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R Schiemann

Publications and source records attributed to R Schiemann.

At least 37 records · Page 2Linked to original sources

[Measuring of the energy turnover in adult swine during feeding of rations with potato starch, potatoes, beets, pressed shreds and coarse fodder as supplements to a basic ration. 2. Evaluation and discussion of the results for further development of energetic feed rating for swine].

Energy metabolism measurings of male castrates of a live weight between 90 and 180 kg after feeding rations with a wide variety in the content of various carbohydrates (crude fibre 36-185, water soluble carbohydrates 25-306, starch 272-683 g/kg DM) formed the experimental basis of the considerations. Energy retention depended significantly on the digestibility and metabolizability of the energy, on energy concentration and the crude fibre content of the rations. By means of multiple regression analyses the energetic effect of 1 g digested matter of the carbohydrate fraction was assessed as follows: 12.9 kJ for starch, 12.1 kJ for disaccharides, 11.5 kJ for the remaining water soluble carbohydrates and 10.4 kJ for bacterially fermentable carbohydrates (BFC). There was a difference between the energetic effective value of starch and BFC. This corresponds completely to the difference in the utilization of metabolizable energy between exclusively precaecal and postileal digestion. The following conclusions are drawn for the further development of the energetic feed evaluation for pigs in the framework of the GDR feed evaluation system: --There are to be differentiated fixed values for the retention of digestible carbohydrates for the fractions starch, water soluble carbohydrates (pectin) and bacterially fermentable carbohydrates. --The influence of the digestibility of the energy in the ration on the energetic retention effect of BFC is small. The integration of these variables into an estimation equation for the energetic feed value is therefore not necessary.

Animal Feed↗

[The effect of the protein level of feed on the energy maintenance requirement of rats during the course of growth and after the conclusion of the intensive growth phase using different feeding regimens].

In two experiments with male Wistar rats energy metabolism was measured on the feeding level of maintenance in the course of growth and in various adult periods after the application of feed mixtures with various protein-carbohydrate quotas (10, 40 and 70% crude protein) according to two different feeding regimes. While there was a change of protein levels between the animal groups in periods 1 to 3 and 8 to 10 from one period to the other, the protein levels in periods 4 to 7 and 11 to 13 remained the same for each animal group. Irrespective of the feeding regime, a dependence of the energy maintenance requirement on the nutrients according to the expected values was measured, which result from the different efficiency of ATP synthesis in the oxidative degradation of the nutrients. On an average of the periods maintenance requirement amounted to 357 +/- 21, 399 +/- 16 and 443 +/- 28 kJ/kg LW0.75.d (experiment 1) and 350 +/- 29, 383 +/- 34 and 442 +/- 30 kJ/kg LW0.75.d (experiment 2) for 10, 40 and 70% crude protein in the feed. The relation between the maintenance requirement values was 100:112:124 and 100:109:126. This contrasts with the relative expected values of 100:108:115 and 100:109:116.

Adenosine Triphosphate↗

[Effect of the nutrition level and sex on the energy maintenance requirement of broilers and rats].

In 3 experiments young broiler chickens were supplied on various feeding levels in the growth range between 200 and 2500 g live weight (2.8 and 2.0 in experiment 1, 2.8, 2.3 and 1.8 in experiments 2 and 4, maintenance = feeding level 1.0). In experiments 1 and 2 short-time measurings (30 min) of heat production by means of gas exchange were made at 500, 1000, 1500 and 2000 g live weight in the post-absorptive state and on the maintenance level of feeding. In experiment 1 the heat production of the restrictively fed chickens was in 3 out of the 4 stages of development studied significantly lower by 10-14% than that of the intensively fed ones. In experiment 2 such an effect could not be observed. Fed on the level of energy maintenance, broilers weighing approximately 2000 g (experiment 3) did not show a significant influence of the sex on heat production as a result of 30-minute gas exchange measurings in the post-absorptive state. In experiment 4 24-hour measurings of the energy metabolism were carried out in the growth development in periods of feeding on the maintenance level by means of indirect calorimetry. In the live weight range between 0.9 and 1.3 kg there was only a low, non-significant decrease of the energy maintenance requirement of 4-6% of the highly restrictively fed chickens in comparison to the intensively fed ones. After continued feed restriction (live weight range 1.7-2.2 kg) an energy maintenance requirement reduced by 17% was measured. In an analogously arranged experiment with 24-hour energy metabolism measurings (experiment 5) male Wistar rats in the growth range between 70 and 280 g were supplied on the feeding levels 1.8 and 1.4 resp. In all three periods studied on the feeding level maintenance--beginning at 140-150 g live weight--the highly restrictively fed animals showed a slightly reduced energy maintenance requirement by 8%, 3% (non-significant) and 6% in comparison with the intensively fed animals.

