Metabolizable Energy Requirements Research Articles

Effects of late gestational nutrient restriction on uterine artery blood flow, placental size, and cotyledonary mRNA expression in primiparous beef females.

Fall-calving primiparous beef females [body weight (BW): 451 ± 28 (SD) kg; body condition score (BCS): 5.4 ± 0.7] were individually-fed either 100% (control; CON; n = 13) or 70% (nutrient restricted; NR; n = 13) of metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to parturition. Doppler ultrasonography of both uterine arteries was conducted pre-treatment and every 21 d from days 181 to 265 of gestation. Expelled placentas were collected, and ipsilateral cotyledonary tissue was sampled to assess relative messenger ribonucleic acid (mRNA) expression. Placentas were separated into ipsilateral and contralateral sides, dissected (cotyledonary vs. intercotyledonary), and dried. Data were analyzed with nutritional plane, treatment initiation date, and calf sex (when P < 0.25) as fixed effects. Uterine blood flow included day and nutritional plane × day as repeated measures. We previously reported that post-calving, NR dams weighed 64kg less and were 2.0 BCS lower than CON, but calf birth weight was not affected. Maternal heart rate was less (P < 0.001) for NR dams than CON after nutritional planes began. Nutritional plane did not affect (P ≥ 0.20) uterine artery hemodynamics, but all variables were affected (P ≤ 0.04) by day. Contralateral cotyledonary and placental weight were less (P ≤ 0.04) and contralateral intercotyledonary weight and number of cotyledons tended to be less (P ≤ 0.10) for NR dams than CON, but ipsilateral and whole placental weights were not affected (P ≥ 0.13). Ipsilateral placental weight as a percentage of total placental weight was greater (P = 0.03) for NR dams than CON. Whole placental cotyledonary:intercotyledonary weight was less (P = 0.01) for NR dams than CON. Placental efficiency was not affected (P = 0.89) by nutritional plane. Cotyledonary relative mRNA expression of GLUT3 and SNAT2 was greater (P ≤ 0.05) and relative expression of GLUT1, GLUT4, and NOS3 tended to be greater (P ≤ 0.07) for NR dams than CON. Nutritional plane did not affect (P ≥ 0.13) relative mRNA expression of GLUT5, 4F2hc, CAT1, LAT1, LAT2, VEGFA, FLT1, KDR, GUCY1B3, and PAG2. Despite less contralateral placental growth, beef heifers experiencing late gestational nutrient restriction maintained uterine artery blood flow and total placental mass and had 4 nutrient transporters and 1 angiogenic factor upregulated in cotyledons, all which likely contributed to conserving fetal growth.

PSI-15 Effect of feeding intact protein from soybean meal instead of crystalline amino acids on energy and nitrogen balance by growing pigs

Abstract The objective was to test the hypothesis that feeding intact protein from soybean meal (SBM) to growing pigs instead of crystalline amino acids (AA) increases nitrogen (N) retention, digestible energy (DE), and metabolizable energy (ME). A control corn-SBM diet and three diets, in which the inclusion rate of SBM was reduced and 3, 4, or 5 crystalline AA (i.e., Lys, Met, Thr, Trp, Val) were added, were formulated. The concentration of standardized ileal digestible AA was constant among diets, but crude protein was reduced as crystalline AA were added. Pigs were limit fed at 3.2 times the ME requirement for maintenance. Forty pigs (initial body weight = 20.5 kg; SD = 2.4) were allotted to the 4 diets using a randomized complete block design with 2 blocks of 20 pigs with five pigs per diet in each block. Pigs were housed in metabolism crates with pans and screens that allowed for quantitative collection of feces and urine for 4 d after 5 d of adaptation. Samples of diets, feces, and urine were analyzed for gross energy (GE) and N. The statistical model included diet as fixed effect and block as random effect, and pig was the experimental unit. Contrasts coefficients were used to determine linear and quadratic effects of reducing dietary protein. Results indicated that apparent total tract digestibility (ATTD) of dry matter (DM) decreased (quadratic, P = 0.027) and ATTD of GE tended to decrease (quadratic, P = 0.076; Table 1) as SBM inclusion was reduced in the diets. Absorbed N, retained N (g/d), and ATTD of N were decreased (linear, P &amp;lt; 0.001) as SBM decreased in diets, but retention of N (% of intake and % of absorbed) increased (linear, P &amp;lt; 0.001) as SBM decreased in diets. The DE decreased (linear, P = 0.007) as SBM decreased in diets, whereas SBM had no effect on ME. Dietary SBM also had no effect on ME to GE ratio, but ME to DE increased (linear, P = 0.008) by reducing SBM in diets. In conclusion, diets containing intact protein from SBM had greater ATTD of GE and N, and greater DE, but reduced N retention rate when compared with diets containing crystalline AA. However, daily protein retention could not be maintained when crystalline AA rather than SBM were used to furnish the digestible AA in the diets, which may have negative consequences on carcass quality.

