1. Introduction
Successful rearing of larval fish is the most critical stage in the production cycle for many species. Heros severus (Heckel) is a freshwater tropical cichlid native to the Amazon region in South America and Singapore in Southeast Asia [1] . Since no artificial feed formulation is yet available to completely substitute for Artemia (Leach), feeding live prey to young fish larvae still remains essential in commercial hatchery operations [2] .
The use of Artemia (Leach) nauplii is well established due to its many advantages: year-round availability as on-the shelf cysts; good nutritional value for some fish; and relatively easy improvement through simple enrich- ment techniques [3] . Nutritional deficiencies have been another concern when using brine shrimp. Some stocks of Artemia (Leach) nauplii have shown a deficiency in eicosapantaenoic acid (EPA; 20:5n-3) and doccosahexanoic acid (DHA; 22:6n-3) [4] . The essential fatty acids (EFA) for fish are broadly recognized to comprise polyunsaturated fatty acids (PUFA) with carbon chain lengths of 18 and HUFA with carbon chain lengths of 20 and 22, of both the n-3 and n-6 series. Hence, these fatty acids must be provided in the diet to meet the fish’s requirements. Several studies have demonstrated the positive effect of enriched live food on the growth, survival performance of various aquaculture species [5] - [7] . Also use of Artemia (Leach) enriched with long-chain unsaturated fatty acids for larvae and fry develops non-specific mechanisms of fish immunity and increases their resistance to diseases and environmental stresses. Gapasin et al. [5] studied effect of live food enriched with fatty acid on fish (Chanos chanos (Forsskål)) and their role in increasing the stress resistance of larvae and Ashraf et al. [8] considered effect of enriched diet with fatty acids on the survival rate and salinity stress on the fish side Silverstein (Menidia beryllina (Cope)). Also in Iran, Noori et al. [7] studied the effect of enriched Artemia (Leach) with fatty acids on the resistance to salinity stress in Iranian stergeon fish, Acipencer persicus, (Borodin). Also, Sorgent et al. [9] reported that in freshwater fish, linolenic acid and linoleic acid are more than saltwater fish [9] .
The name “canola” was chosen by the board of the Rapeseed Association of Canada in the 1970s. The “can” part stands for Canada and “ola” refers to oil. Canola was developed through conventional plant breeding from rapeseed. Rapeseed is the highest-producing oil seed crop in the United States. The major customers of canola seed are Japan, Mexico, China, and Pakistan, while the bulk of canola oil and meal goes to the United States, with smaller amounts shipped to Mexico, China, and Europe [10] .
The objective of this study was to investigate canola oil in enhancing severum larval growth, survival and resistance to environmental stresses of temperature and oxygen deficiency and fatty acid composition temperature stress (up 24˚C).
2. Material and Methods
2.1. Fish
In July 2011, severum, Heros severus (Heckel), larvae at the first feeding stage (swim up) were purchased from Spanta Co., Mahyana Ryapars, Iran, and transferred in the Fisheries Laboratory, Department of Natural Resources, Isfahan University of Technology. 480 uniformly sized yolk-sac larvae (3 mg ± 0.83) were randomly divided into 6 groups (two treatments, three replicates) of 80 individuals. Fishes of each group were transferred in to a 35 liter tank. Aeration was applied through a number of narrow pipes terminating to bubbliers. Culture tanks were cleaned daily, and physic-chemical parameters were measured every morning prior to feeding. Water quality was maintained within optimum range: temperature (27.1˚C ± 1˚C), dissolved oxygen (5.76 ± 0.96 mg/L), pH (8.43 ± 0.59), total ammonia (0.02 mg/L), total hardness (165 ± 8 mg/L Caco3) and the photoperiod was set at 12L: 12D cycle (light period from 8 - 20 hours) and light intensity was kept at 40 lux at the tank surface. Dead larvae were removed twice daily and counted.
2.2. Hatching and Enrichment of Artemia (Leach) Nauplii
Artemia cysts (Urmia Lake, Iran) were hatched following standard procedures [11] [12] . Newly hatched Artemia (Instar I) nauplii (200,000 nauplii/L) were divided in batches in 5 L plexiglass tanks. The enrichment protocol followed the method of Clawson and Lovell [13] . 0.5 g of lecithin was dissolved in 100 ml 50˚C water and then 5 g canola oil was mixed it. It was homogenized using a blender and stored in the refrigerator for 1 week. 0.5 mL of the enrichment suspension (assuming a density of 200 Artemia per mL) was added per liter to the incubation water at the onset of the enrichment period. Another 0.5 ml/L of the enrichment diet was added 12 hours before harvesting and nauplii were harvested after 24 hours [14] . Newly hatched Artemia nauplii served as the control [3] .
