The potential of dried, low-hatch, decapsulated Artemia cysts for feeding prawn post-larvae

Low-hatch, decapsulated Artemia cysts were assessed as feed for Penaeus indicus post-larvae (PL) 1–15 days old and the problems resulting from the incorporation of decapsulated cysts into compounded feeds were evaluated. Growth and survival of PL fed on decapsulated cysts (AC) were comparable with Artemia nauplii fed PL (control) and significantly (p < 0.05) higher than observed amongst PL fed on two granulated commercial diets (G150 and G300) or a commercial flake feed (AC-F) incorporating decapsulated cysts (80%). PL fed on artificial diets showed poor growth and delay in metamorphosis. However, survival of PL fed on AC-F was significantly higher (p < 0.05) than that observed amongst granulated feeds. Decapsulated cysts processed into a granulated feed (AC-G) or dried at 90°C (AC-90) also resulted in slow growth and survival when fed to PL. Overall, artificial feeds showed poor water stability and significantly higher leaching of soluble protein and carbohydrates than decapsulated cysts. AC-90 cysts also showed a high level of bursting and leaching of material. This indicates that low-hatch Artemia cysts retain a living membrane after commercial decapsulation and drying prevents loss of highly digestible nutrients, which allows PL growth equal to that on PL fed live Artemia nauplii. Survival of PL was negatively correlated with leaching of soluble protein (p < 0.05), but no correlation was observed for leaching of carbohydrates or between growth and loss of both soluble nutrients. Hence, availability of digestible protein is critical and may influence survival of early stages of post-larval development. Water stability of artificial feeds is an essential factor in promoting efficient nutrition of PL, but other aspects related to heating during processing of feeds also appear to have a deleterious effect on nutritional quality of compounded feeds. Commercially dried, encapsulated Artemia cysts from low-hatch strains remain alive and are highly nutritious for feeding early stages of post-larval prawn but even after death may support acceptable survival when incorporated into a flake diet. © Rapid Science Ltd. 1998     

Optimal first feed organism for South African mud crab <Emphasis Type="Italic">Scylla serrata</Emphasis> (Forskål) larvae

It is not known whether rotifers or Artemia nauplii are the best first food for South African mud crab Scylla serrata larvae. In order to test this, larvae were fed with five different test diets. These were rotifers for the first 8 days and newly hatched EG^® type Artemia nauplii (San Francisco Bay) from day 6 onwards (treatment R6A); newly hatched EG^® type Artemia nauplii throughout the rearing period (treatment EG); newly hatched Vinh-Chau strain (Vietnam) Artemia nauplii throughout the rearing period (treatment VC); decapsulated cysts of EG^® type Artemia throughout the rearing period (treatment DECAP); or decapsulated cysts supplemented with low densities of Artemia EG type Artemia nauplii (treatment MIX). Two experiments were conducted approximately 1 month apart using larvae from two different female crabs. Although results showed it is possible to rear S. serrata larvae through metamorphosis on Artemia nauplii exclusively, larval performance (development, survival and successful metamorphosis) was enhanced by the inclusion of rotifers as a first feed.No significant difference in performance was recorded between larvae fed on the two strains of Artemia nauplii. Larvae fed on decapsulated cysts in treatments DECAP and MIX performed poorly, but there were indications that decapsulated cysts and other inert diets may have potential as supplements to live food in the rearing of S. serrata larvae.     

Nutritional evaluation of decapsulated cysts of fairy shrimp (Streptocephalus dichotomus) for ornamental fish larval rearing

The suitability of decapsulated cysts of the fairy shrimp, Streptocephalus dichotomus as a sole diet was evaluated for the ornamental angelfish Pterophylum scalare larvae. Brine shrimp, Artemia sp., and microworms, Panagrellus redivivus, were used as comparison foods. The results indicate an appreciable weight gain of 15.22±1.69 mg and a growth (length) of 0.876±0.03 cm in experimental fish fed decapsulated fairy shrimp cysts compared with the growth and weight of fish fed other foods. The influence of the experimental diets was further reflected in the composition of fatty acid and amino‐acid profiles of the experimental fish. Angelfish larvae readily consumed the decapsulated cysts and utilized them efficiently during the early days of exogenous feeding.     

