William P. Weiss

The mineral requirements or recommendations generated by various NASEM committees are used by many ration formulation programs. The current NASEM dairy requirement system uses the factorial approach (requirements for maintenance, lactation, gestation, and growth) for most minerals but when data or equations were not available to estimate factorial requirements the committee used available data to estimate adequate intake values. The current beef NASEM uses the factorial method for Ca and P and recommendations for the other minerals. The factorial method works well for Ca and P because adequate data are available to estimate absorption coefficients (AC) and maintenance requirements. In addition, feeding Ca and P above requirements have few if any positive effects. For many other minerals the factorial method is problematic. Estimating both the maintenance requirement and AC can be extremely difficult and inaccuracies in those values have a major impact on accuracy of total dietary requirements. Some minerals have positive effects on health, production and reproduction when fed above factorially determined requirements. For those minerals response models rather than or in addition to requirement models are more appropriate. The AC is in the denominator of the factorial equation and converts absorbed requirements into dietary requirements. The AC for trace minerals is small, often <0.1, and small changes in a low AC can have substantial effects on dietary requirements. Although accurate AC are essential for the factorial method to work, woefully few data are available on the true absorption of trace minerals. Because of antagonism to absorption (e.g., negative effect of S on absorption of Cu, Mn, Se, and Zn) equations will be needed to estimate AC under different dietary conditions but current data is inaccurate to generate equations. The systems currently used will almost always prevent clinical mineral deficiencies, but because of uncertainties, most nutritionists formulate diets to exceed and often far exceed established recommendations. This leads to increased costs, potential antagonism, and increased manure excretion of environmentally important minerals. More accurate systems for estimating mineral requirements will optimize animal performance and health while keeping costs in check and reduce environmental damage.

Inorganic sources of Mg are commonly used in dairy cow diets, but their availability varies significantly. This study assessed the relative availability of 4 commonly used inorganic Mg sources and a novel alkalinizing proprietary mineral blend [PMB; Multesium (GLC Minerals, LLC, Green Bay, WI, USA)]. The study was a duplicated 6 × 6 Latin square, with 12 nonlactating, non-pregnant Holstein dairy cows assigned to a square based on BW and parity. Cows were fed 90% of their voluntary DMI (diet contained 0.21% Mg). Each experimental period lasted 7 d. On d 2 of each period, urinary catheters were fitted. Total urine collection started on d 3 for 48 h with samples collected and measured every 12 h. On d 4, 30 g of Mg were administered as boluses with gelatin capsules: negative control (one empty capsule), magnesium oxide (MgO), magnesium sulfate (MgSO₄), calcium magnesium hydroxide [CaMg(OH)₄], calcium magnesium carbonate [CaMg(CO₃)₂], and PMB [a blend of Ca and Mg sources that includes CaMg(CO₃)₂, CaMg(OH)₄, and MgO]. Blood samples were collected at 0, 1, 2, 3, 12, and 24 h after treatment administration on d 4 of each treatment period. Urine and blood samples were analyzed for Mg and Ca concentration. Statistical analyses were conducted with PROC GLIMMIX including treatment, time, period, square, treatment × time, treatment × period, and time × period as fixed effects, and cow nested within square as a random effect in the model. Urinary Mg excretion for 4 of the Mg sources studied [PMB, MgO, CaMg(OH)₄, and MgSO₄] increased significantly, representing an increase of at least 40.8% relative to control. The supplementation of CaMg(CO₃)₂ did not significantly increase relative to control. There were no significant changes in blood Mg concentration with treatment; but, a significant treatment × time effect was observed. Calcium-rich sources [PMB, CaMg(OH)₄, CaMg(CO₃)₂] had lower blood Mg concentrations at 12 or 24 h after treatment than control and CaMg(CO₃)₂. Based on urinary Mg excretion 24 h after treatment, 4 of the Mg sources evaluated (including PMB) showed a similar availability, however, the availability of the commercial CaMg(CO₃)₂ source included in our study was similar to the negative control (no-supplemented cows).

