Nursery Studies Methods | Results | Publications
Grow-Finish Studies Methods | Results | Publications
Nitrogen Balance Methods | Results
Validation Study (Large scale) for Nursery & G/F Methods | Results (available early 2016)
Incorporating this data into models
Dr. Charles Maxwell, Dr. Jennie Popp, and Dr. Richard Ulrich - University of Arkansas; Dr. Scott Radcliffe - Purdue University, and Dr. Mark Hanigan - Virginia Tech
Maximizing feed grade amino acid (FGAA) use and reducing dietary crude protein in swine diets has been shown to dramatically reduce nitrogen excretion in both nursery and growing/finishing swine which could substantially reduce nitrous oxide (N2O) emissions associated with manure management in swine production. The global warming potential of N2O is about 298 times that of CO2 (carbon dioxide). Reducing the crude protein (CP) content of grower and finisher diets has also been repeatedly shown to enhance carcass quality by elevating intramuscular fat. While some crystalline amino acids are already commonly used in pork production the maximum level of CP reduction, in conjunction with the optimum amino acid inclusion rate, has not been sufficiently determined for widespread acceptance by the swine industry.
Hypothesis: Reducing dietary CP while maintaining amino acids (AA) at equivalent Standardized Ileal Digestibility (SID) ratios by supplementing feed grade AA will reduce nitrogen (N) excretion and greenhouse gas (GHG) emissions (N2O from manure) without impacting swine performance or carcass yield.
Studies were conducted at multiple sites. One was the University of Arkansas wean-to-finish facilities and the second at the Purdue Swine Environmental Research Building (SERB). See the videos above for more on these facilities). The data generated was utilized in modelling work at Virginia Tech. The model was ultimately incorporated into the Swine Environmental Footprint Calculator.
To evaluate maximum replacement of CP with FGAA, 320 weaned pigs were allotted to gender-balanced pens in a wean-to-finish facility (8 pigs/pen). Within blocks, pens were randomly assigned to 1 of 5 dietary treatments. Diets were formulated to maintain constant ME and SID Lys across treatments with SID Lys set at 95% requirement (PIC Nutrient Specification Manual, 2011). Diets were formulated to meet the SID AA ratio recommendations for other indispensable AA (SID) for nursery pigs through the 6th limiting AA (PIC Nutrient Specifications Manual, 2011). For each phase, Ctrl diets were devoid of FGAA, whereas Lys HCl was added in equal increments at the expense of CP (SBM, fish meal [FM], and poultry meal [PM] in phase 1, FM and PM in phase 2, and SBM in phase 3). This formulation procedure resulted in diets that were below the His and Phe/Tyr SID requirement for the highest level of CP reduction. CP and Lys inclusion levels were analyzed.
A second three phase nursery study was conducted with pigs weaned at 21 d to further evaluate limits of CP reduction in nursery diets and compare performance in pigs fed diets based on formulation on an ME vs. NE basis. The study involved 7 pigs/pen and 7 replicates/treatment. Dietary ingredients were similar to those used in experiment 1, except soy protein concentrate was used to replace fish meal. Dietary treatments were: 1), Control diet formulated on an ME basis and with FGAA used to meet the “Trp Set Point” without adding feed grade Trp in phase 1 and 2 and 0.02 % added Trp in phase 3; 2) Diet formulated on an ME basis and to meet the “His Set Point” without added feed grade His; 3) As 2 with diets formulated on a NE basis.
Pigs fed RCP 1, RCP 2, and RCP 3 diets in phase 1, 2 and 3, and for the overall study had similar ADG and BW but growth performance declined for pigs fed RCP 4 diets (Table 5; Quadratic effect, P < 0.01). A similar response was observed in ADFI in all time periods except phase 1 where ADFI was similar among treatments. In phase 1, G:F ratio followed a similar response (Quadratic effect, P < 0.01), but decreased linearly in phase 2 (P < 0.08), 3, and overall (P < 0.01). It should be noted that the RCP 4 diet was below requirement for SID His:Lys and Phe/Tyr:Lys which might explain the decrease in performance. The results of this study establishes that a high inclusion of feed grade Lys at the expense of intact proteins can be fed without decreasing ADG and ADFI except at the highest level of FGAA where the requirement for all IDAA was not met. However, G:F was generally reduced at the higher inclusion rates of FGAA, particularly in phase 3.
No differences were observed in ADG, ADFI, or G:F (Table 6) in any phase or overall in pigs fed diets formulated on an aggressive FGAA inclusion (His Set Point) based on ME (Trt.2) or NE (Trt. 3) compared to pigs fed AA inclusion levels currently used in swine industry (Trt. 1). These results indicate that in nursery pigs, one should be able to use a His Set Point in formulating AA based diets without concern for pig performance.
