scholarly journals 44. A higher dose of phytase with application of a full matrix has the potential to reduce feed costs and maintain performance in grower-finisher pigs

2021 ◽  
Vol 12 (2) ◽  
pp. 206
Author(s):  
A. Wilkinson ◽  
D.J. Henman ◽  
C.J. Brewster ◽  
T. McDonald ◽  
J.C. Kim
Keyword(s):  
Full Matrix ◽  
Feed Costs

scholarly journals Divergent ⇒ complex amplitudes in two dimensional string theory

2021 ◽  
Vol 2021 (2) ◽  
Author(s):  
Ashoke Sen
Keyword(s):  
Scattering Amplitudes ◽  
String Theory ◽  
Matrix Model ◽  
Two Dimensional ◽  
Full Matrix ◽  
Instanton Contribution ◽  
The Matrix ◽  
Theory Result ◽  
The One ◽  
Remarkable Agreement

Abstract In a recent paper, Balthazar, Rodriguez and Yin found remarkable agreement between the one instanton contribution to the scattering amplitudes of two dimensional string theory and those in the matrix model to the first subleading order. The comparison was carried out numerically by analytically continuing the external energies to imaginary values, since for real energies the string theory result diverges. We use insights from string field theory to give finite expressions for the string theory amplitudes for real energies. We also show analytically that the imaginary parts of the string theory amplitudes computed this way reproduce the full matrix model results for general scattering amplitudes involving multiple closed strings.

Effects of extending the grazing season in beef production systems

2001 ◽  
Vol 2001 ◽  
pp. 116-116 ◽  
Author(s):  
B.J. O’Neill ◽  
M.J. Drennan ◽  
P.J. Caffrey
Keyword(s):  
Production Systems ◽  
Rural Environment ◽  
Environment Protection ◽  
Beef Production ◽  
Grazing Season ◽  
Protection Scheme ◽  
Grass Silage ◽  
Feed Costs ◽  
The Cost ◽  
Eu Support

The cost of grazed grass is less than half that of grass silage (O’Kiely, 1994) and incomes from beef production are low and largely dependent on EU support schemes. Thus the income from beef production could be incresed by reducing feed costs through increasing the proportion of grazed grass in the diet and optimising the use of the various support schemes. The objective of this two-year study was to examine the effects on the performance of yearling cattle of turnout to pasture three weeks earlier than normal. This was examined within two suckler beef production systems. One was a standard system similar to that outlined by Drennan (1993) and the second was compatible with the Rural Environment Protection Scheme (REPS).

Studies in aryltin chemistry. Part 6. Crystal and molecular structures of tetra(p-methylsulphonylphenyl)tin(IV) and tetra(p-methylsulphinylphenyl)tin(IV) monohydrate

1990 ◽  
Vol 68 (8) ◽  
pp. 1277-1282 ◽  
Author(s):  
Ivor Wharf ◽  
Michel G. Simard ◽  
Henry Lamparski
Keyword(s):  
Least Squares ◽  
Crystal Structures ◽  
Direct Method ◽  
Molecular Structures ◽  
Water Molecules ◽  
Monoclinic Space Group ◽  
Molecular Symmetry ◽  
Asymmetric Unit ◽  
Full Matrix ◽  
Space Group

Tetrakis(p-methylsulphonylphenyl)tin(IV) and tetrakis(p-methylsulphinylphenyl)tin(IV) n-hydrate have been prepared and their spectra (ir 1350–400 cm−1; nmr, 1H, 13C, 119Sn) and X-ray crystal structures are reported. The first compound is monoclinic, space group C2/c, Z = 4, with a = 21.589(6), b = 6.207(3), c = 22.861(11) Å, β = 93.80(3)° (22 °C); the structure was solved by the direct method and refined by full-matrix least squares calculations to R = 0.043 for 2755 observed reflections. It has 2 molecular symmetry with the methyl group and one oxygen atom completely disordered in both CH3S(O2) groups in the asymmetric unit. The second compound is tetragonal, space group P42/n, Z = 2, with a = b = 15.408(6), c = 6.379(2) Å (−100 °C); the structure was solved by the Patterson method and refined by full-matrix least squares calculations to R = 0.060 for 1209 observed reflections. It has [Formula: see text] molecular symmetry with the whole asymmetric unit disordered. Water molecules occupy positions on parallel 42 axes but molecular packing requirements prevent all sites having 100% occupancy giving n ~ 1 for the hydrate. Keywords: Tetra-aryltins, crystal structures, sulphone, sulphoxide, hydrogen-bonding.

