施氏鲟幼鱼对饲料中部分营养素的需求与利用研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
施氏鲟(Acipenser schrenckii)是目前世界上现存的27种鲟鱼之一,具有个体大、病害少、生长速度快、肉质鲜美等特点。近年来,施氏鲟养殖在我国迅速发展,已形成了较大养殖规模,产业前景广阔。但关于施氏鲟的营养与饲料研究非常有限,仅涉及蛋白质、脂肪等少数几种营养素的需求和部分脂肪源的评价,本文研究了施氏鲟幼鱼对饲料中磷、维生素A、维生素E和维生素C的需要量以及不同糖源、脂肪源和共轭亚油酸对施氏鲟幼鱼的营养生理作用,为该鱼的配合饲料配制提供依据。具体研究内容和结果如下:
     1.施氏鲟幼鱼对磷需要量的研究
     以Ca(H_2PO_4)_2·H_2O为磷源,配制含磷水平分别为0.18%(对照组),0.40%,0.71%,0.98%,1.38%和1.66%的6组等能等氮纯化饲料,每组饲料饲喂3个重复,每个重复饲养20尾初始体质量约为4.7g的幼鱼。经过8周的饲养后,对生长、饲料效率、成活率、幼鱼肌肉常规组成及脊椎骨灰分和钙磷含量进行分析。结果表明,随饲料中磷含量的升高,鱼体增重率、饲料效率和特定生长率显著增加(P<0.05),直至0.98%组达最大,然后随着饲料磷含量的增加,这些指标显著降低(P<0.05);试验各添加组的成活率显著高于对照组(P<0.05),但各添加组间没有显著差异(P>0.05);饲料添加磷对鱼体肌肉水分、粗蛋白质和粗脂肪含量无显著影响(P>0.05);当饲料磷含量在0.71%~1.66%之间时,脊椎骨中灰分、钙和磷含量差异不显著(P>0.05),但显著高于对照组和0.40%试验组(P<0.05)。经过折线回归分析得出,为维持施氏鲟幼鱼最佳生长和骨骼磷水平,饲料中磷的需要量为0.88%~1.00%(占干饲料)。
     2.施氏鲟幼鱼对维生素A需要量的研究
     试验以酪蛋白和脱脂豆粕为蛋白源,糊精为糖源,玉米油和豆油为脂肪源的半纯化饲料为基础饲料。试验饲料中的维生素A共设7个梯度,分别为:10(对照组)、258、510、1050、2020、4100和8300 IU/kg。每一梯度设3个重复,每个重复放养20尾初始体质量为12.09±0.22 g的施氏鲟,养殖8周,研究维生素A对施氏鲟幼鱼生长性能、肌肉组成、肝脏和肌肉中维生素A积累量、血清过氧化物歧化酶(SOD)和溶菌酶活性的影响。结果表明:用对照组饲料饲喂的试验鱼表现出厌食、游动迟缓的缺乏症状,其它各组则未出现这些症状;饲料中维生素A含量对增重率、饲料效率、肝体指数影响显著(P<0.05),且在1050 IU/kg组时,各值均达到最高值;肌肉成分不受维生素A含量影响;当饲料中维生素A含量在10~4100 IU/kg时,肌肉和肝脏中的维生素A含量随饲料中维生素A增加而增加,但饲料中维生素A含量超过4100IU/kg时,这些指标不再增加;血清中溶菌酶和SOD活力都随维生素A的增加而增加,在1050IU/kg组,这两种酶的活力均达最高,而高于此浓度时(>1050IU/kg),酶活力出现降低趋势。对饲料中维生素A含量和施氏鲟增重率进行折线回归,施氏鲟获得最佳生长时,饲料中维生素A最低需求量为923 IU/kg。
     3.施氏鲟幼鱼对维生素E需要量的研究
     以酪蛋白、明胶和白鱼粉为蛋白源,配制成7组半纯化试验饲料,饲料中维生素E添加量分别为0(对照组)、20、50、100、200、500和1000mg/kg,每一梯度设3个重复,投喂体质量为10.10±0.31g的施氏鲟幼鱼8周,考察不同维生素E添加量对幼鱼生长及组织维生素E含量的影响,并确定施氏鲟幼鱼对维生素E的需要量。结果表明,随着饲料中维生素E添加量的增加,幼鱼的增重率、饲料效率、特定生长率、存活率和肥满度显著增加(P<0.05),当饲料中维生素E添加量为200mg/kg时,这些指标达到最高水平,随维生素E添加量的进一步增加,其增重率、饲料效率、肥满度又显著降低(P<0.05),而特定生长率差异不显著(P>0.05);对照组幼鱼肝体指数显著高于各添加组(P<0.05)。肌肉和肝脏中维生素E水平随饲料维生素E添加量的增加而显著上升(P<0.05),当添加量≥100mg/kg时,肝脏中维生素E水平无显著变化(P>0.05),同时当添加量≥200mg/kg时,肌肉中维生素E水平也无显著变化(P>0.05);对照组幼鱼肌肉中粗脂肪含量显著高于各添加组(P<0.05),而饲料中添加维生素E≥100mg/kg时,肌肉中粗蛋白质含量较对照组有显著提高(P<0.05)。对特定生长率与饲料中维生素E水平进行折线回归分析得出施氏鲟幼鱼对饲料中维生素E的需要量为187.4mg/kg。
     4.施氏鲟幼鱼对维生素C需要量的研究
     以包膜维生素C为维生素C源,配制8种维生素C水平(0.1,58.2,110.4,221.8,350.2,475.6,698.4和906.2 mg/kg)的试验饲料,每一饲料设3个重复,每重复放养10尾初始体质量为7.25±0.33g施氏鲟,养殖8周。结果显示:8周试验期间,各组试验鱼没有维生素C缺乏症状出现,存活率均为100%;维生素C对施氏鲟的生长影响显著(P<0.05),饲料维生素C从0.1mg/kg升到110.4mg/kg时,施氏鲟的增重率和特定生长率显著升高,饲料系数显著降低,但饲料维生素C超过110.4mg/kg,施氏鲟增重率、特定生长率和饲料系数变化不显著;饲料维生素C不超过221.8mg/kg时,肝脏、肌肉中的维生素C含量和血清溶菌酶的活性随饲料维生素C含量增加而增加;血清皮质醇浓度随饲料维生素C增加而显著降低。饲料中维生素C含量对特定生长率和肝脏中维生素C含量进行折线回归法分析,维持施氏鲟幼鱼最佳生长的饲料维生素C含量为110.4mg/kg;肝脏中维生素C含量达最大时饲料维生素C需要量为239.7mg/kg。
     5.不同糖源对施氏鲟幼鱼生长和部分生理生化指标的影响
     以葡萄糖、果糖、麦芽糖、蔗糖,糊精、α-淀粉和玉米淀粉为糖源,分别配制含22%的7组等氮等能的试验饲料,每组饲料设3个平行,每个平行放养20尾初始体质量为4.70±0.08g的幼鱼,饲养8周,研究不同糖源对施氏鲟幼鱼生长性能及血糖、肝糖原和消化道内淀粉酶活性等生理生化指标的影响。结果表明:不同糖源对施氏鲟幼鱼的增重率、特定生长率和饲料效率有显著影响(P<0.05),各组增重率依次为糊精、α-淀粉>葡萄糖、玉米淀粉>麦芽糖>蔗糖、果糖;特定生长率和饲料效率的变化规律和增重率类似;糖源对幼鱼的蛋白质和糖的消化率影响显著(P<0.05),各组蛋白质消化率依次为果糖>葡萄糖、麦芽糖、糊精>玉米淀粉>α-淀粉,糖的消化率依次为果糖、葡萄糖>麦芽糖>糊精>α-淀粉>玉米淀粉;不同糖源对施氏鲟幼鱼肌肉中的水分、粗脂肪和灰分含量有显著影响(P<0.05),对粗蛋白质含量无显著影响(P>0.05);不同糖源对幼鱼在饱食后的不同时间段血糖和肝糖原含量影响显著(P<0.05);在饱食后的不同时间点内,各组的胃淀粉酶活性均为先上升后下降,瓣肠的淀粉酶活性为先升高后降低再升高后降低,十二指肠淀粉酶活性为先下降后上升再下降,各组的淀粉酶活性均受糖源的显著影响(P<0.05),在肝脏中未检出淀粉酶活性。以增重率和特定生长率为参考指标,施氏鲟幼鱼饲料中适宜的添加糖源为糊精和α-淀粉。
     6.不同脂肪源对施氏鲟幼鱼生长、血脂和体脂肪酸的影响
     在饲料中分别添加10%的7种不同来源的脂肪(鱼油、葵花油、牛油、猪油、菜籽油、玉米油和大豆油),饲养初始体质量约为9.83 g的施氏鲟幼鱼8周。试验分7组,每组3个平行,每个平行20尾鱼。研究饲料中7种不同来源脂肪对施氏鲟幼鱼生长、血脂和体脂肪酸成分的影响。结果表明:增重率以大豆油组最高,达到了611.29%,葵花油组最低为451.57%,显著低于其它各组(P<0.05);饲料效率以葵花油组最低为86.58%,显著低于其它6组(P<0.05),其余6组差异不显著(P>0.05)。肥满度、脏体指数以鱼油组最低,与其它六组差异显著(P<0.05);肝体指数各组间差异不显著(P>0.05)。鱼油和大豆油两组鱼血清中胆固醇、甘油三酯和低密度脂蛋白胆固醇含量在7组中相对较低。肌肉中总n-3系多不饱和脂肪酸比例以鱼油组最高,与其它六组差异显著(P<0.05),总n-6系多不饱和脂肪酸比例以大豆油组为最高,鱼油组最低。综合比较,施氏鲟饲料中脂肪以添加大豆油最好,鱼油次之,葵花油最差。
     7.共轭亚油酸对施氏鲟幼鱼的降脂作用研究
     为探讨共轭亚油酸(CLA)对饲料诱导的高脂质施氏鲟的生理作用,试验分两阶段进行:第一阶段,试验鱼随机分两组,分别投喂对照组饲料和强化饲料(高糖饲料)6周,建立高脂质施氏鲟模型;第二阶段,将试验鱼随机分成对照组、高脂模型组+CLA组(在对照饲料中添加分别CLA0、0.5%、1.0%和2.0%),试验期6周,测定CLA对饲料诱导的高脂施氏鲟生长性能、体脂和血脂水平的影响。结果表明:添加1.0%和2.0%CLA的鱼体特定生长率与对照组相比显著降低(P<0.05),各试验组存活率和饲料效率无显著差异(P>0.05);添加2.0%CLA的试验组的鱼体脂肪含量低于对照组和各添加组(P<0.05),但后者之间鱼体脂肪含量差异不显著(P>0.05),鱼体水分、蛋白质含量和肝体指数各组间无显著差异(P>0.05);添加CLA2.0%的试验组与对照组相比,肝脏脂肪含量显著降低(P<0.05),但与其它各组差异不显著(P>0.05);添加CLA各组的鱼体肥满度较对照组显著降低(P<0.05);添加1.0%和2.0%CLA试验组鱼体血清总胆固醇含量显著低于其它组(P<0.05),2.0%CLA组试验鱼血清高密度脂蛋白胆固醇较对照组显著降低(P<0.05),添加CLA的各试验组血清甘油三酯和低密度脂蛋白胆固醇含量较对照组均无显著性差异(P>0.05)。试验得出:饲料中添加CLA对饲料诱导的高脂施氏鲟具有降低生长、减少鱼体和肝脏脂质积累以及调节血脂水平的作用,其作用效果以添加2.0%的CLA最大。
Amur sturgeon, Acipenser schrenckii, is one of the 27 existing Acipenseriformes species and a large riverine species native to Amur River, and has become the most popular sturgeon species for aquaculture in China because of its rapid growth, tasty quality and relatively few problems with diseases. So far, some studies were conducted on the lipid and protein requirement and evaluation of some lipid sources for Amur sturgeon. However, little information is available on the requirements and utilizations of the fish for dietary nutrients. Hence, the present study was conducted to investigate dietary requirements of phosphorus, vitamin A, vitamin E, and vitamin C and evaluate the effects of different carbohydrate, lipid sources and conjugated linoleic acid on growth and physiological performance for juvenile sturgeon. The contents are as follows:
     1. Dietary phosphorus requirement of juvenile Acipenser schrenckii