The Use of Decapsulated Cysts of the Brine Shrimp Artemia as Direct Food for Carp Cyprinus carpio L. Larvae

Decapsulated Arremia cysts have been evaluated as a direct food source for larvae of the carp Cyprinus carpio L. All decapsulated cyst diets gave excellent survival of carp larvae during the first two weeks of culturing. Unlike traditionally brine-stored decapsulated cysts, dried Artemia embryos provided growth results comparable to those obtained with freshly hatched Artemia nauplii. Furthermore, except for Artemia embryos that lost their hatchability after long-term storage in air, several other inactivation treatments, simulating improper harvesting and processing of cysts, did not produce a significant decrease in the nutritional quality of the decapsulated cysts.
Using decapsulated cysts 89 a direct food source for carp larvae, instead of nauplii, the quantity of cysts needed can be reduced by about 25% to 35% after one and two weeks of culturing, respectively. Moreover, the use of decapsulated cysts advances the possible commercialition of poor-hatching and less expensive cyst products for culture of carp larvae.     

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

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

Lipid Nutrition and Feeding of Cobia Rachycentron canadum Larvae

This study examined the fatty acid composition of cobia Rachycentron canadum eggs and yolksac larvae, as well as the ovaries of wild caught females as an initial guide to lipid nutritional requirements. A 2-wk feeding study also was conducted to investigate the effectiveness of four dietary treatments on the growth and survival of cobia larvae. Cobia eggs in the tailbud stage contained 31.4 ± 1.3 μg lipid/egg. After hatching, the amount of lipid decreased significantly (P < 0.05) from 28.3 ± 0.3 to 23.2 ± 0.1 μg lipid/larvae during the yolksac larval stage (days 1 to 3 after hatching). Ovaries from wild caught adults and captive spawned eggs and yolksac larvae contained high levels of PUFAs with docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), and arachidonic acid (ARA) accounting for approximately 80% of the total suggesting that cobia larvae may have a high dietary requirement for these fatty acids. For the feeding study, larvae were fed: 1) Artemia only; 2) enriched rotifers for 1 d only + microparticulate diet (day 313); 3) enriched rotifers for 3 d (day 3–5) + Artemia (day 3–13); and 4) enriched rotifers for 6 d (day 3–8) + Artemia (day 3–13). Cobia larvae began feeding on rotifers 3 d after hatching and on newly hatched Artemia nauplii by the fifth day following the onset of exogenous feeding (day 7). On day 7, no differences in larval growth were found among larvae fed rotifers for 3 versus 6 d, whereas larvae fed only Artemia or rotifers for I d followed by microparticulate diet were significantly smaller (P < 0.05) and did not survive beyond day 9 and 13, respectively. The results of the feeding study indicate that cobia larvae require rotifers for a minimum of 4 d following the onset of exogenous feeding.     

Decapsulated Artemia cysts as dietary supplement for juvenile crayfish (Pacifastacus leniusculus, Astacidae) at different food supply frequencies from the onset of exogenous feeding under controlled conditions

Considering that the use of decapsulated Artemia cysts as direct food for juvenile crayfish could be an alternative to live nauplii, a 100-day experiment was carried out under controlled conditions to evaluate the effects of cysts, comparing with nauplii, as supplement to a dry diet for salmonids on the survival and growth of juvenile signal crayfish (Pacifastacus leniusculus) from the onset of exogenous feeding (stage 2). The reduction of feeding frequency was also tested. According to a bifactorial design, six treatments, differing in the supplement and feeding frequency, were tested: the dry diet supplemented with Artemia nauplii or decapsulated cysts was supplied once a day, once every two days and once every three days. Survival rates ranged from 56.7% to 81.7%, rising significantly with increasing the feeding frequency. The highest growth (12.94 mm carapace length and 593.08 mg weight) was reached by the crayfish that received the dry diet supplemented with cysts once a day, with significant differences from the rest of the treatments. Considering the supplement, the cysts supported significantly higher growth than the nauplii. Regarding the feeding frequency, growth was higher when the food was supplied once a day, showing significant differences from the other two frequencies (once every two days and once every three days). This study shows that decapsulated cysts are better dietary supplement than live nauplii. In crustacean culture, this is the first report of successful use of Artemia cysts from the onset of exogenous feeding.     