Lignin is a polyphenolic polymer that is an important factor in limiting fiber digestibility by ruminants. The objective of the current study was to evaluate lignin's effects on whole animal energy utilization in diets similar in NDF content. A low-lignin (LoLig) diet was formulated to contain 32.5% NDF (DM basis) and 9.59% lignin (NDF basis) and the high-lignin (HiLig) diet was formulated to contain 31.0% NDF (DM basis) and 13.3% lignin (NDF basis). These diets were randomly assigned and fed to 12 late-lactation (mean ± SD; 214 ± 14.9 DIM) multiparous Jersey cows (mean ± SD; 435 ± 13.9 kg) in a 2-period crossover design. Cows fed the LoLig treatment consumed more DM than cows on the HiLig diet (mean ± SD; 19.9 vs. 18.7 ± 0.645 kg/d) and the LoLig diet was concurrently of a greater gross energy concentration (mean ± SEM; 4.27 vs. 4.23 ± 0.03 Mcal/kg). As expected, increasing the concentration of lignin resulted in a reduction in total-tract NDF digestibility (45.5% vs. 40.4% ± 0.742%). Increasing lignin also resulted in a reduction in the digestibility of starch (97.7 vs. 96.3 ± 0.420) and CP (65.0 vs. 60.0 ± 0.829). Lignin also decreased the concentration of digestible energy (2.83 vs. 2.63 ± 0.04 Mcal/kg) and ME (2.52 vs. 2.36 ± 0.05 Mcal/kg), but the concentration of NE_L was similar (1.81 vs. 1.75 ± 0.06 Mcal/kg). Increasing the concentration of lignin also reduced yields of ECM (33.7 vs. 30.0 ± 0.838 kg/d), milk protein (1.00 vs. 0.843 ± 0.027 kg/d), and milk fat (1.30 vs. 1.19 ± 0.058 kg/d). Decreasing the dietary lignin concentration did not affect daily methane emissions, averaging 391 ± 29.6 L/d. Results of this study indicate that feeding a diet greater in lignin decreases the digestibility of nutrients and provides less energy for production responses and that energy supplied from digestible NDF may be less than predicted by some nutrition models.

Summary: Dairy ration models predict the gross energy (GE) concentration of the diet using a 4.20 Mcal/kg coefficient for both feed neutral detergent fiber (NDF) and starch. The use of this GE concentration for starch has been validated; however, to our knowledge, the GE concentration of NDF has never been previously analytically determined using bomb calorimetry. The current study reports the GE concentration of feed NDF to be 4.03 ± 0.245 Mcal/kg. The high variation in GE concentration among feed NDF residues is likely a function of variable NDF chemical composition across individual feeds. The GE concentration of fecal NDF has also never been characterized. We hypothesized that the GE concentration of fecal NDF would be greater than the GE concentration of feed NDF because fecal NDF would be enriched in lignin; however, these were similar (averaging 3.94 ± 0.0245 Mcal/kg).

This experiment investigated the effects of feeding low and high supplies of vitamin A (VA) during the transition period on plasma metabolites, prevalence of ketosis, and early milk production. In a randomized complete block design, 42 prefresh Holstein cows and 21 heifers were blocked by parity and calving date and assigned to 1 of 3 dietary treatments (n = 21 per treatment unless noted): CON, a transition diet with supplemental VA (75,000 IU/d) to meet the requirement; LVA, a transition diet with no supplemental VA; or HVA, a transition diet receiving supplemental VA (187,500 IU/d) 2.5 times greater than the requirement. Experimental periods were prepartum (-14 d prepartum), postpartum (1 to 30 d in milk), and carryover period (31 to 58 d in milk; common lactating diet with adequate VA was fed). Differences in dry matter intake in the pre- and postpartum periods and milk yield were not detected among treatment. Milk fat, protein, and lactose yields were similar among treatments and not affected by VA. Somatic cell count increased linearly with increasing VA. Body weight and body condition score decreased postpartum, but no VA effect was observed. Plasma retinol concentrations (n = 10 per treatment) decreased at d 2 postpartum and increased as lactation progressed, but the concentrations were unaffected by treatment. Plasma β-carotene (n = 10 per treatment) had a treatment by time interaction and its concentration decreased after parturition and remained low for 2 wk. Plasma fatty acids and β-hydroxybutyrate did not differ among treatments. Milk retinol concentration and yield (n = 10 per treatment) increased as VA supply increased. Segmented neutrophils (%) decreased, and lymphocytes (%) increased in blood with increasing VA supply. In conclusion, providing different supplies of VA did not affect production, mobilization of body fat, and risk of ketosis; however, excessive VA supply may have negatively affected the immune response, in part contributing to increased milk somatic cell counts during early lactation.

