33 resultados para RATION
em Chinese Academy of Sciences Institutional Repositories Grid Portal
Resumo:
The effect of ration on growth and energy budget of Chinese longsnout catfish was investigated in a growth trial. Fish of initial body weight of 6.5 g were fed at six ration levels (RLs): starvation, 0.8%, 1.6%, 2.4%, 3.2% of body weight per day, and apparent satiation for 8 weeks. Fish were weighed biweekly to adjust feed amount. The results showed that specific growth rate in wet weight, protein and energy increased logarithmically with increased RLs. The relationship of specific growth rate in wet weight (SGRw, % day(-1)) and RL (%) was a decelerating curve: SGRw=-0.62+3.10 Ln(RL+1). The energy budget equation at satiation was: 100 IE=12.94 FE+5.50(ZE+UE)+40.07 HE+41.49 RE, where IE, FE, (ZE+UE), HE, RE are food energy, faecal energy, excretory energy, heat production and recovered energy respectively. Body composition was slightly but significantly affected by ration size except for protein content. The most efficient ration based on the relationship between RL and feed efficiency ratio in energy (FERe) was 1.8% of body weight per day.
Resumo:
Two growth trials using a range of ration sizes from starvation to maximum feeding suggested that linear relationships existed between specific growth rate and ration size for Nile tilapia and givel carp, Continuous measurement of activity showed that activity level, in terms of distance swum per day, was not affected significantly by ration size in both Nile tilapia and gibel carp. (C) 2001 The Fisheries Society of the British Isles.
Resumo:
Nile tilapia weighing 8.29-11.02 g were fed a practical diet at seven ration levels (starvation, 0.5, 1, 2, 3, 4% body weight per day and satiation) twice a day at 30 degrees C. Feed consumption, apparent digestibility, nitrogenous excretion and growth were determined directly, and heat production was calculated by difference of energy budget. The relationship between specific growth rate in wet weight (SGR(w), percentage per day) and ration size (RL, percentage per day) was a decelerating curve described as SGR(w) = 2.98 (1 - e(-0.61(RL-0.43))). The apparent digestibility coefficients for dry matter and protein showed a decreasing pattern with increasing ration while the apparent digestibility coefficient of energy was not significantly affected by ration size. The proportion of gross energy intake lost in nitrogenous excretion tended to decrease with increasing ration. Feed efficiency was highest, and the proportion of gross energy intake channelled to heat production was lowest, at an intermediate ration level (2% per day). The energy budget at the satiation level was: 100IE = 16.9FE + 1.2(ZE + UE) + 62.3HE + 19.6RE, where IE, FE, (ZE + UE), HE and RE represent gross energy intake, faecal energy, excretory (non-faecal) energy loss, heat production and recovered energy (growth), respectively. (C) 1997 Elsevier Science B.V.
Resumo:
Growth and energy budget were measured for three sizes(2.4, 11.1 and 22.5 g) of juvenile white sturgeon Acipenser transmontanus held at 18.5 degrees C and fed tubificid worms at different levels ranging from starvation to ad libitum. For each size-class, specific growth rate increased linearly with increasing ration, and conversion efficiency was highest at the maximum ration. Growth rate decreased with increasing fish size at the maximum ration, but increased with size al each restricted ration. Conversion efficiency increased with increasing ration for each size-class and was usually highest at the maximum ration. Faecal production accounted for 3.2-5.2% of food energy. The proportion of food energy lost in nitrogenous excretion decreased with increasing ration. With increases in ration, the allocation of metabolizable energy to metabolism decreased, while that to growth increased. Fish size had no significant effect on the allocation of metabolizable energy to metabolism or growth. Al the maximum ration, on average 64.9% of metabolizable energy was spent on metabolism, and 35.1% on growth. (C) 1996 The Fisheries Society of the British Isles
EFFECT OF RATION SIZE ON THE GROWTH AND ENERGY BUDGET OF THE GRASS CARP, CTENOPHARYNGODON-IDELLA VAL
Resumo:
Young grass carp (12-13 g) were kept at five ration levels ranging from starvation to ad libitum feeding at 30-degrees-C. They were fed duckweed. Food consumption, absorption efficiency and growth were determined directly, and metabolism and nitrogenous excretion calculated indirectly from energy and nitrogen budgets, respectively. The relationship between specific growth rate and ration size was linear. Absorption efficiency for energy was not affected by ration size and averaged 50.6 +/- 0.57% (mean +/- s.e.). Depending on ration size, energy lost in excretion accounted for 4.5-5.9% of the food energy, energy channelled to metabolism accounted for 34.4-48.3% of the food energy, and energy retained as growth accounted for 6.7-11.9% of the food energy. Regardless of ration, a constant proportion of food energy (30.7%) was accounted for by feeding metabolism (total metabolism minus fasting metabolism). The energy budget at the maximum ration was: 100 C = 49.1F + 4.5U + 3.6R(fa) + 30.9R(fe) + 11.9G, where C, F, U, R(fa), R(fe) and G represent food consumption, faecal production, excretion, fasting metabolism, feeding metabolism and growth, respectively.
