Feeding juvenile Artemia enriched with ascorbic acid improves larval survival in the spiny lobster Jasus edwardsii

Newly hatched Jasus edwardsii phyllosoma were fed unenriched Artemia [endogenous ascorbic acid (AA) concentration of 166 μg g^?1 dry weight (dw)], Artemia supplemented with algae (AA concentration 594 μg g^?1 dw) or with ascorbyl‐2‐polyphosphate (A2P) (AA concentration 11 737 μg g^?1 dw) to examine possible benefits of AA enhancement on culture. Plain or algal‐enriched Artemia were fed continuously for 28 days in two treatments during the study. Four other treatments received A2P‐enriched Artemia on a progressive basis starting from the commencement of the trial (D‐0), the third (D‐3), sixth (D‐6) or ninth day (D‐9) of Stage I (14 days) and similarly during Stage II (14 days). Prior to the commencement of A2P supplementation, plain Artemia were supplied to these animals. By Stage III (28 days feeding), algal, D‐0 and D‐3 phyllosoma had attained the largest size. The uptake and retention of AA by Stage III phyllosoma appeared to be dose‐dependent with the highest concentration of AA incorporation evident in D‐0 phyllosoma (1816 μg g^?1 dw), while algal and plain phyllosoma contained the lowest concentrations (600 and 300 μg g^?1 dw, respectively). Survival at Stage III was highest in D‐0 phyllosoma (89%) and lowest in plain phyllosoma (51%). There was a positive relationship between phyllosoma AA concentration and larval survival (R² = 0.8328, P < 0.0001). D‐0 phyllosoma had the lowest stress index when subjected to an osmotic/temperature activity test, indicative of better survival in culture compared to plain, algal and D‐9 phyllosoma, which had consistently higher indices. A negative relationship existed between phyllosoma AA concentration and stress indices at Stage III (R² = 0.9263, P < 0.0001), suggesting that AA from the Artemia diet conferred stress resistance.     

Uptake and metabolism of a particulate form of ascorbic acid by Artemia nauplii and juveniles

A study was conducted to establish whether a particulate form of ascorbic acid (AA), ascorbyl‐2‐phosphate (A2P), could be used to enrich Artemia. In the first experiment, we examined the efficiency of A2P conversion to and maintenance of AA by juvenile Artemia (1.5 mm, 5‐day‐old) held at 9000 L^?1 and 28 °C for 24 h. Maximal uptake and assimilation was >10 000 μg AA g^?1 dry weight (dw) (representing >1%Artemia dw) at enrichment rates of ≥1.2 g A2P L^?1. In the second experiment, a similar biomass of instar II/III nauplii (1 mm, 2‐day‐old) and juvenile (2.5 mm, 8‐day‐old) Artemia were enriched for 6 or 24 h at 28 °C before starvation for 6 or 24 h at 18 or 28 °C. At 0 h and after 6 and 24 h enrichment, AA levels were 485, 3468 and 11 080 μg g^?1 dw in nauplii and 122, 4286 and 12 470 μg g^?1 dw in juveniles. When Artemia nauplii or juveniles were enriched for 6 h and starved for 6 h at 18 or 28 °C, there was no significant reduction in AA. Continuation of starvation to 24 h at 18 and 28 °C reduced the level of AA to 3367 and 2482 μg g^?1 dw in nauplii and 3068 and 2286 μg g^?1 dw in juveniles. After 24 h enrichment, 6 h of starvation at 18 and 28 °C reduced AA to 8847 and 7899 μg g^?1 dw in nauplii and to 9053 and 8199 μg g^?1 dw in juveniles. Continuation of starvation to 24 h at 18 and 28 °C further reduced AA levels in nauplii to 6977 and 4078 μg g^?1 dw and to 7583 and 5114 μg g^?1 dw in juveniles. This study demonstrated that A2P could be assimilated as AA in the body tissue of different‐sized Artemia in a dose‐dependant manner and AA was depleted during starvation depending on time and temperature.     

