Net Energy Requirement For Maintenance Research Articles

Effect of supplementing zilpaterol hydrochloride during different periods on energetics, growth performance, carcass traits and fatty acid profile in meat of finishing lambs

To determine the effect of adding β2 agonist zilpaterol hydrochloride during different periods on growth performance, dietary energetic, carcass traits and fatty acid profile, forty male lambs Pelibuey × Katahdin (37.70 ± 0.83 kg) were blocked by body weight and randomly assigned to pens. Treatments consisted in: 1) control, no zilpaterol supplementation, 2) zilpaterol supplementation for 20 d (ZIL20), 3) zilpaterol supplementation for 30 d (ZIL30), and 4) zilpaterol supplementation for 40 d (ZIL40). Compared with control treatment, zilpaterol supplementation increased final live weight (FLW) (3.5 %; P = 0.0563), average daily gain (ADG, 14.8 %; P = 0.0598) and gain:feed ratio (10.3 %; P = 0.0324). As well as hot carcass weight (6.1 %; P = 0.0064), dress out percentage (2.6 %; P = 0.0139) and Longissimus dorsi muscle area (13.7 %; P = 0.0015). Compared to control group, zilpaterol increased (P = 0.0413) observed vs. expected dietary of NEm (net energy requirements for maintenance) and NEg (net energy requirements for growth) (5.7 and 8.1 %, respectively). Twenty days of zilpaterol treatment improved FLW (4.4 %, P = 0.0566) and tended to improve ADG (17.4 %, P = 0.0718) when compared to control group. Only intramuscular fat showed a positive linear effect (P = 0.0006) in stearic fatty acids proportion and negative linear effect (P = 0.0585) in araquidonic fatty acid proportion. We conclude that zilpaterol hydrochloride improved variables of growth performance, energy retention and carcass traits with noticeable effects from 20 d of zilpaterol supplementation.

The Energy Contents of Broken Rice for Lactating Dairy Cows.

This study aimed to evaluate (1) the net energy for lactation of broken rice in dairy cows and (2) the effects of broken rice substituting in diets on feed intake, nutrient energy utilization, and milk production. An energy metabolism experiment was conducted using a respiration chamber system in four multiparous Holstein crossbred cows (88.6% Holstein × 11.4% Native Thai; body weight of 438 ± 16.0 kg; 70 ± 31 days in milk) according to a 4 × 4 Latin square design with four 21-d periods. The four dietary treatments included a basal diet substitution with broken rice at 0%, 12%, 24%, and 36%. Increasing the substitution rate of broken rice in the diet resulted in unaffected feed intake, milk yield and composition, and energy balance (p > 0.05); however, a linear increase in the digestibility of dry matter, organic matter, and neutral detergent fiber (p < 0.05). The estimated net energy for lactation of broken rice was 8.68 MJ/kg. The net energy requirement for maintenance was estimated at 504 kJ/kg of metabolic body weight. Our results indicated that broken rice is a good energy-feed resource and that increasing the proportion in the diet up to 36% had no adverse effect on dairy cows' production performance.

Relationship between feed efficiency and resilience in dairy ewes subjected to acute underfeeding

Selection of dairy sheep based on production levels has caused a loss of rusticity, which might compromise their future resilience to nutritional challenges. Although refocusing breeding programs toward improved feed efficiency (FE) is expected, more-efficient ewes also seem to be more productive. As a first step to examine the relationship between FE and resilience in dairy sheep, in this study we explored the variation in the response to and the recovery from an acute nutritional challenge in high-yielding Assaf ewes phenotypically divergent for FE. First, feed intake, milk yield and composition, and body weight changes were recorded individually over a 3-wk period in a total of 40 sheep fed a total mixed ration (TMR) ad libitum. Data were used to calculate their FE index (FEI, defined as the difference between the actual and predicted intake estimated through net energy requirements for maintenance, production, and weight change). The highest and lowest FE ewes (H-FE and L-FE groups, respectively; 10 animals/group) were selected and then subjected to the nutritional challenge (i.e., withdrawing the TMR and limiting their diet only to the consumption of straw for 3 d). Afterward, sheep were fed again the TMR ad libitum. Temporal patterns of variation in performance traits, and ruminal fermentation and blood parameters were examined. A good consistency between FEI, residual feed intake, and feed conversion ratio was observed. Results supported that H-FE were more productive than L-FE sheep at similar intake level. Average time trends of milk yield generated by a piecewise model suggest that temporal patterns of variation in this trait would be related to prechallenge production level (i.e., H-FE presented quicker response and recovery than L-FE). Considering all studied traits, the overall response to and recovery from underfeeding was apparently similar or even better in H-FE than in L-FE. This would refute the initial hypothesis of a poorer resilience of more-efficient sheep to an acute underfeeding. However, the question remains whether a longer term feed restriction might impair the ability of H-FE ewes to maintain or revert to a high-production status, which would require further research.