Freeze‐dried forms of mosquito larvae for feeding of Siamese fighting fish (Betta splendens Regan, 1910)

Live diets are preferably used for rearing Siamese fighting fish (Betta splendens Regan, 1910) since they provide superior growth over the dry feed. In the current study, three different preparations of mosquito larvae were prepared (frozen at ?20°C, F–20; freeze‐dried and kept at 4°C, FD4; freeze‐dried and kept at ambient temperature, FDAT) and were individually fed to 1‐month‐old red male fighting fish (1.18 ± 0.01 g initial body weight) over 6 weeks duration. At the end of experiment, there were no significant differences in growth performance and feed utilization across three dietary treatments (p ? 0.05). Specific activity of lipase was significantly lower in fish fed FD4 and FDAT than with the F–20 diet, while no differences in other enzymes were observed. The fish fed with FDAT diet significantly increased in viscerosomatic index relative to F–20 and FD4 treatments. Significant improvements in skin redness and flesh quality (RNA and RNA/protein ratio) were observed in the fish fed with FDAT diet relative to the other treatments. This preferred FDAT treatment also maintained the carcass composition. Analysis of digestive enzymes in FDAT mosquito larvae demonstrated the presence of protein‐, carbohydrate‐, and lipid‐digesting enzymes after 1 month of storage. The findings from our experiments indicate that the freeze‐dried form (FDAT) of mosquito larvae is suitable for rearing Siamese fighting fish. However, effective preparation protocol and appropriate storage times should be further studied.     

Laboratory investigation of daily food intake and gut evacuation in larvae of African catfish <Emphasis Type="Italic">Clarias gariepinus</Emphasis> under different feeding conditions

Temporary accumulation of ascorbic acid 2-sulfate (AAS) was measured to estimate food intake and gut evacuation in larvae of African catfish. Fish larvae were fed decapsulated cysts of Artemia containing AAS. In a first experiment it was found that no biosynthesis of AAS occurs in the larvae of this species. In a second experiment, the gut contents of the fish larvae fed were calculated as they changed during development. In a third experiment, the gut evacuation rate of fish larvae was determined during continuous and discontinuous feeding regimes in the first five days after the start of exogenous feeding. Food consumption by catfish larvae increased from 46.5% of their body dry weight (BDW) on day 1 after the start of exogenous feeding to 53.8% BDW on day 3. Thereafter, food consumption decreased to 27.8% BDW on day 5. A similar pattern was observed for gut evacuation, which increased during the first days of exogenous feeding and decreased as fish growth continued. The rate of gut evacuation in a continuous feeding regime was significantly higher (P < 0.05) than that under discontinuous feeding. On day 1 post-hatch and 7 h after first food ingestion the fish larvae evacuated 87% of the food in continuous feeding compared with 43% under discontinuous feeding. It was found that gut emptying differs during larval development. Under continuous feeding, on days 1 and 3 post-hatch and 11 h after the first meal 90% of the food was evacuated compared with 71% evacuated on day 5. The advantages and limitations of the AAS method for estimation of food consumption by fish larvae are discussed.     

