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1.
Abstract.— The present study was conducted to investigate the effects of dietary supplementation of β‐1,3 glucan and a laboratory developed feed stimulant, BAISM, as feed additives for juvenile olive flounder, Paralichthys olivaceus. Eight experimental diets were formulated to be isonitrogenous and isocaloric and to contain 50.0% crude protein and 16.4 kJ of available energy/g with or without dietary β‐1,3 glucan and BAISM supplementation. β‐1,3 glucan (G) and BAISM (B) were provided at 0% in the control diet (G0B0) and at 0.05% G + 0.45% B (G0.05B0.45), 0.05% G + 0.95% B (G0.05B0.95), 0.1% G + 0.90% B (G0.1B0.9), 0.10% G + 1.90% B (G0.1B1.9), 0.15% G + 1.35% B (G0.15B1.35), 0.15% G + 2.85% B (G0.15B2.85), and 0.30% G + 2.70% B (G0.3B2.7) in experimental diets. After the feeding trial, fish fed G0.1B0.9, G0.1B1.9, and G0.15B1.35 diets had higher percent weight gain (WG), feed efficiency ratio (FER), specific growth rate (SGR), protein efficiency ratio (PER), and condition factor (CF) than those fed G0B0, G0.05B0.45, G0.05B0.95, G0.15B2.85, and G0.3B2.7 diets (P < 0.05); however, there was no significant differences among fish fed G0.1B0.9, G0.1B1.9, and G0.15B1.35 diets. Fish fed G0.1B0.9 and G0.1B1.9 diets had higher chemiluminescent responses (CL) than those fed the other diets (P < 0.05). Lysozyme activity of fish fed G0.1B0.9 diet was significantly higher than that of fish fed the other diets (P < 0.05). These results indicated that the optimum dietary supplementation level of β‐1,3 glucan and BAISM could be approximately 0.10% β‐1,3 glucan + 0.90% BAISM (G0.1B0.9) of diet based on WG, FER, SGR, PER, CF, CL, and lysozyme activity in juvenile olive flounder, P. olivaceus.  相似文献   
2.
A 10‐wk feeding trial was conducted to evaluate the potential use of fermented fisheries by‐products and soybean curd residues mixture (FFSM) as a partial replacement for fish meal (FM) in the diet of juvenile olive flounder, Paralichthys olivaceus. Five experimental diets were formulated with FFSM replacing 0, 15, 30, 45, and 60% of the FM protein (FFSM0, FFSM15, FFSM30, FFSM45, and FFSM60, respectively). Juvenile olive flounder averaging 5.99 ± 0.08 g (mean ± SD) were randomly distributed into aquaria at 15 fish/aquarium, with three replicate aquaria for each experimental diet. Weight gain (WG) of fish fed FFSM0, FFSM15, and FFSM30 was significantly higher than that of fish fed FFSM45 and FFSM60 (P < 0.05). Also, WG of fish fed FFSM45 was significantly higher than that of fish fed FFSM60 (P < 0.05). There were no significant differences in WG among fish fed FFSM0, FFSM15, and FFSM30 (P > 0.05). Specific growth rate (SGR) of fish fed FFSM15 was significantly higher than that of fish fed FFSM45 and FFSM60 (P < 0.05). Also, SGR of fish fed FFSM0, FFSM15, FFSM30, and FFSM45 was significantly higher than that of fish fed FFSM60 (P < 0.05). There were no significant differences in SGR among fish fed FFSM0, FFSM15, and FFSM30 and among those fed FFSM0, FFSM30, and FFSM45 (P > 0.05). Feed efficiency (FE) and protein efficiency ratio (PER) of fish fed FFSM60 were significantly lower than those of fish fed FFSM0, FFSM15, FFSM30, and FFSM45 (P < 0.05); however, there were no significant differences in FE and PER among fish fed FFSM0, FFSM15, FFSM30, and FFSM45. Hepatosomatic index of fish fed FFSM0, FFSM15, and FFSM30 was significantly higher than that of fish fed FFSM60 (P < 0.05); however, there were no significant differences among fish fed FFSM0, FFSM15, FFSM30, and FFSM45 and among those fed FFSM45 and FFSM60. No significant differences were observed in condition factor and survival rate among all dietary groups tested. The whole‐body proximate composition averaged 75.0 (% dry matter basis [DM]), 8.66 (% DM), 16.38 (% DM), and 76.1%, for crude protein, crude lipid, ash, and moisture, respectively. Based on growth performance, the FFSM could replace up to 30% FM protein by the ANOVA test; however, broken‐line model analysis indicated 28.7% as an optimum replacement level in juvenile olive flounder diets.  相似文献   
3.