The previous nursery experiment (Experiment 1; Bass et al., 2013) conducted to evaluate feeding reduced CP diet with the highest levels of FGAA to nursery pigs resulted in poor growth performance, especially G:F ratio in phase 3 and the overall nursery period. In the previous study, experimental diets were formulated to meet the 95% of SID Lys requirement for nursery pigs. Also, RCP 4, which was formulated with the highest level of FGAA, did not meet the His and Phe requirement Lys/NE.
In conclusion, unlike the previous study, growth performance of nursery pigs was not affected by the higher level of FGAA and lower dietary CP. This may be due to different SID His:Lys and SID Phe+Tyr:Lys ratios used in diet formulation or different protein source used in each study. In the second nursery study, all diets were formulated based on 100 % or excess of SID Lys requirement for nursery pigs, and were formulated to meet the His and Phe+Tyr requirement. In addition, soy protein concentrate (SPC) was used in the second study during phase 1 and 2, replacing menhaden fish meal used in nursery study one.
Each experiment was conducted following a five phase grow-finish protocol. Pigs were fed 1 of 4 or 5 diets and 10 ppm of Paylean was fed during the final 3-week finishing phase-Phase 5. During phase 1 through 5, individual pig BW, and pen feed disappearance were measured over each phase to allow calculation of ADG, ADFI and G:F by phase. Tenth rib, ¾ midline back fat measurements and loin muscle area were estimated at study initiation and at the end of each phase via ultrasound to allow estimation of carcass lean gain. When the average of all blocks was 129-134 kg all pigs were individually weighed, tattooed, transported to, and harvested at a commercial pork packing plant according to industry accepted procedures. Longissimus muscle (LM) and fat depths at the 10th rib were measured on-line with a Fat-O-Meater probe and individual hot carcass weight was recorded.
A total of 420 pigs were blocked within gender and randomly allotted to pens with 6 pigs/pen. Within blocks, pens of pigs were randomly assigned to 1 of 5 dietary treatments (7 reps/treatment/gender). Diets were formulated by incrementally increasing levels of Lys with corresponding reductions in CP. Pigs were randomly allotted to the following diets:
RCP 1 to 4 were then formulated to have stepwise and equally spaced increased Lys with corresponding reductions in CP between RCP 1 and 4. Diets 2-4 were supplemented with FGAA as needed to meet AA needs based on AA minimum ratios. Dietary CP and Lys inclusion levels were analyzed.
Diets were formulated to 95% of the average SID Lys requirement for barrows and gilts (PIC Nutrient Specifications Manual, 2011), and exceeded the SID AA/Lys ratio recommendations for other IDAA by 2 percentage points.
Distillers dried grains with solubles (DDGS) were included in all diets at the 20% level, with the exception of phase-5 finishing diets which was devoid of DDGS.
In experiment 1, diets were formulated on an ME basis and as soybean meal was reduced in diets, the calculated Lys/NE decreased which may explain some of the increase in fat deposition in pigs fed ME based diets formulated by decreasing soybean meal and including high levels of FGAA. Therefore, experiment 2 was conducted to establish the efficacy of using a “Set Point SID requirement” of sequentially reducing CP by adding FGAA to meet the SID IDAA/Lys ratio as a means of establishing the practical limits of CP reduction and AA replacement without impacting growth performance, carcass composition or quality in growing and finishing pigs fed NE based RCP diets. Diets were formulated starting with a Ctrl diet that approximates acceptable inclusion levels of FGAA currently used in industry, followed by sequentially formulating three additional dietary treatments, each based on the next limiting AA. Diets in this study were formulated on a constant NE basis within phase. DDGS was included in all diets. The SID His requirement in the highest RCP diet was met in each phase without added feed grade His.
There were a total of 9 replicates/treatment with pigs housed 6 pigs/pen. Sex within pen was balanced. Diets were formulated as in experiment 1 which were:
All diets were supplemented with FGAA to meet IDAA recommended levels. Note that feed grade His was not added to any diet.
Body weights of pigs decreased linearly with decreasing dietary CP during phase 1, 2, and 3 (P < 0.01; Table 7). Additionally, BW increased and then decreased quadratically during phase 3 (P = 0.09), 4 (P < 0.04), and 5 (P < 0.01) with BW decreasing significantly in pigs fed RCP 4. When Paylean was included in the Phase 5 diets, barrows fed the Ctrl diet had greater ADG than Ctrl-fed gilts, but RCP 1-, RCP 2-, and RCP 3-fed gilts had greater ADG than their castrated male counterparts (Quadratic gender × reduced CP diet, P = 0.08; Figure 1A) Both ADG and G:F decreased linearly (P ≤ 0.06) during phase 1 and 2. Furthermore, gain efficiency increased 4.6 % in gilts between Ctrl and RCP 2 before decreasing to similar G:F values between Ctrl and RCP 4; however, G:F remained relatively unchanged in barrows across the 5 dietary treatments (Quadratic gender × reduced CP diet, P = 0.04; Figure 1B).