Determination of energy and protein requirements of preweaned dairy calves: A multistudy approach

The first studies concerning nutrient requirements for preweaned dairy calves were from the 1920s and 1930s; however, few studies were published in the following decades. We aimed to determine energy and protein requirements of preweaning Holstein and Holstein × Gyr dairy calves in a multistudy meta-regression. We used a database composed of individual measurements of 166 preweaned male calves (138 submitted to treatments and 28 used as the reference group) from 4 studies that used the methodology of comparative slaughter. Animals with less than 15/16 of Holstein genetic composition were considered crossbred Holstein × Gyr, whereas other animals were considered Holstein. Net energy requirements for maintenance (NEM) were determined by the regression between heat production and metabolizable energy intake (MEI). The metabolizable energy requirements for maintenance were calculated by the iterative method, and the efficiency of use of metabolizable energy for maintenance was obtained by NEM divided by the metabolizable energy requirements for maintenance. Net energy requirements for gain (NEG) were estimated using a regression of the retained energy (RE) as a function of empty body weight (EBW) and empty body gain (EBG). The efficiency of use of metabolizable energy for gain was estimated by the regression of RE as a function of MEI, but with partitioning the MEI into MEI from liquid feed and MEI from starter feed. Additionally, the effect of a liquid feed (milk or milk replacer) was tested on the slope of the regression. The metabolizable protein requirements for maintenance (MPM) were estimated using the intercept of the regression between the metabolizable protein intake (MPI) and average daily gain. The MPM was determined as the ratio between the intercept and the metabolic body weight. Net protein requirements for gain (NPG) were estimated by the regression between retained protein, EBG, and RE. The efficiency of use of metabolizable protein for gain was estimated by the regression of the retained protein as a function of MPI, but with partitioning the MPI into MPI from liquid feed and MPI from starter feed. Additionally, the effect of a liquid feed (milk or milk replacer) was tested on the regression slope. Breed did not influence any of the nutrient requirements' estimates. The NEM was estimated as 70.2 kcal/metabolic body weight per day. The efficiency of use of metabolizable energy for maintenance observed was 66%. The NEG was estimated by the equation NEG = 0.0901 × EBW0.75 × EBG0.9539. The efficiency of use of metabolizable energy for gain was estimated as 57.6, 49.3, and 41.2% for milk, milk replacer, and starter feed, respectively. The MPM was estimated as 4.22 g/EBW0.75 per day, and the NPG was determined by the equation: NPG = 30.06 × EBG + 70.98 × RE. The efficiency of use of metabolizable protein for gain was estimated as 71.9, 59.2, and 44.4% for milk, milk replacer, and starter feed, respectively. We concluded that no differences were observed in energy and protein requirements between Holstein and Holstein × Gyr crossbred cows. The efficiencies of use of metabolizable energy and protein are greater for milk when compared with milk replacer and starter feed. Therefore, we propose that the equations generated herein should be used to estimate energy and protein requirements of preweaned Holstein and Holstein × Gyr crossbred dairy calves raised under tropical conditions.

Net energy requirement for maintenance of crossbred beef heifers (Bos taurus x Bos indicus) as measured with the washed-rumen technique and indirect calorimetry

The aim of this work was to determine the net energy requirement for maintenance (NEm) of commercial crossbred beef heifers. Six crossbred (Bos taurus x Bos indicus) heifers cannulated in the dorsal sac of the rumen and with an initial body weight (BW) of 414 ± 52 kg were used. Heifers had an adaptation period to ration and management of 28 days. They were fed daily with a maintenance ration based on chopped Taiwan grass (Pennisetum purpureum) and a supplement, except on the days of fasting heat production (FHP) measurements. Cattle were fasted with the washed-rumen technique. All contents (dry, liquids) in the reticulo-rumen were evacuated through the rumen cannula. After rumen evacuation, heifers were fasted for 12 h and subsequently, oxygen (O2) consumption was measured for 23 h in open-circuit respiration chambers. FHP was calculated by the energy equivalent of each liter of O2 consumed (19.7 kJ/L). FHP measurements were made 4 times per animal (4 periods) with 13 days of rest between measurements to reestablish feed intake. Mean O2 consumption and FHP (n = 24) were 1,587 ± 231 L/d (CV = 14.54%) and 399.6 ± 58 kJ/kg0.75/d (CV = 14.69%), respectively. The data derived from the present study may contribute to the improvement in the estimates of net energy requirements for maintenance of commercial crossbred beef cattle in the tropics.

Energy Requirements of Beef Cattle: Current Energy Systems and Factors Influencing Energy Requirements for Maintenance.