The effect of PUFA enriched Artemia on growth, survival and lipid composition of western rock lobster, Panulirus cygnus, phyllosoma

Western rock lobster, Panulirus cygnus, phyllosoma were grown from hatching to stage IV. Larvae were fed with Artemia enriched with a (i) base enrichment (Base) containing 520 g kg^?1 squid oil or tailor made enrichments in which oils high in polyunsaturated fatty acid (PUFA) have been added at the expense of squid oil. These treatments were (ii) base enrichment supplemented with docosahexaenoic acid (DHA) rich oil, (iii) base enrichment supplemented with arachidonic acid (AA) rich oil, or (iv) base enrichment supplemented with DHA and AA (D + A) rich oils. Total survival of phyllosoma to stage IV was high, with no significant difference between treatments (range 12.3–17.5%). By stage IV, the larvae fed the DHA or AA enriched Artemia were significantly larger (3.33 mm length) than larvae fed the Base or D + A enriched Artemia (3.18–3.24 mm length). Phyllosoma were sampled at stages II and III for biochemical analysis. The major lipid class (LC) in all phyllosoma was polar lipid (PL) (88.9–92.4%), followed by sterol (ST) (6.2–9.7%). Triacylglycerol (TAG), free fatty acid (FFA) and hydrocarbon/wax ester were minor components (≤1%) in all phyllosoma samples. In contrast, the major LC in all enrichments and enriched Artemia was TAG (76.3–85.1% and 53.4–60.2%, respectively), followed by PL (11.4–14.8% and 30.6–38.1% respectively). The main fatty acids (FA) in phyllosoma were 16:0, 18:1n‐9, 18:1n‐7, 18:0, AA, eicosapentaenoic acid (EPA) and DHA. Addition of AA, and to a lesser extent DHA, to enrichments resulted in increased levels of those FA in Artemia and phyllosoma compared with the Base enrichment. This was particularly evident for stage III larvae. Comparatively, elevated growth for phyllosoma to stage IV was achieved with DHA and AA enriched diets. Our findings highlight the importance of lipids and in particular essential long‐chain PUFA, as nutritional components for phyllosoma diets.     

Effects of starvation and feeding on the fatty acid profiles of Stage I phyllosoma of the spiny lobster, Jasus edwardsii

Fatty acid analyses were conducted on newly hatched and 8‐day‐old‐starved and fed Stage I phyllosoma larvae of the spiny lobster, Jasus edwardsii. Fed animals were offered excess 1.5 mm juvenile Artemia (enriched using the alga Isochrysis galbana, Tahitian isolate, T. iso.). After 8 days, there were significant increases in larval dry weight and the proportion of lipid in fed phyllosoma, whereas these parameters decreased in starved phyllosoma. The abundance of the saturated fatty acids 16 : 0 and 18 : 0 increased in both starved and fed phyllosoma, whereas the main monounsaturated fatty acids 16 : 1n‐7, 18 : 1n‐9 and 18 : 1n‐7 increased with feeding but decreased with starvation. There were no significant differences in the relative proportions of the highly unsaturated fatty acids (HUFAs) arachidonic (AA, 20 : 4n‐6), eicosapentaenoic (EPA, 20 : 5n‐3) and docosahexanoic (DHA, 22 : 6n‐3) acids between newly hatched and starved animals, whereas quantitatively DHA decreased with starvation and feeding. The DHA/EPA ratio was significantly lower in the starved and fed phyllosoma (0.5) compared with that found in the newly hatched phyllosoma (0.9). The lipid profiles of the newly hatched, starved and fed phyllosoma contained large amounts of n‐6 fatty acids resulting in low n‐3 : n‐6 ratios (2.8, 2.7 and 1.6 respectively). The importance of these results and the ability of enriched Artemia to provide a suitable fatty acid profile for this species are discussed.     