     Six experimental isonitrogenous and isoenergetic purified diets were formulated containing increasing contents of phosphorus (0.18%, 0.40%, 0.71%, 0.98%, 1.38% and 1.66%, respectively). Monocalcium phosphate was used as dietary phosphorus source, casein and glutin as protein source, dextrin as carbohydrate source, and soybean oil and maize oil as lipid source, respectively. Each experimental diet was fed to triplicate groups of 20 Amur sturgeon juveniles with initial weight approximately 4.7g in 400-1 aquaria and maintained at 25.6±2.0℃for 8 weeks. The results showed that the weight gain rate, feed efficiency and specific growth rate of the juveniles increased significantly with the increasing of the dietary phosphorus level (P<0.05). These values reached the peak when the juveniles were fed the diet supplemented with 0.98% phosphorus, and then decreased significantly with the further increases of the dietary phosphorus level (P<0.05). The survival rate of the fish fed the control diet (0.18% phosphorus diet) was significantly lower than that of the fish fed the other diets (P<0.05). Supplementation of dietary phosphorus had no significant effect on the muscle moisture, crude protein, or crude lipid content of the juveniles (P>0.05). The fish fed the diets supplemented with 0.71%-1.66% dietary phosphorus had significantly higher ash, calcium, and phosphorus contents in vertebra than those fed the control diet and the 0.40% phosphorus diet (P<0.05). Broken-line regression analyses of specific growth rate and vertebrae phosphorus against dietary phosphorus level indicated that the dietary phosphorus requirement for optimal growth and phosphorus content in vertebra of juvenile Amur sturgeon was 0.88%-1.00% of dry diet.
     2. Dietary vitamin A requirement of juvenile Acipenser schrenckii
     The experiment was conducted to determine the dietary vitamin A requirement of juvenile Amur sturgeon by formulating seven semipurified diets containing 10, 258, 510, 1050, 2020, 4100 and 8300 IU vitamin A (as retinol acetate) kg~(-1) diet, respectively. Each experimental diet was fed to triplicate groups of 20 early juveniles with initial average weight 12.09±0.22g in 405-1 aquaria and maintained at 25.0±2.0℃for 8 weeks. Fish fed the basal diet (10 IU vitamin A kg~(-1) diet) exhibited bad appetite and activity, whereas these signs were not observed in any group fed diets supplemented with vitamin A. Weight gain, feed efficiency and hepatosomatic index increased significantly with the increases of dietary vitamin A level, which reached the peak at vitamin A 1050 IU kg~(-1) diet, and then decreased. The muscle chemical compositions were not affected by dietary vitamin A levels. Vitamin A concentrations in liver and muscle increased significantly as vitamin A levels increased within a range of 10-4100 IU kg~(-1) diet and above this, didn't change significantly. The activities of lysozyme activities and super oxide dismutase (SOD) in serum were the highest when the content of vitamin A was 1050 IU kg"1 diet. Either deficit or excess (>1050 IU kg~(-1)) of vitamin A in the diet would reduce the activities of the two enzymes. Broken-line regression analysis of weight gain against dietary vitamin A level showed that juvenile Amur sturgeon required a minimum of 923 IU vitamin A kg~(-1) diet for maximal growth.
     3. Dietary vitamin E requirement of juvenile Acipenser schrenckii
     The effects of dietary vitamin E (dl-α-tocopheryl acetate) on growth performance and tissue vitamin E content of juvenile Amur sturgeon had been investigated. Triplicate groups of experimental fish with initial body weight (10.10±0.31)g were cultured and fed by semi-purified diets with seven levels of vitamin E supplements (0, 20, 50, 100, 200, 500 and 1000 mg/kg diet) at 10.46% dietary lipid for 8 weeks. The weight gain, feed efficiency, specific growth rate, survival rate and condition factor significantly (.P<0.05) increased concomitantly with increasing of supplemented vitamin E level and reached their peaks on the group fed with 200mg vitamin E/kg diet, respectively. With the further increase of supplemented vitamin E level, the weight gain, feed efficiency and condition factor significantly (P<0.05) decreased, whereas the specific growth rate had no significant (P>0.05) differences among treatments. Hepatosomatic index of the control group was significantly (P<0.05) higher than that of the other treated groups. The vitamin E content in liver and muscle significantly (P<0.05) increased concomitantly with increasing of supplemented vitamin E level. No significant (P>0.05) changes were found on vitamin E content in liver of groups fed with > 100 mg vitamin E/kg diets and on that in muscle of groups fed with≥200 mg vitamin E/kg diets. The crude lipid content in muscle of the control group was significantly (P<0.05) higher than that of the other treated groups, and the crude protein content in muscle of groups fed with >100mg vitamin E/kg diets were significantly (P<0.05) higher than that of the control group. The broken-line regression analysis of specific growth rates against dietary vitamin E levels suggested that the vitamin E requirement of juvenile Acipenser schrendkii for optimal growth might be 187.4 mg/kg diet.
     4. Dietary vitamin C requirement of juvenile Acipenser schrencki
     An 8 weeks growth experiment was conducted to determine the effects of dietary vitamin C on survival, growth, tissue ascorbic acid content, activity of serum lysozyme and serum cortisol concentration of Amur sturgeon with initial weight of 7.25±0.33g. Eight practical diets were formulated to contain 0.1, 58.2, 110.4, 221.8, 350.2, 475.6, 698.4 and 906.2 mg ascorbic acid equivalent kg-1 diet, supplied as enveloped ascorbic acid. Each diet was fed to triplicate groups of fish in aquarium, and each aquarium was stocked with 10 fish. Fish were fed four times daily to apparent satiation for 8 weeks. The water temperature fluctuated from 19.5 to 25.5 during the experimental period. The results showed that: No gross deficiency signs were observed in any of experimental fish. Survival rate was not significantly affected by the dietary vitamin C (P>0.05). Weight gain rate (from 514.46 to 680.31%), special growth rate (from 3.24 to 3.67 % day-1) and feed conversion ratio (from 0.85 to 0.70) were significantly affected by the dietary vitamin C (P<0.05). The vitamin C contents in liver and muscle positively correlated with the vitamin C in diets. The activities of serum lysozyme significantly increased with increasing dietary vitamin C, while the serum cortisol content significantly decreased. The Broken-line regression analysis showed the breakpoints were at 110.4 mg kg-1 based on maximal special growth rate, 279.4mg kg-1 on liver maximum storage of ascorbic acid.
