中华鲟幼鱼循环饥饿后的补偿生长和体成分变化

研究中华鲟(Acipenser sinensis)幼鱼循环饥饿后的补偿生长和体成分变化。实验设4个循环饥饿组(T1:饥饿1 d,饱食投喂3 d;T2:连续饥饿2 d,饱食投喂4 d;T3:连续饥饿4 d,饱食投喂6 d;T4:连续饥饿7 d,饱食投喂8 d)和1个对照组(T0:每天饱食投喂)。结果显示:在水温21.5～25.4℃条件下,T1组末重和特定生长率均超过对照组,表现为超补偿生长;T2组末重和特定生长率均接近对照组,表现为完全补偿生长,T1、T2组食物转化率均显著高于对照组;T3、T4组实际摄食水平均明显高于对照组,但表现为不能补偿生长。4个循环饥饿组幼鱼肝体比及脏体比均显著高于对照组。各组肌肉蛋白质和脂肪含量下降,同时水分和灰分含量上升;从饥饿2 d组开始,蛋白质和脂肪含量显著低于对照组,且蛋白质含量比脂肪含量下降幅度更大。     

饥饿和补偿生长对红鲫幼鱼生长和体组分的影响

分析了饥饿和冉投喂处理后红鲫（Carassius auratus red variety）幼鱼的生长和体组分变化。饥饿状态下,红鲫幼鱼体重、比肝重、肥满度和肝体指数下降,各饥饿组体重均与同期对照组存在极显著差异（P〈0．01）,其中饥饿15d组体重与初始体重存在极显著差异（P〈0．01）,肝糖原、粗蛋白和粗脂肪含量下降,水分和灰分含量上升;再投喂后,除饥饿15d组肝糖原与对照组仍有极显著差异外,其他各项指标均恢复到与对照组无显著差异。实验过程中,各饥饿组食物转化率均明显高于对照组,且与对照组存在极显著差异（P〈0．01）,其中饥饿10d组最高,达到了24．38％。结果表明,红鲫幼鱼存在完全补偿生长能力,其完全补偿生长是通过提高食物转化率（FCE）来实现的,短期饥饿时将糖原和粗脂肪作为主要能源物质。     

千年笛鲷幼鱼的饥饿和补偿生长

研究了在22.5～31.9 ℃条件下,千年笛鲷幼鱼在不同饥饿时间（0、2、4、6、9、11 d）处理后再投喂的补偿生长。千年笛鲷幼鱼的体重在短时间（2～6 d）的饥饿后下降不大,9 d以上的饥饿可导致幼鱼的体重明显下降。经过饥饿11 d后,鱼体蛋白质含量明显下降,脂肪含量略有下降,灰分含量有所上升,水分含量明显上升,表明千年笛鲷幼鱼在饥饿过程中主要依靠消耗蛋白质作为能量来源。恢复投喂后,各组的鱼体生化组成均恢复到对照组水平。饥饿11 d组鱼在恢复投喂后全部死亡,半致死时间为10～11 d。结果表明：饥饿2 d组的千年笛鲷幼鱼在恢复生长过程中具有超补偿生长能力,该补偿现象通过提高食物转化率达到;饥饿4 d组幼鱼具有完全补偿生长能力;饥饿6 d组幼鱼仅有部分补偿生长能力;饥饿9 d组幼鱼不具有补偿生长能力;饥饿11 d组幼鱼为饥饿致死。图5表1参13     

