival were obtained, with no interaction between these effects. On 11 dph and 15 dph, growth was generally maximized at the intermediate light intensities (50 and 100 Ix) and minimized at the extremes (5 and 1,000 Ix). By 15 dph, growth was higher at 34 ppt than at 24 ppt. Survival to 15 dph showed trends similar to those of growth. Survival was higher at 100 Ix (avg. = 46%, range = 41–54%) than at 5 Ix (avg. = 11%, range = 6–17%) and higher at 34 ppt (avg. = 43%, range = 3145%) than at 24 ppt (avg. = 17%, range = 8–38%). Whole‐body osmolality (mOsmol/kg) was significantly lower in larvae reared at 24 ppt (avg. = 304, range = 285–325) through 11 dph than in larvae reared at 34 ppt (avg. = 343, range = 296–405). Larvae reared under the extreme light intensity treatments (5 and 1,000 Ix) at 34 ppt appeared to exhibit osmoregulatory stress, particularly on 11 dph, when a marked increase in whole‐body osmolality was observed. The mid‐intensity treatments (50 and 100 Ix) at 34 ppt optimized growth and survival of larval southern flounder in this study; and elicited the most stable osmotic response. These conditions appear to be consistent with those that southern flounder larvae encounter in nature during this early developmental period.     

Applying the ontogeny of digestive enzyme activity to guide early weaning of pigfish,Orthopristis chrysoptera (L.)

Weaning marine fish larvae from live prey to a dry microdiet is an important step towards optimizing the commercial production, but early weaning is constrained by the lack of sufficient digestive enzymes at first feeding. This study quantified the activity of five digestive enzymes throughout the larval period of pigfish (Orthopristis chrysoptera [L.]) to assess ontogenetic changes in digestive abilities, and then trials were conducted that determined the optimal time for weaning. The activity of all digestive enzymes was low or undetectable at first feeding (3 days post hatching, dph; 2.5 mm standard length, SL). A substantial increase in activity occurred at 5.7 mm SL (17 dph), 6.9 mm SL (21 dph), 7.7 mm SL (23 dph), 8.4 mm SL (25 dph) and 11.2 mm SL (30 dph) for bile salt‐dependent lipase, trypsin, chymotrypsin, amylase and acid protease respectively. During the weaning experiment, larvae were co‐fed live prey and microdiet beginning 15 dph (4.8 mm SL). Live prey was withdrawn from the diet at 24, 28, 32 or 36 dph, with the control receiving live prey and microdiet throughout (to 43 dph). There were no significant differences in mean final SL among treatments, but survival was significantly lower when larvae were weaned at 24 dph compared to 32–43 dph. Based on the digestive enzyme activity and survival, weaning larval pigfish at 32 dph (11.7 mm SL) when reared at 24°C is recommended.     

Influence of larval co-feeding with live and inert diets on weaning the tongue sole Cynoglossus semilaevis

The tongue sole Cynoglossus semilaevis, an inshore fish in China, has showed great potential in aquaculture recently. However, poor survival was recorded during the period of weaning from live Artemia to artificial diets. In this paper, the influence of co‐feeding larvae with live and inert diet on weaning performance was described. The C. semilaevis larvae were reared at 21 ± 1 °C and fed four different feeding regimes from 6 days post‐hatching (dph): A, Artemia (10 individuals mL^?1); B, Artemia (5 individuals mL^?1); C, mixed diet (10 Artemia individuals mL^?1 and 12 mg L^?1 inert diet); and D, mixed diet (5 Artemia individuals mL^?1 and 12 mg L^?1 inert diet). Rotifers were also supplied in all cases during the first days of feeding. Mixed diets of commercial formulated feed and live prey (rotifers and Artemia) allowed larvae to complete metamorphosis, achieving similar specific growth rate (SGR) (18.5 ± 1.4% and 18.7 ± 1.6%) and survival (40 ± 7.6% and 48.5 ± 6.8%) compared with larvae fed on live feed alone (SGR of 18.3 ± 1.2%, 19.3 ± 1.9% and survival of 41.2 ± 11.3%, 38 ± 4.9%). However, in metamorphosed fish, when live feed was withdrawn on 31 dph, there was significant difference (P < 0.05) in survival and growth among treatments. Metamorphosed fish, previously fed mixture diets during larval stages, had similar survival (62.1 ± 7.6% and 62.8 ± 3.9% for regimes C and D, respectively) but higher than that obtained for fish that previously fed on live feed (49.3 ± 2% and 42.1 ± 3.9% for regimes A and B, respectively) after weaning (day 60). The SGR of weaned fish previously fed live feed was similar (3.1 ± 0.6% and 2.92 ± 0.6% for regimes A and B, respectively) but lower than that recorded for fish that was fed from day 6 to day 30 on the mixed diet (4.5 ± 1.1% and 4.9 ± 0.3% for regimes C and D, respectively). It is suggested that weaning of C. semilaevis from early development would appear to be feasible and larval co‐feeding improves growth and survival.     