     5. Effects of different carbohydrate sources on growth, some physiological and biochemical indexes of juvenile Acipenser schrencki
     Juvenile Amur sturgeon were fed with 7 groups of isonitrogenous and isoenergetic diets containing 22% glucose, fructose, maltose, sucrose, dextrin,α-starch and corn starch respectively, for 8w to study the effects of differents dietary carbohydrate sources on growth, plasma glucose, liver glycogen concentration and the amylase activity of alimentary tract of juvenile Amur sturgeon. Each group had 3 replicates, and one replicate contained 20 fish (mean weight, 4.70±0.08g). The results showed: Weight gain rate (WG), specific growth rate (SGR) and feed efficiency (FE) of sturgeon were significantly (P < 0.05) affected by the different dietary carbohydrate sources. The effect of different dietary carbohydrate sources on the WG was dextrin,α-starch > glucose, corn starch > maltose > sucrose, fructose; SGR and FE had similar show to WG. Digestibility of sturgeon was significantly (P<0.05) affected by feeding different carbohydrate sources, on carbohydrate digestibility was glucose, fructose > maltose > dextrin >α-starch > corn starch; on protein digestibility was fructose > glucose, maltose, dextrin > corn starch >α-starch. Moisture, crude ash and crude lipid of muscle of sturgeon were significantly (P < 0.05) affected by the different dietary carbohydrate sources, but crude protein had no significantly difference (P>0.05). Plasma glucose and liver glycogen concentration of sturgeon were significantly (P<0.05) affected by the different dietary carbohydrate sources in different period after satiation. In different period after satiation, in stomach, amylase activity increased first and then decreased; in duodenum, the activity droped at first, then performed as same as in stomach; in intestinal valve, the activity increased at first then decreased, and performed again; the amylase activity of alimentary tract was significantly (P<0.05) affected by feeding different carbohydrate sources. In liver, no amylase activity had been detected. According to WG and SGR, the appropriate carbohydrate in diet of Amur sturgeon was dextrin andα-starch.
     6. Effects of dietary lipids on the performance of growth, serum lipids and tissue fatty acid composition of juvenile Acipenser schrencki
     An 8-week growth experiment was conducted to test seven lipids on juvenile Amur sturgeon. The fish (initial body weight 9.83 g) in triplicate groups were fed with 10 % of each lipid included into basic diet in fiberglass tanks. Seven dietary lipids were fish oil, sunflower oil, tallow, lard oil, colza oil, corn oil and soybean oil repectively. The results showed that: The weight gain rate of fish fed soybean oil diet was the highest (611.29%) and group of sunflower oil was the lowest (451.57%) which were significantly lower than other groups. The lowest feed efficiency was also observed at group of sunflower oil which had significant difference from the other 6 groups. Fish fed with fish oil had the lowest condition factor and gut somatic index which were significantly lower than those of the other groups (P<0.05).There was no significant difference in hepatopancreas somatic index of the fish. The concentrations of cholesterol, triglyceride and low density lipoprotein cholesterol in serum of group fish oil and soybean oil were comparatively low in the 7 groups. The ratios of total n-3 polyunsaturated fatty acids in lipid of muscle of fish fed fish oil were significantly higher than those of fish fed other lipids (P<0.05), while the highest and the lowest ratios of total n-6 polyunsaturated fatty acids were observed in the fish fed soybean oil and fish oil, respectively. Compared comprehensively, the best dietary lipid to juvenile Amur sturgeon was soybean oil, the next in order was fish oil, while sunflower oil was minimal.
     7. Study on effects of conjugated linoleic acid on weight losing and lipid lowering of juvenile Acipenser schrencki
     The experiment was conducted to investigate the effects of dietary conjugated linoleic acid (CLA) on growth, body lipid level and serum lipids in juvenile Amur sturgeon. Groups of fish were fed controlled and enriched diets for 6 weeks to gaint high-lipid groups. Then, juvenile Amur sturgeons were randomly divided into control group and high-lipid +CLA groups (0, 0.5, 1.0, 2.0% CLA/control diet respectively). At the end of experiment, SGR decreased significantly by 1.0% and 2.0% CLA supplement (P<0.05). CLA had no effect on survival rate and FCR; CLA addition reduced condition factor among treatments. No differences were detected in body moisture, protein, and HSI, The lipid contents in liver reduced at 2.0% CLA feeding; TC decreased in serum when the fish were fed 1.0% and 2.0% CLA, and HDL-C decreased when supplied with 2.0% CLA, while, TG and LDL-C were silimar among treatments. In conclusion, the fortified CLA was effective in lowering growth, body lipid and blood lipids of juvenile Amur sturgeon, and the maximum effect on these appeared at the 2.0% CLA supplemented group.
引文
1.Frances S S,Eleanor N W.营养学-概念与争论.(王希成 主译).北京:清华大学出版社,2002:130
    2.艾庆辉,麦康森,王正丽.维生素C对鱼类营养生理和免疫作用的研究进展.水产学报,2005,29(6)
    3.安国利,冯程强,王长法.灭活疫苗对鲤鱼血清溶菌酶活力和腹腔吞噬细胞活性的.山东师范大学学报.1999,14(2):175-179
    4.蔡春芳,陈立侨,吴萍.饲料糖种类和水平对异育银鲫肝糖原代谢的影响.中国水产科学,2003,10(1):55-59
    5.曹瑞,王枫,季爱玲.共轭亚油酸对肥胖大鼠肝脏脂质代谢的影响.解放军预防医学杂志,2006,24(2):88-91
    6.曾红,任泽林(译).鱼类的营养需要(NRC).北京:中国农业科技出版社,1993
    7.常青,熊邦喜,龙良启.池养鳗鲡血液生化成分分析.水利渔业,1997,92:16-18.
    8.陈细华.鲟形目鱼类生物学与资源现状.北京:海洋出版社,2007,92-95
    9.荻野珍吉(郑长义,戴宏宗译).鱼类的营养与饲料.台北:养鱼世界杂志社,1984
    10.杜立强.脂肪水平对史氏鳃摄食生长的影响.[硕士学位论文].河北:河北师范大学,2004
    11.段铭,高宏伟,郝黎明.不同脂肪源对肉仔鸡肝脏中脂肪代谢相关基因表达的影响.中国畜牧杂志,2003,39(6):7-9
    12.冯健,覃志彪.4种不同脂肪源对太平洋鲑生长和体组成的影响.水生生物学报,2006,30(3):256-261
    13.甘玲,陈晓春.共轭亚油酸的降脂功能及其对生化参数的影响.动物科学与动物医学,2003,20(10):48-50
    14.高淳仁,雷霁霖.不同脂肪源对真鲷幼鱼生长、存活及体内脂肪酸组成的影响.中国水产科学,1999,6(3):55-60
    15.高露姣,陈立侨,宋兵.饥饿和补偿生长对施氏鲟幼鱼摄食、生长和体成分的影响.水产学报,2004,28(3):279-284
    16.高露姣,陈立侨,赵晓勤.施氏鲟幼鱼的饥饿和补偿生长研究-对消化器官结 构和酶活性的影响.中国水产科学,2004,11(5):413-419