Simple SummaryThe accurate estimation of energy requirements for present-day genotypes under current feeding conditions is crucial for improving profitability and reducing the environmental impact of the beef industry. Equations for predicting energy requirements of beef cattle according to the Agricultural and Food Research Council (AFRC) are outdated and require an urgent update. The results from literature review confirmed previous reports on the under prediction of energy requirements for maintenance by the AFRC, especially for growing animals. This may have consequences on the efficiency of use of the dietary energy on productive functions. Although much less research has been conducted over the last decade on energy metabolism for suckler cows, the existing data appears to be relevant as a valid reference for updating AFRC recommendations. The present review also revealed the lack of data on the contribution of both animal and diet-related factors influencing on energy requirements for beef cattle and thus conclusions on this regard are difficult to draw.The present review compared features of the UK system for predicting energy requirements in beef cattle with a number of feeding systems developed from research institutes consortiums around the world. In addition, energy requirements for maintenance calculated from studies conducted at the Agri-Food and Biosciences Institute (AFBI) in Northern Ireland since the 1990s were compared with compiled data from recent peer-review papers published over the last decade (2009–2020). The mean metabolisable energy requirement for the maintenance (MEm) of growing cattle was 0.672 MJ/kg0.75 according to values obtained from calorimetry studies conducted at AFBI. This value is respectively 8.2 and 19.5% greater than the MEm values obtained by the Agricultural and Food Research Council (AFRC), and the National Academies of Sciences, Engineering and Medicine (NASEM) equations, but it is in close agreement with the Institut National de la Recherche Agronomique (INRA) approach, when assuming a Bos taurus bull (300 kg LW) and an efficiency for converting energy for maintenance (km) of 0.65. Most of the literature data on energy requirements for the maintenance for this animal category were obtained from studies conducted with Bos indicus animals and their crossbreds in Brazilian conditions with this confirming lower requirements of these animals when compared to pure Bos taurus cattle. A simulation of the total ME requirements calculated for an Angus × Friesian steer (LW = 416 kg) offered good quality grass silage, indicated that both AFRC and NASEM systems overestimate (38.5 and 20.5%, respectively) the observed efficiency of converting ME for growth (kg). When the total ME requirements (maintenance + growth) were assessed, both systems underpredicted total ME requirement in 15.8 and 22.1 MJ/d. The mean MEm requirements for suckler cows obtained from the literature (0.596 MJ/kg0.75) is on average 19.1% greater than predictions given by both AFRC and INRA (lactation) equations when considering a 550 kg cow and a km value of 0.72. Although no differences in net energy requirements for maintenance (NEm) were detected between dry and lactating suckler cows, as expected the later displayed greater variation as a result of differences in milk production. On this regard, the INRA model recognise increased NEm requirements for lactating animals compared to dry cows. The re-evaluation of the concept of diet metabolisability and the analysis of existing data on compensatory growth responses are recommended for future updates of the British system (AFRC) having in to account the particularities of grass-based systems in the UK.

Determination of maintenance energy requirement and responses of dry ewes to dietary inclusion of lucerne versus concentrate meal

An accurate value for metabolizable energy (ME) requirement for maintenance (MEm) is essential to enable sheep husbandry practice to reach its potential. The objectives of the study were to use calorimetry chamber data of dry ewes (Hu × thin-tail Han F1 crossbred) to develop updated MEm, examine effects of substituting concentrate feed with lucerne hay on energy partitioning, and explore the relationships between energy utilization and fasting heat production (FHP). Data were collected from three experiments. In Exps. 1, 2a and 2b, lucerne hay was used to replace concentrates in three levels (0:40%, 15:25% and 30:10%), with diets containing 60% maize stover (Exp. 1), fresh rye forage (Exp. 2a) or dry rye forage (Exp. 2b). Within each experiment, diets were isoenergetic (digestible energy, DE) and isonitrogenous. Exp. 3 aimed at evaluating effects of three BW levels on nutrient utilization of dry ewes offered diets containing 60% maize stover, 15% lucerne hay and 25% concentrates. Energy metabolism data were measured using the respiration calorimeter chamber technique in all three experiments, followed by the measurement of FHP in Exps. 1, 2b and 3. The MEm derived from the linear regression between energy balance (EB) and ME intake was 0.440 MJ/kg BW0.75. The average FHP was 0.326 MJ/kg BW0.75. The fasting metabolism, net energy requirement for maintenance (NEm) and MEm were estimated to be 0.336, 0.359 and 0.511 MJ/kg BW0.75, respectively, through adjustment of FHP using fasting urinary energy output, activity allowance and efficiency of ME use for maintenance. The FHP was negatively correlated to EB/metabolic BW, ME/gross energy (GE), ME/DE, EB/GE intake and EB/ME intake, while positively correlated to HP/GE intake, HP/ME intake and CH4-E/GE intake. Compared to zero lucerne hay diet, the 15% lucerne hay intake decreased HP (MJ/d), and had no negative effects on EB (MJ/d) or energy utilization efficiencies. The results indicate that nutrient requirement standards currently used across the world are likely to underestimate MEm for dry ewes, and the selection of low FHP ewes for breeding has the potential to improve sheep production efficiency.

Animals selected for postweaning weight gain rate have similar maintenance energy requirements regardless of their residual feed intake classification.