In a randomized complete block design, 40 lactating Holstein cows (average 98 d in milk and 41 kg/d of milk yield) were randomly assigned to 1 of 4 diets: (1) containing soybean meal as the major protein supplement (CON diet); (2) CON diet with high-protein dried corn distillers grains at 20% on a dry matter (DM) basis by replacing mainly soybean meal (DG diet); (3) DG diet except that high-protein dried corn distillers grains with yeast bodies (extracted after corn ethanol production) was used (DGY diet); or (4) DG diet supplemented with sodium bicarbonate and potassium carbonate to elevate the dietary cation and anion difference (DCAD; DG-DCAD diet). The DCAD of CON, DG, DGY, and DG-DCAD were 185, 62, 67, and 187 mEq/kg of DM, respectively. The experiment began with a 10-d covariate period and then cows were fed the experimental diets for 5 wk (2-wk diet adaptation and 3-wk data collection periods). Dry matter intake and milk yield were measured daily, and spot urine and fecal samples were collected in the last week of the experiment to measure nutrient digestibility; N, S, and P utilization and excretion; and in vitro NH₃ and H₂S emissions from manure. All data were analyzed using the MIXED procedure of SAS (random effect: block; fixed effects: diets, repeated week, and interactions). During data collection, DM intake was not different among treatment groups, but milk yield tended to be lower (42.4 vs. 39.9 kg/d) for DG, DGY, and DG-DCAD versus CON, which could have been caused by decreases in organic matter and neutral detergent fiber digestibility. Milk protein yield tended to be lower (1.33 vs. 1.24 kg/d) for DG, DGY, and DG-DCAD versus CON. Milk fat yield was lower (1.26 vs. 1.55 kg/d) for DG and DGY versus CON, but that for DG-DCAD (1.43 kg/d) did not differ from CON. Similarly, energy-corrected milk was lower (38.0 vs. 43.3 kg/d) for cows on DG and DGY versus those on CON, but it did not differ between DG-DCAD (40.7 kg/d) and CON. Urinary and fecal N excretion were greater for DG, DGY, and DG-DCAD compared with CON due to greater dietary crude protein content and N intake. However, NH₃ emissions did not differ across treatments. Intakes of dietary P and S were greater for DG, DGY, and DG-DCAD, resulting in greater excretion of those in manure and greater H₂S emissions from manure compared with CON. These data suggest that the negative effects of feeding distillers grains on production of lactating cows can be partly explained by a decrease in nutrient digestibility (milk yield) and excessive anion load (milk fat). The milk fat response to DG-DCAD suggests that milk fat depression observed with a diet with high content of distillers grains can be partially alleviated by supplementation of cations. In the current study, we observed no beneficial effects of DG containing yeast bodies.

Reducing the dietary cation-anion difference (DCAD) reduces urine pH and, therefore, has potential to lower NH3 emissions from manure. We determined the effects of decreased DCAD on dry matter intake, production, nutrient digestibility, manure characteristics, and NH3 emissions from manure. An in vitro incubation study was conducted to evaluate the degree of reduced urine pH on manure pH and NH3 emissions from manure. In this study, urine pH was directly decreased from 8.5 to 7.5, 6.5, and 5.5 by adding sulfuric acid, which resulted in decreases in manure pH when manure was reconstituted with the fecal-to-urine ratio of 2:1 (as-is basis). The manures from urine at pH 7.5, 6.5, and 5.5 decreased NH3 emissions linearly by 19, 33, and 36%, respectively, compared with the manure from unacidified urine. An animal study was conducted with 27 mid-lactation Holstein cows in a randomized complete block design. Cows were blocked by parity and days in milk and assigned to 1 of 3 different DCAD diets: (1) HDCAD, a diet with DCAD of 193 mEq/kg of dry matter (DM); (2) MDCAD, a diet with 101 mEq/kg of DM; and (3) LDCAD, a diet with 1 mEq/kg of DM. A commercial anionic product (predominantly ammonium chloride) partly replaced urea, soybean meal, soyhulls, and corn grain in MDCAD and LDCAD to lower DCAD. The experiment lasted 7 wk (1-wk covariate followed by 6-wk data collection). Spot urine and fecal samples were collected for manure incubation. Data were analyzed using the MIXED procedure of SAS in a randomized block design. Dry matter intake and milk yield were not altered by treatments. No difference in milk fat content was observed among treatments, but fat yield tended to decrease linearly (1.00 to 0.86 kg/d) as DCAD decreased, resulting in a tendency for decreasing energy-corrected milk yield (35.1 to 32. kg/d). Milk protein content increased (3.00 to 3.14%) as DCAD decreased, but milk protein yield was riot affected. Total-tract digestibility of DM, organic matter, and neutral detergent fiber did not differ among treatments. Digestibility of crude protein tended to decrease as DCAD decreased. There was no difference in fecal and urine N excretion among treatments, but fecal N as proportion of N intake tended to increase as DCAD decreased. Urine pH decreased linearly from 8.42 for HDCAD to 8.11 arid 6.41 for MDCAD arid LDCAD, respectively, resulting in decreased manure pH (7.57, 7.40, and 6.96 for HDCAD, MDCAD, and LDCAD, respectively). The cumulative NH3 emissions from manures over 6 d tended to decrease linearly as DCAD decreased (461 to 390 mg/kg of manure), but the decrease was only nunierical when calculated on a cow basis (i.e., g/cow). In conclusion, lowering DCAD has potential to reduce NH3 emission from manure of lactating cows. However, a tendency for decreased milk fat yield and energy-corrected milk yield suggests that DCAD of 1 mEq/kg of DM may be too low, and more studies are needed to examine relatively less reduced DCAD to determine production responses in addition to NH3 emission from manure.