饥饿和补偿生长对史氏鲟幼鱼摄食、生长和体成分的影响

报道了饥饿和再投喂对史氏鲟幼鱼摄食、生长以及生化组成的影响.22±2℃条件下,随着饥饿时间延长,幼鱼白肌的RNA/DNA比值不断减小,体重逐渐下降,后者与同期对照组之间存在极显著性差异(P<0.01).饥饿7d,鱼的肝糖原和肌糖原含量显著降低(P<0.05),但随着饥饿时间的延长,肝糖原和肌糖原含量则出现不同程度的回升;脂肪含量和蛋白质含量分别在饥饿14d和21d时下降幅度最大,提示史氏鲟幼鱼动用储存物质的顺序依次是糖原、脂肪和蛋白质.而饥饿过程中鱼体水分和灰分含量则有所上升.恢复投食后,饥饿幼鱼的摄食强度增大,生长加快,其中7d、14d饥饿组幼鱼的RNA/DNA比值达到或接近正常投喂组水平,但21d饥饿组的比值仍明显低于正常投喂组(P<0.05).恢复投食30d后,7d和14d饥饿组幼鱼体重接近对照组(P>0.05),21d饥饿组的终体重未能赶上对照组(P<0.05),这表明史氏鲟幼鱼的补偿生长随饥饿时间不同而异.试验结束时,各处理组鱼体生化组成与正常投喂组没有显著差异(P>0.05).     

饥饿后再投喂对哲罗鱼生长和体成分的影响

在14-18℃条件下,对平均初始体重（35.15±1.06）g的哲罗鱼（Hucho taimen）进行了不同时间的饥饿处理和再投喂的恢复生长实验。实验共设5个处理组,分别为S0组（对照组,持续投喂56d）、S1组（饥饿7天后再投喂49d）、S2组（饥饿14天后再投喂42d）、S3组（饥饿21天后再投喂35d）和S4组（饥饿28天后再投喂28天）,每组30尾鱼,研究再投喂后体重和体成分（粗蛋白、粗脂肪、水分和灰分）的变化。实验结果显示：与持续投喂组相比,饥饿7d后哲罗鱼体重下降了11.52%;饥饿14d后体重下降了17.09%;饥饿21d和28d后体重分别下降了26.24%和36.07%。恢复投喂结束时饥饿7d组体重赶上了对照组,饥饿14d组体重超过了对照组,饥饿21d和28d组体重低于对照组。在饥饿和恢复投喂过程中其体成分呈规律性变化：在各试验组饥饿后,鱼体躯干脂肪含量下降,躯干水分和灰分含量升高,蛋白质含量略有下降。恢复投喂后各营养成分逐渐恢复。     

饥饿和恢复投喂对翘嘴鲌幼鱼摄食、生长及体成分的影响

研究了在20.3~24.8℃条件下分别饥饿0 d、4 d、8 d、12 d和16 d后恢复投喂16 d对翘嘴鲌(Culter al-burnus)幼鱼摄食、生长及体成分的影响。结果显示:随着饥饿时间延长,幼鱼体质量损失率显著增大;肝体指数变小,水分和灰分含量逐渐升高;粗脂肪含量在饥饿前期下降较快,饥饿后期下降速率降低,各饥饿组与对照组差异显著(P<0.05);粗蛋白含量饥饿前期下降缓慢,饥饿4 d、8 d组与对照组差异不显著(P>0.05),饥饿后期下降明显,饥饿12 d、16 d组与对照组有显著差异(P<0.05);比能值不断下降,除饥饿4 d组外,各饥饿组与对照组都有显著差异(P<0.05)。恢复投喂后,各饥饿组鱼体生化组成和鱼体比能值均恢复至对照组水平,恢复投喂期间各饥饿处理组的摄食率显著高于对照组(P<0.05)。结果表明:饥饿4 d、8 d组翘嘴鲌幼鱼具有完全补偿生长能力;饥饿12 d、16 d幼鱼仅有部分补偿生长能力。     

饥饿和补偿生长对点带石斑鱼幼鱼摄食和生长的影响

在水温29.2±0.2℃条件下,对点带石斑鱼幼鱼(1.832±0.03 g)进行了不同时间的饥饿后再供食的恢复生长试验。对照组(S0)持续投喂30 d,饥饿组S2、S4、S6、S8和S10分别饥饿2 d、4 d、6 d、8 d和10 d后再分别恢复投喂28 d、26 d、24 d、22 d和20 d。结果表明:饥饿组在恢复投喂后,体重迅速增重,且S2的体重超过了S0,但两者体重差异不显著(P>0.05),而其他各饥饿组的体重均显著低于S0和S2组(P<0.05)。点带石斑鱼经饥饿再恢复投喂,其特殊生长率和摄食率均显著高于S0(P<0.05);食物转化率呈波动变化,各饥饿组的食物转化率大部分均低于S0。比较分析认为,S2为完全补偿生长,其他各试验组为部分补偿生长,且这种补偿生长效应主要是通过恢复生长阶段提高摄食水平来实现。     