Data of comparative slaughter were used to determine Nellore bulls' net energy requirements classified as efficient or inefficient according to residual feed intake (RFI) and selection lines (SL). Sixty-seven Nellore bulls from the selected (SE) and control (CO) lines of the selection program for postweaning weight gain were used. The animals underwent digestibility trials before being submitted to the finishing trial. Sixteen bulls were slaughtered at the beginning of the finishing trial, and their body composition was used as the baseline for the remaining animals. For body composition determinations, whole empty body components were weighed, ground, and subsampled for chemical analyses. Initial body composition was determined with equations developed from the baseline group using shrunk body weight, fat, and protein. The low RFI (LRFI) and CO animals had a lower dry matter (DMI) and nutrient intake (P < 0.05) than high RFI (HRFI) and SE animals, without alterations in digestibility coefficients (P > 0.05). During the finishing trial, DMI remained lower for LRFI and CO animals. Growth performance was similar between RFI classes, except for empty body weight gain that tended to be higher for LRFI than HRFI (P = 0.091). The SE animals had less fat content on the empty body (P = 0.005) than CO. Carcasses tended to be leaner for LRFI than HRFI (P = 0.080) and for SE than CO (P = 0.066) animals. LRFI animals retained more energy (P = 0.049) and had lower heat production (HP; P = 0.033) than the HRFI ones. Retained energy was not influenced by SL (P = 0.165), but HP tended to be higher for SE when compared to CO (P = 0.075) animals. Net energy requirement for maintenance (NEm) was lower for LRFI than HRFI (P = 0.009), and higher for SE than CO (P = 0.046) animals. There was an interaction tendency between RFI and SL (P = 0.063), suggesting that NEm was lower for LRFI+CO than HRFI+CO (P = 0.006), with no differences for SE (P = 0.527) animals. The efficiency of ME utilization for maintenance (km) of LRFI and HRFI animals were 62.6% and 58.4%, respectively, and for SE and CO were 59.0% and 62.1%, respectively. The breeding program for postweaning weight has not improved feed efficiency over the years, with RFI classification not being a promising selection tool for SE animals. Classification based on RFI seems to be useful in animals that have not undergone the breeding program, with LRFI animals having lower energy requirements than the HRFI ones.

Ergot alkaloids reduce circulating serotonin in the bovine.

Ergot alkaloids can interact with several serotonin (5-hydroxytryptamine [5-HT]) receptors provoking many physiological responses. However, it is unknown whether ergot alkaloid consumption influences 5-HT or its metabolites. Thus, two experiments were performed to evaluate the effect of ergot alkaloid feeding on 5-HT metabolism. In exp. 1, 12 Holstein steers (260 ± 3 kg body weight [BW]) were used in a completely randomized design. The treatments were the dietary concentration of ergovaline: 0, 0.862, and 1.282 mg/kg of diet. The steers were fed ad libitum, kept in light and temperature cycles mimicking the summer, and had blood sampled before and 15 d after receiving the treatments. The consumption of ergot alkaloids provoked a linear decrease (P = 0.004) in serum 5-HT. However, serum 5-hydroxytryptophan and 5-hydroxyindoleacetic acid did not change (P > 0.05) between treatments. In exp. 2, four ruminally cannulated Holstein steers (318 ± 3 kg BW) were used in a 4 × 4 Latin square design to examine the difference between seed sources on 5-HT metabolism. Treatments were: control-tall fescue seeds free of ergovaline, KY 32 seeds (L42-16-2K32); 5Way-endophyte-infected seeds, 5 way (L152-11-1739); KY31-endophyte-infected seeds, KY 31 (M164-16-SOS); and Millennium-endophyte-infected seeds, 3rd Millennium (L108-11-76). The endophyte-infected seed treatments were all adjusted to provide an ergovaline dosage of 15 μg/kg BW. The basal diet provided 1.5-fold the net energy requirement for maintenance. The seed treatments were dosed directly into the rumen before feeding. The experiment lasted 84 d and was divided into four periods. In each period, the steers received seeds for 7 d followed by a 14-d washout. Blood samples were collected on day 0 (baseline) and day 7 for evaluating the treatment response in each period. A 24 h urine collection was performed on day 7. Similar to exp. 1, serum 5-HT decreased (P = 0.008) with the consumption of all endophyte-infected seed treatments. However, there was no difference (P > 0.05) between the infected seeds. The urinary excretion of 5-hydroxyindoleacetic acid in the urine was not affected (P > 0.05) by the presence of ergot alkaloids. In conclusion, the consumption of ergot alkaloids decreases serum 5-HT with no difference between the source of endophyte-infected seeds in the bovine.

Feeding behavior, water intake, and energy and protein requirements of young Nellore bulls with different residual feed intakes.