    17.高露姣,陈立侨.不同脂肪源饲料对施氏鲟幼鱼生长的影响.海洋渔业,2004,26(3):210-214
    18.高露姣,施兆鸿,艾春香.不同脂肪源对施氏鲟幼鱼血清生化指标的影响.海洋渔业,2005,27(4):3 19-323
    19.高芃,顾光,马宁.共轭亚油酸减肥作用的人体试食试验研究.上海预防医学杂志,2004,16(9):421-423
    20.龚晨睿,马良,田辉.共轭亚油酸对大鼠血脂水平的调节作用及其机理的研究.中国比较医学杂志,2003,13(4):204-206
    21.郭冉,刘永坚,田丽.不同糖源对南美白对虾(Penaeus vannamei)生长、成活率和虾体组成的影响.中山大学学报(自然科学版),2005,44(3):90-92
    22.贺利民,吕岱竹,吴莉宇.高效液相色谱法同时测定无骨海鱼中的维生素A、D和E.分析试验室.2004,23(5):77-79
    23.贺喜,戴秋仲,李剑波,等.共轭亚油酸对动物体脂代谢的影响及其作用机制.饲料工业,2006,27(2):58-61
    24.侯永清,李绍钰.饲料中添加维生素E对畜禽肉质的影响.饲料博览,2001,(9):30-32
    25.胡国宏,朱世成,张俊辉,等.养殖史氏鲟幼鱼的含肉率和鱼肉营养成分分析.大连水产学院学报,2003,18(1):70-71
    26.黄鹤忠,丁磊,宋学宏.青鱼和草鱼葡萄糖耐量的比较研究.中国水产科学,2005,12(4):496-500
    27.黄真理,常剑波.鱼类体长与体质量关系中的分形特征.水生生物学报,1999,23(4):330-336
    28.李爱杰.水产动物营养与饲料学.北京:中国农业出版社,1996:26-36
    29.李同庆,郝玉江,安瑞永,等.饲料蛋白水平对史氏鲟幼体消化率的影响.淡水渔业,2002,32(5):51-54
    30.李同庆.蛋白水平对史氏鳃摄食生长的影响.[硕士学位论文].河北:河北师范大学,2002
    31.梁萌青,季文娟.中国对虾发育阶段维生素A需要量的研究.海洋与湖沼,1999,30(2):150-154
    32.刘洪杰,毛兴华.牙鲆幼鱼对n-3高度不饱和脂肪酸的吸收及与生长关系的初 步研究.海洋与湖沼,1999,30(3):238-244.
    33.刘键,赵德树.史氏鲟的生物学特性及其人工繁殖技术.水利渔业,2006,26(1):26-28
    34.刘树青,江晓路,牟海津.免疫多糖对中国对虾血清溶菌酶、磷酸酶和过氧化物酶的作用.海洋与湖沼,1999,30(2):278-283
    35.刘威,方定志.高淀粉膳食诱导高甘油三酯血症大鼠血浆及肝脏磷脂含量变化的研究.四川大学学报(医学版),2007,38(1):129-131
    36.刘玮,Kofi Fynn-Aikins.饲料中D-葡萄糖含量对白鲟稚鱼的生长、脂肪合成酶及肝组成的影响.江西科学,1993,11(2):94-101
    37.刘玮,徐萍,任本根,龚纲明.不同脂肪源饲料对草鱼稚鱼生长的影响.水产学报,1995,19(4):362-365
    38.龙勇,李林春.鲟鱼消化生理和营养需求研究进展.农业高等专科学校学报,2007,17(3):108-111
    39.吕实波,徐建华,孙成玺.共轭亚油酸对肥鼠的减肥作用等.营养学报,2004,26(3):235-236
    40.毛翠风,庄平,刘健.长江口中华鲟幼鱼的生长特性.海洋渔业,2005,27(3):177-181
    41.母昌考,王春琳.鱼类必需脂肪酸营养研究现状.饲料工业,2003,24(6):44-46
    42.农业部畜牧兽医局,全国饲料工业协会,全国饲料工业标准化技术委员会等.饲料工业标准汇编(上册).北京:中国标准出版社,2002:70-92,243-247
    43.任泽林,陈义林,霍启光.氧化鱼油对鲤鱼(Cyprinus carpio)肉质的影响.饲料广角,2004,19:37-40
    44.沈文英,张利红,郑永萍,周刘琴,郑建平.饥饿对银鲫血液组分和卵巢发育的影响.动物学研究,2003,24:441-444.
    45.舒晓亮,施尧,刘晓丽.n-6/n-3脂肪酸不同的食用油对大鼠血清微量元素的影响.上海医学,2006,29(1):26-29
    46.田丽霞,刘永坚,冯健,等.不同种类淀粉对草鱼生长、肠系膜脂肪沉积和鱼体组成的影响.水产学报,2002,26(3):247-251
    47.万文菊,侯水生.不同饱和度脂肪酸日粮对北京鸭生产性能的影响.山东畜牧兽医,2003,4:5-6
    48.王道尊,潘兆龙,梅志平.不同脂肪源饲料对青鱼生长的影响.水产学报,1989, 13(4):370-374
    49.王镜岩,朱圣庚,徐长法.生物化学(第三版).北京:高等教育出版社,2002
    50.王军,苏金全,邵勋.免疫添加物对大黄鱼血液白细胞数量及吞噬功能的影响.海洋科学,2001,5(9):44-46
    51.王雷,李光友,毛远兴.口服免疫药物对养殖中国对虾病害防治作用的研究.海洋与湖沼,1994,25(5):486-492
    52.巫淼鑫,邬国英,韩瑛.6种食用植物油及其生物柴油中脂肪酸成分的比较研究.中国油脂,2003,28(12):65-67
    53.吴凡,文华,蒋明等.维生素B_(12)对草鱼幼鱼生长、体组分和造血机能的影响.吉林农业大学学报,2007,29(6):695-699
    54.吴锐全,肖学铮,黄樟翰.鲟鱼的营养需求和饲料.水利渔业,1999,19(5):21-22
    55.伍莉,陈鹏飞,陈建.施氏鲟消化酶活性的初步研究.南农业大学学报,2002,24(2):179-183
    56.肖懿哲,林金忠.施氏鲟饲料脂肪的最适量研究.水利渔业,2001,21(5):4-5
    57.肖懿哲,苏永全.史氏鲟饲料脂肪的最适合量.水产学杂志,2001,14(1):21-24
    58.邢浩春.维生素B6对史氏鲟幼鱼摄食生长及能量收支的影响.[硕士学位论文].河北:河北师范大学,2005
    59.徐杰,胡国华,张大勇.大豆种子脂肪酸组分的研究进展.大豆科学,2005,24(1):61-66
    60.徐乐宗.史氏鲟养殖技术讲座:史氏鲟人工繁殖技术.齐鲁渔业,2003,20(8):53-55
    61.徐立红,陈专,徐盈.用高效液相色谱法测定鱼样中的维生素D_3和E.水生生物学报,1994,18(2):192-193
    62.徐新章,何珍秀,付培峰.不同脂肪源对幼蟹生长的影响.饲料工业,1997,18(5):16-18
    63.薛秀恒,王志耕,王菊花.共轭亚油酸强化乳对小鼠体脂及血脂的影响.营养学报,2006,28(2):120-123
    64.杨艳梅,陈炳卿.共轭亚油酸的代谢及其对脂类代谢的影响.卫生毒理学杂志,2002,16(4):239-241
    65.杨雨虹,郭庆,黄金善.鲤鱼饲料磷的需要量研究.东北农业大学学报,2006,37(1):48-51
    66.叶继丹,卢彤岩,刘洪柏.六种鲟鱼消化酶活性的比较研究.水生生物学报,2003,27(6):590-595
    67.叶继丹,张文源,孙大江,等.配合饲料饲养史氏鲟幼鱼的试验研究.水产学杂志,1998,11(1):34-39
    68.叶继丹,张文源,孙大江.配合饲料饲养史氏鲟幼鱼的试验研究.水产学杂志,1998,11(1):34-39
    69.叶元土.淡水鱼类营养与饲料配制技术发展趋势与存在问题分析(下).饲料广角,2005,10:32-36
    70.游文章,黄忠志,廖朝兴.草鱼对饲料中磷需要量的研究.水产学报,1987,11(4):285-292
    71.于信勇.史氏鲟的生物学特性及其养殖技术.科学养鱼,2000,3:16-17
    72.袁骐.养殖史氏鲟不同部位氨基酸组成.氨基酸和生物资源氨基酸和生物资源,2006,28(1):25-28
    73.张桂珍,李广生,王凡.硒和维生素E对喂克山病病区粮大鼠胰岛素、C肽水平的影响及其发生机制.营养学报,1993,15(3):266-270
    74.张文斌.共轭亚油酸对脂肪代谢的影响及其作用机制.国外医学卫生学分册,2004,31(3):175-179
    75.赵婕,王俊香,徐静,范效琴.肝硬化患者肠外营养时的脂肪酸代谢研究.临床医药实践杂志,2005,14(4):275-277
    76.赵美清,冯利东,王翠莲.心脑血管疾病患者脂蛋白(a)与红细胞流变性关系的研究.医学研究杂志,2006,35(2):49-50
    77.赵万鹏,刘永坚,潘庆.草鱼摄食后皿糖和肝糖原质量分数的变化.中山大学学报(自然科学版).2002,41(3)
    78.赵万鹏.草鱼摄食后肝胰脏组织淀粉酶活性的变化.水产科学,2002,21(6):13-15
    79.中国标准出版社第二编辑室.中国环境保护标准汇编水质分析方法.北京:中国标准出版社,2006:73-77,124-129,149-153,489-491
    80.中华人民共和国卫生部,中国国家标准化管理委员会.中华人民共和国国家标准食品卫生检测方法理化部分(一).北京:中国标准出版社,2004
    81.中华人民共和国卫生部,中国国家标准化管理委员会发布.食品卫生检验方法理化部分(一).北京:中国标准出版社,2004:25-46
    82.周俊,文华,何瑞国,刘伟.中华鲟摄食不同水平的两种糖后淀粉酶活性的变化.大连水产学院学报,2007,22(1):27-31
    83.周萌,曹俊明,吴建开.军曹鱼幼鱼对饲料中磷需要量的研究.动物营养学报,2005,17(3):62
    84.周文玉,俞春玉,刘建忠.饲料中油脂的质和量对团头鲂生长的影响.上海水产大学学报,1998,7(增刊):292-296
    85.周勇.幼鳖饲料中添加维生素E的实验.河北渔业,2004,3:42-43
    86.1Badinga I,Selberg K T,Dinges A C,et al.Dietary conjugated linoleic acid alters hepatic lipid content and fatty acid composition in broiler chickens.Poultry Science,2003,82(1):111-116
    87.Agnisola C,Mckenzie D J,Taylor E W,Bolis C L,Tota B.Cardiac performance in relation to oxygen supply varies with dietary lipid composition in sturgeon.American Journal of Physiology.1996,27:417-425
    88.Aoe H T,Mimura T S,Komo A.Requrement of young carp for vitamin A.Bull.Jap.Soc.Sci.Fisheries.1968,34:959-964
    89.Bai S,Lee K J.Different levels of dietary DL-α-tocopherol acetate affect the vitamin E status of juvenile Korean rockfish(Sebasres schlegeli).Aquaculture,1998,161:405-414
    90.Bandarra N M,Nunes M L,Andrade A M,et al.Effect of dietary conjugated linoleic acid on muscle,liver and visceral lipid deposition in rainbow trout juveniles (Oncorhynchus mykiss).Aquaculture,2006,254:496-505
    91.Bassaganya R J,Hontecillas M R,Bregandabl K,et al.Effect of dietary conjugated linoleic acid in nursery pigs of dirty and clean environments on growth,empty body composition,and immune competence.Journal of Animal Science,2001,79(3):714-721
    92.Berge G M,Ruyter B,Torbjφrn(?)sg(?)rd.Conjugated linoleic acid in diets for juvenile Atlantic salmon(Salmo salar):effect on fish performance,proximate composition,fatty acid and mineral content.Aquaculture,2004,237:365-380
    93.Bobban S A,Rebecca L A,Steven R B,et al.Effect of dietary lipid source on the growth,tissue composition and hematological parameters of largemouth bass(Micropterus salmoides).Aquaculture,2006,(255):210-222
    94. Boyd C E. Phosphorus dynamic in ponds, Proc Annu Conf Southeast Assoc Game Fish Comm, 1971,25: 418-426
    
