scholarly journals Maintenance requirements for energy in cross-bred cattle

1975 ◽  
Vol 33 (2) ◽  
pp. 127-139 ◽  
Author(s):  
B. R. Patle ◽  
V. D. Mudgal

1. Twenty-seven energy and protein balances were done using nine cross-bred (Brown Swiss × Sahiwal) mature bullocks in a series of three balance trials. The bullocks were fed 75, 100 and 125 % of the metabolizable energy (ME) and digestible crude protein standard values recommended by the (US) National Research Council (1966). Heat production was estimated by indirect calorimetry, by collection and analysis of respiratory gases2. Utilization of energy for maintenance and fat production was estimated by computing regression of energy balance v. digestible energy (DE) and ME separately on a metabolic body size (kg body-weight (W)0·75) basis. Maintenance energy requirements and efficiency of utilization of ME for lipogenesis were estimated using multiple regression of ME intake, also. Heat production (and thus energy balance) was corrected for excess nitrogen intake3. An attempt was made to measure basal heat production of bullocks so that the net energy requirements for maintenance could be estimated. Extrapolation of the regression line of energy balance v. ME intake below maintenance on a W0·75 basis gave a basal metabolism of 348·09 kJ/W0·75 per d4. Energy requirements for maintenance were (kJ/kg W0·75 per d): 539·43 DE, 448·81 ME and 348·09 net energy. The results of multiple regression gave a requirement of 432·15 kJ ME/kg W0·75 per d for maintenance5. The efficiency of utilization of ME for maintenance was 81·34% while for lipogenesis it was 54·5 %.

1977 ◽  
Vol 37 (1) ◽  
pp. 23-33 ◽  
Author(s):  
B. R. Patle ◽  
V. D. Mudgal

1. Twenty-four energy and nitrogen balances were determined using twenty-four crossbred cows (Brown Swiss × Sahiwal) during their midstage of lactation. Energy balances were estimated by subtracting milk energy and heat production from the metabolizable energy (me) intake. Heat production was estimated by indirect calorimetry, by collection and analysis of respiratory gases. The cows were given amounts corresponding to 90, 110 and 130 % of the me and 90 and 110% of the digestible crude protein (DCP) standards of the (US) National Research Council (1966).2. Energy requirements were estimated by partitioning the me intake for maintenance, milk production and energy gain or loss by multiple regression of energy balance values. Heat production (and thus energy balance) was corrected for excess N intake.3. Energy requirements for maintenance were 585.18, 580.17 and 574.41 kJ me/kg body-weight0.75 per d for cows in negative balance, cows in positive balance and for all cows, respectively.4. The efficiency of utilization of me for milk production was 68.52, 65.48 and 66.12% respectively, for cows in negative balance, for cows in positive balance and all cows. Energy required per kg fat-corrected milk production was 4.580, 4.791 and 4.746 MJ me for the respective groups of cows.5. The efficiency of utilization of me for tissue gain was 67.67 and 64.86 % for cows in positive balance and for all cows respectively.


1990 ◽  
Vol 63 (2) ◽  
pp. 155-163 ◽  
Author(s):  
C. Prieto ◽  
J. F. Aguilera ◽  
L. Lara ◽  
J. FonollÁ

Sixteen adult castrated male goats of the Granadina breed, with initial live weights ranging from 26.0 to 33.3 kg were used in two experiments to determine their protein and energy requirements for maintenance. Digestibility, nitrogen and energy balance measurements were made during the experiments. Two diets, which were based on pelleted lucerne (Medicago sativa) hay alone or on this forage and barley, were individually given at about maintenance level once daily. Gas exchange was measured using open-circuit respiration chambers. Fasting heat production was also determined. By regression analysis endogenous urinary N and maintenance requirements for N were estimated to be 119 mg/kg body-weight (W)0.75 per d and 409 mg total N/kg W0.75 per d respectively. Fasting heat production was 324 kJ/kg W0.75. The energy requirement for maintenance was calculated by regression of energy balance on metabolizable energy (ME) intake and a value of 443 kJ/kg W0.75 per d was found. The overall efficiency of utilization of ME for maintenance was 0.73.