This study aimed to determine feeding behavior, water intake (WI), and energy requirements of high- and low-residual feed intake (RFI) Nellore bulls. Data were collected from 42 weaned Nellore bulls (initial body weight [BW] 260 ± 8.1 kg; age 7 ± 1.0 mo) housed in a feedlot in group pens that contained electronic feeders, waterers, and a scale connected to the waterers. The individual dry matter intake (DMI), WI, and BW were recorded daily. The indexes of average daily gain (ADG), feed efficiency (gain to feed ratio), and RFI were calculated based on the data collected. The number of feeder and waterer visits and the time spent feeding or drinking water per animal per day were recorded as feeding behavior measures. Energy requirements for maintenance and gain were calculated according to the BR-CORTE system. Low-RFI bulls had lower DMI (P < 0.01) than high-RFI bulls, and no differences (P > 0.05) were observed between the two groups regarding WI, performance, and feeding behavior measurements. The net energy requirements for maintenance, metabolizable energy for maintenance, and efficiency of metabolizable energy utilization were 63.4, 98.6 kcal/metabolic empty body weight (EBW)0.75 daily, and 64.3%, respectively, for low-RFI bulls, and 78.1, 123.9 kcal/EBW0.75 daily, and 63.0%, respectively, for high-RFI bulls. The equations obtained for net energy for gain (NEg) were: NEg (Mcal/EBW0.75) daily = 0.0528 × EBW0.75 × EBG0.5459 for low-RFI and 0.054 × EBW0.75 × EBG0.8618 for high-RFI bulls, where EBG is the empty body gain. We did not observe any difference (P > 0.05) regarding the composition of gain in terms of protein or fat deposition between the two groups. Both groups also presented similar (P > 0.05) carcass and non-carcass traits. Therefore, our study shows that low-RFI Nellore bulls eat less, grow at a similar rate, and have lower maintenance energy requirements than high-RFI bulls. We also suggest that the lower feed intake did not compromise the carcass traits of more efficient animals, which would reduce production costs and increase the competitiveness of the Brazilian beef sector on the world market.

Short-term feed intake regulation of dairy cows fed a total mixed ration or grazing forage oats

The integration of feeding behaviour with hepatic and endocrine–metabolic signals provides insights for a better understanding of short-term intake in dairy pasture-based systems. Therefore, the objective was to quantify hepatic and endocrine–metabolic signals before and after the first daily feeding event relating to feeding behaviour in a total mixed ration (TMR) versus a grazing pasture-based diet. During 15 days of adaptation and 5 days of measurements, 14 multiparous Holstein cows (days in milk = 148 ± 12.7; liveweight = 535 ± 10.9 kg; body condition score = 2.8 ± 0.08 (1–5 scale); milk yield = 28.9 ± 3.32 kg) were assigned to two treatments in a randomised block design: PAS = pasture (herbage allowance = 45 kgDM/cow.day; dry matter (DM) = 21%, net energy requirements for maintenance and lactation = 6.7 MJ/kgDM) + concentrate (0.9% of liveweight) or TMR (55:45 forage:concentrate ratio, as-dry basis; DM = 40%, net energy requirements for maintenance and lactation = 7.2 MJ/kgDM) ad libitum in a free stall facility. The DM intake of the first feeding event, feeding behaviour, and total DM intake and milk production, were measured. Blood and liver samples were taken before and after the first feeding event for hormones and metabolites determination. Comparing TMR versus PAS cows, total DM and net energy requirements for maintenance and lactation intake, milk production, and energy balance were greater (P &amp;lt; 0.05), eating and rumination activities were lower (9.2%, P &amp;lt; 0.01; 2.4%, P = 0.06 respectively) and resting activity was greater (11.6%, P &amp;lt; 0.01), whereas duration and DM intake of the first feeding event did not differ. The insulin:glucagon ratio and liver adenosine triphosphate:adenosine diphosphate ratio increased (P &amp;lt; 0.05), and plasma glucose decreased (P &amp;lt; 0.05) after the first feeding event only in TMR cows, probably due to greater flux of propionate to the liver. A negative correlation between post-feeding liver adenosine triphosphate:adenosine diphosphate ratio and post-feeding liver acetyl coenzyme A (r = –0.82, P = 0.045) was also observed only in TMR cows. It is concluded that hepatic and metabolic signals known to support the hepatic oxidation theory in TMR-fed cows appear not to affect the cessation of the first feeding event in mid-lactation cows grazing a pasture-based diet. Further research is required to relate intake rate, flux of nutrients to liver and its response in hepatic metabolism in grazing dairy cows.

148 Residual feed intake and body weight gain relate to feeding behavior in Nellore bulls: Implications for performance and maintenance requirements