Early weaning of southern flounder, Paralichthys lethostigma, larvae and ontogeny of selected digestive enzymes

There is considerable interest in rearing Southern flounder, Paralichthys lethostigma, for commercial production and for stock enhancement. Both goals depend upon excellent larval nutrition for the production of robust juveniles. The current use of live prey for larviculture is an expensive and time consuming process that can be alleviated by weaning larvae onto dry feed. A study was conducted to assess the potential for early weaning of southern flounder larvae onto a microdiet (MD). In addition, the activity of selected digestive enzymes was measured during ontogeny to evaluate the digestive capabilities of the larvae over time. Pancreatic enzyme activities (U larva^− 1) were very low or undetectable at hatching and a marked increase in activity was not observed until the larvae reached 4 mm (~ 11 dph) in standard length for chymotrypsin (24–44,000) and 6 mm (~ 25 dph) for amylase (< 1–24), trypsin (1–18) and bile salt-dependent lipase (0–443). Acid protease activity (~ 1.0) was detected once the larvae were 8.5–9.0 mm (37–39 dph) in length although a sizeable increase in activity (> 10.0) was not observed until after complete metamorphosis (> 11.0 mm; 40–45 dph). Feeding regimes employed for the weaning study consisted of a live feed control (C) and a combination of live feed and MD in which the addition of the MD was initiated on 11 dph and live feed terminated on 17 (T17), 23 (T23) or 29 (T29) dph. At the end of the study (35 dph), mean standard length and the percent of settled fish were significantly greater for fish in the control treatment (8.3 mm; 21.1%) than for fish fed any combination of live prey and MD (6.4 mm; 2.0%). Average survival was 27.7% and no significant differences were noted among treatments. However, the number of fish exhibiting spinal deformities, lordosis, was significantly lower in the control and T29 treatments (1.7%) than the T17 and T23 treatments (25%). The results of this study indicate that southern flounder larvae readily wean onto dry feed prior to the onset of metamorphosis. However, decreased growth and a high incidence of lordosis emphasize the need for the development of a more appropriate MD for this species when digestive enzyme activities are relatively low and gastric digestion is absent.     

Effects of light intensity on growth,feeding activity and development in common sole (Solea solea L.) larvae in relation to sensory organ ontogeny

The effects of four light intensities (1000 lx, 500 lx, 50 lx, 3 lx) on growth, survival and feeding activity in common sole (Solea solea L.) larvae were studied from 4 to 51 days post hatching (dph). During the pelagic larval stage (4–12 dph), larvae reared at 3 lx showed a lower growth. From 19 onwards, the larvae reared under 3 lx displayed a significant (P ≤ 0.05) higher SGR than the other treatments and a higher final weight compared to 1000 lx and 500 lx. Survival rate was higher under intermediate light intensities (500 and 50 lx). Larvae reared at 3 lx displayed a significant delay in the degree of metamorphosis compared to the other treatments, while at 33 dph metamorphosis was completed under all treatments. Histological examination revealed the importance of vision and light in the first feeding of this species, while after metamorphosis, the full development of other sensory organs indicated that feeding activity is also mediated by chemosensory perception. Results indicate that high light intensity seems to be more suitable during the pelagic larvae, while the opposite would ensure better growth from the onset of metamorphosis to the benthic phase.     