81 Effects of udder quarter location on colostrum yield, nutrients, and immunoglobulin G in beef heifers

Abstract We hypothesized that colostrum total nutrients and immunoglobulin G (IgG) would not be affected by side of the udder, but that they would be greater in the rear versus the front half of the udder due to difference in volume of colostrum produced. Complete colostrum yield was collected individually from each quarter pre-suckling [40.5 ± 21.0 min (SD)] from fall-calving crossbred beef heifers (body weight = 472 ± 34 kg; body condition score (= 5.3 ± 0.4) that were either individually-fed 100% (control; n = 12) or 70% (nutrient restricted; n = 12) of NASEM metabolizable energy and metabolizable protein requirements from d 160 of gestation to calving. Analysis of colostrum lactose, protein, triglycerides, and free glucose was performed using colorimetric assays on a UV-visible light microplate reader. Colostrum IgG was analyzed using a commercially available ELISA kit. Quarter yield, nutrient or IgG concentration, and total nutrients or IgG were analyzed using the mixed procedure of SAS with fixed effects of udder location, nutritional plane, and their interaction in the model. Nutritional plane was not part of the current objective, but was included to account for variation in colostrum yield due to nutrient restriction, as we have previously reported. Separate statistical comparisons were made between the front and rear quarters and between the right and left quarters of the udder, with each quarter considered a sampling unit within each experimental unit (half) for both analyses. The interaction of udder location × nutritional plane did not affect (P ≥ 0.11) any variable. Nutrient restriction decreased (P ≤ 0.03) colostrum yield, total lactose, and total free glucose compared with controls. Front quarters produced less volume (P &amp;lt; 0.001; 36.2% of total); total lactose, protein, and free glucose (P ≤ 0.02; 34.3 to 43.3%); and total IgG (P &amp;lt; 0.001; 33.7%) than rear quarters. Front quarters tended to produce less (P = 0.07; 43.3%) total triglycerides than rear quarters. Lactose concentration was 10.5% greater (P = 0.05) in front compared with rear quarters, but other nutrient or IgG concentrations were not affected (P ≥ 0.18). Udder side did not affect total volume (P = 0.78), total nutrients (P ≥ 0.36), or total IgG (P = 0.79). The left side represented 50.7% of the total volume and 50.1 to 53.4% of total nutrients and IgG produced. Concentration of nutrients and IgG also were not affected (P ≥ 0.31) by udder side. In conclusion, colostrum did not differ between udder sides, but, relative to front quarters, rear quarters produced greater nutrient and IgG yield due to greater colostrum volume with minimal differences in nutrient or IgG concentrations.

PSIV-A-4 Effect of late gestational nutrient restriction on locomotor activity of beef heifers

Abstract The objective of this study was to determine the effects of nutrient restriction on locomotor behavior during late gestation. Fall-calving crossbred beef heifers were moved to 3.7 × 15.8 m partially-covered pens and individually-fed 100% (control; n = 13) or 70% (nutrient restricted; n = 13) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from d 160 of gestation to calving. Diets were based on chopped sorghum sudan hay fed in Calan gates and supplemented to meet targeted nutritional planes. IceQube accelerometers (iceRobotics, Edinburgh, UK) were placed on the left hind fetlock between d 158 and 168 of gestation to determine standing time, lying time, step count, number of lying bouts, and motion index. Daily behavior data were averaged for 5 distinct periods (period 1: IceQube placement to d 180 of gestation; period 2: d 181 to 201 of gestation; period 3: d 202 to 222 of gestation; period 4: d 223 to 243 of gestation; and period 5: 244 to 264 of gestation). Days in which animals were moved from their pens were excluded from the data set, resulting in an average of 17.2 ± 2.35 d per period. Data were analyzed with fixed effects of nutritional plane, period, and their interaction in the model. Maternal sire and day of treatment initiation were included as covariates. The number of lying bouts was affected (P = 0.02) by the nutritional plane × period interaction. Within period, there was no effect (P ≥ 0.20) of nutritional plane on lying bouts. Lying bouts in control heifers decreased (P = 0.008) from period 1 to 2, whereas lying bouts in nutrient restricted heifers decreased (P = 0.002) from period 1 to 2 before increasing (P = 0.02) again from period 2 to 3. Motion index and step count were affected (P ≤ 0.05) by nutritional plane, where both were greater in control heifers. Motion index and step count were affected (P &amp;lt; 0.001) by period, while standing time and lying time tended to be affected (P ≤ 0.09) by period. Motion index and step count decreased (P &amp;lt; 0.001) between periods 1 and 2 and periods 3 and 4 but increased (P ≤ 0.004) between periods 2 and 3 and periods 4 and 5. Standing time decreased (P = 0.02), while lying time increased (P = 0.02), between periods 3 and 4. These data suggest that nutrient restricted heifers may have reduced locomotor behavior in late gestation compared with control heifers. Throughout all periods of gestation, control heifers took more daily steps and had a greater motion index, suggesting that nutrient availability in late gestation may directly impact locomotor behavior of beef heifers.

