The effects of birth weight and estimated breeding value for protein deposition on nitrogen efficiency in growing pigs

The effects of birth weight (BiW; low BiW [LBW] vs. high BiW [HBW]) and estimated breeding value (EBV) for protein deposition (low EBV [LBV] vs. high EBV [HBV]) on N retention, N efficiency, and concentrations of metabolites in plasma and urine related to N efficiency in growing pigs were studied. At an age of 14 wk, 10 LBW–LBV (BiW: 1.07 ± 0.09 [SD] kg; EBV: −2.52 ± 3.97 g/d, compared with an average crossbred pig with a protein deposition of 165 g/d), 10 LBW–HBV (BiW: 1.02 ± 0.13 kg; EBV: 10.47 ± 4.26 g/d), 10 HBW–LBV (BiW: 1.80 ± 0.13 kg; EBV: −2.15 ± 2.28 g/d), and 10 HBW–HBV (BiW: 1.80 ± 0.15 kg; EBV: 11.18 ± 3.68 g/d) male growing pigs were allotted to the experiment. The pigs were individually housed in metabolism cages and were subjected to an N balance study in two sequential periods of 5 d, after an 11-d dietary adaptation period. Pigs were assigned to a protein adequate (A) or protein restricted (R, 70% of A) regime in a change-over design. Pigs were fed 2.8 times the energy requirements for maintenance. Nontargeted metabolomics analyses were performed in urine and blood plasma samples. The N retention (in g/d) was higher in the HBW than in the LBW pigs (P < 0.001). The N retention (in g/[kg metabolic body weight (BW^0.75) · d]) and N efficiency, however, were not affected by the BiW of the pigs. The N retention (P = 0.04) and N efficiency (P = 0.04) were higher in HBV than in LVB pigs on the A regime but were not affected by EBV in pigs on the R regime. Restricting the dietary protein supply with 30% decreased the N retention (P < 0.001) but increased the N efficiency (P = 0.003). Nontargeted metabolomics showed that a hexose, free amino acids (AA), and lysophosphatidylcholines were the most important metabolites in plasma for the discrimination between HBV and LBV pigs, whereas metabolites of microbial origin contributed to the discrimination between HBV and LBV pigs in urine. This study shows that BiW does not affect N efficiency in the later life of pigs. Nitrogen efficiency and N retention were higher in HBV than in LBV pigs on the A regime but similar in HBV and LBV pigs on the R regime. In precision feeding concepts aiming to further optimize protein and AA efficiency in pigs, the variation in EBV for protein deposition of pigs should be considered as a factor determining N retention, growth performance, and N efficiency.     

Energy metabolism of growing broilers in relation to the environmental temperature

7 experiments with 6 chickens each (origin Tetra B) in the live weight range between greater than 100 and less than 300 g and up to 1800 g were carried out at environmental temperatures (ET) of 35, 30, 25 (2 experiments) 20 (2 experiments) and 15 degrees C. In the course of each experiment the chickens alternatively received feed mixtures containing 20 and 40% crude protein (3 animals/variant) for maintenance and weight gain (semi ad libitum). Energy metabolism was measured according to indirect calorimetry over a total of 645 metabolism periods. In the temperature range studied there was no compensation between thermoregulatory heat and heat from other metabolic processes. The partial utilization of metabolizable energy for energy retention in the body was independent of ET and remained in the limits between 71 and 73%. Energy utilization was dependent on the protein content of the feed. It decreased from 75 to 69% with the increase of the protein content from 20 to 40%. Energy requirement for protein retention varied between 1.67 and 1.89 kJ metabolizable energy/kJ and was independent of ET. Energy requirement (metabolizable energy) for the maintenance of the energy balance was independent of the protein content of the feed. It increased from 433 kJ/kg LW0.75.d at 35 degrees C to 693 kJ/kg LW0.75.d at 15 degrees C ET. The relationship between heat production and ET is parabolic. The thermoneutral temperature decreased from 35 to 25 degrees C in the course of development. In the live weight range of 300-500 g thermoregulatory heat production had its maximum with 19 kJ/kg LW0.75.d.K and decreased in the further development to 10-13 kJ/kg LW0.75.d.K.     