The objective was to assess the effect of prepartum vaccination timing relative to pen change with an ac-idogenic diet at 28 or 21 d before expected parturition (dpp) on lying time (LT), prepartum serum energy status (glucose, IGF-1, and nonesterified fatty acids), urine pH, and serum Ca at calving in pregnant Holstein dairy cows. Pregnant multiparous Holstein cows (n = 308) from 1 large dairy herd were randomly allocated into 1 of 3 treatment groups at 35 +/- 3 dpp as follows: (1) vaccination at 28 dpp and pen change at 21 dpp (V28PC21; n = 108), (2) vaccination and pen change at 28 dpp (V28PC28; n = 99), and (3) vaccination and pen change at 21 dpp (V21PC21; n = 101). When cows changed pens, an acidogenic diet was introduced. Every other week, a group of 43 to 53 animals were enrolled and electronic data loggers (IceQube, IceRobotics) were fitted to the hind leg of individual cows to as-sess their LT. Blood samples were collected at 28, 26, 21, 19, 14 dpp and at calving. Parity, body condition score, days dry, and gestation length were not different among groups. Overall, V28PC28 cows had 7 additional days in prepartum pens consuming an acidogenic diet compared with V28PC21 or V21PC21 cows. Regard-less of treatment group, cows in the far-off pen had 43 min/d less LT (709 vs. 753 min/d) and increased day-to-day coefficient of variation of LT (0.21 vs. 0.10) compared with cows within the prepartum pen. On average, for the 7 d following vaccination alone (28 to 22 dpp period), V28PC21 cows had-22 min/d less LT compared with V21PC21 cows. Serum concentrations of glucose, nonesterified fatty acids, and IGF-1 were altered following vaccination alone, pen change alone, or vaccination plus pen change with an acidogenic diet before calving. At calving, V28PC21 cows had greater glucose concentrations (6.45 mmol/L) compared with V21PC21 cows (5.76 mmol/L), with V28PC28 cows intermediate (6.11 mmol/L). The assessment of Ca sta-tus at calving revealed that V28PC21 cows had greater Ca concentration (2.34 mmol/L) with lower subclini-cal hypocalcemia (<2.0 mmol/L; 17.3%) compared with V21PC21 cows (2.17 mmol/L and 31.9%), with V28PC28 cows intermediate (2.28 mmol/L and 25.2%). Serum concentrations of IGF-1 at calving were also greater for V28PC21 (3.43 nmol/L) cows compared with V21PC21 (2.69 nmol/L), with V28PC28 cows intermediate (3.07 nmol/L). Overall, V28PC21 cows had greater serum glucose, IGF-1, and-46% reduc-tion in subclinical hypocalcemia (from 31.9 to 17.3%) compared with V21PC21 cows but did not differ from V28PC28 cows (25.2%). These findings provided evi-dence that vaccinating cows at 28 dpp, followed 7 d later by pen change with an acidogenic diet at 21 dpp, would be beneficial.