Animal Feed↗

[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.

Animals↗

[The energy preservation requirements of growing pigs of different sexes fed normal and high protein diets. 5. Comparison with the results obtained from castrated pigs, sows and boars].

In one experiment each with castrated pigs, sows and boars (hybrid pigs of line 150), two groups of six animals received rations containing 17 and 45% crude protein resp. over the complete test period from 35 to 130 kg (castrated pigs), 150 kg (sows), 170 kg live weight (boars) and passed alternatively through a total of 60 metabolism periods on growth and 48 on maintenance level. There were significant differences between the 3 categories of animals with regard to energy maintenance requirement in the relation of 100:105:110 for castrated pigs less than sows less than boars. In contrast to the estimated values derived from previous studies for energetic maintenance requirement of 650 kJ/kg LW0.62.d the measured values for all 3 animal categories are by approximately 50% higher. The protein content did not have an influence on the maintenance requirement of metabolizable energy of the animals. The utilization of metabolizable energy of the two rations for body energy retention corresponds to the expectations with regard to its dependence on nutrients. The requirement of metabolizable energy for protein and fat retention is 1.7:1.0. The energy content of the weight gain of boars was, on average, 85% of that of castrated pigs and sows. The studies of blood parameters did not show any deviations in the parameters tested.

Animal Feed↗

[The energy utilization of root vegetables and their processed products by adult swine].

The energetic utilization of raw and steamed sugar beets, raw carrots and fresh conserved or dried sugar beet pulp was measured at 8 adult pigs each with the application of the respiration experiment method. The experiment was laid out according to the difference method with 4 periods of basic rations per animal. The digestibility of the energy of the 5 feedstuffs (sequence as above) was measured as 85, 87, 83, 67 and 69% and energy retention as 10.1, 9.8, 9.1, 8.2 and 8.1 MJ/kg DM. In comparison to earlier measurings (Schiemann et al., 1966) digestibility was by 4%, relatively, lower. Under consideration of the difference in the digestibility of energy, there is very good agreement in energy retention.

Animal Feed↗

[The energy utilization of coarse feed by adult swine].

The energetic utilization of 12 technically dried roughages (6 legumes, 5 grasses, 1 straw) with a wide variation of the chemical composition (crude fibre content 190-395, crude protein content 61-266 g/kg DM) was tested with 8 adult pigs each by means of the respiration test technique. The experiments were laid out according to the difference method with 3-4 basal ration period per animal. The digestibility of the energy of the feedstuffs (except straw) ranged from 40-60%, the partial utilization of the metabolizable energy from 63 to 74%.

Animal Feed↗

[Methodologic studies for the measurement of kinetic parameters of the metabolism of whole body protein in association with measurements of energy metabolism in rats].

In 3 successive experiments with growing rats the suitability of pulse labelling with [15N]glycine, linked with a 14C labelling by means of [14C]lysine (experiment 3), was tested for the determination of kinetic parameters of the protein metabolism of the whole body by the application of the compartment model in comparison with pulse labelling with a 15N amino acid mixture (experiment 2) and long-time labelling with 15N with 15N labelled wheat in the feed (experiment 1) under standardized experiment conditions. In simultaneously carried out measurings of energy metabolism with parallel groups of animals the comparability of the metabolic development was studied. The ascertained values of protein synthesis rate, protein catabolism rate and re-utilization rate showed insignificant differences only between the 3 15N tracer variants (with certain limitations for the 'protein turnover' (P)-group of experiment 2) in comparison with errors of the applied methods, from which conclusions can be drawn for the suitability of [15N] glycine as tracer, at least under the experiment conditions tested. The protein synthesis and degradation rates ascertained from 14CO2 excretion in experiment 3 were clearly below those average values ascertained with 15N. The differences in the average heat production between the main periods of the 3 experiments were statistically insignificant.

Animal Feed↗

[The energy requirement of heifers. 4. Comparison of the digestibility and rumen physiologic parameters in heifers and full-grown sheep].

In 159 comparative studies with fully grown sheep and heifers of the digestibility and of rumen physiologic values at a variation of the feed ration in the crude fibre content between 112 and 318 g, in the crude protein content between 94 and 194 g and in the content of nitrogen free extractive between 484 and 641 g/kg DM is provided that the digestibility of energy in heifers was, on average, 4 digestibility units lower than in sheep. The corresponding values for the digestibility of crude protein and crude fibre are 12 and 3.5 digestibility units. Due to the lower methane energy excretion of the heifers the difference at the level of metabolizable energy is reduced to 1.5% of the gross energy. The level of the differences in digestibility is influenced by the development of the young cattle and the composition of the rations. In young cattle of the live weight range between 100 and 150 kg the digestibility of the energy is 6-8 units lower than in sheep. A higher crude fibre content in the ration diminishes the difference in the digestibility of energy and the nutrients between the two animal species.