Assessment of temperature or salinity effects on larval development by catecholamine‐induced metamorphosis of hatchery‐reared flat oyster,Ostrea angasi (Sowerby 1871) larvae

A need to improve larval rearing techniques led to the development of protocols for catecholamine‐induced settlement of flat oyster, Ostrea angasi, larvae. To further refine these techniques and optimize settlement percentages, the influence of salinity or temperature on development of O. angasi larvae was assessed using epinephrine‐induced metamorphosis. Larvae were reared between salinities of 15–35 and temperatures between 14.5 and 31°C. The greatest percentage survival, growth, development occurred when larvae were reared between 26 and 29°C and between salinities of 30 and 35. Larvae reared outside this salinity and temperature range exhibited reduced growth, survival and/or delayed development. Short‐term (1 h) reduction in larval rearing temperature from 26°C to 23.5°C significantly increased larval metamorphosis without affecting larval survival. Short‐term (1 h) increase in larval rearing temperature from 26°C to 29 and 31°C decreased larval survival and metamorphosis. To ensure repeatability in outcomes, tests showed that larvae sourced from different estuaries did not vary significantly in their metamorphic response to short‐term temperature manipulation and epinephrine‐induced metamorphosis.     

Early-weaning diets for gilthead sea bream (Sparus aurata L.) and their potential use in Hellenic marine fish hatcheries

The purpose of this experiment has been to evaluate the suitability of commercially available early-weaning microdiets (MDs) for the production of sea bream early juveniles and in comparison with late-weaning protocols already in use by Hellenic marine fish hatcheries. Four sea bream experimental groups were allocated in rearing tanks of a commercial Hellenic marine fish hatchery. Each group represented a different protocol (A, B, CA, and CB) based on the combination of two different early-weaning MDs (A and B) and a late-weaning diet (C). In addition, the late-weaning protocols have received Artemia instar II only and not Artemia instar I. In protocol A, Artemia instar I first feeding and the early-weaning diet A were administered at 17 days post-hatch (17 dph). In protocol B, Artemia instar I first feeding started at 15 dph and the early-weaning diet B was administered at 18 dph. In the C protocols, Artemia instar II first feeding started at 20 dph and the early-weaning diets (A or B) were administered at 25 dph. All protocols have received the late-weaning diet C only after the 50th dph. The experiment lasted for 65 days. By the end of the experiment, early-weaning protocol A and late-weaning protocol CB had similar wet weights, but still lower to the wet weights recorded for the late-weaning protocol CA. These results cannot be explained solely by the nutritional profile of each weaning diet. The larval fatty acid profile of each protocol and at various time intervals reveals the importance that the succession of Artemia, rotifers, and MDs has for each protocol and not just the nutritional profile of the weaning diets, per se.     