Energy requirements of young female cattle. 6. Energy requirements

Results taken from 6 experiments with young female cattle comprising 477 metabolism periods served the derivation of the animals energy requirement in the development range greater than 125 kg live weight according to the factorial method. The energy requirement per kg LW0.75 and day, calculated from metabolism data, was independent of the stage of development and the intensity of feeding. It averaged 455 +/- 66 kJ metabolizable energy/kg LW0.75.d and 250 +/- 37 kJ NEFcattle/kg LW0.75.d respectively. The partial energy requirement for live weight gain, expressed in net energy fat, was equivalent to the energy content of the live weight gain. Energy retention and thus energy requirement per kg live weight gain increased with the live weight and reached a maximum of 26 MJ. Energy retention per kg live weight gain largely depended on the intensity of feeding and the stage of gravidity. Restrictive energy supply and progressing gravidity decreased energy content in the weight gain. The influences mentioned were taken into consideration on the derivation of the partial requirement for live weight gain. Equations were developed for the estimation of the energy requirement of young female cattle, which can be applied to both gravid and non-gravid cattle.     

Energy metabolism of growing rats in relation to the environmental temperature

8 experiments were carried out with 9 albino rats each (Wistar line, bred at the institute) in the live weight range between 70 and 200 g and at environmental temperatures (ET) of 34, 32, 30, 28, 26, 24, 22 and 20 degrees C. In the course of each individual experiment the rats were alternatively fed for maintenance and weight gain (semi ad libitum) with feed mixtures containing 10, 25 and 40% crude protein (3 animals/variant). Energy metabolism was measured according to the method of indirect calorimetry over a total of 780 metabolism periods. In the temperature range studied there was no compensation between thermoregulatory heat and heat from other processes of the metabolism. The partial utilization of metabolizable energy for energy retention in the body was independent of ET and ranged between 73 and 80% for the 7 experiments with ET between 32 and 20 degrees C. Energy utilization depended on the protein content of the feed and decreased from 81 to 79 or 73 resp. when the protein content increased from 10 to 25% or to 40% resp. Energy requirement for protein retention varied between 1.61 and 2.09 kJ metabolizable energy/kJ and was independent of ET. Energy maintenance requirement (measured at 28, 30 and 32 degrees C) increased with the growing protein content from 415 to 439 and 447 kJ/kg LW0.75.d resp. (regression analysis) and from 411 to 420 and 432 kJ/kg LW0.75.d (measuring at maintenance level). The relative weight gain with the increased protein content of the feed largely corresponds to the expected values according to the efficiency of ATP synthesis in the oxidative degradation of nutrients. The relationship between heat production and ET is parabolic. In the live weight range studied the average thermoneutral temperature (TNT) was 32 degrees C. It decreased during the course of development from 34 to 30 degrees C. TNT decreased with the growing protein content of the feed. Thermoregulatory heat production depended on both environmental temperature and the stage of development. Its average value in the development range studied decreased with an increase of the environmental temperature by 2 K each, starting from 20 degrees C and rising to 32 degrees C, in the following linear sequence: 23.3, 21.0, 16.8, 12.5, 8.3, 4.0 and 0.3 kJ/kg LW0.75.d.K.     