    95. Bullis S P. Clinical of pathology of temperate freshwater and estuarine fish. In: Fish Medicine, Stoskpf, 1993: 232-239
    
    96. Chevance F V, Farmer L J. Release of volatile odor compounds from full and low-fat frankfurters. J Agric Food Sci, 1999,47(12): 5161-5168
    
    97. Cites: Document AC. 16.7.2.16th Meeting of the Cites Animals Committee Shepherdstown, 2000: 11-15
    
    98. Clerton P, Troutaud D, verlhac V, GabaudanJ, Deschaux P. Dietary vitamin E and rainbow phgocyte functions: effect on gut and on head kidney leukocytes. Fish and Shellfish Immunology. 2001, 11: 1-13
    
    99. Cofino C, Magni S, Pastorelli G. Effect of conjugated linoleic acid on meat quality,lipid metabolism, and sensory characteristics of dry-cured hams from heavy pigs. J Anim Sci, 2003, 81: 2219-2229
    
    100. Corino C, Mourot J, Magni S. Influence of dietary conjugated linoleic acid on growth, meat quality, lipogenesis, plasma leptin and physiological variables of lipid metabolism in rabbits. J Anim Sci, 2002, 80(4): 1020-1028
    
    101. Cowey C B, Degener E, Tacon A G The effect of vitamin E and oxidized fish oil on the nutrition of rainbow trout (Salmo gairdneri) grown at natural, varying water temperature. Br J Nutr, 1984, 51: 443-451
    
    102. Cruz-suarez L E, Ricque M D, Pinal M D. Effect of diferent carbohydrate sources on the growth of Penaeus vannamei: economical inpact. Aquaculture, 1994, 123:349-360
    
    103. Cuesta A, Esteban M A, Meseguer J. Changes in some innate de-fence parameters of sea Bream induced by retinol acetate. Fish.Shellfish.Immunol. 2002, 13(4): 279-291
    
    104. Cui Y, Hung S S O, Zhu X. Effect of ration and body size on the energy budget of juvenile white sturgeon. Journal of Fish Biology, 1996, 49: 863-876
    
    105. Dabrowski K, Ascorbic acid in aquatic organisms. CRC press, 2001: 288
    
    106. Dabrowski K, Matusiewicz M, Blom J H. Hydrolysis, absorption and bioavailability of ascorbic acid esters in fish. Aquaculture, 1994, 124: 169-191
    
    107. Dabrowski K. Gulonolactone oxidase is missing in teleost fish. Biol Chem Hoppe-seyler, 1990, 371: 207-214
    
    108. Dandapat J, Rao K J. Dietary vitamin E modulates antioxidant defense system in giant fresh-water prawn, Macrobrachium rosenbergii. Comp Biochem Physiol, 2000,127: 101-115
    
    109. Dedi J, Takeuchi T, Hosoya K, Watanabe T, Seikai T. Effect of vitamin A levels in Artemia nauplii on the caudal skeleton formation of Japanese flounder Paralichthys olivaceus. Fish.Sci.1998, 64(2): 334-345
    
    110. Deng D F, Hemre G I, Storebakken T, Shiau S Y, Hung S S O. Utilization of diets with hydrolyzed potato starch, or glucose by juvenile white sturgeon (Acipenser transmontanus), as affected by Maillard reaction during feed processing.Aquaculture, 2005, 248: 103-109
    
    111. Deng D F, Hung S S O, Conklin D E. White sturgeon (Acipenser transmontanus) require both n-3 and n-6 fatty acids. Aquaculture, 1998, 161: 333
    
    112. Deng D F, Redsite S, Hung S S O. Glycemic and glycosuric responses in white sturgeon (Acipenser transmontanus) after oral administration of simple and complex carbohydrates. Aquaculture, 2001, 199: 107-117
    
    113. Deng D F. Carbohydrate utilization by white sturgeon (Acipenser transmontanus).(Ph D dissertation). California: University of California, 1999
    
    114. Deng D F. Qualitative requirement of essential fatty acid for white sturgeon (Acipenser transmontanus). (MS dissertation). California: University of California,1996
    
    115. Dong F D, Stale R, Silas S O H.Glycemic and glycosuric responses in white sturgeon (Acipenser transmontanus) after oral administration of simple and complex carbohydrates. Aquaculture, 2001, 199: 107-117
    
    116. Dugan M E R, Aalhus J L, Schaefer A L. The effect of linoleic acid on fat to lean repactitioning and feed conversion in pigs. Can J Anim Sci, 1997, 77(4): 723-725
    
    117. Falahatkar B, Soltani M, Abtahi B, Kalbassi M R, Pourkazemi M. Effect of dietary vitamin C supplementation on performance, tissue chemical composition and alkaline phosphatase activity in great sturgeon (Huso huso). Journal of Applied Ichthyology, 2006, 22 (1): 283-286
    
    118. Feng J, Jla G Studies on the Fatty Liver Diseases Resulted from Different Levels in Sciaenops ocellatus Diets. Acta Hydrobiologica Sinica, 2005, 29(1): 61-65
    
    119. Figueiredo S A C, Rema P, Bandarra N M. Effect of dietary conjugated linoleic acid on growth, nutrient utilization, body composition, and hepatic lipogenesis in rainbow trout juveniles (Oncorhynchus mykiss). Aquaculture, 2005, 248: 163-172
    
    120. Fontagne S, Bazin D, Breque J, Vachot C, Bernarde C, Rouault T, Bergot P. Effect of dietary oxidized lipid and vitamin A on the early development and antioxidant status of Siberian sturgeon (Acipenser baeri) larvae. Aquaculture, 2006, 257:400-411
    
