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Summary The growth of river catfish Mystus nemurus (Cuvier & Valenciennes) larvae fed four isocaloric diets (4200 kcal kg−1) with different protein levels during weaning was determined. Diets containing 45, 50, 55, and 60% protein were formulated by linear programming using amino acid profiles based on that of 2‐day‐old river catfish larvae. Artificial diets were fed to the larvae beginning at day 5 after being initially fed Artemia nauplii for 4 days. The larvae thrived solely on artificial diets from day 8 to day 16. On the other hand, the control larvae were fed Artemia nauplii from day 1 to day 16. Results of the feeding trial showed that growth and survival of M. nemurus larvae given the diet containing 60% protein were high and comparable to those of the larvae given only live food (control). Larvae fed the 55% protein diet had significantly lower growth and survival than the larvae on the control and 60% diets but significantly higher growth and survival rates than did larvae fed with 45 and 50% protein diets. Carcass moisture and total lipids after 16 days of feeding did not differ significantly (P > 0.05), but body protein increased with increasing dietary protein. Body protein of the control larvae was similar to that of larvae given the 60% protein diet.

Growth of three strains of Oreochromis niloticus L. fry exposed to salinity stress in the presence of an internal reference fish were compared. The Central Luzon State University (CLSU) strain was obtained from the Freshwater Aquaculture Center, CLSU, Philippines. The ISRAEL strain was acquired from the Philippine government's Bureau of Fisheries and Aquatic Resources National Freshwater Fisheries Technology Center (BFAR‐NFFTC), Munoz, Nueva Ecija. The National Inland Fisheries Institute (NIFI) strain was obtained from the NIFI, Bangkok, Thailand. Eight to nine full‐sib families (replicates) per strain were split into two groups. One group was grown in freshwater for 2 weeks, acclimated to 32 ppt and reared for 2 weeks and finally grown in freshwater for another 2 weeks. Another group was contemporaneously grown in freshwater polyethylene tanks for 6 weeks. Each replicate family included a size‐matched internal reference population of red tilapia strain. Two‐way analysis of variance (anova) revealed no significant strain differences (P=0.081; r2=0.106). However, analysis of covariance with the internal reference strain used as a covariate showed significant (P=0.049; r2=0.638) strain effects on specific growth (based on standard length measurements). The ISRAEL strain showed consistently better growth rate in both saline and freshwater environments than the NIFI and CLSU strains. We estimated the statistical power of the two‐way anova (ϕ=√(k′−1)(factor MS−s2)/(k′s2); Zar 1984) to be ∼0.30. There was a 70% probability of a Type II error and no true difference in the growth of the three strains was detected. The use of internal reference strain as a covariate improved the r2 from 0.106 to 0.638 and increased the efficiency of the test in detecting a true difference. Other strain comparison studies in our laboratory at the Southeast Asian Fisheries Development Center Aquaculture Department showed that the ISRAEL strain shows better growth than the NIFI and CLSU strains in a crowding stress tolerance experiment, when fed only with rice bran and under restrictive feeding regimes.

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