Growth and lipid composition of phyllosomata of the southern rock lobster, Jasus edwardsii, fed enriched Artemia

Newly hatched phyllosoma larvae of Jasus edwardsii were on‐grown to stage V. Using triacylglycerol‐rich marine oil nutrient sources and microalgae, Artemia were enriched with the major polyunsaturated fatty acids (PUFA) to ratios similar to that of wild‐caught phyllosomata. Artemia enriched by different methods were fed to cultured phyllosomata. At each stage animals were counted, measured and sampled for lipid analyses. Survival was highest from stages II to III (62–86%), with mean total survival at 3–12%. From stages I to V larvae increased in mass (0.2–2.2 mg) and total length (2.1–5.8 mm), and decreased in total lipid. The major lipid class in all phyllosomata was polar lipid, followed by sterol, with no triacylglycerol detected. The main fatty acids were 18:1(n‐9)c, 18:2(n‐6), 16:0, 18:0, eicosapentaenoic acid [EPA; 20:5(n‐3)], 18:1(n‐7)c, arachidonic acid [AA; 20:4(n‐6)] and docosahexaenoic acid [DHA; 22:6(n‐3)]. On‐grown phyllosomata had levels of AA and EPA similar to that of wild phyllosomata, but contained markedly lower levels of DHA. Strategies for enhancement of DHA levels will be needed for culture of rock lobster phyllosomata.     

Ingestion of artificial diets with different textures as determined by the inert marker ytterbium oxide during culture of early‐stage phyllosoma of the spiny lobster,Jasus edwardsii

Instar 1 and 2 Jasus edwardsii (Decapoda; Palinuridae) phyllosoma larvae were fed an artificial diet formulation (based on fish and mussel) consisting of three different gelatin combinations (firm, 4% inclusion; medium, 2% inclusion; and soft, no gelatin). The diet contained ytterbium oxide (Yb₂O₃; 1% inclusion), an inert heavy metal marker, which was used to confirm diet consumption in instar 1 and 2 phyllosoma. Over a 6‐h feeding period, instar 1 phyllosoma showed a preference for the soft and medium diets as opposed to the firm diet, but this effect was not significant with instar 2. The artificial diets remained palatable over the duration of the experiments, suggesting leaching did not influence diet attractiveness. It is suggested that diets comprising softer food items such as microencapsulated pellets or gelatinous formulated diets and pastes are most suitable for early‐instar phyllosoma. Furthermore, it is also suggested that Yb₂O₃ is a potentially useful marker for ongoing quantitative work on diet utilization in lobster larvae.     

Effect of Artemia enrichment on the growth and survival of Pacific bluefin tuna Thunnus orientalis (Temminck & Schlegel) larvae

This study was carried out to investigate the suitability of Artemia enriched with docosahexaenoic acid (DHA) and choline as live food on the growth and survival rate of the Pacific bluefin tuna (PBT; Thunnus orientalis) larvae. The PBT larvae were fed either Artemia enriched with oleic acid (Diet 1), DHA (Diet 2), DHA+choline 1.0 mg L^?1 (Diet 3) and DHA+choline 2.0 mg L^?1 (Diet 4) or striped knifejaw larvae (Diet 5, reference diet), in duplicate for 12 days. Enrichment of Artemia with DHA significantly increased the DHA levels to 13.9, 13.8 and 12.5 mg g^?1 on a dry matter basis in Diets 2, 3 and 4 respectively; however, the levels were significantly lower than the reference diet (26.9 mg g^?1 dry matter basis; Diet 5). Although growth and survival rate were significantly improved by the enrichment of Artemia with DHA and choline, the improvement was negligible compared with the enhanced growth and survival rate of the fish larvae‐fed group (P<0.05). The results demonstrated that enriched Artemia does not seem to be the right choice to feed the PBT larvae perhaps because of the difficulties in achieving the correct balance of fatty acid with higher DHA/EPA from Artemia nauplii.     