Resumo:
Various borates, vanadates, niobates, antimonates, titanates, zirconates and CaS doped with Dy3+ were prepared. Factors which have an effect on the yellow-to-blue intensity ratio (Y/B) of Dy3+ emission are reported. Y/B increases with decreasing Z/r or electronegativity of the next-neighbour element M in the complex oxides Dy-O-M. The greater the degree of covalency between Dy3+ and O2-, the greater Y/B is. When Dy3+ is located at a site with an inverse centre and high symmetry, Dy3+ displays no luminescence. It seems that Y/B of Dy3+ located at a site deviated from an inverse centre is greater than that of Dy3+ located at a site without an inverse centre. Y/B does not vary much with the variation in concentration of Dy3+ when Dy3+ is substituted for an element with the same valency, but it does depend on the concentration of Dy3+ when Dy3+ is substituted for an element with a different valency in the matrix, because defects are formed in this case.
Sensitivity Analysis of Dimensionless Parameters for Physical Simulation of Water-Flooding Reservoir
Resumo:
A numerical approach to optimize dimensionless parameters of water-flooding porous media flows is proposed based on the analysis of the sensitivity factor defined as the variation ration of a target function with respect to the variation of dimensionless parameters. A complete set of scaling criteria for water-flooding reservoir of five-spot well pattern case is derived from the 3-D governing equations, involving the gravitational force, the capillary force and the compressibility of water, oil and rock. By using this approach, we have estimated the influences of each dimensionless parameter on experimental results and thus sorted out the dominant ones with larger sensitivity factors ranging from10-4to10-0 .
Resumo:
This is the first part of direct numerical simulation (DNS) of double-diffusive convection in a slim rectangular enclosure with horizontal temperature and concentration gradients. We consider the case with the thermal Rayleigh number of 10^5, the Pradtle number of 1, the Lewis number of 2, the buoyancy ratio of composition to temperature being in the range of [0,1], and height-to-width aspect ration of 4. A new 7th order upwind compact scheme was developed for approximation of convective terms, and a three-stage third-order Runge-Kutta method was employed for time advancement. Our DNS suggests that with the buoyancy ratio increasing form 0 to 1, the flow of transition is a complex series changing fromthe steady to periodic, chaotic, periodic, quasi-periodic, and finally back to periodic. There are two types of periodic flow, one is simple periodic flow with single fundamental frequency (FF), and another is complex periodic flow with multiple FFs. This process is illustrated by using time-velocity histories, Fourier frequency spectrum analysis and the phase-space rajectories.
Resumo:
针对啁啾脉冲放大技术建成的钛宝石激光装置,提出一种获得高重复率激光脉冲列的方法.通过改变钛宝石再生放大器中泡克耳斯盒电光开关的传统工作模式,使得腔内放大的脉冲从某特定时刻起,每当在腔内往返一次就以一定的倒出比例(倒出率)倒出腔内脉冲能量的一部分,从而可以在有限的时间段内产生高重复率的啁啾激光脉冲列.基于Franz-Nodvik放大理论,建立了该高重复率再生放大器的理论模型,通过数值计算,系统地分析了初始增益、倒出时刻、倒出率对输出的脉冲序列的影响.在抽运功率为35mJ、倒出率为1/2的实验条件下,通过腔外
Resumo:
实验采用三倍频Nd:YAG(波长355nm,脉宽8ns,频率30Hz)脉冲激光器作为抽运光源,在ZnO纳米粉末(直径~100nm)中发现了类似激光现象.并用环形腔理论模拟了ZnO的颗粒密度对平均自由程的影响,从理论上证明在纳秒级激光器的抽运下,ZnO纳米粉末也可以发射激光.