Methodologic studies on protein metabolism and bioenergetics of protein deposition in growing animals. 4. Energy metabolism in chickens in connection with measurement of parameters of protein metabolism

In connection with the measuring of parameters of the protein metabolism in parallel experiments, the energy metabolism of 6 chickens (origin Tetra B) in the live weight range between approximately 100 and 1,800 g was determined under conditions of restricted energy supply. 3 animals each received a feed mixture containing 20% (animal group 1) and 38% (animal group 2) crude protein. The amount of feed was daily increased by 1.5 g DM. The digestibility of energy and nitrogen was independent of the age. 66.3 +/- 3.3% and 64.0 +/- 5.0% resp. of the metabolisable energy were utilised for protein and fat retention. The energy maintenance requirement, determined at a live weight of 2,000 g, was independent of protein supply and averaged in the two animal groups 434 +/- 40 kJ metabolisable energy/kg live weight 0.75 . d. The result of multiple regression was, for the growth period investigated, an energy maintenance requirement of 403 +/- 32 kJ metabolisable energy/kg live weight 0.75 . d. 1.77 and 1.38 J metabolisable energy resp. were required for 1 J protein or fat retention. The energy requirement for protein retention was independent of the degree of protein supply. The results from the measuring of energy metabolism are discussed in connection with the kinetic parameters of protein metabolism ascertained in parallel experiments.     

The energy maintenance requirement of growing pigs of different sexes given normal and high protein diets. 1. Experiments in castrates

Energy retention was measured alternately at 12 barrows, fattening hybrids of line 150 (150 X (L X E], at maintenance level (4 periods) and growth feeding (5 periods) in the live weight range between 32 and 134 kg, 6 animals each received rations with 17 and 45% crude protein resp. during the complete experimental period. The nutrition level did not have a significant influence on the digestibility level of the feed. The experiments carried out at maintenance level showed that the maintenance requirement of metabolizable energy in the experiments with 17% crude protein in the ration was 941, in the experiments with 45% crude protein in the ration 913kJ ME/kg LW0.62 and on average 927 kJ ME/kg LW0.62. Including the experiments with growth feeding one can conclude from a regression analysis, largely in agreement with the measured values, that 955 kJ ME/kg LW0.62 is the energy maintenance requirement. These values of maintenance requirement are by 50% higher than those derived from previous measurings. In contrast to expectations, the increase of protein concentration in the ration did not result in a higher energy maintenance requirement. The utilization of metabolizable energy for retention amounted to 74% for rations with a normal protein content and to 65% for those with a high protein content. The multiply regressive evaluation showed a utilization of metabolizable energy for fat retention of 79% and for protein retention of 53%.     

The energy metabolism of swine at a feed level of "live weight equilibrium"

10 castrated pigs each of a live weight (LW) of 35 kg and 115 kg were fed over 28 and 40 days resp. in a way that a live weight equilibrium was achieved. The pigs were kept individually and at a low mobility on perforated floors of zinc-plated sheet iron at an air temperature of 19 degrees C. The weighing 35 kg received 668 kJ ME/kg LW 0.75 per day and one half of the animals weighing 115 kg 635 kJ ME/kg LW 0.75 in a diet consisting of barley and bran. The other half of the animals weighing 115 kg received 514 kJ ME/kg LW 0.75 per day in a ration consisting barley, bran and dried skim milk. The crude protein content of the rations was 12.6 and 17.1% resp. of the DM, the crude fibre content amounted to 8-10% of the DM. Energy excretion in faeces and urine was calorimetrically measured. Up to the end of the experiment LW and the weight of the empty body (without ingesta) remained unchanged. For the measuring of energy retention, 4-5 zero animals each were analysed before the experiments. The pigs weighing 35 kg showed a daily loss of 39 g fat in the course of the 40-day experiment. The calculation of the energy balance showed that an intake of 790 kJ ME/kg LW 0.75 was necessary. This maintenance requirement, rather high in comparison with values from literature, can be explained with the emission of body heat on sheet iron floors and a crude fibre content of 9% in the rations. The pigs of the two groups of 115 kg LW were at an energy equilibrium at both nutrition levels. The lower maintenance requirement of the group fed with dried skim milk cannot exclusively be explained by the higher energetic utilization of the milk protein in the ration. The reason should be the more advanced age of the animals of the milk group. Although they had nearly the same live weight, their empty bodies contained 41% fat, the pigs of the barley/bran group, however, only 34%, both before and after the experiment.     