PSIV-A-7 Effects of late gestational nutrient restriction of beef heifers on small intestinal crypt depth in neonatal calves

Abstract We hypothesized that late gestational nutrient restriction would impair small intestinal development in neonatal calves, including crypt cell depth and proliferation. Fall-calving crossbred beef heifers [body weight (BW) = 466 ± 30 (SD) kg; BCS: 5.4 ± 0.5] bred to a single sire were individually-fed 100% (control; n = 10) or 70% (nutrient restricted; n = 12) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from d 160 of gestation to calving. Calves were removed from their dams immediately post-calving and fed artificial colostrum and milk replacer relative to body weight until euthanasia at 48.7 ± 0.4 h of age. The gastrointestinal tract was removed, and proximal jejunum samples were dissected from each calf and immersion-fixed in 10% neutral buffered formalin. Tissues were embedded in paraffin blocks and cut into 5-µm sections that were mounted on glass slides. Slides were incubated with Ki-67 (marker of nuclear proliferation) and counterstained with Hematoxylin using an autostainer. Images were taken at 5× magnification using an upright microscope. QuPath software was used to measure crypt depth, starting at the base of the crypt region and ending at the furthest cluster of Ki-67 positive cells, perpendicular to the base of the mucosa. For each calf, 10 crypt depth measurements were taken from 4 images, resulting in 40 crypt depth measurements that were averaged. Nutritional plane was a fixed effect in the model, and maternal sire, date of study initiation, and calf sex (when P &amp;lt; 0.25) were considered covariates. We previously reported that calves born to nutrient restricted dams weighed less (P ≤ 0.05) at birth and 48 h than calves born to control dams. Small intestinal mass tended to be less (P = 0.11) in offspring of nutrient restricted dams but was not affected (P = 0.58) when expressed relative to body weight. Calves born to nutrient restricted dams also tended to have less (P = 0.11) small intestinal mass relative to brain weight. Maternal nutrient restriction did not affect (P = 0.95) jejunal crypt depth. Additionally, crypt depth relative to body weight was not affected (P = 0.20) by nutrient restriction. Although crypt depth was not affected, further analysis of proliferation and morphology will help to understand the relationship between maternal nutrient restriction and small intestine development in neonatal calves.

Energy requirement for primiparous Holstein × Gyr crossbred dairy cows

Our objective was to estimate the requirements of metabolizable energy (ME) and net energy for the maintenance (NEm) of lactating and dry cows, the efficiency of ME utilization for milk production (kl) and tissue gain (kg), and the use of body energy mobilization for milk production (kt) throughout the lactation of primiparous crossbred Holstein × Gyr cows, using open-circuit respiration chambers. Twenty-nine primiparous Holstein × Gyr crossbred cows with an initial BW averaging 563 ± 40.1 kg and 2.5 ± 0.09 years old were used throughout lactation and dry periods. The cows were kept non-pregnant throughout the study to eliminate possible confounding factors. Apparent digestibility assays, followed by calorimeter measurements, were performed 6 times throughout the lactation period. In the dry-off period, the cows were also evaluated but fed with restricted intake (DMI = 1.1% BW/d) to achieve heat production close to maintenance. After 21 d of diet adaptation, an apparent digestibility assay followed by calorimeter measurements was performed. Parameter estimates for lactation period were obtained by mixed models including lactation stage as repeated measures. For restricted feeding at dry-off and fasting period assays, the requirements were estimated by exponential regression. For whole lactation, the values of MEm and NEm were 0.588 and 0.395 MJ/BW0.75, respectively. The efficiencies klkgkt were 0.672, 0.771, and 0.814, respectively. However, MEm and NEm were higher in early and mid-lactation than late, while kl was higher in early than other lactation stages. Dry and non-pregnant cows had MEm of 0.434 MJ/BW0.75 and NEm of 0.351 MJ/BW0.75 for maintenance level, and MEm of 0.396 MJ/BW0.75 and NEm of 0.345 MJ/BW0.75 for fasting metabolism level and efficiency of ME utilization for maintenance was 0.80. Our findings confirmed that F1 crossbred Holstein × Gyr dairy cows have differences in energy requirement and efficiency throughout the lactation stages, suggesting the use of different values in each stage. The estimated values of energy requirement for maintenance and efficiencies for primiparous lactating crossbred Holstein × Gyr were similar to those reported in the literature in specific studies and requirements systems.

Increasing midtarsal joint stiffness reduces triceps surae metabolic costs in walking simulations but has little effect on total stance limb metabolic cost

The human foot’s arch is thought to be beneficial for efficient gait. This study addresses the extent to which arch stiffness changes alter the metabolic energy requirements of human gait. Computational musculoskeletal simulations of steady state walking using direct collocation were performed. Across a range of foot arch stiffnesses, the metabolic cost of transport decreased by less than 1% with increasing foot arch stiffness. Increasing arch stiffness increased the metabolic efficiency of the triceps surae during push-off, but these changes were almost entirely offset by other muscle groups consuming more energy with increasing foot arch stiffness.

Late gestational nutrient restriction in primiparous beef females: Performance and metabolic status of lactating dams and pre-weaning calves.