Artemia prey size and mode of presentation: Effects on the survival and growth of phyllosoma larvae of southern rock lobster (Jasus edwardsii)

Performance of phyllosoma of thesouthern rock lobster (Jasus edwardsii)was examined after feeding Artemia-baseddiets. Survival and growth of newly-hatchedlarvae cultured to Stage III were lower(p < 0.05) when fed 0.8 mm Artemia than1.5 mm or 2.5 mm Artemia alone or 1.5 mmArtemia in combination with pieces ofmussel (Mytilus edulis planulatus) gonad.This could not be attributed to deficiencies inthe composition of fatty acids but appeared tobe due to the inability of larvae to capturesufficient appropriate-sized, enrichedArtemia for their nutritional requirements.There was an indication that survival andgrowth were higher between Stages III and Vwhen fed 2.5 mm Artemia than 1.5 mmArtemia alone or in combination with musselpieces. However, Stage VI larvae grew to asimilar size at Stage VIII when fed 1.5 mm or2.5 mm Artemia. Unexpectedly, larvae fedthe combination of 1.5 mm Artemia plusmussel supplement had lower survival than foundpreviously, and generally lower than when fed 1.5 mm Artemia alone. This was despitean apparent nutritional profile (lipid contentand fatty acid composition) of mussel more akinto that of newly-hatched phyllosoma thanenriched Artemia. On the other hand,survival and growth to Stage VIII were higherwhen larvae were fed alginate pelletscontaining Artemia than when fed 1.5 mmor 2.5 mm Artemia alone.     

Relative bioavailability of zinc in supplemental inorganic and organic sources for Nile tilapia Oreochromis niloticus fingerlings

A 90‐day feeding experiment was conducted with sex reversed Nile tilapia (Oreochromis niloticus) fingerlings fed purified or practical diets supplemented with different zinc sources to evaluate fish growth performance and zinc and iron retention in fish bones, fillets, liver, skin and eyes. The relative bioavailability value (RBV) of zinc in the supplemental sources tested was also calculated. Fish were fed with isonitrogenous and isoenergetic purified or practical diets supplemented with 150 mg Zn kg^?1, as zinc sulphate monohydrate (ZnSO₄), zinc oxide (ZnO) or zinc amino acid complex (Zn‐AA). The feeding trial was conducted in 30, 50 L aquaria where four 0.66 ± 0.01 g (mean ± SD) fingerlings were initially stocked. No significant differences were observed for any growth performance variables (P > 0.05). In practical diets, only ZnSO₄ and ZnO presented bone zinc retention similar to that for the standard zinc source. Zinc concentration in the bone of fish fed practical diet supplemented with Zn‐AA (171 ± 3.62 μg g^?1) was significantly lower than that verified for the practical diets supplemented with the standard zinc source (200 ± 17.7 μg g^?1) or with ZnSO₄ (204 ± 19.9 μg g^?1). Assuming the concentration of zinc in bones as the response criterion, the supplemental zinc RBV from ZnSO₄ (105%) was higher than the RBV for Zn‐AA (95.1%) or ZnO (94.9%). Iron concentration in the bones of animals fed the non‐zinc‐supplemented purified diet was significantly higher than that observed for purified diet supplemented with Zn‐AA (P < 0,05). The results of the present work allowed us to conclude that ZnSO₄ in relation to ZnO or Zn‐AA was the supplemental zinc source with higher zinc bioavailability to Nile tilapia.     

Delivery of HUFA, probionts and biomedicine through bioencapsulated Artemia as a means to enhance the growth and survival and reduce the pathogenesity in shrimp Penaeus monodon postlarvae