The energy metabolism of growing swine in a live weight range of 10-50 kg. 3. Energy maintenance requirement of growing swine]

Investigations into the energy maintenance requirement yielded the following results: For the energy maintenance requirement (EMR) in dependence on live weight (LW) using the relation EMR = aLWb from 13 experiments, an exponent of the live weight of 0.647 +/- 0.054 (0.57 to 0.73) was found out. Increasing the protein content in the feed from approximately 17 to approximately 45% in 6 experiments lowered the energy maintenance requirements about 14, 4, 6, 2, 6 and 12% respectively. The animals' development had no influence on the difference. The amount of the energy maintenance requirement varied greatly between the experiments. Exclusively in the experiments with barrows, a lowest value of 634 and a highest value of 931 kJ metabolizable energy per kg LW0.62.d was measured. On average of 19 comparisons the energy maintenance requirement derived from growth and maintenance periods by means of regression analysis was significant (alpha = 0.05), about 4% higher than the energy maintenance requirement measured on maintenance level directly.     

Effect of dietary boron on growth performance, calcium and phosphorus metabolism, and bone mechanical properties in growing barrows.

An experiment was conducted to evaluate the effects of dietary boron (B) on growth performance, bone mechanical properties, and calcium (Ca) and phosphorus (P) metabolism in pigs. Thirty-six barrows were weaned at approximately 21 d of age and randomly assigned to receive one of three dietary treatments. Treatments consisted of 1) low-B basal diet (control), 2) basal + 5 mg B/kg diet, and 3) basal + 15 mg B/kg diet. Boron was supplemented as sodium borate. Barrows remained on their respective experimental diets throughout the nursery (35 d) and growing (30 d) phases of production. Blood samples were obtained from each barrow at the end of each phase. Following the 30-d growing period, eight barrows per treatment were transferred to stainless steel metabolism crates. Barrows had an adjustment period of 7 d, followed by a 7-d total collection of urine and feces. All barrows were fed at 90% of the previous ad libitum grower intake of the control animals during the adjustment and collection periods. At the end of the 7-d collection period, barrows were killed and femurs and fibulas were harvested for the assessment of bone mechanical properties. During the nursery phase, ADG and ADFI were increased (P < 0.05) by B supplementation. Boron did not affect (P = 0.34) feed efficiency during the nursery phase. During the growing phase, ADG and ADFI were increased (P < 0.05) by B supplementation. Boron did not affect (P = 0.97) feed efficiency during the growing phase. Boron did not affect (P = 0.44) bone ash percentage, but B supplementation increased (P < 0.05) bone ash P. Ultimate shear force of the fibula was increased (P < 0.05) in barrows supplemented with 15 mg B/kg diet compared to barrows fed diets supplemented with 5 mg B/kg diet. Apparent absorption and retention of Ca and P were not affected (P > 0.05) by dietary B. These data indicate that B supplementation to pigs can increase growth and bone strength without greatly affecting Ca and P metabolism.     

公鸡和母鸡氮代谢及氮维持需要量的比较研究

试验采用氮平衡试验研究产蛋高峰期罗曼公、母鸡的氮维持需要量(Nm),并分析公、母鸡氮代谢的变化规律。试验选取27周龄健康的公、母鸡各30只,分别分为5个处理,每处理6个重复,每个重复1只试鸡,对公、母鸡分别饲喂5个不同粗蛋白质水平的试验日粮。结果表明:相同蛋白水平处理组的公鸡氮食入量和氮沉积率均高于母鸡的结果。母鸡和公鸡的氮食入量(NI)与氮沉积量(NB)间的回归方程分别为NB=0.3743NI-0.1589(R2=0.79)和NB=0.6228NI-0.3151(R2=0.85)。母鸡和公鸡的氮维持需要量分别为每天0.4245g和0.5059g;每千克体重0.2364g和0.2754g;每千克代谢体重0.2739g和0.3208g。     