Fall-calving primiparous beef females [body weight (BW): 451 ± 28 (SD) kg; body condition score (BCS): 5.4 ± 0.7] were individually-fed 100% (control; CON; n = 13) or 70% (nutrient restricted; NR; n = 13) of estimated metabolizable energy and metabolizable protein requirements from day 160 of gestation to calving. Post-calving, all dams were individually-fed tall fescue hay supplemented to meet estimated nutrient requirements for maintenance, growth, and lactation in Calan gates until day 149 of lactation, which limited calves to milk only. From day 150 of lactation until weaning at day 243, dams and calves were group-fed in drylots. Dam BW and metabolic status were determined every 21 d, and BCS and backfat (BF) were determined every 42 d of lactation until weaning. Pre-weaning calf BW, size, and metabolic status were determined every 21 d. Data were analyzed with nutritional plane, calving date, and calf sex (when P < 0.25) as fixed effects. Circulating metabolites included day and nutritional plane × day as repeated measures. We previously reported that post-calving, NR dams were 64kg and 2.0 BCS less than CON, but calf BW and size at birth were not affected. During the first 147 d of lactation, NR dams gained more (P < 0.01) BW than CON and increased (P < 0.01) BCS, while CON decreased (P ≤ 0.01) BCS and BF. Previously, NR dams had lower (P < 0.01) circulating triglycerides on day 1 of lactation, tended to have lower (P = 0.08) triglycerides on day 21, and had lower (P ≤ 0.04) non-esterified fatty acids (NEFA) on days 21 and 243 than CON. Maternal glucose and urea N were not affected (P ≥ 0.73). At weaning, NR dams weighed 17kg less (P = 0.15), were 0.67 BCS lower (P < 0.01), and tended to have less (P = 0.06) BF. Calves born to NR dams weighed less (P = 0.02) than CON by day 42 of age and were 13% smaller (P < 0.01) at weaning. Calf girth measures diverged (P ≤ 0.05) by day 21 of age, and skeletal size measures were less (P ≤ 0.08) for calves born to NR dams at most timepoints after day 63 of age. Calves born to NR dams tended to have lower (P = 0.09) circulating urea N pre-weaning than CON, but glucose, triglycerides, and NEFA were not affected (P ≥ 0.16). In summary, first-parity beef females that were nutrient restricted during late gestation experienced compensatory growth and gained body condition during lactation but were still thinner at weaning. Nutrient restriction reduced pre-weaning calf growth, likely due to decreased milk production.

Estimating the magnitude and sensitivity of energy fluxes for stickleback hosts and Schistocephalus solidus parasites using the metabolic theory of ecology.

Parasites are ubiquitous, yet their effects on hosts are difficult to quantify and generalize across ecosystems. One promising metric of parasitic impact uses the metabolic theory of ecology (MTE) to calculate energy flux, an estimate of energy lost to parasites. We investigated the feasibility of using metabolic scaling rules to compare the energetic burden of parasitism among individuals. Specifically, we found substantial sensitivity of energy flux estimates to input parameters used in the MTE equation when using available data from a model host-parasite system (Gasterosteus aculeatus and Schistocephalus solidus). Using literature values, size data from parasitized wild fish, and a respirometry experiment, we estimate that a single S. solidus tapeworm may extract up to 32% of its stickleback host's baseline metabolic energy requirement, and that parasites in multiple infections may collectively extract up to 46%. The amount of energy siphoned from stickleback to tapeworms is large but did not instigate an increase in respiration rate in the current study. This emphasizes the importance of future work focusing on how parasites influence ecosystem energetics. The approach of using the MTE to calculate energy flux provides great promise as a quantitative foundation for such estimates and provides a more concrete metric of parasite impact on hosts than parasite abundance alone.

Integrative transcriptomics and proteomics profiling of Arabidopsis thaliana elucidates novel mechanisms underlying spaceflight adaptation

Spaceflight presents a unique environment with complex stressors, including microgravity and radiation, that can influence plant physiology at molecular levels. Combining transcriptomics and proteomics approaches, this research gives insights into the coordination of transcriptome and proteome in Arabidopsis’ molecular and physiological responses to Spaceflight environmental stress. Arabidopsis seedlings were germinated and grown in microgravity (µg) aboard the International Space Station (ISS) in NASA Biological Research in Canisters – Light Emitting Diode (BRIC LED) hardware, with the ground control established on Earth. At 10 days old, seedlings were frozen in RNA-later and returned to Earth. RNA-seq transcriptomics and TMT-labeled LC-MS/MS proteomic analysis of cellular fractionates from the plant tissues suggest the alteration of the photosynthetic machinery (PSII and PSI) in spaceflight, with the plant shifting photosystem core-regulatory proteins in an organ-specific manner to adapt to the microgravity environment. An overview of the ribosome, spliceosome, and proteasome activities in spaceflight revealed a significant abundance of transcripts and proteins involved in protease binding, nuclease activities, and mRNA binding in spaceflight, while those involved in tRNA binding, exoribonuclease activity, and RNA helicase activity were less abundant in spaceflight. CELLULOSE SYNTHASES (CESA1, CESA3, CESA5, CESA7) and CELLULOSE-LIKE PROTEINS (CSLE1, CSLG3), involved in cellulose deposition and TUBULIN COFACTOR B (TFCB) had reduced abundance in spaceflight. This contrasts with the increased expression of UDP-ARABINOPYRANOSE MUTASEs, involved in the biosynthesis of cell wall non-cellulosic polysaccharides, in spaceflight. Both transcripts and proteome suggested an altered polar auxin redistribution, lipid, and ionic intracellular transportation in spaceflight. Analyses also suggest an increased metabolic energy requirement for plants in Space than on Earth, hence, the activation of several shunt metabolic pathways. This study provides novel insights, based on integrated RNA and protein data, on how plants adapt to the spaceflight environment and it is a step further at achieving sustainable crop production in Space.