One of the major problems in the shrimp culture industry is the difficulty in producing high-quality shrimp larvae. In larviculture, quality feeds containing a high content of highly unsaturated fatty acids (HUFA) and ingredients that stimulate stress and disease resistance are essential to produce healthy shrimp larvae. In the present study, Penaeus monodon postlarvae (PL15) were fed for 25 days on an unenriched Artemia diet (control; A) or on a diet of Artemia enriched with either HUFA-rich liver oil of the trash fish Odonus niger (B), probionts [Lactobacillus acidophilus (C1) or yeast-Saccharomyces cerevisiae (C2)] or biomedicinal herbal products (D) that have anti-stress, growth-promoting and anti-microbial characteristics. P. monodon postlarvae fed unenriched Artemia exhibited the lowest weight gain (227.9 ± 8.30 mg) and specific growth rate (9.95 ± 0.05%), while those fed the HUFA-enriched Artemia (B) exhibited the highest weight gain and specific growth rate (362.34 ± 12.56 mg and 11.77 ± 0.08%, respectively). At the end of the 25-day rearing experiment, the shrimp postlarvae (PL40) were subjected to a salinity stress study. At both low and high (0 and 50‰) salinities, the group fed the control diet (A) experienced the highest cumulative mortality indices (CMI) 935.7 ± 2.1 and 1270.7 ± 3.1, respectively. Those fed diet D showed the lowest stress-induced mortality, and CMI were reduced by 31.1 and 32.3% under conditions of low and high salinity stress, respectively. A 10-day disease challenge test was conducted with the P. monodon postlarvae (PL40–PL50) by inoculating the shrimp with the pathogen Vibrio harveyi at the rate of 10⁵–10⁷ CFU/ml in all rearing tanks. P. monodon postlarvae fed probiont-encapsulated Artemia diets (C1 and C2) exhibited the highest survival (94.3 and 82.3%, respectively) and lowest pathogen load (V. harveyi) in hepatopancreas (5.2 × 10² ± 9.0 × 10 and 4.6 × 10² ± 9.0 × 10 CFU g⁻¹, respectively) and muscle (2.0 × 10² ± 6 × 10 and 1.7 × 10² ± 8.6 × 10 CFU g⁻¹, respectively) tissues. The shrimp that were fed the unenriched Artemia (Control; A) showed the lowest survival (26.33%) and highest bacterial load in the hepatopancreas (1.0 × 10⁵ ± 5 × 10³ CFU g⁻¹) and muscle (3.6 × 10⁴ ± 6 × 10² CFU g⁻¹). The shrimp fed the herbal product (D)-enriched Artemia also exhibited enhanced survival and reduced V. harveyi load in the tissues tested compared to the control diet (A) group. The results are discussed in terms of developing a quality larval feed to produce healthy shrimp larvae.     

Survival of blue king crab Paralithodes platypus Brandt, 1850, larvae in cultivation: effects of diet, temperature and rearing density

Blue king crab (Paralithodes platypus) larvae were cultivated to test the effects of diet, temperature and rearing density. Dietary treatments included no feeding (unfed), Artemia nauplii enriched with diatoms Thalassiosira nordenskioeldii (THAL), unenriched Artemia fed in addition to Thalassiosira (A+THAL) and a control diet of Artemia enriched with frozen Isochrysis paste (ISO 6). Trials were conducted at 6 °C, and a rearing density of 10 zoea L^?1, with six replicates per treatment. The ISO 6 diet was also tested at 3 °C (ISO 3) and 9 °C (ISO 9), and at densities of 20 (ISO 20) and 40 (ISO 40) zoea L^?1. Survival of zoea larvae fed the A+THAL diet (91.7%) was significantly higher than all others, whereas unfed zoea larvae died within 2 weeks. Temperature and rearing density had no significant effects on survival. Time required to reach stage C1 was significantly greater at 3 °C (109 days) than at 6 °C (70 days), but did not decrease further at 9 °C. After reaching the postlarval (glaucothoe) stage, half of the replicates in the ISO 20 and ISO 40 treatments were fed continuously, but survival did not differ significantly from unfed glaucothoe. We conclude that blue king crab larvae are not lecithotrophic and can be cultivated with high survival using the proper diet. These techniques can be used to produce large numbers of juvenile crab for laboratory research, or could be modified for use in stock‐enhancement programmes.     

Hatchery performance of early benthic juvenile American lobsters (Homarus americanus) fed enriched frozen adult Artemia diets

One of the main factors hindering aquaculture production of American lobsters (Homarus americanus) is the need for a cost‐effective and nutritionally sound diet. Live Artemia results in good growth, but is expensive and is a constant source of contamination. Frozen Artemia, although lower in cost, generally results in decreased survivorship and growth relative to live Artemia. The recent advent and mass production of enriched frozen Artemia products may provide for a cost‐effective and nutritionally complete food source for culturing American lobsters. Here, commercially available frozen adult Artemia enriched with either n‐3 fatty acids, or Spirulina was fed to juvenile American lobsters, and their growth and survivorship for three months was compared with that of animals fed unenriched frozen adult Artemia. Both enriched Artemia products produced survivorship superior to that for animals fed unenriched Artemia. Results for growth were equivocal although animals fed the Spirulina‐enriched Artemia had the greatest condition factor. Although more costly by the end of the experiment, enriched diets were more economically efficient than unenriched Artemia. This research demonstrates that enriched feedstuffs are cost‐effective over longer time intervals, and benefits may continue beyond the hatchery‐rearing phase. Enriched diets may also yield animals with a better condition factor, which may further influence their survivorship when released to the wild in enhancement programmes.     