Consequences of nutritional and husbandry factors on the heat production of rats and broilers. 2. Effect of environmental temperature on the heat production of fully grown broilers and rats

In an experiment with broilers (origin Tetra B) and with rats (albino, Wistar line) with 2 animals each, heat production was ascertained by measuring CO2 production and O2 consumption over 20 minutes after their feeding 18 h and 1 h before the beginning of measuring at ambient temperatures of 30, 25, 20, 15 and 10 degrees C. Every variant was followed through over 6 h/d in 12 measuring sections. The feed amount/ánimal and day was adapted to energy maintenance requirement. At the beginning of the experiments the broilers and rats were 14 and 21 weeks old resp. and weighed 2.2 kg and 220 g resp. The variation of the ambient temperature did not influence the heat production of the broilers. In contrast to this, the time of feeding in relation to the beginning of measuring had a distinct effect on heat production. Whereas a heat production of 342 +/- 34 kJ/kg LW0.75.d was ascertained in the postabsorptive state 18 h after the last feed intake, it increased by 11% to 393 +/- 32 kJ/kg LW0.75.d when measuring began 1 h after feeding. The very act of feed intake increased heat production by 75%. Rats showed a distinct increase of heat production caused by a decreasing ambient temperature. In the temperature range of 30-25 degrees C the increase was shallower than in the range of 25-10 degrees C. Per 1 degrees C below 25 degrees C heat production increased by 30 kJ/kg LW0.75.d. The increase was independent of the metabolism level, which was influenced by the feeding variants. The results are discussed in connection with Rubner's theory of heat compensation.     

The energy metabolism of growing swine in the body weight range of 10-50 kg. 2. Nitrogen and energy metabolism

Investigations were carried out about nitrogen and energy metabolism feeding rations with 17-24 and 44-47% crude protein content on maintenance and growing level to castrated male hybrid pigs of line 150. In growing periods the N deposition amounted to 10 g/animal.d (15 kg live weight), 18 g/animal.d (30 kg LW) and 21 g/animal.d (greater than 40 kg LW) on lower protein feeding level. In experiments with higher protein feeding level the corresponding results were 17, 22 and 22 g N deposition/animal.d. The partial utilization of metabolizable energy for deposition amounted to 70% for the rations with 17-24% protein content and to 59% for the rations with 44-47% protein content, without correlation to the animals development and the alternation in the protein feeding level. The results of regression analysis about maintenance requirement were 814, 775 and 806 kJ metabolizable energy/kg LW0.62.d in trials feeding rations with 17-24% crude protein content as well as 764, 846 and 818 kJ metabolizable energy/kg LW0,62.d in trials feeding rations with 44-47% crude protein content. 1,5-1,8 MJ metabolizable energy were used per MJ protein energy deposition and 1,3-1,4 MJ per MJ fat energy deposition respectively. The energy deposition per kg live weight gain amounted to values between 9 (10 kg LW) and 18 MJ (60 kg LW).     