    121. Fracalossi D M, Allen M E, Yuyanma L K. Ascorbic acid biosynthesis in Amazonian Fish. Aquaculture, 2001, 192: 321-332
    
    122. Friedman A, Sklan D. Vitamin A and immunity. Nutr immunol, 1993, 197(8): 120
    
    123. Fynn-aikins K, Hung S S O, Liu W, Li H. Growth, liopgenesis and liver composition of junvile white sturgeon {acipenser transmontanus) fed different levels of D-glucose. Aquaculture, 1992, 105: 61-72
    
    124. Fynn-Aikins K, Hung S S O, Liu W, Li H. Growth, lipogenesis and liver composition of juvenile white sturgeon {Acipenser transmontanus) fed different levels of D-glucose, Aquaculture, 1992, 105: 61-72
    
    125. Gatlin D M, Bai S C, Erickson M C. Effect of dietary vitamin E and synthetic antioxidants on composition and storage quality of channel catfish . Aquaculture,1992, 106: 323-332
    
    126. Gershanovich A D, Kiselev G A. Growth and haematological response of sturgeon hybrids Russian sturgeon {Acipenser gueldenstaedti brandt) x beluga (Huso huso L.) to protein and lipid contents in the diet. Comparative Biochemistry and Physiology,1993, 106: 591-586
    
    127. Greene D H S, Selivonchiek D P. Lipid metabolism. Fish Prog Lipid Res, 1987, 26:53-85
    
    128. Halver J E. The vitamins. In: Halver J E (Ed.), Fish Nutrition. Academic Press, New York, 1989, 40
    
    129. Halver J E. The vitamins. In: Halver J E, Hardy R W Eds., Fish Nutrition, 3rd ed.. California: Academic Press, 2002: 61-141
    
    130. Hamer K, Lie O. Minimum requirement of vitamin E for Atlantic salmon (Salmo salar L.), at first feeding . Aquac Res, 1995, 26:175-184
    
    131. He L M, Lu D Z, Wu L Y. Simultaneous determination of vitamin A, D and E in the boneless seawater fish by high performance liquid chromatography. Chinese Journal of Analysis laboratory 2004, 23: 77-79(in Chinese).
    
    132. Hemre G I, Deng D F, Wilson R P, Berntssen M H G Vitamin A metabolism and early biological responses in juvenile sunshine bass (Morone chrysopsxM.saxatilis) fed graded levels of vitamin A. Aquaculture, 2004, 235: 645-658
    
    133. Hernandez H L H, Teshima S, Ishikawa M, Alam M S, Koshio S, Tanaka Y. Dietary vitamin A requirements of juvenile Japanese flounder (Paralichthys olivaceus) Aquac. Nutr, 2005, 11:3-9
    
    134. Hernandez L H, Teshima S I, Koshio S, Ishikawa M, Tanaka Y, Alam M S. Effect of vitamin A on growth, serum anti-bacterial activity and transaminase activities in the juvenile Japanese flounder(Paralichthys olivaceus). Aquaculture, 2007, 262:444-450
    
    135. Herold M A, Hung S S O, Fynn-Aikins K. Apparent digestibility coefficients of carbohydrates for white sturgeon. The progressive fish-culturist, 1995, 57: 137-140
    
    136. Hilton J W. Hypervitaminosis A in rainbow trout (Salmo gairdneri): toxic signs and maximum tolerable level. J Nutr, 1983, 113: 1737-1745
    
    137. Hu C J, Chen S M, Pan C H, Huang C H. Effect of dietary vitamin A or P-carotene concentrations on growth of juvenile hybrid tilapia, Oreochromis niloticusxO.aureus. Aquaculture, 2006, 253: 602-607
    
    138. Huang C H, Lin W Y. Effect of dietary vitamin E level on growth and tissue lipid peroxidation of soft-shelled turtle, Pelodiscus sinensis. Aquae Res, 2004, 35(10):948-954
    
    139. Hughes K P, Soares J H. Efficacy of phytase on phosphorus utilization in practical diets fed to striped bass (Monroe saxatilis). Aquae Nutr, 1998, 4: 130-140
    
    140. Hung S S O, Deng D F. Sturgeon, Acipenser spp. In: Webster C D and Lim C ed.,Nutrient requirement and feeding of finfish for aquaculture. CABI Publishing, 2002,344-357
    
    141. Hung S S O, Fynn-Aikins, Lutes P B, Xu P. Ability of juvenile white sturgeon (Aispenser transmontanus) to utilize different carbohyduate. Journal of Nutrition, 1989,119:727-733
    
    142. Hung S S O, Groff J M, Lutes P B, Alkins F K F. Hepatic and intestinal histology of juvenile white sturgeon fed different carbohydrates. Aquaculture, 1990, 87(15):349-360
    
    143. Hung S S O, Groff J M, Lutes P B, Fynn-Aikins K. Hepatic and intestinal histopathology of juvenile white sturgeon fed different carbohydrates. Aquaculture,1990, 87: 349-360
    
    144. Hung S S O, Storebakken T, Cui Y, Tian L, Einen O. High-energy diets for white sturgeon (Aicpenser tranmontanus). Aquaculture Nutrition, 1997, 3: 281-286
    
    145. Hung S S O. Carbohydrate utilization by white sturgeon as assessed by oral adminstration tests. Journal of Nutrition, 1991c, 121: 1600-1605
    
    146. Hung S S O. Nutrition and feeding of hatchery-produced juvenile white sturgeon (Acipenser transmontanus): an overview. In: Williot, P ed. Proceedings of the First International Symposium on the Sturgeon. France: Cemagef, 1991, 65-77
    
    147. Hung S S O. Sturgeon, Acipenser spp. In: Wilson, R P ed., Handbook of Nutrient Requirements of Finfish. Florida: CRC Press, 1991b, 153-160
    
    148. Hutchins C G, Rawles S D, Gatlin EDM. Effect of dietary carbohydrate kind and level on growth, body composition and glycemic response of juvenile sunshine bass (Morone chrysops Yx. saxatilis). Aquaculture, 1998, 161: 187-199
    
    149. Kang J X, Leaf A. The cardiac an tiarrhythmic effect of polyunsaturated fatty acid.Lipids, 1996, 31: 41-44
    
    150. Kaushik S J, Breque J, Balanc D. Apparent amino acid availability and plasma free amino acid levels in Siberian Sturgeon (Acipenser baeri). Comparative Biochemistry and Physiology, 1994,107: 433-438
    
    151. Kaushik S J, Brequr J, Bland. Requirement for protein and essential amino acid and their utilization by Siberian sturgeon (Acipenser Barel). In: Willot P, ed., Acipenser.France: Cemagref, 1991: 25-39
    
    152. Kaushik S J, Luquet P, Blanc D, Paba A. Studies on the nutrition of Siberian sturgeon (Acipenser baeri).Utilization of digestible carbohydrates by sturgeon.Aquaculture, 1989, 76: 97-107
    
    153. Keeton J T. Low-fat meat products-technological problems with processing. Meat Sci, 1993, 36: 261-267
    
    154. Kennedy R, Campbell P J, Porter A, Tocher D R. Influence of dietary conjugated linoleic acid (CLA) on lipid and fatty acid composition in liver and flesh of Atlantic salmon (Salmo salar). Comparative Biochemistry and Physiology, Part B, 2005, 141:168-178
    
    155. Ketola H G, Richmond M E. Requirement of rainbow trout for dietary phosphorusand its relationship to the amount discharged in hatchery effluents. Am Fish Soc,1994, 123: 587-594
    
    156. Kim J D, Kim K S, Song J S. Optimum level of dietary monocalcium phosphate based on growth and phosphorus excretion of mirror carp (Cyprinus carpio).Aquaculture, 1998, 161: 337-344
    
    157. Kitamura S, Suwa T, Ohara S, Nakagawa K. Studies on vitamin requirements of rainbow trout: III Requirement of vitamin A and deficiency symptoms. Bull Jpn Soc Sci Fish 1967, 33: 1126-1131
    
    158. Kocabas A M, Gatlin III D M. Dietary vitamin E requirement of hybrid striped bass (Morone chrysops female xM saxatilis male). Aquac Nutr, 1999, 5: 3-7
    
    159. Lall S P. The minerals. In: Halver J E, Hardy R W eds., Fish Nutrition 3rd ed. San Diego CA: Academic Press, 2002: 259-308
    
    160. Lee S M, Kyoung D K, Santosh P L. Utilization of glucose, maltose, dextrin and cellulose by juvenile flounder (Paralichthys olivaceus). Aquaculture, 2003, 221:427-438
    
    161. Li T Q, Hao Y J, An R Y, Gao Y J. Effect of feed protein content on digestibility of juvenile (Acipenser schrenckii) for various nutritive components. Freshwater Fisheries (in Chinese), 2002, 32: 51-54
    