Effects of supplementation of decapod zoea to Artemia basal diet on fatty acid composition and digestive gland histology in common octopus (Octopus vulgaris) paralarvae

The present study aimed to evaluate the effect of the supplementation of different crab zoeas to enriched Artemia basal diet for Octopus vulgaris paralarvae during the first month of life. Paralarvae were fed using enriched Artemia nauplii alone and Artemia co‐fed either first zoea stages of Grapsus adscensionis or Plagusia depressa. The experiment was carried out over a period of 28 days, in 0.12 m³ tanks with a flow‐through rearing system. Growth in dry weight as well as mantle length and width were assessed weekly. Additionally, prey and paralarvae fatty acid composition and digestive gland (DG) histology were evaluated. Addition of low amounts of crab zoeas (approx. 100 indv. L^?1 day^?1) provided during critical life stages of O. vulgaris proved to be good enough to improve paralarvae growth and survival in comparison with those fed exclusively on enriched Artemia. These results were supported by the finding of a higher number of glycoprotein absorption vacuoles in the DG from paralarvae co‐fed crab zoeas, suggesting a higher feeding activity. In addition, fatty acid analysis of crab zoea showed that these are good sources of dietary arachidonic and eicosapentaenoic acids during the octopus planktonic life stage, whereas the low docosahexaenoic (DHA) content suggests the use of additional DHA sources or higher zoea densities to meet paralarvae nutritional demand to carry out a successful metamorphosis to benthic life.     

Weaning requirements of larval mulloway,Argyrosomus japonicus

Mulloway (Argyrosomus japonicus) is an emerging aquaculture species in Australia, but there is a need to improve the production technology and lower costs, including those associated with larval rearing and live feeds. Three experiments were conducted to determine appropriate weaning strategies from live feeds, rotifers (Brachionus plicatilis) and Artemia, to cheaper formulated pellet diets. Experiment 1 examined the effects of feeding Artemia at different levels [0%, 50% or 100% ration of Artemia fed from 18 days after hatching (dah); based on current hatchery protocols] and a pellet diet from two larval ages (14 or 23 dah). In addition, rotifers were supplied to larvae in all treatments for the duration of the experiment (14–29 dah), at which time all larvae were successfully weaned onto the pellet diet. No significant (P>0.05) differences existed between the growth of fish fed a 50% and 100% ration of Artemia; however, fish fed a 0% ration of Artemia had significantly (P<0.05) reduced growth. The time of pellet introduction had no significant (P>0.05) effects on the growth of larvae. Experiments 2 and 3 were designed to determine the size [total length (TL), mm] at which mulloway larvae selected Artemia equally or in preference to rotifers, and pellet (400 μm) equally or in preference to Artemia respectively. Each day, larvae were transferred from a holding tank to experimental vessels and provided with rotifers (2 mL^?1), Artemia (2 mL^?1) or a combination of rotifers (1 mL^?1) and Artemia (1 mL^?1) (Experiment 2), and Artemia (2 mL^?1), a pellet diet or a combination of Artemia (1 mL^?1) and a pellet diet that was broadcast every 15 min (Experiment 3). After 1 h, a sub‐sample of larvae was randomly selected from each replicate vessel (n=5) and the gut contents were examined under a light microscope. Mulloway larvae began selecting Artemia equally to rotifers at 5.2 ± 0.5 mm TL and selected pellets equally to Artemia at 10.6 ± 1.8 mm TL. Our results have led to the establishment of weaning protocols for larval mulloway, which optimize larval growth while reducing feed cost by minimizing the amount of Artemia used during production.     