2.3. Treatments
After 7 days of acclimation to the condition, fish were divided in two treatments (in a completely randomized design with 3 replicates per treatment) were: 1) larvae fed newly hatched Artemia nauplii and 2) larvae fed canola oil enriched Artemia nauplii. The fish larvae in all treatments were fed 4 times per day for 18 days. Then all groups of fish were switched to the commercial diet for an additional period of 18 days.
2.4. Sampling
Feeding was stopped six hours prior to sampling fish for chemical analysis, survival and growth measurement on days 18 and 36. All fish from each replicate were harvested at weekly intervals, bulk-weighted and the total length (TL) was taken. The amount of feed given per group was recorded and used to calculate feed conversion ratios (FCR) [15] . Ninety fish per treatment (30 fish per replicate tank) and 3 replicate of enriched and unenriched Artemia nauplii (200 thousand Artemia nauplii for each replicate) were randomly collected on days 7 and 28. Samples were oven-dried at 60˚C for 24 h then stored at −20˚C. These dried samples were later analyzed for fatty acid methyl esters [16] , using gas chromatography (GC) (Agilent 6890N). Results were expressed as % total body dry weight. Also the number of surviving fish was recorded and used for calculating mortality. At the end of feeding trial all fish each tank were taken and their weights and lengths were measured. Specific growth rates (SGR), feed conversion ratios (FCR) and survival rate were calculated as following:
SGR =100 × (Ln final weight − Ln initial weight)/day [17]
FCR = feed intake (g)/weight gain (g) [15]
Survival = 100 × (initial fish number − dead fish number)/(initial fish number)
2.5. Resistance to Environmental Stresses
Thirty severum larvae were subjected to temperature stress test following the method described by [18] [19] . The test involved immersing fish, 10 fish larvae/replicate in 34˚C (as high temperature) and 16˚C (as low temperature) for a period of one hour. Sixty severum larvae (20 larvae/replicate) of each treatment were exposed for 2 and 5 min under low oxygen tension [18] [19] . The mortality was recorded at every 1 h interval sup to 24 h.
2.6. Statistical Analysis
At the end of the experiment the number of surviving fish was recorded and used for calculating mortality. Diet effects on total length, SGR, FCR, survival, weight, and environmental stress were analyzed using independent T test at confidence level 5% (P = 0.05) (SPSS version 9).
3. Results
Fatty acid contents of newly hatched and enriched Artemia are shown in Table 1. The individual fatty acid levels of linolenic (w3) and linoleic (w6) acid were consistently higher in the canola oilenriched nauplii than in the newly hatched nauplii. The HUFA and EPA levels (2.15% and 2.15% ± 0.07) were highest in newly Artemianauplii.
Fatty acid content of severum larvae is shown in Table 2. The EPA (3.37% ± 0.07%) level in treatment 1 was generally high compared to treatment 2 (2.8% ± 0.25%). The PUFA level was significantly different in all treat- ments (P < 0.05), with highest PUFA observed in treatment 2 (P < 0.05). The HUFA level was high in treatment 1 (Table 2).
Fatty acid content of canola oil is shown in Table 3. The linoleic (18:2n-6) and linolenic acid (18:3n-3) levels in canola oil were generally high compared to EPA and DHA. The HUFA level was zero in canola oil.
Severum fedwith Artemia enriched with canola oil (treatment 2) exhibited significantly higher (P < 0.05) growth compared to treatment 1 (fed newly Artemia nauplii) after 18 and 36 days of culture (Table 4). After 36 days of culture, survival significantly differed among the treatments (P < 0.05). The highest survival was observed in treatment 1 (Table 4).
When 36-day-old severum were subjected to temperature stress, mortality rate of the severum fed with Artemia
Table 1. Certain fatty acids (%) of newly Artemia nauplii (A), Artemia enriched with canola oil (B).
Values in each row with different superscripts are significantly different (P < 0.05). Data are mean ± SD (n = 3); SFA = saturated fatty acid; USFA = unsaturated fatty acid; HUFA = highly unsaturated fatty acid and PUFA = poly unsaturated acid; tr = trace.
Table 2. Whole-body fatty acid composition (%) of 18-day old severum larvae fed of different diets.
Values in each row with different superscripts are significantly different (P < 0.05). Treatment 1: severum larvae fed with newly Artemianauplii; Treatment 2: severum larvae fed with Artemia enriched with canola oil; Tr = trace.
Table 3. Certain fatty acids (%) of canola oil.
Table 4. Average total weight and lengtha, Specific growth rate (SGR), food conversion ratio (FCR) and percent survival of fish fed various dietary treatments. Values are mean ± standard deviation (n = 10).