肉牛真胃灌注不同水平的葡萄糖和酪蛋白对日粮氮代谢调控的研究

３头带有瘤胃和真胃瘘管的肉牛（３７５±２５ｋｇ）饲喂全羊草以满足维持需要,设计３个对比试验,每个试验均向瘤胃内持续灌注高乙酸摩尔比例（７５％）的混合ＶＦＡ。试验１,真胃每天持续灌注１００ｇ,２５０ｇ和４００ｇ葡萄糖;试验２,真胃每天持续灌注２００ｇ,３００ｇ和４００ｇ酪蛋白;试验３,真胃每天持续灌注２５０ｇ葡萄糖与２００ｇ,３００ｇ,４００ｇ酪蛋白组成的混合物。连续７天灌注后测定氮平衡。试验结果表明,真胃灌注葡萄糖、酪蛋白及两者的混合物均能增加氮沉积和可消化氮转化为沉积氮的效率（ＲＮ／ＤＮ）,经回归分析,可消化氮转化为沉积氮的效率（ｙ,％）与真胃葡萄糖灌注量（ｘ,ｇ／天）之间存在线性正相关,回归方程为ｙ＝２５．０８２＋０．１０６９ｘ（ｒ＝０．９８９,ｎ＝４）;与真胃酪蛋白灌注量（ｘ,ｇ／天）之间存在曲线正相关,回归方程分别为ｙ＝３３．４７０＋３．３８２１ｎｘ（ｒ＝０．９７０,ｎ＝４）;与真胃葡萄糖和酪蛋白混合物的灌注量（ｘ,ｇ／天）之间也存在曲线正相关,回归方程为：Ｙ＝３５．８７０＋４．０７９ｌｎｘ（ｒ＝０．９８５,ｎ＝４）。真胃灌注葡萄糖和酪蛋白的混合物比单独灌注葡萄糖时氮的转化效率提高了１９．４１％（Ｐ?     

Impact of betaine on pig finishing performance and carcass composition

Two experiments were conducted to evaluate the effect of betaine supplementation of finishing diets on growth performance and carcass characteristics of swine. Experiment 1 included 288 pigs in a 2 x 2 x 3 factorial arrangement of treatments consisting of barrows and gilts of two genetic populations fed diets with 1.25 g/kg supplemental betaine from either 83 or 104 kg to 116 kg and control pigs fed betaine-devoid diets. Pigs were housed three pigs per pen with eight replicate pens per treatment. Diets were corn-soybean meal-based with 300 ppm added choline. Genetic populations differed (P < 0.05) in fat depth (2.24 vs 2.93 cm) and longissimus muscle depth (53.8 vs 49.1 mm) at 116 kg. Betaine reduced feed intake (P < 0.05); however, real-time ultrasound measurements were not affected. In Exp. 2, 400 pigs were used in a 2 x 2 x 2 factorial arrangement of treatments to evaluate the effect of sex (barrow or gilts), betaine (0 or 1 g/kg of diet), and crude protein (CP) (0.70% lysine = 12.7% CP or 0.85% lysine = 15.0% CP) when fed from 60 to 110 kg live weight. Pigs had been assigned to either a high- or low-protein feeding regimen at an average initial weight of 11.3 kg and were maintained on their respective protein levels throughout the experiment. For a 56-d period from 61.7 kg to 113.6 kg, pigs were fed diets with 300 ppm added choline. Within each protein level, pigs were randomly assigned to diets containing 0 or 1 g/kg betaine. Pigs were group-housed (four to five pigs per pen). Pig weight and feed intake were recorded every 28 d. Real-time ultrasound measurements were recorded initially and at d 28 on 64 pigs, and on all pigs prior to slaughter. Growth rate was fastest and feed intake greatest for barrows (P < 0.05) and for pigs receiving 12.7% crude protein. A crude protein x betaine interaction (P < 0.05) was observed from d 28 to 56 with pigs fed the 15% CP diet growing fastest when supplemented with 1 g/kg betaine, and pigs receiving the 12.7% CP diet growing fastest when the diets contained 0 g/kg betaine. Gilts more efficiently (P < 0.05) converted feed into body weight gain, as did pigs receiving the 12.7% CP diet (P < 0.05). Longissimus muscle area and fat measurements were unaffected by betaine or dietary protein on d 28. However, by d 56 betaine reduced average fat depth in barrows (P < 0.05; 3.21 vs 3.40 cm), but not in gilts. Betaine may be more effective at altering body composition in barrows than in gilts.     