Resumo:
近年来,种群空间分布格局日益为生态学家所重视,已成为生态学发展最快的领域和生态学理论发展的核心之一,群落的植被盖度和生物多样性是生态学研究的常用指标。植物种群分布格局及群落特征是种群和群落对环境条件长期适应和选择的结果,一方面决定于植物自身的生物学特性,另一方面与种群和群落分布的生境密切相关,对于揭示植被对环境的适应规律及它们之间的相互关系具有十分重要的意义。 本文以油蒿种群为研究对象,沿着鄂尔多斯高原从东至西的降水梯度(336~249mm),应用传统的分布格局检验法以及点格局方法进行油蒿种群分布格局的研究;采用Gleason 指数、Shannon-Wiener 指数、Pielou 指数和Simpson 指数分析比较油蒿群落的生物多样性。从格局分析的尺度问题、严密性以及聚集程度变化趋势等几个方面,对本文采用的种群分布格局分析方法进行比较,为种群分布格局分析方法的选择提供参考。 种群分布格局分析结果表明沿着降水递减的梯度,在小尺度上油蒿种群分布格局表现为由均匀分布向随机分布转变的趋势;在大尺度上则表现为由随机分布向聚集分布转变的趋势。沿降水逐渐减弱的梯度上,油蒿种群的聚集程度逐渐增强。降水梯度对油蒿种群分布格局的影响一方面由油蒿本身的生物学特性决定,在降雨量小的地区,油蒿母株周围幼苗的存活率高,呈现聚集分布格局,而降雨量大的地区,油蒿幼苗存活概率比较平均,形成随机分布格局;其次,降雨量较大的地区,土壤水分资源较充足,油蒿个体较大,个体之间以竞争关系为主,聚集程度较低,降雨量少的地区,油蒿个体较矮小,个体之间为共同抵御恶劣生境,呈现聚集分布的格局。 群落FPC 和生物多样性指数与年平均降水量的回归分析结果显示,降水量越大,植被盖度越高,物种丰富度越大,群落物种分布均匀程度和优势度越低。充足的降雨促进油蒿群落的发育,草本层植物长势更好,生物量增加,群落的结构趋于复杂。 传统的分布格局检验方法和点格局方法在油蒿种群分布格局分析应用中得到的结果具有高度一致性,然而在实际工作中,这些方法之间具有各自的优劣和适应性。 建议在选取种群分布格局的分析方法时,要充分考虑研究目的,根据具体的物种和实验环境确定采用的方法。需在各细微尺度上做种群分布格局分析时,点格局方法优于传统的分析方法;在大范围取样及对工作效率要求较高时,方差均值比率法和聚集强度指数法更适合。由于聚集强度指数法在进行结果判定时比较模糊,建议优先选择方差均值比率法,将聚集强度指数法作为参考。降雨的减少显著改变了植物种群的空间分布格局和群落结构及物种组成,在进行生态恢复时可以参照本文的分析结果进行恢复植被的合理配置。
Resumo:
Silver carp (Hypophthalmichthys molitrix) and bighead carp (Aristichthys nobilis) were used as a new pen-cultureed biomanipulation technique to control algal blooms in Meiliang Bay of Lake Taihu. In order to evaluate the capacity of these two fishes to decrease algal blooms, diel feeding samplings were carried out in May (without algal blooms) and September (with algal blooms) in 2005. Based on estimated food consumption by the Elliott-Persson model, silver carp increased daily food consumption from 2.07 g dry weight per 100 g wet body weight in May before the outbreak of algal blooms to 4.98 g dry weight per 100 g wet body weight in September during algal blooms outbreak. However, no obvious variation of food consumption was observed in bighead carp during the study period. This species 1.88 and 1.54 g dry weight of plankton per 100 g wet body weight in May and September, respectively. Silver carp had a higher feeding capacity for plankton than bighead carp. Biotic factors (i.e., fish size and conspecific competition with natural species in the lake) may affect the feeding behaviors of both carps as well as seasonal variation of plankton communities in the pen.
Resumo:
Three large fish pens (0.36 km(2) of each) stocked with silver and bighead carp were set up in Meiliang Bay for controlling toxic Microcystis blooms. The responses of plankton communities and food consumption of silver and bighead carp were studied. Crustacean zooplankton were significantly suppressed in the fish pens. Total phytoplankton biomass, Microcystis biomass and microcystin concentration were lower in the fish pens than in the surrounding lake water, but the difference was not statistically significant. The present stocking density of silver plus bighead carp (about 40 g/m(3) in July) was likely too low to achieve an adequate control of Microcystis. Silver carp fed mainly on phytoplankton but bighead carp mainly on zooplankton: mean zooplankton contribution in the gut was 31.5% for silver carp and 64.7% for bighead carp. Compared with previous studies, both carp species preyed upon more zooplankton because of the abundant food resource. Daily rations of silver and bighead carp were estimated by Egger's model in the main growing season. Filtration rate was calculated from the daily ration and the density of plankton in the lake. During May-October, filtration rates of silver and bighead carp for phytoplankton were 0.22-1.53 L g(-1) h(-1) and 0.02-0.68 L g(-1) h(-1), respectively, and filtration rates for zooplankton were 0.24-0.44 L g(-1) h(-1) and 0.08-1.41 L g(-1) h(-1), respectively. Silver carp had a stronger ability of eliminating phytoplankton than bighead carp. To achieve a successful bioniampulation with a minimum effect of ichthyoeutrophication, the stocking proportion of bighead carp should be controlled in the future practice. (c) 2007 Elsevier B.V All rights reserved.
Resumo:
The icefish (Neosalanx taihuensis) of Lake Chaohu, China, foraged almost exclusively on crustacean zooplankton in both spring and summer. The icefish showed diurnal feeding periodicity, with peak feeding in the morning. No food was observed in icefish guts collected at night. Our results indicate that that the icefish was a particulate feeder and light intensity greatly affected its foraging on zooplankton. Daily consumption of zooplankton by icefish varied significantly both diurnally and among seasons, which ranged from 0.22 to 2.23 g (wet weight) per 100 g wet fish weight at temperatures between 16.3 degrees C (spring) and 28.8 degrees C (summer).