2001 ◽  
Vol 136 (4) ◽  
pp. 451-459 ◽  
Author(s):  
R. J. EARLY ◽  
O. MAHGOUB ◽  
C. D. LU

Energy requirements for maintenance and growth were estimated by comparative slaughter in Omani male lambs during the hot summer months (July–October: maximum temperature, 48 °C). Weaned lambs (n = 10 per diet) were fed one of three totally mixed, 160 g CP/kg DM diets that contained 600, 400 or 200 g rhodesgrass hay/kg for low (9·98 MJ/kg, medium (10·3 MJ/kg) and high (11·4 MJ/kg) energy contents, respectively. All diets were balanced to meet the minimum nutritional needs for maximum growth. The trial lasted for 113–114 days. The purpose of having three diets was to induce a broad spectrum of growth rates that could be used in regression analysis (tested for linear, quadratic and exponential effects). Metabolizable energy (ME) intake was regressed on live weight (LW), empty body weight, tissue energy and tissue protein gain and vice versa. Coefficients of determinations were not significantly improved by quadratic or logarithmic regressions over linear relationships. Geometric mean regressions were used to control further biases due to major axis dependence when Y is regressed on X or vice versa. Based on tissue energy gain, the best estimates of ME required for maintenance (MEm) and gain (MEg) were 526 kJ/kg LW0·75/d and 42·1 kJ/kg LW0·75/g LW gain, respectively. Net energy values for maintenance (NEm) and gain (NEg) were 278 kJ/kg LW0·75/d and 20·6 kJ/kg LW0·75/g LW gain, respectively. These equations predicted MEm and NEm requirements that were similar to or slightly greater than those established by the US National Research Council (1985) and the UK Agricultural and Food Research Council (1993) for growing male lambs. The MEg and NEg requirements were substantially greater (by 43–89%) in this respect. Efficiency values were calculated as net energy available for maintenance or gain divided by the metabolizable energy available for maintenance or gain. The efficiency of metabolizable energy used for maintenance and gain was 0·50 and 0·52, respectively, and did not appear to be much different from values for other breeds of sheep in temperate climates. Dietary energy concentrations did not affect the efficiency of energy deposition. The data suggest that Omani sheep in hot climates have greater NEg requirements, and consequently MEg requirements, than other breeds of sheep in temperate climates.


1973 ◽  
Vol 53 (3) ◽  
pp. 471-477
Author(s):  
D. I. DICKIE ◽  
J. W. WILTON ◽  
T. D. BURGESS

Four studies and populations of beef animals were used to evaluate different methods of expressing energy requirements by comparing actual to predicted gains of bulls and steers fed in Ontario. Large differences between predicted and actual gains occurred. Based on a total of 503 animals, gains predicted by the net energy method (National Academy of Sciences–National Research Council. 1970. Nutrient requirements of domestic animals. 4. Nutrient requirements of beef cattle. (4th rev.). Nat. Acad. Sci., Publ. ISBN 0-309-01754-8; Washington, D.C.) were approximately 20% below the actual gains but exceptions within treatment groups were evident. Three hundred and twenty-five individually fed bulls were used to compare the accuracy with which gains were predicted from equations using total digestible nutrients (National Academy of Sciences–National Research Council. 1963. Nutrient requirements of domestic animals. 4. Nutrient requirements of beef cattle. Nat. Acad. Sci., Publ. 1137, Washington, D.C.) net energy (National Academy of Sciences–National Research Council. 1970. Nutrient requirements of domestic animals. 4. Nutrient requirements of beef cattle. (4th rev.). Nat. Acad. Sci., Publ. ISBN 0-309-01754-8, Washington, D.C), and metabolizable energy (Agricultural Research Council. 1965. The nutrient requirements of farm animals. No. 2. Ruminants. London, England). The metabolizable energy method predicted gains most accurately.


1994 ◽  
Vol 74 (1) ◽  
pp. 97-102 ◽  
Author(s):  
Z. Jiang ◽  
R. J. Hudson

Seasonal energy intakes of 6- to 14-mo-old wapiti hinds were determined in energy balance trials under pen and field conditions in winter, spring and summer. Six animals grazed native pastures supplemented with alfalfa hay when pasture availability declined in winter. Another six were penned and fed alfalfa-barley pellets to maximize growth throughout the year. Season and diet-specific metabolizable energy requirements for maintenance and liveweight gain were determined from regression of metabolizable energy intake on gain. Daily maintenance requirements of penned wapiti ranged from (mean ± SE) 473 ± 35 kJ kg−0.75 in winter to 728 ± 78 kJ kg−0.75 in summer. On spring and summer pasture, daily ecological maintenance requirements ranged from 900 ± 26 to 984 ± 37 kJ kg−0.75. Energy requirements for gain were the same in pen and field trials, ranging from 25 ± 6 to 33 ± 5 kJ g−1 in winter and from 40 ± 6 to 43 ± 12 kJ g−1 in spring and summer. This study provides basic information on the metabolizable energy needs of wapiti and insights into how their seasonal requirements can be optimally met. Key words: Elk, metabolizable energy requirement, growth, physiological maintenance, ecological maintenance, seasonality, energy balance


2019 ◽  
Vol 97 (7) ◽  
pp. 3056-3070 ◽  
Author(s):  
Emily A Petzel ◽  
Evan C Titgemeyer ◽  
Alexander J Smart ◽  
Kristin E Hales ◽  
Andrew P Foote ◽  
...  

