We discuss issues raised by Serebrov, et al. in a recent paper regarding systematic effects in the beam neutron lifetime experiment performed at NIST. We show that these effects were considered in ...the original analyses and that our corrections and systematic uncertainties were appropriate. We point out some misconceptions and erroneous assumptions in the analysis of Serebrov, et al. None of the issues raised in Serebrov, et al lead us to alter the value of the neutron lifetime reported previously.
Abstract
Rumen fluid from three beef steers (480 ± 10 kg), fitted with rumen canulae, were used to investigate the impact of Ca dose and olive meal on in vitro rumen fermentation characteristics. ...Steers were fed a high concentrate finishing diet for 21d, and rumen fluid was collected from each steer 2h post-feeding. A 2 x 4 factorial arrangement of treatments was used for this experiment. Factors included: 1) 0 or 5% olive meal and 2) Ca dose: 0, 0.02, 0.04, and 0.08% Ca from CaCl2. A McDougall’s buffer-rumen fluid mixture (1:1; 30 mL) was added to conical tubes containing 0.5g of the ground basal diet and incubated at 39°C for 0, 4, 8, and 12h (5 replicates per treatment per time point). After incubation, supernatant was removed for VFA analysis and the remaining digesta was dried to determine DM disappearance (DMD). At 4 and 8h post incubation digestion tubes containing 0.04% Ca had greater (P < 0.001) DMD when compared to all other Ca doses. At 12h post incubation, DMD was greater (P < 0.001) in digestion tubes containing 0.02% and 0.08% Ca compared to all other Ca doses. At 8h post incubation, molar proportions of acetic acid were greater (P < 0.03) in digestion tubes containing olive meal compared to no olive meal and were greater (P < 0.001) in digestion tubes containing 0.08% Ca compared to all other Ca doses. At 12h post incubation, isobutyric acid (P < 0.01) and butyric acid (P < 0.02) were greater in digestion tubes containing 0.02% and 0.04% Ca compared to all other Ca doses. Butyric acid was lesser (P < 0.02) with olive meal inclusion at 12h. Total VFA concentrations were similar across treatments. These data suggest that Ca and olive meal can impact in vitro fermentation characteristics.
Abstract
Eighty-three American Wagyu steers (725 ±10.7 kg) were used to evaluate the effects of olive byproduct supplementation on feedlot performance and carcass characteristics. We hypothesized ...that with supplementation of olive byproduct would improve feedlot performance and longissimus muscle intramuscular fat composition. Steers were blocked by initial body weight (BW) and randomly assigned within block to one of two treatments. Treatments consisted of: 1) Control diet (basal ration with no olive byproduct) + 1 kg of supplemental cracked corn per animal per day, or 2) Control diet + 1 kg of supplemental olive byproduct per animal per day. Steers were housed in feedlot pens (n=4 steers/pen; 11 replicates/treatment) and fed a traditional American Wagyu finishing diet (DM basis: 68.4% DM, 14.3% CP; 74.8% TDN, 1.16 Mcal/kg NEg, 5.3% crude fat). Diets were delivered to pens, once daily, in the morning in amounts to allow ad libitum access to feed over a 24 h period. Olive byproduct and cracked corn were top-dressed to the appropriate treatment pens immediately after delivery of the basal ration. Steers were individually weighed on d -1 and 0, and approximately every 28 d throughout the 177 d experiment. Equal numbers of steers per treatment were slaughtered throughout the experiment and carcass data were collected. Data were analyzed using a mixed effects model of SAS (SAS Inst. Inc.) for a randomized complete block design. Steers receiving olive byproduct had a lower final BW (P < 0.01) when compared to steers receiving the control diet. Longissimus muscle long chain fatty acids C18:1 and C:22:0 were greater (P < 0.05) and C18:0 lesser (P < 0.05) in controls when compared to steers supplemented with olive byproduct. Under the conditions of this experiment, feeding olive byproduct reduced final BW and had minimal impacts on longissimus muscle fatty acid composition.