Abstract This study determined feed intake behavior, performance, feed efficiency, and maintenance requirements of bulls with high and low residual feed intake and body weight gain. Data were collected from 42 weaned Nellore bulls (initial BW 260 ± 8.1 kg; age 7 ± 1.0 mo) housed in a feedlot in a group pen that contained electronic feeders. Individual dry matter intake (DMI) was recorded daily and body weight (BW) was measured every 28 d over a 140-day period. Indexes of average daily gain (ADG), feed efficiency, and residual feed intake (RFI) were calculated. Residual feed intake and gain (RFIG) was calculated according to previously published equations. Frequency of meals, duration per visit, and time spent feeding per day were recorded as feeding behavior measures. Maintenance requirements were calculated according to the BR-CORTE system. High RFIG bulls had lower DMI (P &amp;lt; 0.01), lower final BW (P &amp;lt; 0.01), and were more feed efficient (P &amp;lt; 0.01) than low RFIG bulls, but both groups had similar ADG (P = 0.55). No differences in feeding behavior were observed between the two groups (P &amp;gt; 0.05). The net energy requirements for maintenance, metabolizable energy for maintenance, and efficiency of metabolizable energy utilization were 76.5, 122.68 kcal/EBW0.75 daily, and 62.4%, respectively for high RFIG bulls, and 89.2, 143.76 kcal/EBW0.75 daily, and 62.0% for low RFIG bulls. This study reveals that low RFIG bulls are less feed efficient and have greater maintenance requirements than high RFIG bulls (0.16 ± 0.006 and 0.18 ± 0.006, respectively). As low RFIG eat more, and in beef cattle, feeding behavior is associated with methane emissions, we suggest further research evaluating this relationship be conducted. In addition, selection for high RFIG cattle would improve feed efficiency, reduce production costs, and could potentially reduce methane emissions.

Energy requirements and efficiency of energy utilization in growing dairy goats of different sexes

The aim of this study was to investigate the effects of sex on the requirements for maintenance and efficiency of energy utilization in growing Saanen goats. A database from 7 comparative slaughter studies that included 238 Saanen goats was gathered to provide information for the development of prediction equations of energy requirements for maintenance and efficiency of energy utilization. The experimental design provided different levels of metabolizable energy intake (MEI) and empty body weight (EBW). The data were analyzed so that sex (e.g., intact males, castrated males, and females; n = 98, 80, and 60, respectively) was a fixed effect, and blocks nested in the studies and goat sex were random effects. For the development of linear and nonlinear equations, we used the MIXED and NLMIXED procedures in SAS (SAS Institute Inc., Cary, NC). Nonlinear regression equations were developed to predict heat production (HP, kcal/kg0.75 of EBW; dependent variable) from MEI (kcal/kg0.75 of EBW; independent variable). Using the comparative slaughter technique, the net energy requirement for maintenance (NEM) was calculated as the value of HP at MEI equal to zero. Additionally, NEM was evaluated based on the degree of maturity. The metabolizable energy requirement for maintenance was calculated as the value at which HP is equal to MEI. Efficiency of ME utilization for maintenance (km) was calculated as the ratio between NEM and the metabolizable energy requirement for maintenance. Efficiency of energy utilization for growth (kg) was assumed to be the slope of the linear regression of retained energy (RE) on MEI above the maintenance stage (model intercept equal to 0). Efficiencies of RE as protein (kp) and as fat (kf) were calculated using the multiple linear regression of MEI above the maintenance (model intercept equal to 0) on RE as protein and as fat, respectively. Sex affected NEM (75.0 ± 1.76 kcal/kg0.75 of EBW for males and 63.6 ± 2.89 kcal/kg0.75 of EBW for females) and sex did not affect km (0.63). In contrast, sex no longer affected NEM when degree of maturity was considered on its estimation. The kg was different between sexes (0.31 for castrated males and females, and 0.26 for intact males), but kp (0.21) and kf (0.80) were similar between sexes. These results may be useful for improving robustness of the energy requirement recommendations for dairy goats.

Oscillating and static dietary crude protein supply: II. Energy and protein requirements of young Nellore bulls.

:The objective of this study was to evaluate whole body chemical composition and energy and protein nutrient requirements for maintenance and gain of Nellore bulls. Fifty young bulls, with an average age of 7 ± 1 mo and initial body weight (BW) of 260.0 ± 8.1 kg, were used in this experiment. Four bulls were used as baseline reference animals and were slaughtered at the beginning of the experiment. Four bulls were fed at maintenance (12 g dry matter [DM]/kg of BW), whereas 42 bulls were divided into six groups (n = 7/group) and were randomly assigned to the following dietary treatments 105 (low [LO]), 125 (medium [MD]), or 145 (high [HI]) g crude protein (CP)/kg DM, LO to HI (LH), LO to MD (LM), or MD to HI (MH) oscillating CP at a 48-h interval for 140 d. At the end of the experiment, bulls were slaughtered and samples of the whole body were collected. All samples were lyophilized, ground, and composed as percentage of component of empty body weight (EBW) from each bull. A power model was used to estimate carcass, non-carcass components, and gastrointestinal content of the shrunk body weight (SBW), and CP and water present in the empty body, whereas an exponential model was used to estimate adipose tissue and ether extract (EE) present in the EBW. Nonlinear regression equations were developed to predict heat production from metabolizable energy (ME) intake and retained energy (RE). The net energy requirements for maintenance and ME for maintenance were 77 and 122.75 kcal/EBW0.75/d, respectively. The efficiency of ME utilization for maintenance was 62.7%. The equation obtained for net energy for gain (NEg) was: NEg (Mcal/EBW0.75/d) = 0.0535 × EBW0.75 × EBG0.7131, where EBG is the empty body gain, and the efficiency was 24.25%. Net protein requirement for growth (NPg) was: NPg (g/d) = 227.372 × EBG – 19.479 × RE. There was a linear increase for carcass, CP, and water present in the EBW as the animal grew. The EE deposition exponentially increased as EBW increased.