AbstractTwo experiments were conducted to measure rates of ruminal disappearance, and energy and nutrient availability and N balance among cows fed corn husks, leaves, or stalks. Ruminal disappearance was estimated after incubation of polyester bags containing husks, leaves or stalks in 2 separate ruminally cannulated cows in a completely randomized design. Organic matter (OM) that initially disappeared was greatest for stalks and least for husks and leaves (P < 0.01), but amounts of NDF that initially disappeared was greatest for husks, intermediate for stalks, and least for leaves (P < 0.01). Amounts of DM and OM that slowly disappeared were greatest in husks, intermediate in leaves, and least in stalks (P < 0.01). However, amounts of NDF that slowly disappeared were greatest in leaves, intermediate in husks, and least in stalks (P < 0.01). Rate of DM and OM disappearance was greater for leaves, intermediate for husks and least for stalks, but rate of NDF disappearance was greatest for stalks, intermediate for leaves, and least for husks (P < 0.01). Energy and nutrient availability in husks, leaves, or stalks were measured by feeding ruminally cannulated cows husk-, leaf-, or stalk-based diets in a replicated Latin square. Digestible energy lost as methane was less (P = 0.02) when cows were fed leaves in comparison to husks or stalks, and metabolizable energy (Mcal/kg DM) was greater (P = 0.03) when cows were fed husks and leaves compared with stalks. Heat production (Mcal/d) was not different (P = 0.74) between husks, leaves, or stalks; however, amounts of heat produced as a proportion of digestible energy intake were less (P = 0.05) among cows fed leaves in comparison to stalks or husks. Subsequently, there was a tendency (P = 0.06) for net energy available for maintenance from leaves (1.42 Mcal/kg DM) to be greater than stalks (0.91 Mcal/kg DM), and husks (1.30 Mcal/kg DM) were intermediate. Nitrogen balance was greater when cows were fed leaves, intermediate for husks, and least for stalks (P = 0.01). Total tract digestion of NDF was greater (P < 0.01) for husks and leaves compared with stalks. Husks had greater (P = 0.04) OM digestibility in comparison to stalks, and leaves were intermediate. Apparently, greater production of methane from husks in comparison to leaves limited amounts of energy available for maintenance from husks even though total-tract nutrient digestion was greatest when cows were fed husks or leaves.


1958 ◽  
Vol 195 (3) ◽  
pp. 654-658 ◽  
Author(s):  
F. W. Hill ◽  
L. B. Carew ◽  
A. van Tienhoven

Increased fat production in diethylstilbestrol-treated chicks was found to be due primarily to increased energy consumption and to a lesser extent to preferential synthesis of fat at the expense of protein tissue. This was shown in experiments comparing normal and estrogen-treated male chicks with respect to gains in live weight, fat and protein at two planes of nutrition, and the yield of metabolizable and productive (net) energy which they obtained from the diet. It was found that the fattening effect could not be due to increased digestibility, increased net energy yield from absorbed nutrients, or lowered heat production. Under the influence of estrogen, total tissue gain expressed in Calories was increased, and was composed of greater fat gain and lower protein gain. Tissue energy gains were a linear function of metabolizable energy consumption. This relationship predicted equal tissue energy gains under pair-feeding conditions, which was confirmed experimentally.


Author(s):  
Bonjin Koo ◽  
Olumide Adeshakin ◽  
Charles Martin Nyachoti

Abstract An experiment was performed to evaluate the energy content of extruded-expelled soybean meal (EESBM) and the effects of heat treatment on energy utilization in growing pigs. Eighteen growing barrows (18.03 ± 0.61 kg initial body weight) were individually housed in metabolism crates and randomly allotted to one of three dietary treatments (six replicates/treatment). The three experimental diets were: a corn-soybean meal-based basal diet and two test diets with simple substitution of a basal diet with intact EESBM or heat-treated EESBM (heat-EESBM) at a 7:3 ratio. Intact EESBM was autoclaved at 121°C for 60 min to make heat-treated EESBM. Pigs were fed the experimental diets for 16 d, including 10 d for adaptation and 6 d for total collection of feces and urine. Pigs were then moved into indirect calorimetry chambers to determine 24-h heat production and 12-h fasting heat production. The energy content of EESBM was calculated using the difference method. Data were analyzed using the Mixed procedure of SAS with the individual pig as the experimental unit. Pigs fed heat-EESBM diets showed lower (P &lt; 0.05) apparent total tract digestibility of dry matter (DM), gross energy, and nitrogen than those fed intact EESBM. A trend (P ≤ 0.10) was observed for greater heat increments in pigs fed intact EESBM than those fed heat-EESBM. This resulted in intact EESBM having greater (P &lt; 0.05) digestible energy (DE) and metabolizable energy (ME) contents than heat-EESBM. However, no difference was observed in net energy (NE) contents between intact EESBM and heat-EESBM, showing a tendency (P ≤ 0.10) toward an increase in NE/ME efficiency in heat-EESBM, but comparable NE contents between intact and heat-EESBM. In conclusion, respective values of DE, ME, and NE are 4,591 kcal/kg, 4,099 kcal/kg, and 3,189 kcal/kg in intact EESBM on a DM basis. It is recommended to use NE values of feedstuffs that are exposed to heat for accurate diet formulation.