Weaning of bullseye puffer (Sphoeroides annulatus) from live food to microparticulate diets made with decapsulated cysts of Artemia and fishmeal

Two experiments were carried out to test microparticulate diets forweaning hatchery-produced larvae and juveniles of bullseye pufferSphoeroides annulatus. The diets were formulated with differentprotein sources: diet 1 with a combination of decapsulated cysts ofArtemia and fishmeal, and diet 2 with a combination offishmeal, squid, tuna gonad and shrimp meal. In the first experiment60-days-old fish were weaned with the microdiets over five days. Fishsurvival after 11 weeks of feeding was 92% for diet 1, 85%for diet 2, and 95% for the control fish fed Artemianauplii. Once it was determined that bullseye puffer can be adequatelyreared with artificial dry diets, diet 1 was used to test earlier timesfor weaning to reduce the period of Artemia feeding. In thesecond experiment, three different times were tested for initiation ofweaning in sibling fish larvae, i.e., at 29, 34, and 39 days post-hatch.Small differences in weight, length and survival were found amongweaning treatments after 23 days of feeding. When weaned at day 29post-hatch, fish larvae grew from an initial weight of 38.4 mg andlength of 11.1 mm to a final weight and length of 405.7 mg and 25.1 mmrespectively. Final survival in this treatment was 49.3%. Thereduced period of Artemia feeding would provide an economicalalternative for the species to take into consideration for its cultureat commercial scale.     

Development of First-Feeding Protocols for Indoor Larviculture of Largemouth Bass (Micropterus salmoides)

Largemouth bass (LMB) Micropterus salmoides fry do not accept prepared diets at first feeding. Fry are initially reared in fertilized ponds on natural live foods until large enough to be feed trained. Unpredictable weather patterns and depletion of natural forages can affect nursery pond survival. A series of experiments was conducted to investigate the use of Artemia nauplii prepared diets and optimal feeding schedules to raise LMB fry from first feeding through habituation to a commercial dry diet. In Studies 1, 2, and 3, swim-up fry were transferred to a recirculating system and stocked into either 3-L (Studies 1 and 2) or 10-L (Study 3) acrylic aquaria. Study 1 screened candidate diets to evaluate whether LMB fry could be transitioned directly to prepared diets or if they required live foods. In Study 2 the optimum duration for feeding live Artemia (1, 2, or 3 weeks) and the appropriate size of commercial diets (<200 or 200–360 μm) were evaluated. Study 3 was designed to identify the best transitional feed. Results from Study 1 indicate that fry fed Otohime-A (<200 μm) and decapsulated Artemia cysts performed better than those fed other diets tested. However, survivals were low (6%–8%) indicating a need for live feed initially. In Trial 2, fry fed live Artemia nauplii for two weeks and then transitioned to a 200–360 μm diet (Otohime-B) performed better than other diet combinations tested. In Study 3, survival was significantly higher in treatments using decapsulated Artemia cysts or Otohime-B as transitional diets between initial live Artemia feeding and trout starter. These data indicate that LMB fry can be successfully raised from first feeding to fully habituated to a commercial trout starter by feeding live Artemia nauplii for two weeks, followed by a gradual transition to either decapsulated Artemia cysts or Otohime-B for one week, then gradually transitioning to trout starter. Surviving fish were easily transitioned to commercial floating feed (Study 4). This protocol yielded survival rates of approximately 70% and may improve the reliability of LMB fingerling production by eliminating the outdoor nursery pond phase.     

A comparison of artificial and natural foods and their combinations in the rearing of goldfish, Carassius auratus (L.)

Intensive grow‐out of goldfish, Carassius auratus (L.), larvae and juveniles in closed systems requires the control of environmental conditions and feeding. This study investigates the use of different types of live food and combinations of live food and dry food in a series of four rearing experiments. Juvenile goldfish can be weaned from Artemia onto live food at about 24 days after the onset of feeding without causing a reduction in growth and survival. The replacement of Artemia by Daphnia at day 10 appears feasible, as growth and survival were not significantly affected. Fish fed decapsulated Artemia cysts grew better than fish fed live Artemia. Within the first 14 days, goldfish juveniles should be fed at least 155 cysts per fish per day to achieve fast growth and to minimize size variation.     