An eight‐week study was conducted to determine the optimum dietary choline level in juvenile olive flounder, Paralichthys olivaceus. Seven diets were prepared to contain 0, 250, 500, 750, 1,000, 2,000 and 3,000 mg/kg diet. Juveniles (5.9 ± 0.03 g; 5.5 ± 0.4 cm; mean ± SD) were randomly distributed into 21 tanks (25 fish/tank) and fed one of the diets in triplicates. Survival rate of fish fed the diet containing the lowest choline level was significantly lower than those of fish fed the other diets (p < 0.05). Final body weight, weight gain, specific growth rate, feed efficiency and protein efficiency ratio significantly increased with increasing choline levels up to 1,000 mg/kg diet. Whole‐body protein and lipid contents increased in accordance with choline levels up to 750 mg/kg diet, beyond which they plateaued. Liver and muscle lipid contents elevated with increasing choline levels up to 2,000 mg/kg diet. Plasma cholesterol esters, triglycerides, cholesterol and total lipids were significantly influenced by the graded choline levels; however, responses of those indices were not identical. Broken‐line analyses of weight gain and liver choline concentrations responding to the graded choline levels revealed that choline requirements of the juvenile flounder could be between 847 and 1,047 mg/kg diet.  相似文献   
4.
A 10‐wk feeding experiment was conducted to evaluate the potential use of fermented soybean curd residues (FSCR) as an energy source in diets for juvenile olive flounder, Paralichthys olivaceus. Five isonitrogenous and isoenergetic diets were formulated to contain dry soybean curd residues to replace wheat meal (WM) at the levels of 0, 25, 50, 75, and 100% (FSCR0, FSCR25, FSCR50, FSCR75, and FSCR100, respectively). Fish averaging 6.00 ± 0.07 g (mean ± SD) were randomly distributed into 15 aquaria as groups of 15 fish and fed the experimental diets in triplicate at a rate of 4–5% of wet body weight per day twice daily on dry matter basis. At the conclusion of the feeding trial, weight gain (WG) and specific growth rate (SGR) of fish fed diet FSCR25 were significantly higher than those of fish fed diets FSCR50, FSCR75, and FSCR100 (P < 0.05); however, there were no significant differences in WG and SGR among fish fed diets FSCR0 and FSCR25 and among those fed diets FSCR0 and FSCR50. Feed efficiency and protein efficiency ratio of olive flounder fed diet FSCR25 were significantly higher than those of fish fed diets FSCR50, FSCR75, and FSCR100 (P < 0.05); however, there were no significant differences in these parameters among fish fed diets FSCR0 and FSCR25 and among those fed diets FSCR0, FSCR50, FSCR75, and FSCR100. Hematological characteristics, condition factor, hepatosomatic index, and survival rate of fish fed FSCR0 were not significantly different from those of fish fed the other diets. These results indicated that FSCR could replace up to 50% WM as an energy source in juvenile olive flounder diets based on ANOVA test.  相似文献   
5.
This experiment was conducted to study the effects of the graded recombinant bovine somatotropin (rBST) levels on growth, plasma rBST concentrations, and body composition of Korean rockfish, Sebastes schlegeli, and to estimate the optimum oral dosage of rBST. Seven experimental diets were formulated to be isonitrogenous and isocaloric and to contain 49.0% crude protein and 16.7 kJ available energy/g, with 0, 5, 10, 15, 20, 25, or 50 mg rBST/kg body weight (BW)/wk (rBST0, rBST5, rBST10, rBST15, rBST20, rBST25, and rBST50, respectively). After the feeding trial, fish fed all the diets supplemented with rBST showed higher weight gain (WG), feed efficiency (FE), specific growth rate (SGR), and protein efficiency ratio (PER) than those fed the rBST0 diet (P < 0.05). WG of fish fed rBST15, rBST20, rBST25, and rBST50 diets was significantly higher than that of fish fed rBST0 and rBST5 diets (P < 0.05); however, there were no significant differences among fish fed rBST10, rBST15, rBST20, rBST25, and rBST50 diets. FE of fish fed rBST15 and rBST20 diets was significantly higher than that of fish fed rBST0, rBST5, rBST10, and rBST50 diets, and fish fed rBST10, rBST25, and rBST50 diets had significantly higher FE than those fed rBST0 and rBST5 diets (P < 0.05). SGR of fish fed all the diets supplemented with rBST was significantly higher than that of fish fed rBST0 diet (P < 0.05); however, there were no significant differences among fish fed all the diets supplemented with rBST. PER of fish fed rBST15 and rBST20 diets was significantly higher than that of fish fed rBST0, rBST5, and rBST50 diets, and fish fed rBST10, rBST25, and rBST50 diets had significantly higher PER than those fed rBST0 and rBST5 diets (P < 0.05). Whole‐body protein of fish fed rBST15 diet was significantly higher than that of fish fed rBST0, rBST5, and rBST10 diets (P < 0.05); however, there were no significant differences among fish fed rBST15, rBST20, rBST25, and rBST50 diets. Plasma rBST concentrations of fish fed all the diets began to rise at 3 h after oral administration of rBST; the maximum plasma rBST concentration peaked at 12 h and returned to the basal level at 24 h. Broken‐line model analyses of WG and FE were 12.8 and 13.2 mg rBST/kg BW/wk, respectively. These results indicated that the optimum oral dosage could be greater than 12.8 mg rBST/kg BW/wk but less than 13.2 mg rBST/kg BW/wk in juvenile Korean rockfish.  相似文献   
6.