2003 ◽  
Vol 83 (4) ◽  
pp. 787-792
Author(s):  
E. K. Okine ◽  
D. H. McCartney ◽  
J. B. Basarab

The accuracy of predicted CowBytes® versus actual dry matter intake (DMI) and average daily gain (ADG) of 407 Hereford × Angus and Charolais × Maine Anjou (445.6 ± 36 kg) feeder cattle using digestable enery acid detergent fiber (DE) estimated from the (ADF) content [Laboratory analysis method (LAB)] and from values determined in vivo (INVIVO method) was examined. The diet consisted of a 73.3% concentrate diet, 22.0% barley silage, 1.6% molasses, and 3.1% feedlot supplement fed ad libitum (as-fed basis). The calculated DE values of the feed were used to predict the metabolizable energy (ME), net energy of maintenance (NEm), and net energy of gain (NEg) of the diet. These energy values were then used in CowBytes® to predict dry matter intake (DMI), ADG, and days on feed (DOF) necessary to meet targeted quality grade of AA and weights of 522 and 568 kg for the heifers and steers, respectively. There was no effect of gender and prediction method interaction (P > 0.10) on any of the variables measured. There were no (P > 0.05) differences in predicted DMI by either the INVIVO or LAB method but both methods underestimated DMI actually consumed by the cattle by 6.8 and 4.9% (P = 0.007), respectively. Indeed, regression values from these predictive methods and actual DMI were (P < 0.05) different from the one-to-one relationship expected by definition. In spite of the higher actual DMI, the actual ADG of the cattle was 14 and 11% (P = 0.0004) lower than was predicted by either the INVIVO or LAB methods. A possible reason for the lower ADG could be an overestimation of DE of the diet. Thus, if available, users of CowBytes® should use actual DMI from their experience in ration formulation. In addition, the effects of environmental temperature on digestibility of diets should be taken into consideration when using the DE of the diet as determined from in vivo digestibility trials or calculated from chemical analyses in determining the DMI of feedlot cattle. Key words: Beef cattle, performance, CowBytes®, National Research Council


1998 ◽  
Vol 78 (1) ◽  
pp. 107-114 ◽  
Author(s):  
D. R. Ouellet ◽  
J. R. Seoane ◽  
H. Lapierre ◽  
P. Flipot ◽  
J. F. Bernier

Metabolizable energy (ME), net energy for maintenance and net energy for growth of grass silages were evaluated by the comparative slaughter technique using a 2 × 2 × 3 factorial design. Sixty medium frame beef steers (259 ± 29 kg BW) were divided in groups of five and fed during 3 months either Timothy (T) or Bromegrass (B) harvested at stem elongation (S) of the first cut or at boot stage of the aftermath (A). Forages were fed at one of three levels of intake: ad libitum (FF), 80% of FF, or 65% of FF. Silages averaged 26.9% DM, 16.0% CP and 37.7% ADF. Regression of logarithm of heat production (HE) against ME intake were similar for all silages (log HE = 0.00046*ME + 2.4923; r2 = 0.89). From this equation, fasting HE of 311 kJ kg−0.75 d−1, ME for maintenance of 559 kJ kg−0.75 d−1 and efficiency of utilization of energy for maintenance of 56% were determined. Regression of ME intake against retained energy (RE) were similar for all silages. Efficiency of ME utilization for growth was 33% using the regression of ME over RE with a ME requirement for maintenance fixed at 559 kJ kg−0.75 d−1. Net energy for maintenance and growth were similar for all silages, averaging 6.17 and 3.70 MJ kg−1, respectively. The use of a prediction equation based on ADF of forages underestimated ME values of silages by approximately 25%. Moreover, NRC (1984) equations that estimate NE from experimentally estimated ME values tended to overestimate the net energy of our grass silages. Key words: Net energy, grass silages, timothy, bromegrass, beef cattle


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