Great tits (Parus major) in a west European temperate forest show little seasonal variation in metabolic energy requirements

Understanding how birds annually allocate energy to cope with changing environmental conditions and physiological states is a crucial question in avian ecology. There are several hypotheses to explain species' energy allocation. One prominent hypothesis suggests higher energy expenditure in winter due to increased thermoregulatory costs. The "reallocation" hypothesis suggests no net difference in seasonal energy requirements, while the "increased demand" hypothesis predicts higher energy requirements during the breeding season. Birds are expected to adjust their mass and/or metabolic intensity in ways that are consistent with their energy requirements. Here, we look for metabolic signatures of seasonal variation in energy requirements of a resident passerine of a temperate-zone (great tit, Parus major). To do so, we measured whole-body and mass-independent basal (BMR), summit (Msum), and field (FMR) metabolic rates during late winter and during breeding in Belgian great tits. During the breeding season, birds had on average 10% higher whole-body BMR and FMR compared to winter, while their Msum decreased by 7% from winter to breeding. Mass-independent metabolic rates showed a 10% increase in BMR and a 7% decrease in Msum from winter to breeding. Whole-body BMR was correlated with Msum, but this relationship did not hold for mass-independent metabolic rates. The modest seasonal change we observed suggests that great tits in our temperature study area maintain a largely stable energy budget throughout the year, which appears mostly consistent with the reallocation hypothesis.

PSIV-14 Effects of Maternal Nutrient Restriction During Late Gestation on Expelled Cotyledonary Mrna Expression in Primiparous Beef Females

Abstract To determine the effects of late gestational nutrient restriction on expelled cotyledonary mRNA expression, fall-calving Hereford × Simmental-Angus heifers [single-sired; BW: 451 ± 28 (SD) kg; BCS: 5.4 ± 0.7] bred to a single sire were allocated by fetal sex and expected calving date to receive either 100% (control; CON; n = 12) or 70% (nutrient restricted; NR; n = 11) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth. Beginning on d 160 of gestation, heifers were individually fed chopped sorghum sudan hay (1.74 Mcal ME/kg, 6.69% CP, 72.0% NDF; DM basis) and based on individual intakes, supplemented to meet targeted nutritional planes. Calving was observed for all females and placentas were collected at natural expulsion. Immediately after collection (average: 4.5 h post-calving; range: 2.3 to 12.1 h post-calving), 2 representative cotyledons on the ipsilateral side were cleaned with phosphate buffered saline, and cotyledonary tissue was flash frozen. Total RNA was extracted, and RT-qPCR was performed for mRNA expression of glucose transporters (SLC2A1, SLC2A3, SLC2A4), a fructose transporter (SLC2A5), amino acid transporters (SLC1A1, SLC3A2, SLC7A1, SLC7A5, SLC7A8, SLC38A2), angiogenic factors/receptors (VEGFA, NOS3, FLT1, KDR, GUCY1B3), and pregnancy-associated glycoprotein 2 (PAG2). Relative mRNA expression was analyzed with nutritional plane, treatment initiation date, time to cotyledon sampling, and calf sex (when P &amp;lt; 0.25) as fixed effects. We have previously reported that total uterine blood flow during late gestation was not affected (P ≥ 0.20) by nutritional plane or the nutritional plane × day of gestation interaction. Post-calving, NR dams were 64 kg BW less (P &amp;lt; 0.001) and 2.0 BCS less (P &amp;lt; 0.001), but calf birth weight was not affected (P = 0.72) by nutritional plane. Contralateral placental dry weight tended to be less (P = 0.07) in NR dams, but total placental weight was not affected (P = 0.86) by late gestational nutritional plane. Cotyledonary relative mRNA expression of SLC2A3 and SLC38A2 was greater (P ≤ 0.05) and relative expression of SLC2A1, SLC2A4, and NOS3 tended to be greater (P ≤ 0.07) in NR dams compared with CON. Late gestational nutritional plane did not affect (P ≥ 0.13) cotyledonary relative mRNA expression of FLT1, GUCY1B3, KDR, PAG2, SLC1A1, SLC2A5, SLC3A2, SLC7A1, SLC7A5, SLC7A8, and VEGFA. In summary, first parity beef females who experienced late gestational nutrient restriction maintained uterine blood flow and placental mass and had 4 nutrient transporters and 1 angiogenic factor upregulated in cotyledons, all which likely contributed to their conservation of fetal growth.

PSII-19 A Satellite-Based Decision-Support Tool to Optimize Profitability and Environmental Stewardship of Cow-Calf Operations