Post-prandial protease activity in the digestive tract of African catfish Clarias gariepinus larvae fed decapsulated cysts of Artemia

The alkaline proteolytic activity in the gut of African catfish larvae was studied during short time ranges from 30 min to 4 h after ingestion of decapsulated Artemia cysts. The variation in total protease and trypsin activities during the day was monitored during starvation, after one single meal ingestion, and during continuous feeding. In starved larvae the enzymatic activity was low and did not change in time. No significant endogenous secretion of digestive enzymes was detected. The level of alkaline proteolytic activity found in starved larvae was further considered as the basal level. In larvae fed only one meal during the day, the enzyme activity significantly increased from 3 h post-feeding up to a maximum level found 12 h after feeding. In the larvae receiving a meal every 4 h, the effect of feeding on the proteolytic activity was significantly different from the one in fish fed only once a day. The total protease activity in this dietary treatment changed according to the time of feeding and fluctuated around a constant level, which was intermediate between the maximum and the basal level. No rhythmic cycle of enzyme production in the fish was observed when the proteolytic activity was studied during a cycle of 24 h. When specific trypsin activity was measured, a similar pattern was found as with the total protease. The contribution of digestive enzymes from Artemia to the total digestion of food by the catfish larvae was calculated to be less than 1% of the total amount of the proteolytic activity measured in the larval gut.     

Optimal dietary lipid level for large yellow croaker (Pseudosciaena crocea) larvae

A 30‐day feeding experiment was conducted in blue tanks (70 × 50 × 60 cm, water volume 180 L) to determine the effects of dietary lipid levels on the survival, growth and body composition of large yellow croaker (Pseudosciaena crocea) larvae (12 days after hatchery, with initial average weight 1.93 ± 0.11 mg). Five practical microdiets, containing 83 g kg^?1 (Diet 1), 126 g kg^?1 (Diet 2), 164 g kg^?1 (Diet 3), 204 g kg^?1 (Diet 4) and 248 g kg^?1 lipid (Diet 5), were formulated. Live feeds (Artemia sinicia nauplii and live copepods) were used as the control diet (Diet 6). Each diet was randomly assigned to triplicate groups of tanks, and each tank was stocked with 3500 larvae. During the experiment, water temperature was maintained at 23(±1) °C, pH 8.0 (±0.2) and salinity 25 (±2) g L^?1. The results showed that dietary lipid significantly influenced the survival and growth of large yellow croaker larvae. Survival increased with the increase of dietary lipid from 83 to 164 g kg^?1, and then decreased. The survival of larvae fed the diet with 83 g kg^?1 lipid (16.1%) was significantly lower than that of larvae fed other diets. However, the survival in larvae fed the diet with 16.4 g kg^?1 lipid was the highest compared with other artificial microdiets. Specific growth rate (SGR) significantly increased with increasing dietary lipid level from 83 to 164 g kg^?1 (P < 0.05), and then decreased. The SGR in larvae fed the diet with 164 g kg^?1 lipid (10.0% per day) was comparable with 204 g kg^?1 lipid (9.6% per day), but were significantly higher than other microdiets (P < 0.05). On the basis of survival and SGR, the optimum dietary lipid level was estimated to be 172 and 177 g kg^?1 of diet using second‐order polynomial regression analysis respectively.     

Effect of vitamin E and highly unsaturated fatty acid-enriched Artemia urmiana on growth performance, survival and stress resistance of Beluga (Huso huso) larvae