Iodine enrichment of Artemia and enhanced levels of iodine in Atlantic halibut larvae (Hippoglossus hippoglossus L.) fed the enriched Artemia

Flatfish metamorphosis is initiated by the actions of thyroid hormones (TH) and iodine is an essential part of these hormones. Hence, an iodine deficiency may lead to insufficient levels of TH and incomplete metamorphosis. In this study, different iodine sources for enrichment of Artemia were evaluated and the levels of iodine obtained in Artemia were within the range of 60–350 μg g^?1 found in copepods. Larval Atlantic halibut was fed Artemia enriched with either normal DC‐DHA Selco or DC‐DHA Selco (commercial enrichments) supplemented with iodine from days 9 to 60 postfirst feeding. There was no significant difference in growth, mortality or metamorphic development between the groups. The analyses showed that we were able to enrich Artemia with iodine. Further, the larvae‐fed iodine‐enriched Artemia had higher whole body iodine concentration compared to larvae‐fed Artemia without iodine enrichment.     

Evaluation of vitamin C-enriched Artemia nauplii for larvae of the giant freshwater prawn

The effect of high levels of ascorbic acid (AA) delivered through enriched live food has been verified through the successful culture of larval giant freshwater prawn, Macrobrachium rosenbergii. Two successive feeding trials were set up using a control (550 g AA g^–1 DW) and two different AA-enrichment levels in Artemia (1300 and 2750 g AA g^–1 DW). Under standard culture conditions, no differences in growth nor survival could be observed demonstrating that the nutritional requirements are below 550 g AA g^–1 DW, which is the normal level occurring in freshly-hatched Artemia. However, a significantly positive effect could be demonstrated on the physiological condition of the postlarvae, measured by means of a salinity stress test, when vitamin C-boosted live food was administered. Since the AA levels in the predator larvae are linked with the enrichment levels in the live prey, it may be assumed that a positive influence on stress resistance was caused by feeding vitamin C-enriched Artemia. It is expected that under suboptimal conditions, supplementation of high vitamin C levels might also enhance production characteristics.     

The enrichment of rotifers (Brachionus plicatilis) and Artemia franciscana with taurine liposomes and their subsequent effects on the larval development of California yellowtail (Seriola lalandi)

Taurine is an essential or conditionally essential nutrient for many species of marine fish, especially during early development. There is growing evidence that marine fish larvae benefit from taurine‐enriched rotifers; however, it is unknown if larvae benefit from taurine‐enriched Artemia. We investigated the effects of taurine‐enriched rotifers (Brachionus plicatilis) and Artemia franciscana on the growth and whole‐body taurine concentrations of California yellowtail (Seriola lalandi; CYT) larvae. The approach used in this study was to encapsulate taurine within microparticles (liposomes), which were then fed to rotifers and Artemia. We found that feeding taurine liposomes to rotifers and Artemia resulted in taurine concentrations in these prey species that were similar to or above those previously reported in copepods. At the end of the rotifer phase, CYT larvae fed taurine‐enriched rotifers showed increased growth (final dry weights; DW) and had higher whole body taurine concentrations when compared to larvae fed unenriched rotifers. At the end of the Artemia phase, CYT whole body taurine concentrations varied among dietary treatments. Larval lengths and DWs were not significantly different among treatments at the end of the Artemia phase, suggesting that the taurine concentrations of unenriched Artemia were sufficient to support the growth of CYT larvae.     