Abstract Management strategies implemented in cow-calf operations are essential to capitalize on heavier feeder calves, but field data collection can restrict their practical application. A computer program to optimize weaning weight, profitability, and environmental sustainability of grazing cow-calf operations was developed by combining an existing mechanistic nutrition model with pasture biomass estimated using satellite images. Data from the Texas A&amp;M University McGregor Research Center was used as a testbed for the computer model. Pasture forage data from 2016 to 2022 was collected via satellite imagery, and the predicted pasture biomass was adjusted based on third-party algorithms (Sigfarm Intelligence LLC). Nutrient requirements were estimated using the Ruminant Nutrition System (RNS), and a constant pasture nutritive value was obtained. The potential dry matter intake (DMI) was estimated from the initial herd size (input). Actual average weaning weight was used to predict cow milk yield and total metabolizable energy requirements, which was used to estimate the required DMI (DMR). The actual forage allowance was correlated to DMR, and we simulated the forage allowance to support increased DMI and, consequently, increased milk yield to achieve a targeted average weaning weight. Based on Intergovernmental Panel on Climate Change (IPCC) methodology, environmental impact was evaluated from greenhouse gas emission estimates. Our simulations demonstrated that increasing the target weaning weight of a smaller herd with fewer mature cows (757 cows) would produce heavier calves, resulting in a 6% decrease in calf gain per pasture area. Nevertheless, the net income increased in scenarios with heavier weaned calves. The enhanced productivity with heavier weaned calves and fewer cows resulted in a lower carbon emission per kg of produced weaned calves. Based on our simulation, a herd size between 757 and 812 mature cows yielding calves weaned between 280 and 300 kg would be an optimal management strategy for the studied operation. This computer model provides the fundamental framework for a decision-support tool for producers to optimize their cow-calf operations while producing ideal weaned calves for feedlot operations.

Estimation of the metabolisable energy requirements of feedlot light lambs and comparison with the U. S. National Research Council predictions

The aim of the present work was to compare the estimated metabolisable energy requirements (MER) of fattening light lambs raised in feedlot with the U. S. National Research Council (NRC) predictions. Body weight (BW) gain and feed intake were collected from 15 pens (7 lambs/pen) of Manchega male lambs under on-farm conditions over six weeks. The pens were randomly assigned to three dietary treatments (5 pens/treatment) consisting of three concentrates of different composition and barley straw. Feeds were offered for ad libitum consumption throughout the experimental period. Average daily metabolisable energy intake (MEI) was calculated on a weekly basis for each pen from the average daily consumption of concentrate and barley straw and their respective ME contents. Following, the average daily MER was predicted for each pen from the weekly average of both BW and BW gain, according to two models: One including the adjustment of ME for body maintenance (MEm) for the effect of level of MEI on visceral organ tissue energy use as described by NRC (Model 1), and the other excluding such adjustment (Model 2). Model 1 had no mean bias, and exhibited a higher concordance correlation coefficient and a lower underprediction, supporting the need for the upward adjustment of MEm in accordance with MEI to enhance the precision and accuracy of predicted MER. It was concluded that the NRC method was precise and accurate enough to support its application for calculating the MER of feedlot light lambs.

71 Effects of Late Gestational Nutrient Restriction on Calf pre-Weaning Growth, Backgrounding and Feedlot Performance, and Carcass Composition

Abstract Fall-calving Hereford-SimAngus heifers [single-sired; BW: 451 ± 28 (SD) kg; BCS: 5.4 ± 0.7] bred to a single sire were individually fed 100% (control; CON; n = 12) or 70% (nutrient restricted; NR; n = 13) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to calving. Post-calving, all females were fed chopped tall-fescue hay supplemented to meet lactational nutrient requirements in Calan gates to constrain diets of calves to milk only until day 147, then pen-fed in drylots until weaning at day 242 ± 3 (SD). Post-weaning, calves were fed a tall fescue hay-based backgrounding diet in the same large drylots for 53 ± 12 d, then moved to partially covered pens with GrowSafe feeding systems in 2 groups and fed a corn-based feedlot diet (formulated to be 18.3% CP, 1.21 Mcal NEg/kg, DM basis; 89% DM) for 255 ± 3 d (similar days on feed rather than carcass endpoint). Cattle were harvested in a commercial plant, and camera carcass grading was performed. Data were analyzed with maternal treatment, calving date, and calf sex (when P &amp;lt; 0.25) as fixed effects; feedlot group was included for feedlot and carcass measures. We previously reported that birth weight was not affected (P = 0.72), but NR decreased (P &amp;lt; 0.04) milk production by 15%. Calves born to NR dams had reduced ADG from birth to day 147 (P = 0.02), day 147 to weaning (P = 0.08), and birth to weaning (P = 0.003), resulting in NR calves having 13% lighter (P = 0.004) weaning weight. Backgrounding ADG was not affected (P = 0.80) by maternal treatment; thus, feedlot entry BW was 11% less (P = 0.009) in NR calves. On day 28, 56, 84, and 112 on feed, NR calves weighed less (P ≤ 0.09) than control. Final BW was not affected (P = 0.91) by maternal treatment. Feedlot ADG was greater for NR calves from day 168 to slaughter (P = 0.02) and the overall feeding period (P = 0.03), but not before day 168 on feed (P ≥ 0.22). Calves born to NR dams had less (P = 0.02) dressing percentage, but improved (P = 0.02) yield grade and backfat thickness. Hot carcass weight, ribeye area, marbling score, and KPH were not affected (P ≥ 0.26) by maternal treatment. Percent prime, yield grade ≤ 2, and yield grade ≥ 4 were not affected (P ≥ 0.29) by maternal treatment. Overall, late gestational nutrient restriction decreased growth pre-weaning but increased late finishing growth, without affecting backgrounding or early feedlot growth. These cattle had leaner carcasses after similar days on feed, suggesting that late gestational nutrient restriction altered growth patterns or body composition.

