化學分析前,先將樣品120℃蒸壓20 min,混合均勻后105℃干燥24 h。飼料原料、飼料和全魚樣品的水分、粗蛋白、粗脂肪和灰分的測定方法詳見參考文獻(Wang等, 2006)。用Sykam-433氨基酸分析儀(Sykam Company with Limited Liability, Munich, Germany)測定飼料和全魚樣品的氨基酸含量,用Parr-6200熱量計測定(Parr Instrument Company, Moline, IL, USA)測定飼料和全魚樣品的總能。
養殖試驗魚均未出現死亡,PM5組攝食量比對照組、PM1和PM2組高(HSD test, P < 0.05, 見表4)。PM1、PM2、PM3和PM4各組間試驗魚末重和增重無顯著性差異(HSD test, P > 0.05),但比對照組和PM5組高(HSD test, P < 0.05),對照組和PM5組間亦無顯著性差異(HSD test, P > 0.05)。特定生長率和飼料魚粉添加水平的多項方程式為:SGR=?10?5×FL2+0.004×FL+3.091(R2 = 0.85, n = 18, P < 0.05, 見圖1),結果表明當飼料中魚粉添加水平為200 g/kg時,日本海鱸的特定生長率最大。
。ㄔ模篧ang Y, Wang F, Ji W X, et al. Optimizing dietary protein sources for Japanese sea bass (Lateolabrax japonicus) with an emphasis on using poultry by‐product meal to substitute fish meal[J]. Aquaculture Research, 2013.)