This study was conducted to evaluate the dietary α‐tocopherol (vitamin E) requirement in juvenile sea cucumber, Apostichopus japonicus. Sea cucumbers averaging 1.48 ± 0.07 g (mean ± SD) were randomly distributed into 18 rectangular plastic tanks of 20 L capacity in a recirculating system (20 animals per tank). Six semi‐purified experimental diets with average protein and crude lipid levels (dry matter) of 29.7 ± 0.36% and 4.39 ± 0.23% (mean ± SD), respectively were formulated to contain 0 (E4), 15 (E12), 30 (E23), 60 (E44), 120 (E77) and 600 (E378) mg α‐tocopherol/kg diet, supplied as dl‐α‐tocopheryl acetate. Diets were analyzed for α‐tocopherol content by HPLC and the α‐tocopherol levels were 4.01, 12.4, 23.1, 44.3, 77.4 and 378 mg α‐tocopherol/kg diet for E4, E12, E23, E44, E77 and E378 diets, respectively. Casein and defatted fish meal were used as the protein sources in the diets while wheat flour was the carbohydrate source. Sea cucumbers were fed each of the six experimental diets in triplicate groups. At the end of the 14‐week feeding trial, weight gain (WG), specific growth rate (SGR) and feed efficiency (FE) of sea cucumbers fed on E23, E44, E77 and E378 diets were significantly (P < 0.05) higher than those of animals fed on E4 and E12 diets. However, there were no significant differences in WG, SGR and FE among sea cucumbers fed on E23, E44, E77 and E378 diets or among those fed on E4 and E12 diets. Survival of sea cucumbers fed on E44, E77 and E378 diets were significantly higher than those of animals fed on E4, E12 and E23 diets. However, there were no significant differences among sea cucumbers fed on E4, E12 and E23 diets or among those fed on E44 and E77 diets. Whole‐body vitamin E concentration increased with α‐tocopherol content of the diets. Broken line analysis of WG showed an optimum dietary α‐tocopherol requirement of 41 mg α‐tocopherol/kg diet in sea cucumber. These results indicated that the optimum dietary α‐tocopherol requirement in sea cucumber in the form of dl‐α‐tocopheryl acetate could be higher than 23.1 mg α‐tocopherol/kg diet but lower than 44 mg α‐tocopherol/kg diet.  相似文献   
7.
A 14‐wk feeding trial was carried out to evaluate the optimum dietary ascorbic acid (AA) level in juvenile sea cucumber, Apostichopus japonicus. Sea cucumbers averaging 1.49 ± 0.07 g (mean ± SD) were randomly distributed into 18 rectangular plastic tanks of 20 L capacity in a recirculating system (20 animals per tank). Six semipurified experimental diets were formulated to contain 0 (l ‐ascorbyl‐2‐monophosphate [AMP]; AMP0), 30 (AMP24), 60 (AMP48), 120 (AMP100), 240 (AMP206), and 1200 (AMP1045) mg AA/kg diet in the form of AMP using casein as the main protein source. Sea cucumbers were fed each of the six experimental diets in triplicate groups. At the end of 14 wk of feeding trial, weight gain (WG), specific growth rate (SGR), and feed efficiency (FE) of sea cucumbers fed AMP100, AMP206, and AMP1045 were significantly (P < 0.05) higher than those of animals fed AMP0, AMP24, and AMP48. However, there were no significant differences in WG, SGR, and FE among sea cucumbers fed AMP100, AMP206, and AMP1045 and among animals fed AMP0, AMP24, and AMP48. Whole‐body vitamin C concentration increased with AA content of the diets. Broken‐line analysis of WG showed an optimum dietary AA level of 105.3 mg AA/kg diet in sea cucumber. These results indicated that the optimum dietary vitamin C level in sea cucumber in the form of AMP could be greater than 100 mg AA/kg diet but less than 105.3 mg AA/kg diet.  相似文献   
8.