70 Nutrient Restriction During Late Gestation Alters Maternal Circulating Amino Acid Concentrations in Primiparous Beef Females

Abstract We hypothesized that maternal circulating AA concentrations would be reduced by late gestational nutrient restriction, indicating less available nutrients for transport by the uteroplacenta to the growing fetus. Fall-calving Hereford-SimAngus heifers [single-sired; BW: 451 ± 28 (SD) kg; BCS: 5.4 ± 0.7] bred to a single sire were allocated by fetal sex and expected calving date to receive either 100% (control; CON; n = 12) or 70% (NR; n = 13) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to calving. Heifers were individually fed chopped sorghum sudan hay (1.74 Mcal ME, 6.66% CP, 72.0% NDF; DM basis) and based on individual intakes, supplemented to meet targeted nutritional planes. Jugular blood samples were obtained on days 159 (Pre-treatment), 202, and 244 of gestation, and 1 h post-calving to determine serum concentrations of the 20 common AA (except cysteine), 1-methyl histidine, and 3-methyl histidine. Gestational and post-calving AA were analyzed separately with nutritional plane, treatment initiation date, and calf sex (when P &amp;lt; 0.25) as fixed effects. Gestational AA included day and nutritional plane x day using repeated measures. We have previously reported that dam BCS was less (P ≤ 0.04) by day 202 of gestation and dam BW was less (P ≤ 0.01) by day 223 of gestation for NR dams. Post-calving, NR dams were 64 kg BW and 2.0 BCS lless (P &amp;lt; 0.001), but calf birth weight was not affected (P = 0.72) by nutritional plane. Histidine, lysine, and methionine were greater (P ≤ 0.03) in NR dams on day 202 of gestation. Tryptophan and valine were less (P ≤ 0.05) while methionine and total AA tended to be less (P ≤ 0.08) on day 244 of gestation in NR dams. Aspartic acid, glutamic acid, and tyrosine were less (P ≤ 0.03), but 3-methyl histidine was greater (P ≤ 0.01) on days 202 and 244 of gestation in NR dams. 1-methyl histidine was greater (P ≤ 0.05) at all 3 gestational timepoints but leucine was less (P = 0.03) in NR dams during gestation. Post-calving, glutamic acid, leucine, and valine were less (P ≤ 0.04), and methionine, threonine, tryptophan, tyrosine, and total AA tended to be less (P ≤ 0.10) in NR dams. Histidine, 1-methyl histidine, 3-methyl histidine, and serine were greater (P ≤ 0.03) in NR dams post-calving. In summary, late gestational nutrient restriction reduced total maternal circulating AA and altered the maternal serum AA profile, but calf birth weight was not affected. Individual AA that were greater or unaffected in NR dams were likely indicative of body protein catabolism occurring to meet nutrient requirements.

PSII-11 Supplementation of Non-Protein Nitrogen to a Nitrogen-Deficient Diet Increases Lysine Requirement for Nitrogen-Retention

Abstract Low protein (LP) diets have improved nutrient utilization while maintaining animal performance. Regardless, these diets may be limiting in nitrogen (N) content to meet non-essential amino acid (NEAA) requirements, potentially altering essential amino acid (EAA) utilization and requirements. Inclusion of a non-protein nitrogen (NPN) may be beneficial for improving utilization of EAA in LP diets. The objective of this study was to determine the impact of NPN in an N-deficient diet, as indicated by EAA-N:total N ratio (EAA-N:TN) on the Lys requirement for nitrogen retention (NR). A total of 90 growing barrows (initial BW of 20.4 ± 0.46 kg) were randomly assigned to 1 of 10 dietary treatments (n = 9 pigs/treatment) in 9 blocks in a 2 × 5 factorial design. Diets contained no ammonium phosphate (NAP; EAA-N:TN of 0.56) or were supplemented with 1.7% ammonium phosphate (AP; EAA-N:TN of 0.50) with graded levels of dietary lysine [Lys; 0.8%, 0.9%, 1.0%, 1.1% and 1.2% standardized ileal digestible (SID)]. Diets were corn and soybean meal-based and formulated to meet or exceed nutrient requirements according to NRC (2012). Diets were fed at 2.8 × maintenance metabolizable energy requirements in two equal meals per day. A 4-d nitrogen balance collection period was conducted following a 7-d dietary adaptation period. Urine was collected quantitatively, and fresh fecal samples were obtained daily. Nitrogen retention was determined as the difference between N intake and output (fecal and urinary). Linear breakpoint modeling with PROC NLIN was used to estimate Lys requirement. Nitrogen retention was optimized at 1.00% SID Lys (15.6 g/d NR; R2 = 0.68) in pigs fed NAP diets and 1.09% SID Lys (16.4 g/d NR; R2 = 0.61) in pigs fed AP diets. Overall, deficient dietary N reduced NR and Lys requirement, which were increased with NPN supplementation.

Can low-input agriculture in semi-arid Burkina Faso feed its soil, livestock and people?