Mass Production of Juveniles of the Fat Snook Centropomus parallelus in Brazil

A pilot‐scale trial to rear fat snook Centropomus parallelus through larval, weaning and nursery phases was conducted in Florianópolis, Brazil. Eggs (96% fertilization) from captive broodstock, induced to spawn using 50 μg/kg LHRHa were stocked in two 4,000‐L cylindrical fiberglass tanks at a mean density of 19.2 eggs/L. Nannochloropsis oculata was stocked with the eggs and maintained at a mean density of 0.5–1.0 ± 10⁶ cells/mL up to 31 dph (31 dph). Hatching averaged 90%. Larvae were fed rotifers Brachionus rotundiformis enriched with an oil emulsion from 3 dph to 36 dph (30–40 rotifers/mL) and Artermia meta‐nauplii enriched with Selco from 22 dph to 60 dph (mean 2.9 meta‐nauplii/mL). Weaning began at 45 dph with an artificial dry diet NRG (50% protein), supplied together with concentrated and enriched Artemia meta‐nauplii. No critical period of mortality was observed during larval rearing. During the 43 days of weaning and nursery, less than 1% mortality was recorded. Food conversion rate during nursery was 1.17, with a change in the coefficient of variation of mean total length of 1.3%. Specific total growth rate in weight was 13.0 %/d and mean growth in total length and total weight were 0.65 mm/d and 24.0 mg/d over the whole rearing trial respectively. Mean total length and total weight of juveniles were 57.6 ± 0.1 mm and 2.11 ± 0.12 g, respectively, and the length‐weight relationship was W = 8.29931 ± 10–⁵ TL^3.049607 (r= 0.9986). on 88 dph when the trial was terminated. The condition factor on 88 dph was 1.104. On 88 dph a total of 35,000 juveniles were harvested, overall survival was 25.5% with mean final density of 4.4 fishn and biomass of 6.9 kg/m³. The present trial demonstrated the feasibility of mass production of fat snook. Possible improvements necessary for commercial cultivation of fat snook C. parallelus are discussed.     

Breeding and larval rearing of the camouflage grouper Epinephelus polyphekadion (Bleeker) in the hypersaline waters of the Red Sea coast of Saudi Arabia

This is the first report on the successful year-round natural spawning and larval rearing of Epinephelus polyphekadion (Bleeker) in captivity and under hypersaline water conditions of 42-43%₀ salinity in the Red Sea coast of Saudi Arabia. Although the fish spawned naturally once or twice a year during 1992-94 culture period, incorporation of cod-liver oil in the broodstock diet during the 1995 culture period enabled the fish to spawn continuously for 2-3 days in each month during March, April, May and August. The egg fertilization and hatching rates also increased during the 1995 spawning period. The egg fertilization rate varied from 90 to 100% with a mean of 96.5 ± 3.38%. The egg hatching rate varied from 70 to 95% with a mean of 83.1 ± 10.12%. The fertilized egg diameter averaged 757.3 ± 37.36 μm. There was a linear relation between the fertilized egg size and the egg hatching rate. The increase in the hatching rate relevant to the egg size was statistically significant (P < 0.01). The egg development time until hatching lasted for 19 h at 29°C. The newly hatched larval size ranged from 1.55-1.71 mm with a mean of 1.65 ± 0.052 mm in total length. The larval growth was slow in the early stages and the growth curve until metamorphosis showed a curvilinear pattern. Wide variations in larval size, range 22-47 mm with a mean of 33.40 ± 7.01 mm, were observed during the metamorphosis stage at day 50. No significant difference (P > 0.05) in growth and survival was observed between the larvae reared using white and grey coloured tanks. The larval survival up to metamorphosis was 1.6-4.7% with a mean of 2.98 ± 1.56% in the grey coloured tanks and 1.6-1.9% with a mean of 1.73 ± 0.16% in the white tanks. The results demonstrated the possibility of breeding E. polyphekadion under captive culture conditions. However, methods to improve the larval survival have to be pursued further for commercial farming of this species.     

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.     

Effects of two culturing techniques on the growth, survival and larval quality of Dentex dentex Linnaeus, 1758

Common dentex larvae were reared using two culturing techniques, mesocosms and intensive rearing, to determine the principal culture parameters involved in the differences observed in growth, skeletal deformations and survival between the two rearing techniques. In growth, only dry weight of larvae of 40 days post‐hatching (dph) from mesocosms was significantly higher than larvae from intensive rearing. Significant differences were observed in survival at 40 dph (6.58% in mesocosms and 1.58% in intensive rearing) and in the incidence of skeletal deformations, both for percentage of deformed larvae and for some deformation types such as those related to vertebral column and to the caudal complex. Initial larval density and initial prey density and quality are the factors suspected to affect growth and survival performance, while skeletal deformities might also be affected by tank hydrodynamics.     