投喂频率对青鱼幼鱼生长和体成分的影响

为研究不同投喂频率对青鱼生长和体成分的影响,采用自制的配合饲料,在日投喂量相同的情况下,分别以每天1、2、3、4、5次的投喂频率饲养5组青鱼幼鱼(平均初始体质量为0.61 g)45 d。试验结果:随着投喂频率由每天1次增至3次,青鱼幼鱼的终末体质量、增重率、特定生长率、饲料效率、蛋白质效率及蛋白质贮积率均显著提高(P0.05)。但当投喂频率由每天3次增至5次,这些指标在不同投喂组间无显著差异(P0.05)。对全鱼营养成分的分析表明,水分含量在不同投喂组间无显著差异(P0.05),粗蛋白、粗脂肪及灰分含量在不同投喂组间有显著差异(P0.05),其中随着投喂频率的增加,粗脂肪含量呈下降趋势,而灰分含量则呈上升趋势。试验结果表明,青鱼幼鱼适宜的日投喂频率为3次。     

饥饿后再投喂对异育银鲫生长和体成分的影响

在(25±2)℃条件下,对体重(15.6±0.84)g的异育银鲫(Carassius auratus gibelio)进行了不同时间的饥饿处理和再投喂的恢复生长实验。实验把异育银鲫分为4组,为Ⅰ组(持续投喂48 d)、Ⅱ组(饥饿8 d后再投喂40 d)、Ⅲ组(饥饿16 d后再投喂32 d)和Ⅳ组(饥饿24 d后再投喂24 d),每组20尾鱼,研究再投喂后体重和体成分(粗蛋白、粗脂肪、水分和灰分)的变化。结果显示:与持续投喂组相比,饥饿8 d后异育银鲫体重下降了13.28%,饥饿16 d和24 d后体重分别下降了22.36%和33.03%。短期饥饿(Ⅱ)组,再恢复投喂8 d后能实现完全补偿生长,而中长期饥饿组(Ⅲ和Ⅳ)分别在投喂16 d和24 d后表现为部分补偿生长。在饥饿和恢复投喂过程中其体成分呈现规律性变化:各试验组饥饿后,粗蛋白和粗脂肪显著下降,而水分和灰分含量上升,而再投喂后,各营养成分逐渐恢复。Ⅱ组再投喂8 d后,粗脂肪和粗灰份恢复到对照组水平,蛋白质显著低于对照组水平,水分显著高于对照组;再投喂40 d后,粗蛋白和水分亦恢复到对照水平,Ⅲ组恢复投喂16 d后,粗蛋白、粗脂肪和灰分不能恢复到对照水平,恢复投喂32 d后,除灰分外,其余成分皆不能恢复到对照水平。Ⅳ组再投喂24 d后,除水分外,其余各营养成分皆不能恢复到对照水平。结果表明,实现异育银鲫完全补偿生长,其饥饿时间以短时间饥饿8 d为宜。     