Effect of graded nitrogen supplements on egg protein synthesis and body protein retention in broiler hens

In the top laying period (29th/30th week of life) egg protein synthesis and protein retention in the bodies of laying hens were ascertained. Based on egg-N analyses, the relation between N-intake/live weight0.67kg and egg-N discharge/kg LW0.67kg was regressively calculated and described. The subtraction of egg-N discharge/LW0.67kg from N-balance/LW0.67kg made it possible to estimate N-retention/LW0.67kg in the body. From the intersection of this curve with the chi-axis it follows that the broiler hen meets the N-requirement for maintenance and egg production with a daily consumption of 1,264.7 mg N/LW0.67kg, which corresponds to 15.8 g crude protein, and then neither loses nor retains body protein. At a daily intake of this amount of CP (15.8 g) the broiler hen produces 44.1 g egg per day. An energy intake of more than 70 EFUhen/animal and day resulted in fat retention in the broiler hen.     

Supplementation with groundnut haulms for sheep fattening in the West African Sahel

Groundnut haulms along with cowpea hay are major crop residues used for animal fattening in the West African Sahel. In traditional sheep fattening, feeds are always provided ad-hoc and in an unregulated fashion, which is rather wasteful. As a preliminary study to establish the optimal feeding levels of groundnut haulms for profitable sheep fattening, a feeding trial was conducted for 70 days with four levels of groundnut haulms (0, 150, 300 and 450 g/day) and a basal diet of bush hay. The effects of supplementation with groundnut haulms on feed intake, water consumption, live weight changes and economic return were determined. Twenty-four Peuhl Oudah rams with average initial weight of 28.6 kg (SD = 1.4) were randomly allocated to four treatments defined by the four levels of groundnut haulms in the diet. Faeces and urine were collected in weeks 5 and 9 of the trial. Digestible organic matter intake (g/(kg LW)^0.75) and nitrogen intake (g/day) increased linearly with the level of groundnut haulms offered. Sheep that were fed only bush hay lost 18.4 g/day, while those that were offered 150, 300 and 450 g of groundnut haulms gained 1.4, 19.3 and 40.2 g/day, respectively. The gross return ranged from 1883 to 4946 FCFA per ram. Net benefit, after removing the feed and veterinary costs from the gross return, ranged from 368 to 1400 FCFA per ram.     

Comparative Study on Nitrogen Metabolism and the Nitrogen Maintenance Requirement in Lohmann Brown Roosters and Layers

The objective of this study was to investigate the effect of dietary protein level on nitrogen retention and compare nitrogen metabolism in Lohmann Brown adult roosters and layers. The nitrogen maintenance requirement ( Nm ) was determined based on the nitrogen balance. Thirty Lohmann Brown adult roosters and 30 laying hens at 27 weeks of age were randomly divided into five groups of six birds per group. The birds were fed with one of five diets containing 10.46%, 11.77%, 13.79%, 16.77% or 18.29%of crude protein. Nitrogen intake, nitrogen retention and nitrogen retention efficiency were higher in roosters than in laying hens, and the average nitrogen retention rate for groups fed with CP level of 11.77%,13.79%, 16.77% and 18. 29% was improved by 9.14%. The nitrogen maintenance requirement for Lohmann Brown roosters and laying hens at 27 weeks of age were 0.4245 g/d and 0.5059 g/d, respectively,and Nm based on average body weight (BW) and metabolic body weight ( BW0.75 ) was 0.2364 g/kg BW and 0.2739 g/kg BW0.75 for laying hens and 0.2754 g/kg BW and 0.3208 g/kg BW0.75 for roosters, respectively. The regression equations for daily N gain ( NB, protein accretion) vs. daily N intake ( NI )for Lohmann Brown layers and roosters were NB =0.3743NI -0. 1589(R2 =0.79) and NB =0.6228NI -0.3151 (R2 =0.85),respectively. The results of this study indicate that nitrogen intake and nitrogen retention at the same dietary CP level were higher in roosters than in laying hens.     