A 44-day rearing trial was conducted to examine the enrichment of Artemia urmiana nauplii with vitamin E and highly unsaturated fatty acid (HUFA) and its effects on the growth performance, survival and stress resistance of great sturgeon, Huso huso , larvae. Cod liver oil (EPA 18% and DHA 12%) and α-tocopherol acetate were used as lipid and vitamin E sources. Beluga larvae at the first exogenous feeding with 69±5.9 mg body weight were randomly distributed into four treatments and three tanks were assigned to each diet. The test treatments were as follows: larvae fed with HUFA+20% and HUFA+50% (w/w) vitamin E-enriched Artemia nauplii (E1 and E2 groups, respectively), HUFA without vitamin E (HUFA group) and non-enriched Artemia (control group). All treatments fed non-enriched Artemia for the initial 5 days after first feeding and then fed enriched Artemia for 7 days. After the period of enrichment, larvae were fed with daphnia from the 13th to the 40th day. At day 40, submersion in salt water (6 ppt for 4 days and 12 ppt for 2 days) and warm water (33 °C for 2 days) was performed to evaluate larvae resistance to salinity and temperature stress. Final weight, daily growth rate, specific growth rate and weight gain were higher in beluga fed with enriched Artemia . The highest growth rates were observed in E1, whereas survival was not significantly different between groups. Use of vitamin E and HUFA significantly increased fish resistance to a salinity of 12 ppt and the lowest stress resistance was observed in the control group. Stress tolerance was not significantly different at 6 ppt and 33 °C between groups. There was no comparable difference in the haematocrit index under stress conditions. These results indicated that the enrichment of Artemia with essential fatty acids and vitamin E can affect some growth and stress tolerance factors in great sturgeon, Huso huso , larvae.     

Evaluation of Protein Quality in Microbound Starter Diets Made with Decapsulated Cysts of Artemia and Fishmeal for Fish Larvae

Abstract.— The protein quality of carboxymethylcellulose microbound diets (MBDs) made with decapsulated cysts of Artemia andlor fishmeal as protein sources was used as an indicator of their suitability as starter feed for fish larvae. Studies on the proximate, fatty acid and amino acid composition. in vitro protein digestibility. diet solubility, and protein structure were combined with an in vivo feeding experiment with African catfish Clarias gariepinus larvae to evaluate the protein quality of the MBDs and a commercial diet. The growth of catfish larvae was higher when fed Artemia -based MBDs than with fishmeal-based MBDs, despite the higher protein and amino acid content of the latter. The in vitro protein digestibility was high for all the MBDs in comparison to a commercial diet. Differences were found in the protein molecular weight among the diets. Most of the proteins in the fishmeal-based diets had low molecular weight in the range between 7.4 and 49.2 kDa. The Artemia-based MBDs had larger protein fractions between 29.4 and 82 kDa. Decapsulated cysts improved the utilization of the MBDs when used in combination with fishmeal. Besides the effect of chemical attractants, the explanation for the positive effect of Artemia has yet to be elucidated. However, attention should be given to interactions between nutrients (e.g., protein-lipid) in live food, which might have an effect on the functional properties of food proteins.     

Use of decapsulated Artemia cysts in ornamental fish culture

Two series of feeding experiments were conducted to study the feasibility of using decapsulated Artemia cysts for direct feeding to ornamental fish. The first series evaluated the dietary values of the dried and the brine decapsulated Artemia cysts against two conventional live feeds, Artemia nauplii and Moina for adults and fry of the guppy, Poecilia reticulata Peters. In the second series, brine cysts were used for feeding to fry of four other important ornamental fish species, viz. platy, Xiphophorus maculatus (Günther), swordtail, X. helleri (Heckel), molly, P. sphenops Cuvier & Valenciennes and black neon tetra, Hyphessobrycon herbertaxelrodi Géry, and the results were compared with those fed Moina. Evaluation of the performance of the fish fed the various diets was based on stress resistance, growth and survival of the fish. Our findings indicated that decapsulated cysts could be used as a substitute for Artemia nauplii or Moina in freshwater ornamental fish culture. Apart from being a hygienic off‐the‐shelf feed, the direct use of the cysts also signifies a new area of application for low‐hatch cysts in the ornamental fish industry, with concomitant saving in feed costs.     