饵料蛋白能量比对黑鲷幼鱼生长和体成分的影响

取黑鲷(Sparusmacrocephalus)幼鱼960尾,体重(3.39±0.18)g,以鱼粉和豆粕作为蛋白源,鱼油和豆油等比例混合油作为脂肪源,共配制4个蛋白水平(34%、38%、42%、46%),每一蛋白水平设3个脂肪水平(10%、13%、16%),共12种饵料,糖水平保持在16%左右,饵料的蛋白能量比(P/E)在96.76～136.21mg/kcal。黑鲷幼鱼随机分成12组,每组设2重复,实验为期42d。结果表明,对特定生长率(SGR)与饵料系数(FCR)的影响,以较高蛋白组(38%、42%、46%)显著优于低蛋白组(34%)(P<0.05),中、高脂肪组(13%、16%)显著优于低脂肪组(10%)(P<0.05);各组饵料对成活率的影响无显著差异(P>0.05)。当蛋白水平为42%,脂肪水平为16%时,黑鲷幼鱼获得最大特定生长率(3.20)、最高蛋白质效率(2.10)和最小饵料系数(1.14)。全鱼脂肪含量随着饵料中脂肪水平的提高而逐渐升高。在同一饵料蛋白水平内,全鱼蛋白与灰分含量随着饵料脂肪水平的提高呈逐渐升高趋势。经统计分析,饵料中不同蛋白能量比显著影响黑鲷幼鱼生长(P<0.05),饵料中脂肪有明显节约蛋白质的作用(P<0.05)。由生长及体成分的实验结果得出,黑鲷幼鱼的最适饵料蛋白水平为42%,最适蛋白能量比(P/E)为110.37mg/kcal。     

循环饥饿后异育银鲫幼鱼的补偿生长及部分生理生化指标的变化

在(28±1)℃水温条件下,以4种循环饥饿的投喂方式饲养初始体重为1.58 g的异育银鲫(Carassius auratus gibelio)幼鱼,研究其补偿生长和部分生理生化指标的变化。实验分为四组,第一组每天投喂,为对照组,第二组投喂4 d后饥饿1 d,第三组投喂2 d后饥饿1 d,第四组投喂1 d后饥饿1 d,4种方式分别以C、R1/4、R1/2和R1/1表示,试验持续60 d。结果显示,3个试验组的实际摄食率均显著高于对照组(P<0.05),但饲料转化效率均显著低于对照组,导致3个试验组的特定生长率显著下降,体重未赶上对照组,而且饥饿时间越长,体重增长率越低。鱼体的蛋白质、灰分含量未受到投喂方式的显著影响,干物质、脂肪和能量含量随饥饿时间增加显著下降;肥满度、肝体比、ATP酶、SOD酶活性以及谷丙转氨酶和谷草转氨酶活性也随饥饿时间的增加显著下降。     

Compensatory growth,feed intake and body composition of Labeo rohita fingerlings following feed deprivation

Ten‐week study was performed on Labeo rohita fingerlings (av. wt. 3.75 ± 0.06 g) to investigate the nature of compensatory growth. Fingerlings were deprived of food for 0 (control), 1 (D1), 2 (D2) or 3 (D3) weeks and refed to satiation for 5 weeks. The feed deprivation was carried out in D3 group on week 3, 4 and 5; D2 group on week 4 and 5; D1 group on week 5, and refeeding of all the groups were started from week 6 onwards. The D1 and D2 groups caught up in body weight with that of control fish within 2 weeks and 4 weeks of refeeding, respectively, but the D3 group had significantly (P < 0.05) lower body weight than the control after 5 weeks of refeeding. Higher growth efficiency was observed in all the feed deprived groups in the 1st week of refeeding only. Feed intake in D1 group became similar with the control after 5 weeks of refeeding, but the D2 and D3 groups were still hyperphagic when the experiment terminated. Thus, compensatory growth was due to hyperphagia and improved growth efficiency. In conclusion, complete compensatory growth was observed in L. rohita fingerlings after feed deprivation of 1 and 2 weeks.     

Compensatory growth of juvenile black sea bream,Acanthopagrus schlegelii with cyclical feed deprivation and refeeding