    162. Lin J H, Cui Y B, Hung S S O, Shiau S Y. Effect of feeding strategy and carbohydrate source on carbohydrate by white sturgeon (Acipenser transmontanus) and hybrid tilapia (Oreochromis niloticusxO. aureus). Aquaculture, 1997, 148:201-211
    
    163. Lin Y H, Shiau S Y. Dietary vitamin E requirement of grouper (Epinephelus malabaricus) at two lipid levels, and their effect on immune responses. Aquaculture,2005, 248: 235-244
    164. Lygren B, Hamer K, Waagbo R. Effect of induced hyperoxia on the antioxidant status of Atlantic salmon (Salmo salar L) fed three different levels of dietary vitamin E. Aquac Res, 2000, 31: 401-407
    
    165. Mai K, Zhang C, Ai Q. Dietary phosphorus requirement of large yellow croaker (Pseudosciaena crocea R). Aquaculture, 2006, 251: 346-353
    
    166. Maria del S N, Encarnacio'n C, Pablo R, Joan B, Joaquim G, Isabel N. Glucagon and insulin response to dietary carbohydrate in rainbow trout (Oncorhynchus mykiss). General and Comparative Endocrinology, 2004,139: 48-54
    
    167. Mckenzie D J, Piraccini G, Papini N, Bronzi P, Bolis C G, Taylor EW. Oxygen consumption and ventilatory reflex are influenced by dietary lipids in sturgeon. Fish physiology and Biochemistry, 1997, 16: 365-379
    
    168. Medale F, Blanc D, Kaushik S J. Studies on the nutrition of Siberian sturgeon,Acipenser baeri. EL Utilization of dietary non-protein energy by sturgeon.Aquaculture, 1991, 93: 143-154
    
    169. Medale F, Corraze G, Kaushik S J. Nutrition of fanned Siberian sturgeon. In:Gershanovic A D and Smith T I J (eds) Proceedings of the Third Internation Symposium on Sturgeons. Vniro Publishing, Moscow, Russia, 1995: 289-298 pp
    
    170. Mohamed J S, Sivaram V, Christopher R, Marian M P, Murugardass S, Hussain M R.Dietary vitamin A requirement of juvenile greasy grouper (Epinephelus tauvina).Aquaculture, 2003, 219: 693-701
    
    171. Montero D L, Tort L, Robaina J M. Low vitamin E in diet reduces stress resistance of gilthead seabream (Spars aurata) juveniles. Fish Shellfish Immunol, 2001, 11:473-490
    
    172. Moore B J, Hung S S O, Medrano J F. Protein requirement of hatchery-produced juvenile white sturgeon (Acipenser transmontanus). Aquaculture, 1988, 71: 235-245
    
    173. Moreau R, Dabrowski K, Sato P H. Renal L-gulono-l,4-lactone oxidase activity as affected by dietary ascorbic acid in lake sturgeon (Acipenser fulvescens).Aquaculture, 1999, 180: 359-372
    
    174. Moreau R, Dabrowski K. a-tocopherol downergulates gulonolactone oxidase activity in sturgeon. Free Radical Biology and Medicine, 2003, 34: 1326-1332
    
    175. Moreau R, Kaushik S J, Dabrowski K. Ascorbic acid status as affected by dietary treatmen in the Siberian sturgeon (Acipenser baeri Brandt): tissue concentration,mobilization and L-gulonolactone oxidase activity. Fish Physiology and Biochemistry, 1996, 15: 431-438
    
    176. Moren M, Opstad I, Bemtssen M H G, Zambonino I J L, Hamre K. An optimum level of vitamin A supplements for Atlantic halibut (Hippoglossus hippoglossus L.) juveniles. Aquaculture, 2004, 235: 587-599
    
    177. Mottram D S, Edwards R A, Macfie H J H. A comparison of the flavour volatiles from cooked beef and pork meat systems. J Sci Food Agric, 1982, 33(9): 934-944
    
    178. Murai T, Andrews J W. Interactions of dietary a-tocopherol, oxidized menhaden oil and ethoxyquin on channel catfish (Ictalurus punctatus). J Nutr, 1974, 104:1416-1431
    
    179. National Research Council (NRC): Nutrient Requirements of Fish. National Academy Press, Washington DC, 1993
    
    180. Ng W K, Hung S S O, Herold M A. Poor utilization of dietry free anmino acids by white sturgeon. Fish Physiology and Biochemistry, 1996, 15: 131-142
    
    181. Ng W K, Hung S S O. Amino acid composition of whole body, eggs, and selected tissues of juvenile white sturgeon. Aquaculture, 1994, 126: 329-339
    
    182. Noone E J, Roche H M, Nugent A P. The effect of dietary supplementation using isomeric blends of conjugated linoleic acid on lipid metabolism in healthy human subjects. British Journal of Nutrition, 2002, 88: 243-251
    
    183. Nordoy A, Marchioli R, Arnesen H. n-3 polyunsaturated fatty acid and cardiovascular disease. Lipids, 2001, 36: 127-129
    
    184. Ogino C, Takeda H. Requirements of rainbow trout for dietary calcium and phosphorus. Bull Jpn Soc Sci Fish, 1978, 44: 1019-1022
    
    185. Onishi T, Murayama S. Takeuchi M. Changes in digestive enzyme levels in carp after feeding-III. Response of protease and amylase to twice-a-day feeding. Bulletin of the Japanese Society of Scientific Fisheries, 1976,42(8): 921-929
    
    186. Papp Z G, Jeney Z, Jeney G Effect of different levels of dietary vitamin C on growth, ascorbate concentration in some tissue and physiological status of sturgeon hybrid (Acipenser ruthenus L. x Acipenser baeri brandt). In: Gershanovich, A D ,Smith, T I J eds., Proceedings of the Third International Symposium on Sturgeons. Moscow: Vniro Publishing, 1995: 309-313
    
    187. Papp Z G, Saroglia M, Jeney Z, Jeney G, Terova G Effect of dietary vitamin C on tissue ascorbate and collagen status in sturgeon hybrids (Acipenser ruthenus L.xAcipenser baeri brandt). Journal of Applied Ichthyology, 1999, 15: 258-260
    
    188. Pettigrew J E. An economic analysis of feeding conjugated linoleic acid to finishing pigs. 30th Annual Meeting of Proceedings of the American Association of Swine Practitioners. 1999: 149-151
    
    189. Prabir K R, Santosh P L. Dietary phosphorus requirement of juvenile haddock (Melanogra-mmus aeglefinus L.). Aquaculture, 2003, 221: 451-468
    
    190. Qing H A, Kangsen M, Tan B P, Xu W, Zhang W B, Ma H M Liu F Z G. Effect of dietary vitamin C on survival, growth, and immunity of large yellow croaker(Pseudosciaena crocea)
    
    191. R Dabrowski K, Sato P H. Renal L-gulono-1,4- lactone oxidase activity as affected by dietary ascorbic acid in lake sturgeon( Acipenser fulvescens). Aquac, 1999, 180:359 -372
    
    192. Radi E, Abrami G, Serrini G, Mckenzie D, Bolis C, Bronzi P. The role of dietary n-3 fatty acid and vitamin E supplements in growth of sturgeon (Acipenser naccarii).Comparative Biochemistry and Physiology, 1993a, 105: 187-195
    
    193. Rainuzzo J, Reitan K. The significance of lipids at early stages of marine fish: a review. Aquaculture, 1997, 155(2): 103-115
    
    194. Rawles S D, Gatlin III D M. Carbohydrate utilization in striped bass (Morone saxatilis) and sunshine bass (M. chrysopsxM. saxatilis).Aquaculture, 1998, 161:201-212
    
    195. Robbins K R, Norton H W, Baker D H. Estimation of nutrient requirements from growth data. J Nutr, 1979, 109: 1710-1714
    
    196. Roy P K, Lall S P. Dietary phosphorus requirement of juvenile haddock (Melanogrammus aeglefinus L). Aquaculture, 2003, 221: 451-468
    
    197. Saleh G, Eleraky W, Gropp J M. A short note on the effect of vitamin A hypervitaminosis and hypovitaminosis on health and growth of Tilapia nilotica (Oreochromis niloticus). J. Appl. Ichthyol, 1995, 11: 382-385
    
    198. Sargent J, Bell G Recent developments in the essential fatty acid nutrition of fish. Aquaculture, 1999, 177(2): 191-199
    
    199. Schaefer A, Koppe W M, Gunther, K D. Effect of P-supply on growth and mineralization in mirror carp. J Appl Ichthyol, 1995, 11: 397-400
    
    200. Sener E, Yildiz M, Savas E. Effect of Dietary Lipids on Growth and Fatty Acid Composition in Russian Sturgeon (Acipenser gueldenstaedtii) Juvenile.Turk J Vet Anim Sci, 2005, 29: 1101-1107, 10: 32-36
    