Early development of the shortfin silverside Chirostoma humboldtianum (Valenciennes, 1835) (Atheriniformes: Atherinopsidae)

The shortfin silverside Chirostoma humboldtianum has been considered for culture in Mexico, but success has been limited by a poor knowledge of its early development. First synthesis of the early development of the shortfin silverside is presented to determine conditions suitable for rearing. Brooder maturation was induced through photothermal cycles. C. humboldtianum ova were fertilized in vitro. The eggs were incubated in reconstituted water (160-180 mg/L CaCO₃) at 18 °C and 5 gm of NaCl per litre. During the hatching day, 300 shortfin silversides were stocked and followed up until metamorphosis in order to establish the timing of exogenous feeding, changes in food type, growth and development during critical periods for survival, according to the theory of saltatory ontogeny. Free embryos hatched 12 days after fertilization at 18 °C. First critical point for survival is the beginning of exogenous feeding. Free embryos started mixed feeding on day four of post-hatching (dph), point of no-return was presented towards the end of mixed feeding on 6 dph, larval period began at six (dph) when the anus is opened, and metamorphosis to juvenile was presented at 65 dph with a SL of 19.34 ± 2.28 mm, when scales and fins were well developed. Differences in growth between periods were detected: free embryos growth slower than larvae but mouth size depicted a larger growth rate in the former. Cephalic length and mouth size were negatively related to standard length in embryos and larvae. Mouth size was positively related to cephalic length in free embryos but negative in larvae. Results suggest that during the free embryo phase, growth priorities are directed to the development of apparatuses and systems; whereas, during the larval period, energy is directed to growth in length, mouth size and development of fins, which allows them to increase their swimming velocity, grants them a greater capacity to obtain exogenous food and, in consequence, increases fitness for survival.     

Rearing temperature affects Senegalese sole (Solea senegalensis) larvae protein metabolic capacity

The present work examined the short- and long-term effects of three rearing temperatures on protein metabolism and growth trajectories of Senegalese sole larvae using ¹⁴C-labelled Artemia protein as feed. A first feeding trial was performed on larvae reared at 15, 18 and 21 °C (at 26, 17 and 14 days post-hatching (dph), respectively) and a second trial conducted on post-larvae after transfer to the same rearing temperature (~20 °C) (49, 35 and 27 dph, in larvae initially reared at 15, 18 and 21 °C, respectively). Temperature greatly influenced larvae relative growth rate (RGR) and survival, since growth at 15 °C was severely depressed. Protein digestibility and retention was highest at 18 °C during the first trial (85.35 ± 1.16 and 86.34 ± 2.33 %, respectively). However, during the second trial, post-larvae from 15 °C had the highest feed intake and protein digestibility (3.58 ± 1.54 and 75.50 ± 1.35 %, respectively), although retention was similar between treatments. Furthermore, after transfer to 20 °C larvae from 15 °C experienced compensatory growth, which was observed until 121 dph, and confirmed by RGR values, which were significantly higher at 15 ºC than at 21 ºC or 18 ºC. Results from the present study show that Solea senegalensis larval development, survival and protein digestion and retention are highly affected by thermal history.     

The effect of different rotifer feeding regimes on the growth and survival of yellowtail kingfish Seriola lalandi (Valenciennes, 1833) larvae

First feeding success is critical to larval marine finfish and optimization of live feed densities is important for larval performance and the economics of commercial hatchery production. This study investigated various rotifer feeding regimes on the prey consumption, growth and survival of yellowtail kingfish Seriola lalandi larvae over the first 12 days post hatch (dph). The common practice of maintaining high densities of rotifers (10–30 ind. mL^?1) in the rearing tank was compared to a low density feeding technique, where 5–8 ind. mL^?1 of rotifers were offered. A ‘hybrid’ feeding regime offered rotifers at the high density treatment until 5 dph and the lower feeding densities thereafter. There was no significant difference in larval survival (hybrid: 28.9 ± 7%, low density: 17.3 ± 5% and high density: 17.2 ± 9%) or growth (hybrid: 6.12 ± 0.18 mm, low density: 6.03 ± 0.10 mm and high density: 6.11 ± 0.23 mm) between treatments. Rotifer ingestion was independent of rotifer density throughout the trial and increased with larval age, with larvae at 4 dph ingesting 22 ± 1.5 rotifers larvae^?1 h^?1 and by 11 dph ingesting 59 ± 1.6 rotifers larvae^?1 h^?1. These data demonstrate that from first feeding, yellowtail kingfish larvae are efficient at capturing prey at the densities presented here and consequently significant savings in rotifer production costs as well as other potential benefits such as facilitation of early weaning and improved rotifer nutritional value may be obtained by utilizing lower density rotifer feeding regimes.     