A 2 × 3 factorial design was used to reevaluate the dietary protein requirements and to determine the optimum dietary protein to energy (P/E) ratios in Japanese eel, Anguilla japonica, reared in the recirculating system. For each of two experiments, six experimental diets (45P16, 45P17, 45P19, 50P16, 50P17, and 50P19) were formulated and prepared to contain two protein levels (45 and 50%) and three energy levels (16, 17, and 19 kJ/g diet) at each protein level. In the first experiment, glass eel of initial weight 0.1 ± 0.02 g (mean ± SD) were used, while the second experiment was conducted with juvenile eel of initial weight 15.0 ± 3 g (mean ± SD). The first and second experimental periods were 6 and 16 wk for the glass and juvenile eel, respectively. At the end of the first experiment, there were no protein, energy, and their interaction effects. Also, there were no significant differences in weight gain (WG), specific growth rate (SGR), feed efficiency (FE), and protein efficiency ratio (PER) for glass Japanese eel fed all diets. Although there were no significant differences in growth parameters of glass eel fed all experimental diets, these parameters were higher for fish fed 50P16 than for fish fed the other diets. For the second experiment, there were significant protein effects on WG, SGR, and PER (P < 0.05). However, there were neither significant energy effects nor protein and energy interaction effects on WG, SGR, FE, and PER. Fish fed 45P19 had a higher WG, SGR, and PER than did fish fed 45P16, 50P16, and 50P19 (P < 0.05). However, there were no significant differences in growth parameters among fish fed 45P16, 45P17, 50P16, 50P17, and 50P19 and among those fed 45P17, 45P19, and 50P17. These results may indicate that the optimum dietary protein requirement and the P/E ratio could be 44.3% and 24.1 mg protein/kJ (45P19), respectively, in juvenile Japanese eel, based on WG, SGR, and PER.  相似文献   
9.
Two feeding trials using different commercial feeds and different fish sizes were conducted to compare model performance of various regression models on the estimation of optimum feeding rates (OFR; % BW/day) for juvenile olive flounder. Six feeding rates ranging from 1% to 11% in trial I and another six feeding rates ranging from 1% to 6% in trial II were tested. Final body weight, weight gain, feed conversion ratio, condition factor, nutrient gains, and whole‐body lipid and energy contents were significantly influenced by the feeding rates in both trials. The overall responses shown in trial I were generally comparable to those observed in trial II. In trial I, the OFR was estimated to be 7.3%, 5.7%, 9.8% and 10.2% by the one‐slope straight broken‐line, two‐slope straight broken‐line, quadratic broken‐line and quadratic models, respectively. In trial II, the OFR was estimated to be 4.8%, 4.6%, 8% and 8% by the one‐slope broken‐line, two‐slope broken‐line, quadratic broken‐line and quadratic models, respectively. Based on the model selection criteria (R2adj and AICc), the quadratic broken‐line model was selected as the best‐fit model in both trials. This model that describes the dose–response relationship best among the tested models can be recommended when determining an OFR.  相似文献   
10.
Uterine has a pivotal role in implantation and conceptus development. To prepare a conducive uterine condition for possibly new gestation during the estrous cycle, uterine endometrium undergoes dramatic remodeling. In addition, angiogenesis is an indispensable biological process of endometrium remodeling. Furthermore, essential protein expressions related to important biological processes of endometrium remodeling, which are vascular endothelial growth factor (VEGF), myoglobin (MYG), collagen type IV (COL4), fucosyltransferase IV (FUT4), and cysteine‐rich protein 2 (CRP2), were detected in the endometrial tissue reported in many previous studies and recently discovered in histotroph substrates during the estrous cycle. Those proteins, which are liable for provoking new vessel development, cell proliferation, cell adhesion, and cell migration, were expressed higher in the histotroph during the luteal phase than follicular phase. Histotroph proteins considerably contribute to endometrium remodeling during the estrous cycle. To that end, the following review will discuss and highlight the relevant information and evidence of the uterine fluid proteins as endometrial‐secreted factors that adequately indicate the potential role of the uterine secretions to be involved in the endometrial remodeling process.  相似文献   
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