Agriculture in semi-arid Burkina Faso is dominated by mixed crop-livestock smallholder farms with limited investment capacity in production factors, such as improved seeds, fertilizer and equipment. Hence, to make a living, farmers try to make the best use of available resources based on principles of agro-ecology, including crop diversity and nutrient and biomass recycling. We investigated farm-level management of resources (soil, crops and livestock) through time to assess whether the current management options were able to sustain crop and livestock production and fulfil household food requirements. We ran a one-year detailed farm monitoring campaign in collaboration with 22 volunteer farmers representing the diversity of the farming system in our study area. We quantified inputs and outputs in the cropping system (177 fields) for one rainy season. In addition, the weekly dynamics of crop residues left on field were quantified. Moreover, inflow and outflow of resources at farm level were quantified weekly. The cropping system was characterized by a negative nitrogen balance of about 12 kg N/ha/year, with market-oriented farms and large livestock owners having the most negative balance. Legumes grown (sole and intercropping) contributed to alleviate the nitrogen depletion by adding 15 kg N/ha/year to the nitrogen inputs through atmospheric fixation. However, cereal-legume intercropping did not significantly reduce the nitrogen deficit in comparison to sole cereal cropping mainly because of the small proportion of legumes (8%) in intercropped fields. Livestock grazed crop residues left on the soil (739 kg dry matter/ha on average) at a rate of 26 − 76 kg/ha/week, thus strongly reducing the potential for mulching in the region. Livestock protein requirements were rarely met from farm-produced feed with average feed gaps ranging between 40% and 89% of the daily requirements for small and large herd keepers respectively. Large livestock (cattle) owners relied on transhumance during the rainy season, grazing and frequent purchase of crop residues and concentrates to feed their livestock. We estimated that grazed biomass provided on average at least 73% and 58% of metabolizable energy and protein feed requirement of livestock respectively. Concerning food availability, the amount of grain produced was generally enough to fulfil household energy requirements (89–175% of required energy, in kcal), even if households with higher people to land ratio were not self-sufficient. We concluded that the current farm management, even if it provides enough food for the majority of investigated farms, results in soil fertility mining and poor crop livestock production and integration. Our detailed farm data indicate that an appropriate diversity of crops and a better integration of legume crops in the cropping system, associated to improved manure and forage management is needed to sustain crop and livestock production.

Enteric Methane Emissions, Rumen Fermentation Characteristics, and Energetic Efficiency of Holstein Crossbred Bulls Fed Total Mixed Ration Silage with Cassava instead of Rice Straw

This study investigated the effects of substituting rice straw with cassava in total mixed ration silage on feed intake, digestibility, rumen fermentation, ruminating activity, and energy balance. An energy balance experiment was conducted to determine nutrient and energy utilization in dairy bulls. Four Holstein Friesian (HF) crossbred young bulls (93.19% HF × 6.81% Native Thai; average age of 12.08 ± 0.22 months and body weight of 266 ± 9.80 kg) were used in a 4 × 4 Latin square design with four 28-d periods. The four dietary treatments included substituting cassava with rice straw on a 50, 150, 250, and 350 g/kg dry matter basis. Increasing the amount of cassava in the diet resulted in linearly decreased rumination behaviors and enteric methane emissions (p &lt; 0.05) but a linear increase in feed intake and digestibility, total volatile fatty acid concentration, and propionic acid: acetic acid ratio in the rumen fluid (p &lt; 0.05), thus leading to a greater energy balance status (p &lt; 0.01). Our results indicated that replacing cassava with rice straw from 5% to 35% in the ration of Holstein bulls resulted in a substantial reduction in physically effective fiber and chewing time but improved nutrient and energy supply. The metabolizable energy requirement for the maintenance of crossbred dairy bulls was estimated to be 599.9 kJ/kg metabolic body weight and the efficiency of metabolizable energy used for growth was 0.88. We concluded that cassava is a good energy feed resource for Holstein crossbred bulls in the tropics.

Energy utilization and requirement of broiler breeders during the production phase

This study aimed to evaluate energy utilization and propose models for metabolizable and net energy requirements in broiler breeders during the egg production phase. Sixty Cobb500 broiler breeders aged between 29 and 65 wk were randomly assigned to 3 feeding levels. At each age, 6 birds were adapted for 8 d to 3 levels of metabolizable energy intake (MEi), established based on the amount of feed allocated: 1) the amount of feed recommended in the guideline, 2) 25% above, and 3) 25% below. The birds were housed in respirometry chambers for 6 d (1 adaptation, 4 feeding state, 1 fasting) to measure oxygen consumption and carbon dioxide production to calculate heat production (HP) and fasting HP (FHP). Daily measurements of feed intake, egg weight, egg production, and total excreta were recorded. Variables of MEi, HP, and retained energy (RE) in the egg were calculated, while RE in the body and its partitioning into fat and protein in the egg and body were calculated from MEi, total HP (THP), and RE in the egg. Statistical analysis involved linear regression of multiple factors with MEi and age (categorical) as the independent variables. Pearson correlation analysis was conducted to investigate the relationship between visceral mass and the evaluated variables. The study proposed mixed models for developing models of energy requirements for both metabolizable (ME) and net systems (NE). The study found that FHP (average 259 ± 20.08 kJ/kg0.75*d) remained constant throughout the production cycle regardless of the MEi level (P > 0.05). The efficiency of energy utilization for depositing protein and fat in the body changed with the bird's age. The lower error model was considered to select ME requirements for maintenance, egg, and gain efficiencies, disregarding the effect of age. The efficiencies were 0.89, 0.78, and 0.80 for maintenance, gain, and egg production, respectively. The NE was unaffected by age and showed a lower error than the ME model. The NE system was found to be more accurate in expressing the energy requirements of broiler breeders.