Across the entire feeding trial, ADG increased only 2 % between Ctrl and RCP3, but dropped 6 % between RCP3 and RCP4 (Quadratic, P < 0.01). On the other hand, ADFI tended to decreased linearly (P = 0.09) as CP was reduced in swine diets. Gain efficiency increased 4.6 % in gilts between Ctrl and RCP2 before decreasing to similar values between Ctrl and RCP4; however, G:F remained relatively unchanged in barrows across the 5 dietary treatments (Quadratic gender × reduced CP diet, P = 0.04; Figure 1C).
Reducing dietary CP and optimizing the use of FGAA had limited (P ≥ 0.21) effects on HCW, dressing percentage, or LM depth; however, 10th rib fat depth increased linearly (P < 0.01), and fat free lean percentage at study termination decreased linearly as CP was reduced in swine diets (P < 0.02; Figure 1D).
Effects of dietary treatment (Trt.) indicated that ADG decreased linearly with increasing dietary FGAA in phase 3 (Table 8, P < 0.05), 4 (P < 0.10), 5 (P < 0.01) and overall (P < 0.01). Similarly, ADFI decreased linearly in phase 4 (P < 0.05), 5 (P < 0.01) and overall (P < 0.01) with increasing FGAA. Compared to pigs fed the control diet (Trt. 1), G:F in phase 1 increased in pigs fed increasing levels of FGAA at the lower inclusion rates (Trt. 2 and 3) before decreasing to the control level at the highest level of inclusion (Trt. 4, Quadratic effect, P < 0.05). During phase 3, a small, but significant, decrease in G:F was observed with increasing levels of FGAA (Linear effect, P < 0.05). For the overall study, however, a trend for increased G:F was observed (Linear effect, P < 0.06). BW increased at the end of phase 2 with increasing level of FGAA (Quadratic effect, P < 0.06). However, consistent with ADG, BW decreased with increasing dietary FGAA at the end of phase 3, 4 and 5 (Linear effect, P < 0.05, P < 0.01 and P < 0.01, respectively).
As might be expected based on BW, HCW decreased with increasing inclusion of dietary FGAA (Linear effect, P < 0.01). Tenth rib backfat was lower in pigs fed diets formulated to the Val or Ile Set Point (Trt. 2) or the His Set Point (Trt. 4) when compared to those fed diets formulated to the Val and Ile Set Point (Trt. 3).
2013 Midwest American Society of Animal Science (ASAS) meeting Abstract 0224, page 73 (performance and carcass composition)
Significance. This information is timely since the cost of soybean meal is approaching record levels which make substitution of synthetic amino acids for intact protein more economically feasible.
Thirty-two barrows were used to evaluate the effect of feeding reduced CP, AA supplemented diets, on nutrient and VFA excretion. Pigs were randomly allotted to the following diets:
Diets 2 and 3 were formulated to have stepwise and equally spaced reductions in CP between diets 1 and 4. Diets 2-4 were supplemented with FGAA as needed to meet AA needs based on NRC 2012 AA minimum ratios. Four nursery phases and 5 grow-finish phases (21d phases) were fed. Pigs were housed in stainless-steel metabolism pens equipped with a nipple waterer and stainless steel feeder. Collections started with nursery phase 3 and during nursery phases pigs were allowed an eight day adjustment period to the diets followed by a 3 d total collection of feces, urine, and orts. During the grow-finish phases, pigs were acclimated to diets for the first 10 d of each phase, and then feces, urine, and orts were collected for 3 days.
Overall, from d 14-147 post-weaning ADFI was linearly increased as dietary CP was reduced, but no effect of dietary CP concentration on ADG or G:F (Table 9) was observed. Fecal excretion (DM) tended to respond in a quadratic (P = 0.08) fashion with decreasing fecal excretion (DM) up to 2X reduction in CP, but then increasing in 3X fed pigs. Both DE and ME (kcal/kg) were linearly (P < 0.01) reduced as dietary CP was reduced. The linear (P < 0.01) decrease in N intake for pigs fed reduced CP diets was accompanied by linear (P < 0.01) decreases in both urinary and total N excreted. Nitrogen digestibility (%) linearly decreased (P < 0.01) and N retention linearly (%) increased (P < 0.01) with reductions in dietary CP. Overall, there was a linear (P < 0.03) reduction in fecal ammonium as dietary CP was reduced. Total carbon (C) intake and total fecal C excreted tended (P = 0.06) to respond quadratically with an increase in both C intake and C excretion up to the 1X reduced CP diets, followed by a decrease in C intake and increasing C excretion to the 3X diet creating a linear (P < 0.05) decrease in C digestibility as dietary CP was reduced.