Development of Improved Feeding Methods in the Culture of Yellow Tang,Zebrasoma flavescens

Yellow tang, Zebrasoma flavescens, are one of the most heavily traded marine aquarium fish species, with nearly 400,000 individuals collected annually from Hawaii's reefs. Despite recent success culturing this species, significant challenges in the rearing processes remain to be overcome before commercialization is feasible. This study compared two feeding regimens, an original diet treatment, which was initially used to successfully culture yellow tang, and a revised diet, which differed in the timing of the introduction of feed items and weaning periods. Both diet regimens consisted of Parvocalanus crassirostris nauplii, enriched Brachionus rotundiformis rotifers, and Artemia nauplii, followed by a transition to dry and frozen feed items. The revised feeding regimen aimed to considerably reduce the amount of copepods and rotifers needed in the rearing process. Eggs were stocked at 40/L into replicate (n = 3) 200‐L tanks for the feeding regimen trial. A follow‐up rearing study, in which eggs were stocked at 19/L in a single 1000‐L tank, tested the revised feeding method at pilot scale. Fish reared on the revised feeding regimen were observed to grow faster in body length and body depth after 2 wk in culture and transitioned more quickly to juveniles as 41% had completed their transition to juvenile coloration by 70 d after hatch. None of the fish reared under the original feeding regimen attained full juvenile coloration during the study period. Survival was not significantly different between treatments and was 0.13% ± 0.13 and 0.29% ± 0.17 in the original and revised feeding regimens, respectively. In the pilot‐scale study, growth was comparable to that of both treatments in the 200‐L scale trial, but survival was much better at 1.9%. This study successfully shortened the copepod and rotifer feeding periods for yellow tang, while not jeopardizing growth or survival. This outcome enhances the commercialization potential for this and likely other Acanthuridae species.     

Effects of Stocking Density, Salinity, and Light Intensity on Growth and Survival of Southern Flounder Paralichthys lethostigma Larvae

Four separate studies were done on Southern flounder Paralichthys lethostigma larvae during first feeding and metamorphosis to determine the effects of stocking density, salinity, and light intensity on growth and survival. One study used stocking densities of 10, 20, 40, and 80 fish/L during first feeding; the second study compared the growth and survival of larvae stocked at 20 and 33 ppt; and a third experiment evaluated stocking densities of 1/L and 3/L under two different light intensities (1,600 lux vs 340 lux) during metamorphosis. The fourth experiment tested the effects of different salinities (0, 10, 20 and 30 ppt) on larval growth and survival during metamorphosis. Growth and survival (overall 6.9%) were not significantly different ( P > 0.05) for stocking rates up to 80/L. Larvae placed into 20 ppt salinity had survival through first feeding similar to that of larvae raised at 33 ppt. During metamorphosis, light intensity had no effect ( P > 0.05) on growth or survival, but fish stocked at 3/L had significantly lower ( P < 0.05) survival than fish at 1/L. Complete mortality of larvae occurred at 0 ppt. Growth and survival past metamorphosis were not significantly different ( P > 0.05) at 10, 20 and 30 ppt, but unmetamorphosed fish did not survive to day 60 at 10 ppt. Based on these results, practical larviculture of Southern flounder may require a two-step process with high stocking rates (80 fish/L) through first feeding and lower densities (1/L) through metamorphosis. Fingerling production in fertilized nursery ponds might he possible at salinity as low as 20 ppt.