The estimation of utilizable amino acids (uAA) of feeds for ruminants using an in vitro incubation technique

The in vitro incubation technique of Zhao and Lebzien (2000; Arch. Anim. Nutr. 53, 293-302) was used for the estimation of utilizable amino acids (uAA) (sum of amino acids from undegraded feed protein and microbial protein, when N is not limiting) of feeds for ruminants. The rumen fluid from a cow fed only with hay (Expt. 1) and that from a sheep fed with a mixed ration (Expt. 2) was compared with respect to estimation of uAA. In Expt. 1, 30 feeds and feed mixtures were tested and in Expt. 2, 33 feeds and feed mixtures were tested. A close linear relationship was found between the utilizable crude protein (uCP=undegraded feed protein + microbial protein) (X, g/kg) calculated from in vivo experiments and the uAA (Y, g/kg) estimated from in vitro incubations both in Expt. 1: y= 0.95 x-1.39, r2=0.85, p<0.001,n=30; and in Expt. 2: Y=0.85X-6.67,r2= 0.85,p<0.001,n=33. Statistical analysis indicates that there was a significant regressive relationship between uAA determined with the rumen fluid of a sheep (X, g/kg) and uAA determined with the rumen fluid of a cow (Y, g/kg): Y=1.06X+12.4,r2= 0.80,p<0.001,n=27. The results indicate that the in vitro incubation technique of Zhao and Lebzien (2000) can be used for the estimation of uAA of feeds for ruminants. As a rumen-fistulated cow is more expensive than a rumen-fistulated sheep, it is suggested to use a sheep fed a mixed ration as the donor of rumen fluid for the estimation of uAA of feeds with in vitro incubation. Further experiments should be performed to standardize the method and to test the most valid length of the incubation period.     

Protein utilization as well as crude protein and amino acid requirements of broiler hens

After N-balance experiments with broiler hens in the top laying period and the feeding of soybean coarse meal/fish meal protein the protein utilisation values were calculated. The PNu curve and the PEW curve could be described as utilisation values from the N-retention curve (e-function). At an intake of N at which the hen neither decomposed nor retained protein, the utilisation (PNu) for maintenance and egg production was 55.3% and the utilisation of feed protein for egg production 49.4%. Maximum PEW 34.3% could only be ascertained at an N-intake/LW0.67kg of 1500 mg. The corresponding crude protein quota of 18.7 g recommended as crude protein requirement is calculated from this N-quota (xm) and a live weight of the broiler hen of 2804 g. For the same N-quota (xm) and the same live weight of the hens this results in a necessary quota of S-AA of 694 mg per hen and day. Provided the daily feed intake is 145 g and thus the intake of crude protein 18.7 g and that of S-AA 694 mg per hen, the necessary crude protein content of the feed is 130 g per kg original substance and an S-AA concentration which is equivalent to 3.7% of the crude protein (in g/16 g N).     

Energy requirements of pregnant and lactating sows

The energy requirement of pregnant and lactating sows is derived on the basis of extensive experimental studies of the energy metabolism (indirect calorimetry, slaughtering) according to the factorial method. For the first reproduction cycle (RC) 0.41 MJ metabolizable energy (ME) or 0.29 MJ net energy fat, pig (NEFpig) resp. were necessary for energy maintenance requirement for pregnant and lactating sows and, depending on age, 0.44 MJ ME or 0.31 MJNEFpig in the second or third RC and 0.47 MJ ME/kg LW0.75.d or 0.33 MJ NEFpig/kg LW0.75.d in the 4th-8th RC. A linear increase of up to 6% of the energy requirement caused by pregnancy between the 85th and 115th day of pregnancy is taken into consideration. Energy requirement per 1 MJ retention both in pregnancy and lactation is 1.45 MJ ME or 1.03 MJ NEFpig, per 1 MJ milk yield it is 1.33 MJ ME or 0.91 MJ NEFpig. 1 MJ body energy for milk yield corresponds to 1.20 MJ ME or 0.82 MJ NEFpig. Equations describing energy retention in the products of conception, uterus and udder are established as well as equations characterizing the connections between live weight gain or loss and energy content of the gain or loss.