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Results are presented from thin (resistive) shell experiments on HBTX and compared with theoretical (linear and non-linear) studies of the plasma stability. Current pulses of 3--5 ms are obtained, compared with the shell time constant for vertical field penetration of 0.5 ms. Theoretically predicted thin shell modes, phase locked to the wall, are prominent experimentally.

This study evaluated the effect of xylanase supplementation (with or without), feeding method (dry or liquid), and feedstuff (corn distiller's dried grains with solubles [DDGS] or wheat middlings) on apparent total tract digestibility (ATTD) and apparent ileal digestibility (AID) of GE and nutrients, intestinal morphology, ileal and cecal pH, and VFA concentrations. Sixty-four growing pigs (25.87 ± 0.38kg initial BW) were blocked by BW and sex and randomly assigned to 8 dietary treatments. Within each feedstuff, diets were fed either liquid or dry, without or with xylanase (24,000 birch xylan units/kg feed), for 16 d. Diets contained 3.32 and 3.19 Mcal/kg ME for DDGS- and wheat middlings-based diets, respectively. Pigs were fed restricted at 3 times maintenance ME requirements. Liquid diets were prepared by steeping DDGS or wheat middlings with water (1:3, wt/vol) with or without xylanase for 24 h followed by mixing with a basal ingredient mixture and water to achieve a final ratio of 1:2.5 (wt/vol). During steeping of wheat middlings, some fiber degradation occurred. When xylanase was added in dry wheat middlings diets, AID of GE ( < 0.10) and NDF ( < 0.05) increased compared with dry wheat middlings diets without xylanase (64.50 vs. 54.67% and 52.88 vs. 31.69%, respectively), but supplementation of xylanase did not impact AID of GE and NDF when liquid wheat middlings diets were fed. Xylanase in liquid DDGS diets increased ( < 0.05) the AID of NDF compared with liquid DDGS diets without xylanase, but xylanase did not affect AID of NDF in dry DDGS diets. Xylanase in wheat middlings diets improved ( < 0.05) ATTD of GE and N compared with wheat middlings diets without xylanase (80.37 vs. 78.07% and 80.23 vs. 77.94%, respectively). However, there was no effect of xylanase in DDGS diets. Pigs fed DDGS diets had greater concentrations of butyrate in the cecum ( = 0.001) than pigs fed wheat middlings diets (27.6 vs. 20.4 mmol/L). Pigs fed DDGS diets with xylanase had deeper crypts ( < 0.05) in the jejunum than pigs fed DDGS diets without xylanase (98.20 vs. 86.16 μm), but xylanase had no effect in pigs fed wheat middlings diets. Results suggest that liquid feeding and xylanase supplementation had limited potential to enhance nutrient digestibility in pigs fed DDGS-based diets. However, xylanase supplementation in dry wheat middlings-based diets improved the AID of NDF and ATTD of GE and N, but liquid feeding as pretreatment did not further enhance the nutritional value of wheat middlings-based diets.

Crossbred pigs (n = 720; average age = 28 ± 3 days and weight = 9.5 ± 0.3 kg) were used in a 20-day trial in order to determine the influence of phosphorus (P) source and various doses of pharmacological zinc (Zn) on growth performance, plasma minerals and mineral digestibility. Pigs (five intact males and five females per pen) were randomly allotted to treatments in a 3 × 3 factorial arrangement with three sources of dietary P (4.5 g/kg digestible P, 4.5 g/kg digestible P plus 2500 phytase units (FTU)/kg, or 5.5 g/kg digestible P) and three dietary levels of supplemental Zn (0, 1750 or 3500 mg/kg) from ZnO (82% Zn) with eight pens per treatment. Diets were formulated to exceed all nutrient requirements, including calcium (Ca), P and Zn from day 0 to 20. Zn supplementation increased (quadratic P < 0.05) average daily feed intake. There was a significant Zn level × P source interaction on average daily gain and feed conversion ratio (FCR). Pigs fed 4.5 g/kg digestible P without or with 2500 FTU/kg phytase gained more per day (quadratic P < 0.05) and had better FCR (quadratic P < 0.05) when they were fed 1750 mg/kg supplemental Zn. However, pigs fed 5.5 g/kg digestible P gained more per day (linear P < 0.05) and were more efficient (linear P < 0.05) when they were fed 3500 mg/kg supplemental Zn. Plasma Zn and Zn digestibility increased (linear P < 0.05) as pharmacological Zn supplementation increased from 0 to 3500 mg/kg, irrespective of P source. However, Ca, P, sodium (Na), potassium (K) and copper (Cu) digestibility were reduced ( P < 0.05) as pharmacological Zn supplementation increased, and this was mitigated or exacerbated by the supplementation of 5.5 g/kg digestible P or phytase. In conclusion, increasing the dietary inclusion of pharmacological Zn may impact growth performance in young pigs through the interaction with minerals such as Ca, P, Na and K. Pharmacological Zn may reduce Na or K digestibility and indirectly reduce water secretion into the lumen, resulting in an increase in faecal dry matter as pharmacological Zn supplementation in the diet increased.