An 8‐week feeding trial was conducted to evaluate compensatory growth of juvenile black sea bream, Acanthopagrus schlegelii (initial weight 9.56 ± 0.12 g) in fifteen 300 L indoors flow‐through circular fibreglass tanks. Feeding regimes was designed as follows: the control group (fed continuously), and S1, S2, S3 and S4 groups experienced 1, 2, 3 and 4 days of feed deprivation and then refeeding for the remaining days per week respectively. Changes in body weight, specific growth rate (SGR), feed intake (FI) and feed efficiency ratio (FER) were examined biweekly during the trial. At the end of the cyclical feeding periods, survival was not significantly affected by feeding strategy (P > 0.05). Final body weight of fish in S1 group was significantly higher than the control group (P < 0.05) after an 8 weeks trial, and fish in the S2 group reached the same body weight of the control fish (P > 0.05), however, the growth data in the S3 and S4 groups could not catch‐up with the control treatment (P < 0.05). In the first 4 weeks, SGR values of fish with feed deprivation more than 2 days per week were inferior to those of control group (P < 0.05); however, no significant differences of SGR were observed among the groups for the last 4 weeks (P > 0.05). FI increased significantly with the starvation days increasing during the whole feeding trial (P < 0.05). At the periods 2, 4 and 6 weeks, FER values increased significantly with increasing feed‐deprivation days up to S2 group and then levelled off (P < 0.05); however, FER in S2 group was only higher than that in S0 and S1, but no significant differences were found among the other treatments at the end of week 8. Significant differences were found in apparent digestibility coefficients (ADCs) of dry matter and crude protein among the treatments, while ADCs of crude lipid were unaffected. Protein and lipid contents in whole body and dorsal muscle showed declining tendency with increasing food deprivation days, while moisture contents tended to increase (P < 0.05). Serum parameters were markedly affected by feeding regimes except for total protein concentration and thyroxine level. The present results indicated that starvation for 1 and 2 days per week of juvenile black sea bream could achieve over‐compensation and complete compensation respectively. However, in case of longer term feed restriction regime, fish failed to obtain good growth performance.     

Feeding dynamics in fish experiencing cycles of feed deprivation: a comparison of four species

Abstract The temporal dynamics of daily food consumption were examined in individually housed fish that experienced four cycles of 1 week of feed deprivation followed by 2 weeks of feeding to satiation. Four species were compared: European minnows Phoxinus phoxinus: Cyprinidae; three‐spined sticklebacks Gasteosteus aculeatus: Gasterosteidae: gibel carp Carassius auratus gibelio: Cyprinidae; and the longsnout catfish Leiocassis longirostris: Bagridae. The stickleback, carp and catfish showed significant compensatory increases in food intake following deprivation, with the response becoming clearer in successive cycles. The temporal pattern of consumption during the refeeding periods differed between the four species. In sticklebacks, daily intake over a refeeding period initially decreased, but then recovered. In minnows, intake tended to decline over a refeeding period. Gibel carp showed an increase in daily intake on refeeding, but this may have reflected an adverse response to weighing. Over a refeeding period, catfish had a weak tendency to show an initial decline, followed by an increase. These differences are discussed in relation to differences in experimental protocols and biological differences between the species.     

Compensatory growth and body composition of juvenile black rockfish <Emphasis Type="Italic">Sebastes schlegeli</Emphasis> following feed deprivation

ABSTRACT:   Compensatory growth, feeding rate, feed efficiency and chemical composition of juvenile black rockfish (mean weight 1.43 g) were investigated for 35 days after a 14-day feed deprivation treatment under four feeding conditions: one group continuously fed (control) and the other three groups fasted for 5 days (F5), 10 days (F10) and 14 days (F14). All fasted fish were re-fed from day 15. Only F5 achieved the same body weight as the control, indicating that complete compensation occurred in F5. The specific growth rate (SGR) of F5 was the highest at day 21 and then decreased thereafter, showing higher values than the control at days 21, 28 and 42. In contrast, although SGRs of F10 and F14 were higher than that of the control during the whole refeeding period except day 21, they did not catch up the control in body mass, indicating that only partial compensation occurred in F10 and F14. The feeding rate (FR) of all groups except F14 changed in a pattern similar to SGR (Spearman's rank correlation, r _s > 0.9), suggesting that SGR varied depending on FR. Similar feeding efficiencies (FEs) were found in the four groups and they did not vary significantly during the whole refeeding period, suggesting that FE was not the factor affecting SGR. At day 14, the ratios of lipid to lean body mass in F10 and F14 were lower than those in the control and F5, and there was no difference between the control and F5. At day 49, however, only F14 showed a lower value than the other three groups, and there was no difference among the three groups. These results indicate that juvenile black rockfish fasted for 5–14 days can exhibit compensatory growth after refeeding, but timing and degree vary depending on the duration of feed deprivation.     