Within columns values with different superscripts are significantly different (P < 0.05). aInitial weights and lengths of severum larvae 3 (mg) ± 0.83 SD and 6.82 (mm) ± 0.83 SD respectively.
enriched with canola oil (treatment 2) and newly Artemia nauplii (treatment 1) was no significant difference (P > 0.05) in temperature 16˚C and 34˚C (Table 5). The highest mortality was observed in treatment 1. When 36- days-old severum were exposed to oxygen deficiency (5 min), the survival rate was significantly high (P < 0.05) in treatment 2 (75.62% ± 0.66%) compared to treatment 1 (47.5% ± 1.42%) after 24 h (Table 5).
4. Discussion
Several studies have demonstrated the positive effect of enriched live food on the growth performance of various species. HUFA-enriched Artemia nauplii fed to Fenneropenaeus indicus (H. Milne-Edwards), [20] , Sepia
Table 5. Results of temperature stress (34˚C and 16˚C) and oxygen deficiency (2 and 5 min) on mortality rates of different treatments in 36-day-old severum.
Within columns values with different superscripts are significantly different (P < 0.05).
oficinalis (Linnaeus) [17] , and Chanos chanos (Forsskål) [5] exhibited better growth and survival. Gilthead sea bream larvae also grow better if fed rotifers enriched with highly unsaturated n-3 HUFA [21] . Similar to the finding of Tamaru et al. and Hosseinpour et al. [22] in the present study significant differences were found in the growth of severum larvae fed different diets, larvae fed Artemia enriched with canola oil (treatment 2) exhibited significantly higher growth than larvae fed unenriched nauplii (treatment 1) after 36 days of culture (Table 4). Tamaru (1998) used Artemia nauplii enriched with different oils for the production of ornamental fish and significant influences obtained on the growth and survival (P < 0.05). Smith et al. [23] with research on essential fatty acids in the diet Bidyanus bidyanus reported that linolenic acid in the diet increased fish growth rate.
On the other hand, survival of 36 days-old severum fed various diets was significantly different (Table 4). Mortality of the canola oil treated fish was significantly lower than unenriched nauplii fed fish supporting the results of Limanda ferruginea (D. H. Storer) [24] , Peterophylum scalare (Schultze) [25] and Oncorhynchus mykiss (Walbaum) [26] . Akbary et al. [26] concluded that survival rate of rainbow trout larvae fed with enriched Artemia (HUFA + vitamin C) during 29 days of testing (96%) is higher than larvae fed unenriched nauplii (84%) and larvae were fed with commercial food (67%). In the current investigation, the larvae fed by canola oil for 18 days exhibited more resistance to oxygen deficiency (Table 5), compared to treatment 1. When subjected to temperature stress test, 36 days old Heros severus larvae fed canola oil Artemia exhibited no significant difference with larvae fed uneriched nauplii. The mortality in larvae fed enriched Artemia was lower than control Due to the high levels of linolenic acid in treatment 2 supporting the results of Smith et al. [23] , Kiron et al. [4] . [4] reported that n-3 fatty acids are important precursors in the synthesis eicozanoids that is an important mediator in inflammatory reactions and immune responses. When dietary have a deficiency of essential fatty acid n-3, antibacterial activity of macrophage cells is reduced. If macrophages receive linolenic acid, their bactericidal ability will rise. Van Stappen [27] reported that freshwater species would need to the fatty acids linolenic and linoleic and Marine fish species would need to EPA and DHA.
Milkfish larvae given Artemia enriched with HUFA + vitamin C showed better growth and higher survival after a stress test [5] . Ako et al. [18] , Gapasin et al. [5] observed no or few mortalities among fish fed Artemia enriched with menhaden oil (high DHA:EPA ratio) compared to high mortalities among fish fed unenriched Artemia. Red sea bream, Pagrus major, (Temminck & Schlegel) and marble sole Euryglossa orientalis, (Bloch & Schneider) larvae given diets containing DHA and lecithin tolerated temperature and salinity changes, low oxygen and air exposure better than the larvae given DHA and lecithin-free diets [28] . Furuita et al. [29] reported that yellowtail larvae and red sea bream juvenile fed Artemia enriched with DHA exhibited higher survival in the stress test than those fed Artemia enriched with EPA. In the present study, severum larvae fed Artemia enriched with canola oil (Treatment 2) showed better growth and increased resistance to oxygen deficiency than those given unenriched diet (treatment 1). This result is similar to Chanos chanos [5] Sepia officicinalis [17] .
The preceding studies attest the importance of EFA and in fish growth and development. Severum fed with canola oil exhibited significantly (P < 0.05) higher growth than those given unenriched live food after 36 days of culture. When subjected to oxygen deficiency, mortality of the canola oil treated fish was significantly lower (P < 0.05) among the treatment groups. Optimum requirements of these nutrients in severum, however, are not yet known, using of Artemia enriched with long chain polyunsaturated fatty acids in proliferation centers of ornamental fish can increase fish resistance against stress-induced changes in environmental conditions.
Acknowledgements
The author thanks of the Shahidetebari Research Institute Isfahan University of technology for the financial support of this project.
NOTES
*Corresponding author.