Animal Feed↗

[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.

Animals↗

[Nutrient dependence of energy conservation requirements in rats. 4. The influence of protein levels of food on energy conservation requirements of rats during growth and after conclusion of the intensive growth phase].

Albino rats bred in the institute (Wistar line) divided into 3 groups of 9 animals each received, beginning at the age of 4 weeks, feed mixtures with 10, 40 and 70% protein in the rations over a period of 24 weeks divided into 14 subperiods of study. The feed mixture changed cyclically for the groups of animals after each sub-period. Every period was divided into a growth period (8 days) with the rats kept in metabolism cages and a period of feeding on maintenance level (4 days) with the rats kept in respiration chambers. In both periods the temperature was kept constant at 30 degrees C. On 3 days of feeding on the maintenance level the metabolism parameters of energy, C and N metabolism were measured and energy maintenance requirement was ascertained. Both the energy maintenance requirement of the growing rats (up to 200 g live weight) and that of the nearly fully grown and fully grown rats resp. (greater than 200 g live weight) significantly depended on the nutrient composition of the feed mixtures supplied. It increased with the increasing protein and simultaneously decreasing carbohydrate quotas in the feed. On an average of the studies the rats had, in the sequence of 10, 40 and 70% protein content, an energy maintenance requirement of 383 +/- 31 (n = 105), 415 +/- 31 (n = 106) and 459 +/- 36 kJ metabolizable energy/kg LW0.75.d (n = 102). Energy maintenance requirement behaved relatively like 100:108:120. Based on the fact that energy maintenance requirement may be considered the requirement of ATP, relative expectancy values for energy maintenance requirement can be calculated with the energetic efficiency of the ATP synthesis (kJ metabolizable energy/Mol ATP gain) in nutrient catabolism from the relation of the experimentally ascertained nutrient metabolism at a variant supply of protein of 100:110:118. The hypothesis that the efficiency of ATP synthesis in the catabolism of the main nutrients supplying energy can be considered a relative measure of the dependence of the energy maintenance requirement on nutrient composition has been confirmed in this experiment. Different findings in earlier experiments raise the question if those findings were influenced by adaptation effects. An experimental solution of this question is considered important.

Adenosine Triphosphate↗

[The energy requirement of young female cattle. 1. Research overview and body weight development of the animals].

In the period of 1975-1982 6 experiments with young female cattle of various rearing intensities were carried out. The respiration trial technique for the measuring of energy and protein metabolization in connection with the registration of a number of rumen physiologic data were applied together with comparative studies of the digestibility and the rumen fermentation of the rations used with young cattle and with fully grown sheep. The extent of the experiment was characterized by 695 metabolism periods in calves and young cattle as well as by 149 comparative studies of the digestibility and the rumen metabolism of the fully grown sheep. The results ascertained are the basis of the derivation of the energy requirement for the rearing of young female cattle according to factorial criteria. This first out of six papers on these experiments comprises an outline of the experiment arrangement, the material and the methods as well as of the live weight development of the animals. In four of the six experiments there was a continuous monthly registration of the measured values over the complete period of the rearing of the weaned calves up to their calving with four animals each under conditions of extremely high (experiment 1), medium (experiments 5 and 6) and low (experiment 3) rearing intensity. Experiments 2 and 4 provide additional information on rearing periods under special consideration of the gestation period. In experiment 1 the cows were not milked after the first calving, and measuring was continued to the second calving of the animals.

Animal Feed↗

[The energy requirement of young female cattle. 2. Substance and energy metabolism].

The second installment of information on studies over several years of the energy requirement of young female cattle comprises data of the feed intake, the digestibility and metabolizability of the rations used as well as the nitrogen and energy balances of the test animals in six experiments with varying rearing intensities, in which the N, C and energy balances as well as rumen physiologic values were measured monthly using the respiration test technique. Of four experiments, measured values are available over the whole rearing period from calf to calving. The results received from 680 interpretable test periods are-separated for the six experiments--arranged in aggregate form according to live weight range in order to characterize the development of nutrient and energy metabolization processes at various rearing intensities. The results form an essential basis for the derivation of the energy requirement of young female cattle according to factorial criteria.

Animal Feed↗

[Nutrient dependence of energy preservation requirements in rats. 1. Dependence of energy requirements for preservation in fully-grown rats on the type of nutrient offered as the sole energy source].