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Crossbred pigs (n=288; average age=21±3 d and BW=7.1±0.2 kg) were used in a 42-d trial to determine the influence of a microbial phytase and various doses of ZnO on growth performance and serum minerals. Pigs (6 castrated males or females/pen) were randomly allotted to treatments in a 2×3 factorial arrangement with 2 dietary levels of a microbial phytase (0 or 2,500 phytase units/kg) and 3 dietary levels of supplemental ZnO [0, 1750, or 3,500 mg/kg ZnO (72% Zn)] with 4 pens of castrated males and 4 pens of females per treatment. Diets were formulated to exceed all nutrient requirements, including Ca and P from d 0 to 21 (phase 1) and d 22 to 42 (phase 2). Growth performance, serum Zn, and serum P were not influenced (P>0.05) by a ZnO×phytase interaction during phase 1, phase 2, or overall (d 0 to 42). Phytase increased (P=0.01) ADFI and improved (P=0.02) ADG in phase 1 and improved (P=0.01) overall ADG, regardless of the level of ZnO supplemented. Zinc oxide supplementation linearly reduced (P=0.05) ADG, and ZnO at 3,500 mg/kg reduced (quadratic, P=0.04) G:F in pigs (phase 2). During phase 1, phytase increased serum Ca, but only in the absence of ZnO supplementation, which resulted in a ZnO×phytase interaction (P=0.02). Serum Zn was increased (linear, P<0.001) and serum P was decreased (linear, P=0.05) as ZnO supplementation increased in the diet (phase 1). In phase 2, serum Ca was reduced (linear, P=0.04) and serum Zn was increased (linear, P=0.02) as ZnO supplementation increased in the diet. Phytase supplementation increased (P=0.009) serum Zn and increased (P=0.003) serum P (phase 1). There was no influence of phytase supplementation on serum minerals in phase 2. In summary, supplemental ZnO reduced growth performance in this experiment. Phytase supplementation improved ADG in Ca- and P-adequate diets regardless of the level of ZnO supplemented, which may be attributed to the reduction of phytate as an antinutrient. In addition, through phytate hydrolysis, phytase reduced phytate-Zn interactions and increased serum Zn, Ca, and P. However, supplementing ZnO increased serum Zn, which reduced serum P and Ca, indicating Ca-Zn-P precipitation. In addition, phytase increased serum Ca, but only in the absence of Zn, further indicating a complex interaction between Zn, Ca, and P in the blood.

Phytate has been shown to be an antinutrient, and the feeding of high levels of phytase can break down phytate to improve nutrient utilization and pig performance. Dietary xylanase targets arabinoxylan breakdown, thereby improving energy utilization in pigs. However, the effects of simultaneous supplementation have not been clearly determined. Crossbred pigs ( = 45; mean initial weight, 26.4 ± 0.2 kg) were allotted to 1 of 9 treatments to evaluate the effects of both xylanase (endo-1,4-β xylanase [EC 3.2.1.8]) and phytase (6-phytase [EC 3.1.3.26]) supplementation as follows: 1) positive control (PC), a corn-soybean meal-based diet with 15% corn distillers dried grains with solubles, 15% wheat middlings, and 13% corn germ meal; 2) negative control (NC), ME was reduced by 103 kcal/kg from the PC diet by replacement of fat with corn starch; 3) NC + phytase (500 phytase units (FTU)/kg diet); 4) NC + phytase (1,000 FTU/kg diet); 5) NC + phytase (2,000 FTU/kg diet); 6) NC + xylanase (24,000 xylanase units [BXU]/kg diet); 7) NC + phytase (500 FTU/kg diet) + xylanase (24,000 BXU/kg diet); 8) NC + phytase (1,000 FTU/kg diet) + xylanase (24,000 BXU/kg diet); and 9) NC + phytase (2,000 FTU/kg diet) + xylanase (24,000 BXU/kg diet). All diets were formulated to meet nutrient requirements before phytase and xylanase addition to the diets. There were no significant interactions between xylanase and phytase supplementation on growth performance, carcass characteristics, and apparent total tract digestibility (ATTD). The ADG ( < 0.01, quadratic) and G:F ( < 0.05, linear) for the overall period increased as phytase level increased. The ATTD of P increased as phytase supplementation level increased ( < 0.05, linear and quadratic). The ATTD of DM, NDF, ether extract ( < 0.05), and hemicellulose ( = 0.05) increased quadratically as phytase level increased. Estimated carcass lean percentage and lean gain increased ( < 0.05, linear) as phytase level increased. Xylanase supplementation had no effect on growth performance, ATTD, and carcass characteristics. The results demonstrated an improved nutrient digestibility, performance, and carcass response to phytase supplementation beyond P provision because all diets exceeded current P requirement estimates based on standardized total tract digestible P.