PERFORMANCE OF DWARF BROILER BREEDERS IN LAYING CAGES AND FLOOR PENS AND OF NORMAL BREEDERS IN FLOOR PENS

1975 ◽  
Vol 55 (4) ◽  
pp. 741-747 ◽  
Author(s):  
J. H. STRAIN ◽  
A. P. PILOSKI
Keyword(s):  
Body Weight ◽  
Egg Production ◽  
General Pattern ◽  
Female Offspring ◽  
Male Offspring ◽  
Production Cycle ◽  
Feed Conversion ◽  
Broiler Breeders ◽  
Feed Costs

Dwarf broiler breeders in single-bird cages (DC), in floor pens (DF) and normal broiler breeders in floor pens (NF) were compared for their own and their offspring’s performance. No differences were observed in rate of egg production at 147–329 days of age between the NF and DF birds (48 vs. 47%) whereas the DC birds laid at the rate of 40%. Hen-housed egg numbers for the same period followed the same general pattern (NF, 81; DF, 82; DC, 70 eggs/bird). DF and DC birds consumed less feed per dozen eggs than the NF birds (3.4 vs. 4.3 kg/doz). Egg weights in the early part of the production cycle were not significantly different among the groups but at 294 days of age the normal birds laid larger eggs than the dwarfs (65 vs. 62 g). Dwarfs in cages reached 50% production earlier than the DF or NF birds. Female offspring from the three groups grew at the same rate and weighed 1.7 kg at 56 days of age but there were significant differences in feed conversion (NF, 2.46; DF, 2.43; DC, 2.53 kg/kg body weight produced). Male offspring had small but not statistically significant differences in body weight at 56 days (NF, 2.16; DF, 2.12; DC, 2.09 kg) or feed conversion (NF, 2.30; DF, 2.29; DC, 2.34 kg/kg body weight). Mortality in the offspring ranged from 2.7 to 9.2% but did not differ significantly. Income over feed costs per broiler started did not differ from the three groups regardless of the meat price – feed price combination considered. However, when profit was computed on a breeder hen basis, the DF females were more profitable than either the NF or DC females.

The crystal structure of arsenic telluroxide AsTe0.5O2

1993 ◽  
Vol 205 (1) ◽  
Author(s):  
A. C. Stergiou
Keyword(s):  
Crystal Structure ◽  
Least Squares ◽  
Single Crystals ◽  
Direct Methods ◽  
Anomalous Dispersion ◽  
Thermal Parameters ◽  
Trigonal Prism ◽  
Population Parameter ◽  
Full Matrix

AbstractSingle crystals of AsTeSolution of the structure was essentialy effected by direct methods combined with successive Fourier syntheses. The positional and anisotropic thermal parameters were refined by full-matrix least-squares calculations. Absorption and anomalous dispersion corrections were applied to all atoms. The finalThe As atom is coordinated by six O atoms forming a right trigonal prism. The Te atom site is partially occupied by Te atoms with a population parameter 0.5 and surrounded by six O atoms also forming a right trigonal prism. The structure looks like that of NiAs. Each of the AsO

Refinement of the crystal structure of metatorbernite

1993 ◽  
Vol 205 (1) ◽  
pp. 1-7 ◽  
Author(s):  
A. C. Stergiou ◽  
P. J. Rentzeperis ◽  
S. Sklavounos
Keyword(s):  
Crystal Structure ◽  
Least Squares ◽  
Anomalous Dispersion ◽  
Thermal Parameters ◽  
Water Molecules ◽  
Full Matrix ◽  
Absorption Correction ◽  
Atom Position ◽  
Oxygen Atoms

AbstractThe crystal structure of metatorbernite with composition CuThe positional and thermal parameters were refined by full-matrix least-squares calculations. Absorption correction and correction for anomalous dispersion, for all atoms, were applied. The finalThe structure is essentially similar to that described by M. Ross, H. Evans and D. Appleman (1964) for metatorbernite, with a difference in the Cu atom position, which here is 1/4 1/4 0.31 instead of 1/4 1/4 0.80. The U atoms are six-coordinated by two O atoms (uranyl group) and four phosphate – oxygen atoms forming an asymmetrical tetragonal dipyramid. The Cu atoms are six-coordinated by two oxygen atoms of two different uranyl groups and four water molecules forming also an asymmetrical tetragonal dipyramid. The four water molecules form squares Cu(H

Structural Systematics of Rare Earth Complexes. VII. Crystal Structure of Bis(2,2'/6',2␛-Terpyridinium) Octaaquaterbium(III) Heptachloride Hydrate

1994 ◽  
Vol 47 (2) ◽  
pp. 391 ◽  
Author(s):  
CJ Kepert ◽  
BW Skeleton ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Rare Earth ◽  
Single Crystal ◽  
Structural Characterization ◽  
Title Compound ◽  
Room Temperature ◽  
Chloride Ions ◽  
Full Matrix ◽  
X Ray

The room-temperature single-crystal X-ray structural characterization of the title compound (tpyH2)2[Tb(OH2)8]Cl7.~2⅓H2O is recorded. Crystals are triclinic, Pī , a 17.063(5), b 16.243(3), c 7.878(3) Ǻ, α 84.78(2), β 84.39(3), γ 87.81(2)°, Z = 2 formula units; 3167 'observed' diffractometer reflections were refined by full-matrix least-squares procedures to a residual of 0.057. Notable features of interest of the compound are the 'chelation' of chloride ions by the terpyridinium cations , and the existence of a free [Tb(OH2)8]2+ cation in the presence of an abundance of chloride ions.