Heat treatment affects protein quality and protease activity in decapsulated cysts of Artemia when used as starter food for larvae of African catfish Clarias gariepinus (Burchell)

Decapsulated cysts of Artemia subjected to different heat treatments (40, 60, 80 and 96 °C) were fed to African catfish Clarias gariepinus larvae. Heated cysts, untreated cysts and live Artemia nauplii as control constituted the experimental diets. Protein denaturation and solubility, total alkaline protease and specific trypsin activities in the cyst diets were evaluated. The growth of catfish larvae and the proteolytic activity of larval samples during development were also determined. Heat treatment of cysts increased protein denaturation and decreased protein solubility. The protease activity in the cyst diets decreased with higher heating temperatures. The growth of catfish larvae differed according to the diet; higher fish growth was achieved with nauplii and cysts heated at 40 °C. The digestive enzyme activity in larval samples remained similar in all dietary treatments during larval development. The quality of food protein and the way this protein is processed might be more important for successful larval growth than exogenous enzyme supply.     

Growth performance,immunity and intestinal microbiota of swamp eel (Monopterus albus) fed a diet supplemented with house fly larvae (Musca domestica)

Housefly larvae are widely used in livestock breeding industry as a functional feed additive with immunostimulant properties, but their effects as dietary additive are poorly understood in aquatic animals. We conducted an eight‐week rearing experiment to determine the effects of housefly larvae (complete) on growth performance, immunity and intestinal microbiota in swamp eel (Monopterus albus). Dietary treatments were as follows: BD (control group, fed a basal diet), FL7 (fly larvae supplemented once weekly, i.e., 6‐day basal diet, 1‐day larvae) and FL3 (larvae supplemented every third day, i.e., 2‐day basal diet, 1‐day larvae). The final body weight (FBW) and weight gain (WG) of the FL3 group significantly (p < .05) increased. Hepatosomatic index (HSI) and malondialdehyde (MDA) concentration significantly decreased in FL3 and FL7 groups. The expression of immune‐related genes was also influenced by the fly larvae. Aeromonas hydrophila challenge experiment produced higher survival rates in the FL3 (75%) and FL7 (37.5%) groups. Fly larvae also affected the composition of gut microbiota: the abundance of Bacteroides increased, and Pseudomonas decreased, in the treatment groups. Dietary supplementation of housefly larvae has positive effects on the growth and immunity of swamp eel, and we suggest supplementing housefly larvae every third day.     

Response of common carp (Cyprinus carpio) larvae to different dietary levels and forms of supply of medium-chain fatty acids

The effects of dietary medium-chain fatty acids (MCFA) on survival, growth and fatty acid composition of first-feeding carp larvae were investigated in two 21-day feeding trials. In trial 1, one diet CO was supplemented with 10% coconut oil, two diets, M1 and M2 with 1.7 or 4.2% interesterified medium-chain triacylglycerols (MCT), and two other diets T1 and T2 with 1% tricaprylin and 0.7% tricaprin, or 2.5% tricaprylin and 1.7% tricaprin. The five diets were made isolipidic (18% of dry diet) with triolein and compared to a control diet without MCFA. With a low dietary level (1% of dry diet) of caprylic acid (C8:0), final survival and mean weight of larvae fed CO, M1 and T1 were not significantly different from those of control (68 ± 6% and 62 ± 8 mg, respectively). In contrast, with a high dietary C8:0 level (2.5% of dry diet), final survival and mean weight of larvae fed M2 and T2 were markedly decreased (23 ± 2% and 40 ± 8 mg, respectively), without effect of the form of supply. In trial 2, larvae were fed six diets with graded tricaprylin contents (from 0 to 10% in diet). Survival was not significantly affected but growth was decreased by C8:0 levels higher than 2% of dry diet. Fatty acid composition of larval total lipids revealed high levels of lauric and myristic acids in larvae fed coconut oil. Deposition of C8:0 and capric acid (C10:0) was low after MCT feeding, but depended of the form of supply, being higher with pure than with interesterified MCT. Relatively high amounts of C8:0 and C10:0 were recorded in total lipids of larvae fed 10% tricaprylin. It is concluded that high levels of caprylic acid decrease growth but that low levels are well utilised by carp larvae, irrespective of the form of supply.