    201. Shiau S Y, Chen Y. Estimation of the dietary vitamin A requirement of juvenile grass shrimp(Penaeus mondon.) J Nutri, 2000, 130: 90-94
    
    202. Shiau S Y, Shiau L F. Re-evaluation of the vitamin E requirements of juvenile tilapia (Oreochromis niloticusxO. aureus). Anim Sci, 2001, 72: 529-534
    
    203. Shiau S Y. Utilization of carbohydrates in warmwater fish-with particular reference to tilapia (Oreochromis niloticus x 0. aureus). Aquaculture, 1997, 151: 79-96
    
    204. Silass O, Hung F, Kofi F A, Paul B L, Xu R P. Ability of Juvenile White Sturgeon (Acipenser transmontanas) to Utilize Different Carbohydrate Sources. The Journal of Nutrition, 1989, 119: 727-733
    
    205. Sirri F, Tallarico N, Meluzzi A. Fatty acid composition and productive trails of broiler fed diets containing conjugated linoleic acid. Poult Sci, 2003, 82: 1356-1361
    
    206. Skonberg D I, Rasco B A, Dong F M. Fatty Acid Composition of Salmonid Muscle Changes in Response to a High Oleic Acid Diet. Journal of Nutrition, 1994, 124(9):1628-1638
    
    207. Skonberg D I, Yogev L, Hardy R W. Metabolic response to dietary phosphorus intake in rainbow trout. Aquaculture, 1997, 157:11-24
    
    208. Skonberg D I, Yogev L, Hardy R W. Metabolic response to dietary phosphorus intake. In:Tashjian D H, Teh S J, Sogomonyan A, Hung S S O. Bioaccumulation and chronic toxicity of dietary L-selenomethionine in juvenile white sturgeon (Acipenser transmontanus). Aquatic Toxicology, 2006, 79: 401-409
    
    209. Smith S B, Hively T S, Cortese G M. Conjugated linoleic acid depresses the delta9 desaturase index and stearoyl coenzyme A desaturase enzyme activity in porcine subcutaneous adipose tissue. J Anim Sci, 2002, (80): 2110-2115
    
    210. Stephanie F, Didier B, Jeannine B, Christiane V, Cedric B, Thierry R, Pierre B.Effect of dietary oxidized lipid and vitamin A on the early development and antioxidant status of Siberian sturgeon (Acipenser baeri) larvae. Aquaculture, 2006,257:400-411
    
    211. Stuart J S, Hung S S O. Growth of juvenile white sturgeon (Acipenser transmontanus) fed different proteins. Aquaculture, 1989,76: 303-316
    
    212. Suhenda N, Djajadiredja R. Determination the optimum level of vitamin premix for the diet of common carp {Cyprinus carpio L.) fingerlings. In: Cho C Y, Cowey C B,Watanabe T eds., Fish Nutrition in Asia, Ottawa: IDRC, 1985: 130-135
    
    213. Szymczyk B, Pisulewski P M. Effect of conjugated linoleic acid on growth perform an ce, feed conversion efficiency, and subsequent car-cass quality in broiler chickens. Br J Nutr, 2001, 85: 465-473
    
    214. Takeuchi M, Nakazoe J. Effect of dietary phosphorus on lipid content and its composition in carp. Bull Jpn Soc Sci Fish, 1981,47: 347-352.
    
    215. Takeuchi T, Watanabe K, Satoh S. Requirement of grass carp fingerling for a-tocopherol. Nip Sui Gak, 1992, 9: 1742-1749
    
    216. Thompson I, Choubert G, Houlihan D. F, Secombes C J.The effect of dietary vitamin A and astaxanthin on the immunocompetence of rainbow trout. Aquaculture,1995,133:91-133
    
    217. Thompson I, Fletcher T C. The effect of dietary vitamin A on the immunocompetence of Atlantic salmon (Salmo salar L.). Fish Physiol Biochem.1994, 12(6): 513-523
    
    218. Thompson K D,Tatner M F, Henderson R J. Effect of dietary (n-3) and (n-6) polyunsaturated fatty acid ratio on the immune response of Atlantic salmon (Salmo salar L). Aquaculture Nutrition, 2006, 2(1): 21-31
    
    219. Twibell R G, Watkins B A, Brown P B. Dietary Conjugated Linoleic Acids and Lipid Source Alter Fatty Acid Composition of Juvenile Yellow Perch (Perca flavescens).Journal of Nutrition. 2001, 131: 2322-2328
    
    220. Twibell R G, Watkins B A, Rogers L. Effect of dietary conjugated linoleic acids on hepatic and muscle lipids in hybrid striped bass. Lipids, 2000, 35(2): 155-161
    
    221. Twibell R G, Wilson R P. Effect of dietary conjugated linoleic acids and total dietary lipid concentrations on growth responses of juvenile channel catfish, Ictalurus punctatus. Aquaculture, 2003, 221: 621-628
    222. Vielma J, Koskela J, Ruohonen K. Growth, bone mineralization, and heat and low oxygen tolerance in European whitefish fed with graded levels of phosphorus.Aquaculture, 2002, 212: 321-333
    
    223. Wang X J, Choi S M, Park S G. Optimum dietary phosphorus level of juvenile Japanese flounder (Paralichthys olivaceus) reared in the recirculating system. Fish Sci,2005,71: 168-173
    
    224. Wang X J, Kim K W, Bai S C, Huh M D, Cho B Y. Effect of the different levels of dietary vitamin C on growth and tissue ascorbic acid changes in parrot fish (Oplegnathusfasciatus). Aquaculture, 2003, 215: 21-36
    
    225. Watanabe T, Murakami A, Takeuchi L. Requirement of chum salmon held in freshwater for dietary phosphorus. Bull Jpn Soc Sci Fish, 1980,46: 361-367
    
    226. Watanabe T, Takashima T, WadA M. The relationship between dietary lipid levels and a-tocopherol requirement of rainbow trout. Bull Jpn Soc Sci Fish, 1981b, 47:1463-1471
    
    227. Watanabe T, Takeuchi T, Matsui M. Effect of a-tocopherol deficiency on carp: VII.The relationship between dietary levels of linoleate and a-tocopherol requirement.Bull Jpn Soc Sci Fish, 1977,43: 935-946
    
    228. Wei Q, He J, Yang D, Zheng W, Li L. Status of sturgeon aquaculture and sturgeon trade in China: a review based on two recent nationwide surveys. Journal of Applied Ichthyology, 2004, 20: 321-332
    
    229. Wiegand B R, Sparks J C, Parrish F C. Duration of feeding conjugated linoleic acid influences growth performance, carcass traits, and meat quality of finishing barrows.Journal of Animal Science, 2002, 80(3): 637-643
    
    230. Wilson R P, Bowser P R, Poe W E. Dietary vitamin E requirement of fingerling channel catfish. J Nutr, 1984, 114: 2053-2058
    
    231. Wing K N, Phaik K L, Peng L B. Dietary lipid and palm oil source affects growth,fatty acid composition and muscle a-tocopherol concentration of African catfish (Clarias gariepinus). Aquaculture, 2003 (215): 229-243
    
    232. Xie Z, Niu C, Zhang Z, Bao L. Dietary ascorbic acid may be necessary for enhancing the immune response in Siberian sturgeon (Acipenser baerii), a species capable of ascorbic acid biosynthesis. Comparative Biochemistry and Physiology, 2006, 145: 152-157
    
    233. Xu R, Hung S S O, German J B. White sturgeon tissue fatty acid composition are affected by dietary lipids.The Journal of Nutrition, 1993, 123: 1685-1692
    
    234. Xu R, Hung S S O. Effect of dietary lipids on the fatty acid composition of triglycerides and phospholipids in tissues of white sturgeon. Aquaculture nutrition,1996, 2: 101-109
    
    235. Xu X, Storkson J, Kim S. Short-term intake of conjugated linoleic acid inhibits lipoprotein lipase and glucose metabolism but does not enhance lipolysis in mouse adipose tissue. J Nutr, 2003, 1333: 663-667
    
    236. Yasmin A, Takeuchi T, Hayashi M. Effect of conjugated linoleic and docosahexaenoic acids on growth of juvenile tilapia (Oreochromis niloticus).Fisheries Science, 2004, 70(3): 473-481
    
    237. Zhang C, Mai K, Ai Q. Dietary phosphorus requirement of juvenile Japanese seabass, Lateolabrax japonicus. Aquaculture, 2006, 255: 201-209
    
    238. Zhuang P, Boyd K, Zhang L. Overview of biology and aquaculture of Amur sturgeon (Acipenser schrenckii) in china. Journal of Applied Ichthyology, 2002,18(4-6): 659-664
    
    239. Zhuang P, Boyd K, Zhang L.2002. Ontogenetic behavior and migration of Chinese sturgeon (Acipenser sinensis). Environmental Biology of Fishes, 65: 83-97

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700