Arachidonic acid requirements in larval summer flounder, Paralichthys dentatus

The arachidonic acid (20:4n-6,AA) requirements of larval summer flounder weredetermined for the rotifer- and Artemia-feeding stages. Experimental emulsionscontained adequate n-3 highly unsaturated fattyacid (HUFA) ratios and emulsion levels of AAwere set at 0, 3, 6, 9, and 12% (AA0, AA3,AA6, AA9, and AA12). Examination of fatty acidlevels in live feeds and larval tissuesconfirmed the physiological incorporation offatty acids relative to dietary levels. In thefirst experiment, survival, growth, andsalinity tolerance (2-h in 70) were measuredat 18 days after hatch (dah) after feeding thelarvae the various levels of AA. Larvae fedAA6-enriched rotifers were better able tosurvive the salinity tolerance test. AAenrichment up to 12% had no effect on growthand survival. In the second experiment, larvaewere fed AA0- or AA6-enriched rotifers until 23dah, followed by unenriched 24- and 48-h Artemia nauplii until 32 dah. These larvaethen were subdivided and fed AA-enriched Artemia from 33-45 dah. At the end of thisexperiment, larvae fed AA6-enriched rotifershad higher survival, increased growth, andsurvived better in the salinity tolerance test(2-h in 80). The enrichment of Artemiadid not have any effect on these variables.Thus, the provision of AA6-enriched rotifers(10 mg AA g^–1 DW) early in larvaldevelopment may serve to enhance larval stresstolerance at the rotifer stage while alsoincreasing larval survival, growth, and stresstolerance later in the Artemia stage.     

Potential use of Artemia biomass by‐products from Artemia cyst production for the nursing of goby Pseudapocryptes elongatus in Vietnam: effects on growth and feed utilization

The present study was performed to evaluate the effect of using Artemia biomass, by‐product from Artemia cyst production on growth and feed utilization of goby Pseudapocryptes elongatus fingerlings. A control diet containing fishmeal as main protein source was compared with four experimental diets in which fishmeal protein was replaced by increasing dietary levels of Artemia protein, namely 25%, 50%, 75% and 100%. The five test diets were compared with a commercial diet and dried Artemia. All diets were formulated to be equivalent in crude protein (360–370 g kg^?1) and lipid (58–65 g kg^?1). The experiment was conducted in 80 L plastic tanks filled with water at a salinity of 15 g L^?1. Goby fingerlings with 0.21 g initial weight were fed the test diets for 30 days. The results showed that weight gain and specific growth rate of goby were positively correlated with total feed intake. Moreover, growth performances and feed utilization in the fry receiving the commercial feed and fishmeal control diet were similar, both were inferior to the groups fed dried Artemia and the based formulated diets. These results illustrate that both dried Artemia and Artemia‐based feeds can be used for feeding goby fingerlings, indicating the high potential of using locally produced Artemia biomass, which could contribute to reduce the reliance on fishmeal and improve profits for Artemia producers.     

Replacement of live food with a microbound diet in feeding Litopenaeus setiferus (Burkenroad) larvae

Microbound feeds have been well accepted by shrimps and farmers in many penaeid shrimp hatcheries. The present study focused on an adequate level of replacement of Artemia nauplii and microalgae by a microbound diet for rearing Litopenaeus setiferus (Burkenroad) larvae. A microbound diet (MBD) consisting of fishmeal, squid meal, shrimp meal, yeast meal and soybean meal was used. The first experiment was designed to obtain the optimum level of MBD to complete the live feeding schedule, from Protozoea (PZ_III) to Mysis (M_III). The experimental levels of the microbound diet tested were 2, 4, 6 and 8 mg MBD L^?1 day^?1. The next step was to determine the Artemia nauplii replacement level from PZ_I to M_III by MBD. These experiments were carried out either in the presence (Experiment 2) or in the absence of algae (Experiment 3). Four replacement levels were tested: 0% (4 mg MBD L^?1 day^?1: 1 Artemia nauplii mL^?1), 40% (5.5 mg MBD L^?1 day^?1: 0.6 Artemia nauplii), 60% (6.5 mg MBD L^?1 day^?1: 0.4 Artemia nauplii) and 100% (8 mg MBD L^?1 day^?1: 0 Artemia nauplii). In all experiments growth, survival, development, quality index (QI) and performance index (PI), were used to determine the optimum concentration of microbound diet. Results showed that 6 mg MBD L^?1 day^?1 can be recommended as a complement to live food for L. setiferus larvae from PZ_III to M_III. In the presence of algae, maximum growth and survival may be obtained in 40–60% (5.5–6.5 mg MBD L^?1 day^?1) of Artemia nauplii replacement levels. In the absence of algae, the Artemia nauplii replacement resulted in slower development, less salinity resistance, lower growth and lower survival than was obtained in larvae fed with algae.