Significance. The ability to add total fecal and urine collections of the nitrogen manipulation diets across all body weights tested at the University of Arkansas before the diets were tested for greenhouse gas emissions at Purdue University improved the estimation of compounds excreted in fresh manure and then the conversion of these excreted nutrients and compounds during storage in typical deep pit manure structures under the swine facilities (as were measured during the Purdue 12 room study). This research project provided data for a critical link between excretion, storage, and land application.
Large-scale trials are in progress to validate the nursery and grow-finish trials done at Arkansas. The Purdue facility is scaled more similarly to a commercial production system. Gas measurement and monitoring, and separate manure handling systems for each room allowed direct measurements with which to compare previous estimations.
Treatment structure for the experiment was:
All diets were supplemented with Ractopamine during the final 3-4 weeks of the trial, and amino acid concentrations were increased based on estimated increases in lean tissue accretion. However, the overall treatment structure will remain the same. The Experiment involved 24 pens of 10 pigs each per treatment, with 8 manure pits/trt, and 4 rooms per trt. Pen was the experimental unit for all growth performance, feed intake, and carcass data. Pit was the experimental unit for manure excretion data and room is the experimental unit for emission data.
Real-time monitoring of air temperatures included relative humidity, carbon dioxide (CO2), methane (CH4), nitrous oxide (N2O), ammonia (NH3), and hydrogen sulfide (H2S). Total suspended particulates were monitored using gravimetric samplers. The emission and animal performance data were significantly more accurate in this replicated, environmentally-controlled building than is possible commercially, yet still simulate commercial conditions.
Manure from each pit was completely removed to outside storage for volume determination, thorough agitation and sampling at the end of each trial. In addition, core manure samples based on a grid system were obtained at the end of each growth phase. Manure volume in each pit was determined at diet phase changes by taking 6 gridded depth measurements between the slatted floor. Manure samples were analyzed for pH, dry matter, ash, total nitrogen (N), ammonium N, phosphorus (P), carbon (C), and sulfur (S). Data defining the relationship between the reduction in dietary CP with a reduction in manure N and other changes in manure characteristics are essential to model development of the impact of this mitigation strategy on GHG emissions. An additional benefit will be defining the limits of this strategy without impacting animal growth performance under conditions where industry stakeholders have input.
Coming Soon! (first half 2016)
[See also: Virginia Tech modeling efforts] Current nutritional requirement models for swine are focused on partitioning of dietary energy and amino acids to maintenance, growth, gestation, and lactation. Little focus is placed on predicting nutrient excretion, and thus these models cannot be used to provide inputs to an emissions model. Models that predict excretion of energy, protein, and phosphorus have been developed, but have not been evaluated for the accuracy of predictions; and evaluations that have been undertaken focus on predictions of growth and body composition, not nutrient excretion.
GHG emissions from manure storage facilities can be predicted from manure composition, underscoring the need for a robust animal model capable of predicting both animal performance and nutrient excretion. Prediction of GHG emissions from swine manure requires knowledge of N and volatile solids content, neither of which are provided by current NRC predictions.
Data from the nitrogen mitigation growth and nitrogen excretion studies were utilized in enhancement of an animal model capable of predicting swine performance and excretion of nitrogen, carbon, and volatile solids (inputs required by the DNDC model). The growth model developed by the workers at UC-Davis and the recently released Nutrient Requirements of Swine (NRC) eleventh revised edition will be used as a starting point for model development. Equations describing the response to dietary protein and amino acid additions will be evaluated for accuracy, and the effects of Paylean on animal performance and manure nutrient output will be encoded and tested for accuracy. This work is scheduled to precede and utilize data from the UA trial and literature sources. The model will be further evaluated in the 5th year using the Purdue data set.
Dr. Scott Radcliffe
Phone: (765) 496-7718
Dr. Brian Richert
This information is part of the program “Integrated Resource Management Tool to Mitigate the Carbon Footprint of Swine Produced In the U.S.,” and is supported by Agriculture and Food Research Initiative Competitive Grant no. 2011-68002-30208 from the USDA National Institute of Food and Agriculture. Project website: http://www.extension.org/71201.