In two experiments with fully-grown albino rats (Wistar strain) the energetic utilization of glucose, sunflower oil and casein in the maintenance metabolism was determined under thermoneutral conditions of keeping the animals. The relative requirement of metabolizable energy for maintenance was, with either glucose, sunflower oil or casein being the sole energy source of the feed, in experiment 1 100:105:133 and in experiment 2 100:102:135. The absolute values of the maintenance requirement of metabolizable energy were in experiment 1 347 +/- 26, 364 +/- 61 and 460 +/- 33 resp., and in experiment 2 330 +/- 11, 337 +/- 21 and 446 +/- 27 kJ/kg LW 0.75 resp. The results are discussed in connection with the efficiency of ATP synthesis (metabolizable energy/mol ATP gain) in the oxidative decomposition of nutrients.

Adenosine Triphosphate↗

[Nutrient dependence of energy preservation requirements in rats. 2. Effect of the protein level of feed and the environmental temperature on the energy preservation requirement and heat production in fully-grown rats].

The influence of protein in exchange for carbohydrates on the energy maintenance requirement was studied with nearly fully-grown rats at ambient temperatures between 33 and 21 degrees C. The levels of the crude protein content were 10, 25, 40 and 70%. At an ambient temperature of 33 and 30 degrees C energy maintenance requirement increased with the growing protein content in the feed. At a temperature of 30 degrees C the following values of energy maintenance requirement were measured in the sequence of the protein levels mentioned: 330 +/- 11, 347 +/- 18, 360 +/- 15 and 399 +/- 15 kJ metabolizable energy/kg live weight 0.75 X d. The occurring changes largely coincide with the expected values calculated from the efficiency of the ATP synthesis in the oxidative catabolization of protein and carbohydrates. At ambient temperatures of less than 30 degrees C, thermogenous effects after the exchange of protein versus carbohydrates could only be observed partly or not. 30 degrees C in feeding on the maintenance level and 33 degrees C in the state of hunger are estimated as the lower critical temperatures. Below the critical temperatures down to 24 degrees C heat production increased less per 1 degree C temperature decrease both in hungry and fed rats than in the temperature range between 24 and 21 degrees C. By the decrease of the ambient temperature from 24 to 21 degrees C the heat production of the hungry or fed rats increased by 39 or 33 kJ/degrees C X kg live weight 0.75 X d.

Animals↗

[Dependence of energy maintenance requirements on nutrients in rats. 3. Effect of the protein levels of food on the energy maintenance requirements of growing rats].

In addition to earlier experiments with growing rats on the protein levels 10, 25 and 40% crude protein in the dry matter of the feed (Hoffmann et al., 1982 a), two groups of nine male Wistar rats each received feed mixtures with 6 or 25% crude protein resp. and energy metabolism on the energy maintenance level in an N equilibrium or with a positive N balance resp. were measured on 6 levels of live weight between 65 and 250 g and additionally also at subsequent fasting day. Energy maintenance requirement on average of the 6 periods amounted to 381 and 377 kJ metabolizable energy/kg W 0.75 X d on a low or middle protein level resp. and thus did not show changes at the decrease of N retention to values of about zero even with regard to different ATP formation capacities of the nutrients.

Animal Feed↗

[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.

Animals↗

[Energy maintenance requirements and energy requirement for protein retention in growing rats and broilers. 1. Energy maintenance requirements of growing rats].

In 4 experiments with 3 times 3 male Wistar rats each, which received rations with different protein contents (10; 25 and 40% crude protein in the dry matter), in the growth range between approximately 65 and 180 g live weight and with an environmental temperature of 30 degrees C, a total of 226 measurings of the total metabolism were carried out on the energy level maintenance, partly also with the insertion of a fasting day. The most important results were: On the energy level maintenance with the simultaneous catabolisation of body fat there was considerable protein energy retention, which amounted to between 30 and 40% of the retention achieved in the growth periods. The energy maintenance requirement can be determined with good reproducibility (standard mean deviation: +/-6%). The average energy requirement directly measured at the feeding level maintenance of 437 kJ metabolizable energy (ME)/kg live weight 0,75.d (n=224) differs insignificantly from the average value obtained by means of multiple regression analysis from experiment periods with feeding for growth 423 kJ ME/kg live weight 0,75.d (n=437). Consequently it is not necessary to differentiate between energy requirement for maintenance and energy requirement connected correlatively with the live weight (metabolic weight of the body) under conditions of growth. Energy maintenance requirement proved to be insignificantly dependent on the amount of protein in the feed. The relative values of protein quotas of 10, 25 and 40% in the feed were 100, 101 and 103%; the expected values (derived from the efficiency of ATP synthesis in the oxidation of carbohydrates and protein) amount of 100, 104 and 109%. The problem of the thermogenous effect of protein, which is also of great importance to human nutrition urgently requires further experimental investigation. For growing rats the best adaptation of the energy maintenance over the investigated period of development is achieved if the 2/3 potence of the live weight is chosen as the expression of the metabolic body weight. With high probability this can also be transferred to the characterisation of protein metabolisation.

Animals↗