Changes in the proximate composition of juvenile white suckers following re-feeding after a prolonged fast

Cultured juvenile white suckers, Catostomus commersoni, are commonly held over winter without the provision of exogenous feed. This study examined the ability of suckers to recover from prolonged fasting, and the energy partitioning strategies employed during the re-feeding phase. In one trial, white suckers held, without exogenous feed, in commercial lake cages for a prolonged period were fed a semi-moist salmonid diet. Although the fish consumed the feed, they exhibited negligible growth over the 12 weeks of the trial, and there was no evidence of increases in tissue lipid, glycogen or protein. In the second trial, previously well-fed juvenile white suckers were starved for 20 weeks and then re-fed. Condition factor (K), but not body weight was increased during the 8 week trial. However, hepatosomatic index (HSI), hepatic and somatic glycogen, and somatic lipid and protein reserves (expressed as a percentage of tissue) were significantly increased during the re-feeding period. Further, changes in plasma thyroid hormone levels indicated an important role of these hormones in the energy partitioning events. The poor growth of juvenile white suckers in intensive culture may be caused by deleterious changes in feed conversion ability resulting from extended fasting of the fish prior to grow-out.     

Compensatory growth responses in juvenile fat snook,Centropomus parallelus Poey,following food deprivation

The compensatory growth in juvenile fat snook (13.7 g) was evaluated in fish subjected to four treatments: continuously fed (control); subjected to 1 (D1), 2 (D2) and 3 (D3) weeks of food deprivation, followed by a 5‐week re‐feeding period. At the end of food deprivation, the body weights at the different treatments were significantly different and inversely related to the length of the food deprivation period (C=16.425 g; D1=14.024 g; D2=13.542 g; D3=12.228 g). During re‐feeding, no differences were observed in the slopes of body weight growth curves among treatments, indicating failure in full growth compensation. In the first re‐feeding week (week 4), although hyperphagia was observed for all re‐fed groups, better food conversion ratios were detected only for D1 and D2, reflected in an enhancement in the specific growth rates. From week 5 onwards, no differences between treatments and control were detected for any variable. The total food intake was lower for D2 and D3 compared with the control. In the present study, fish showed partial compensatory growth when subjected to a maximum of 2 weeks of food deprivation. Therefore, the food deprivation can promote production losses, even considering a reduction in the total food intake.     

异育银鲫经过低温下停食后的补偿生长

在室内水槽中进行了10周实验,以检验异育银鲫(Carassius auratus gibeli)经过低温下停食后的补偿生长。实验鱼初始体质量为(5.1±0.1)g,分为4组:2组鱼在第1~4周内被停食,在第5~10周分别恢复投喂蛋白能量比为23 g.MJ-1(SL组)和26 g.MJ-1(SH组)的等能饲料;另2组鱼(CL组和CH组)在1~4周内投喂蛋白能量比为23 g.MJ-1的饲料,在第5~10周分别投喂蛋白能量比为23 g.MJ-1(CL组)和26 g.MJ-1(CH组)的饲料。第1~4周内水温控制在14.8~15.2℃,第5~10周内水温控制在24.8~25.2℃。结果表明,第4周结束时SL组和SH组体质量明显低于CL组和CH组;SL组和SH组全鱼水分、蛋白质和灰分百分含量明显高于CL组和CH组,但脂肪含量明显低于后者。恢复投喂期间,SL组在第7~10周内SGR高于CL组,SH组第5~8周内SGR高于CH组,但SL组与SH组,CL组与CH组之间SGR无显著差异(P>0.05)。实验结束时,SL组和SH组的体质量分别低于CL组和CH组,SL组与SH组间及CL组与CH组间体质量无显著差异(P>0.05);SL组和SH组全鱼、躯干和内脏团内蛋白质和灰分含量分别高于CL组和CH组,脂肪含量分别低于CL组和CH组。本实验结果显示,经过低温下停食后,异育银鲫仅表现出部分补偿生长能力,恢复投喂期间增加饲料蛋白质含量未明显增强异育银鲫的补偿生长。[中国水产科学,2007,14(1):113-119]