Effect of age and genetic group on the development of calves weaned at 63 days until one year of age

The development of beef calves born of Charolais (CH), Nellore (N), and Charolais × Nellore crossbred cows with Charolais (CHP) and Nellore (NP) predominance, was evaluated from birth to 12 months of age. The cows were grouped into three age classes: primiparous, young and adult. The net energy requirements for maintenance and gain of the calves were also evaluated, as were the production and availability of energy in the milk of the evaluated cows. We used 93 pairs of contemporary cows and calves maintained in natural pasture. From birth to 21 days of age and from 21 to 42 days of age, the calves of adult cows presented the highest average daily weight gain (ADG), while the calves of young and primiparous cows had similar ADG. The highest net energy requirements for maintenance (NEm) and gain (NEg) were for crossbred and Charolais calves, the latter being similar to Nellore calves. The energy available in the milk of the adult cows was 33% higher than that of primiparous cows. The weight gain of calves was influenced by the age of the cow until weaning. The pre-weaning and post-weaning weights of calves were affected by the genetic group, and adult and young cows produced heavier calves in the pre-weaning period than primiparous cows.

California net energy system for Bos taurus indicus.

The California net energy system (CNES) was the reference for the development of most energy requirement systems worldwide, such as Nutrient Requirements of Beef Cattle (NASEM, Nutrient requirements of beef cattle, 8th Revised ed, 2016) and Brazilian Nutrient Requirements of Zebu and Crossbred Cattle (Valadares Filho, S. C., L. F. C. Silva, M. P. Gionbelli, P. P. Rotta, M. I. Marcondes, M. L. Chizzotti, and L. F. Prados, BR-CORTE: nutrient requirements of zebu and crossbred cattle, 3rd ed, 2016). This review aimed to compare methods used by NASEM and BR-CORTE to estimate the energy requirements for beef cattle. The net energy requirements for maintenance (NEm) of BR-CORTE is based on empty body weight (EBW), whereas NASEM uses shrunk body weight (SBW), but the Bos taurus indicus presents 10% to 8% lower NEm than Bos taurus taurus. We have compared animals with different EBW and SBW but with same equivalent empty body weight/standard reference weight ratio (0.75), as both systems have suggested different mature weights. Both systems predicted similar net energy requirements for gain (NEg) for animals with 1.8 kg of daily gain. However, estimated empty body gain was lower for NASEM estimations when the same metabolizable energy for gain is available. For pregnancy and lactation of beef cows, the NEm and net energy requirements for pregnancy (NEp) of a Zebu cow estimated by BR-CORTE were lower than the values estimated by NASEM. Furthermore, the magnitude of differences between these systems regarding NEp increased as pregnancy days increase. The NASEM and BR-CORTE systems have presented similar values for energy requirement for lactation (0.72 and 0.75 Mcal/kg milk, respectively).

Applying the California net energy system to growing goats1

The aim of this review is to describe the main findings of studies carried out during the last decades applying the California net energy system (CNES) in goats. This review also highlights the strengths and pitfalls while using CNES in studies with goats, as well as provides future perspectives on energy requirements of goats. The nonlinear relationship between heat production and metabolizable energy intake was used to estimate net energy requirements for maintenance (NEm). Our studies showed that NEm of intact and castrated male Saanen goats were approximately 15% greater than female Saanen goats. Similarly, NEm of meat goats (i.e., >50% Boer) was 8.5% greater than NEm of dairy and indigenous goats. The first partial derivative of allometric equations using empty body weight (EBW) as independent variable and body energy as dependent variable was used to estimate net energy requirements for gain (NEg). In this matter, female Saanen goats had greater NEg than males; also, castrated males had greater NEg than intact males. This means that females have more body fat than males when evaluated at a given EBW or that degree of maturity affects NEg. Our preliminary results showed that indigenous goats had NEg 14% and 27.5% greater than meat and dairy goats, respectively. Sex and genotype also affect the efficiency of energy use for growth. The present study suggests that losses in urine and methane in goats are lower than previously reported for bovine and sheep, resulting in greater metabolizable energy:digestible energy ratio (i.e., 0.87 to 0.90). It was demonstrated that the CNES successfully works for goats and that the use of comparative slaughter technique enhances the understanding of energy partition in this species, allowing the development of models applied specifically to goat. However, these models require their evaluation in real-world conditions, permitting continuous adjustments.

LiGAPS-Beef, a mechanistic model to explore potential and feed-limited beef production 2: sensitivity analysis and evaluation of sub-models

The model LiGAPS-Beef (Livestock simulator for Generic analysis of Animal Production Systems – Beef cattle) has been developed to assess potential and feed-limited growth and production of beef cattle in different areas of the world and to identify the processes responsible for the yield gap. Sensitivity analysis and evaluation of model results with experimental data are important steps after model development. The first aim of this paper, therefore, is to identify which parameters affect the output of LiGAPS-Beef most by conducting sensitivity analyses. The second aim is to evaluate the accuracy of the thermoregulation sub-model and the feed intake and digestion sub-model with experimental data. Sensitivity analysis was conducted using a one-at-a-time approach. The upper critical temperature (UCT) simulated with the thermoregulation sub-model was most affected by the body core temperature and parameters affecting latent heat release from the skin. The lower critical temperature (LCT) and UCT were considerably affected by weather variables, especially ambient temperature and wind speed. Sensitivity analysis for the feed intake and digestion sub-model showed that the digested protein per kg feed intake was affected to a larger extent than the metabolisable energy (ME) content. Sensitivity analysis for LiGAPS-Beef was conducted for ¾ Brahman×¼ Shorthorn cattle in Australia and Hereford cattle in Uruguay. Body core temperature, conversion of digestible energy to ME, net energy requirements for maintenance, and several parameters associated with heat release affected feed efficiency at the herd level most. Sensitivity analyses have contributed, therefore, to insight which parameters are to be investigated in more detail when applying LiGAPS-Beef. Model evaluation was conducted by comparing model simulations with independent data from experiments. Measured heat production in experiments corresponded fairly well to the heat production simulated with the thermoregulation sub-model. Measured ME contents from two data sets corresponded well to the ME contents simulated with the feed intake and digestion sub-model. The relative mean absolute errors were 9.3% and 6.4% of the measured ME contents for the two data sets. In conclusion, model evaluation indicates the thermoregulation sub-model can deal with a wide range of weather conditions, and the feed intake and digestion sub-model with a variety of feeds, which corresponds to the aim of LiGAPS-Beef to simulate cattle in different beef production systems across the world.

Estimating digestible energy values of feeds and diets and integrating those values into net energy systems.

The California Net Energy System (CNES) used a combination of measured and tabular metabolizable energy (ME) values and changes in body composition gain to determine net energy requirements for maintenance and gain and their corresponding dietary concentrations. The accuracy of the CNES depends on the accuracy of the feed ME values. Feed or diet ME values can be measured directly but are expensive and require specialized facilities; therefore, most ME values are estimated from digestible energy (DE) values, which are often estimated from the concentration of total digestible nutrients (TDN). Both DE and TDN values are often from tables and not based on actual nutrient analysis. The use of tabular values eliminates important within-feed variation in composition and digestibility. Furthermore, the use of TDN to estimate DE does not account for important variation in the gross energy value of feeds. A better approach would be to estimate DE concentration directly from nutrient composition or in vitro (or in situ) digestibility measurements. This approach incorporates within-feed variation into the energy system and eliminates the issues of using TDN. A widely used summative equation based on the commonly measured feed fractions (ash, crude protein, neutral detergent fiber, and fat) has been shown to accurately estimate DE concentrations of many diets for cattle; however, deficiencies in that equation have been identified and include an overestimation of DE provided by fat and an exaggerated negative effect of intake on digestibility. Replacing the nonfiber carbohydrate term (which included everything that was not measured) in the equation with measured starch concentration and residual organic matter (i.e., nonfiber carbohydrate minus starch) should improve accuracy by accounting for more variation in starch digestibility. More accurate estimates of DE will improve the accuracy of ME values, which will ultimately lead to more accurate NE values.

Energy and protein requirements of crossbred Holstein × Gyr calves fed commercial milk replacer and amino acid supplement

This experiment aimed to estimate the energy and protein requirements for Holstein × Gyr calves up to 60 days of age fed with milk replacer and amino acid supplement. Fifty male calves were used, of which seven were randomly allocated into the reference group and slaughtered at 8 days of age, seven were randomly allocated into the maintenance group slaughtered at 30 days of age, and the 36 remaining calves were included in the experiment at 8 days of age and randomly supplied with four dietary methionine+cysteine:lysine ratios (RMCL; 44%, 48%, 52%, and 56%) through amino acid supplement added as 1 kg/day of milk replacer reconstituted at 13.8% of dry matter. Different RMCL were tested for the models, and there were no significant effects on energy and protein requirements. The net energy requirement for maintenance was 75.2 kcal/empty bodyweight (EBW)0.75.day, with an energy use efficiency for maintenance of 67.38%. The prediction equation of net energy requirement for gain (Mcal/day) was energy retained = 0.0879 × EBW0.75 × empty bodyweight gain (EBWG)0.7580, with an energy use efficiency for gain of 47.57%. The estimated requirements for metabolisable protein for maintenance were 4.83 g/EBW0.75.day. The estimated equation for net protein requirements for gain (g/day) was NPg = EBWG × 246.73 × EBW–0.1204, with a protein use efficiency for gain of 71.55%. The estimated requirements for energy and proteins were greater than the values reported for calves fed with milk. Milk replacers are less efficiently used by calves up to 60 days of age when compared with whole milk.