Crystal and molecular structure of B,B-bis(p-tolyl)boroxazolidine and the orthorhombic form of B,B-diphenylboroxazolidine

1976 ◽  
Vol 54 (20) ◽  
pp. 3130-3141 ◽  
Author(s):  
Steven J. Rettig ◽  
James Trotter
Keyword(s):  
Molecular Structure ◽  
Statistical Analysis ◽  
Hydrogen Bonds ◽  
Crystal And Molecular Structure ◽  
Direct Methods ◽  
Length Variation ◽  
Full Matrix ◽  
Space Group ◽  
Phenyl Rings ◽  
Related Compounds

Crystals of B,B-bis(p-tolyl)boroxazolidine, 1c, are trigonal, a = 25.1028(9), c = 12.4184(7) Å, Z = 18, space group [Formula: see text]. And crystals of B,B-diphenylboroxazolidine, 1a, are orthorhombic, a = 17.6420(4), b = 14.2527(3), c = 10.205(1) Å, Z = 8, space group Pbca. Both structures were solved by direct methods and were refined by full-matrix least-squares procedures to final R values of 0.057 and 0.040 for 2230 and 1828 reflections with I ≥ 3σ(I) respectively. Both molecules have structures similar to related compounds and feature intermolecular N—H … O hydrogen bonds (N … O = 2.982(2) for 1c and 2.896(2) Å for 1a). Bond lengths are: for 1c; O—C, 1.413(3), O—B, 1.478(3), N—C, 1.488(3), N—B, 1.657(3), C(sp3)—C(sp3), 1.501(4), B—C, 1.616(3) and 1.623(3), mean C—C(ar), 1.395, N—H, 0.93(2) and 0.94(2), mean C(sp3)—H, 1.00, and mean C(ar)—H, 1.00 Å; for 1a; O—C, 1.409(2), O—B, 1.476(2), N—C, 1.489(2), N—B, 1.655(2), C(sp3)—C(sp3), 1.507(3), B—C, 1.613(2) and 1.620(2), mean C—C(ar), 1.391, N—H, 0.93(2) and 0.92(2), mean C(sp3)—H, 1.00, and mean C(ar)—H, 0.98 Å. A statistical analysis of the phenyl C—C distances in compounds 1a, 1b, and 1c has provided an example of statistically significant substituent-induced bond length variation in the phenyl rings.

Effects of protected vegetable fats on rumen metabolism and productivity dairy cows

2021 ◽  
Vol 1 (9) ◽  
pp. 68-74
Author(s):  
A. V. Golovin ◽  
Keyword(s):  
Dairy Cows ◽  
Milk Yield ◽  
Milk Fat ◽  
Dry Matter ◽  
Volatile Fatty Acids ◽  
Metabolic Energy ◽  
Black And White ◽  
Rumen Metabolism ◽  
Economic Experiment ◽  
Feed Costs

In a scientific economic experiment conducted in the experimental farm «Klenovo-Chegodaevo» (Moscow) on three groups of Holsteinized black-and-white cows with a milk yield of 7000 kg of milk per lactation, 10 heads in each, it was found that the inclusion in the diet of cows of the experimental groups tested protected fats (hydrogenated and fractionated) in the amount of 300 g per head per day, contributed to the tendency for more intensive metabolic processes in the rumen due to a slight increase in the concentration of volatile fatty acids by 5,6–7,4% and an increase in the mass of microorganisms in the contents of the rumen by 5,4–14,4% (P≥0,05). At the same time, an increase in the concentration of metabolic energy in the dry matter of the cows ration from 10,7 to 11,0 MJ / kg in the period from 21 to 120 days of lactation, due to the inclusion of protected fats in the diet of cows from the experimental groups, contributed to an increase in milk yield 4% fat content for 100 days of the experiment by 9,7% and 11,0% (P≤0,05), compared with the control, as well as the production of milk fat and protein, respectively by 9,6–11,0% (P≤0,05 in the second case) and 7,4–8,3%, feed costs expressed in ME decreased by 4,9–5,2%.

195 Does Feeding a Protease and Probiotic (Bacillus Subtilis) Combination (Syncra® SWI) Result in Improved Growth Performance and Mortality in a Commercial Wean-to-finish Swine Feeding Program?

2021 ◽  
Vol 99 (Supplement_1) ◽  
pp. 77-78
Author(s):  
Trey A Kellner ◽  
Josh Ellingson ◽  
Ana L P de Souza ◽  
Janet C Remus
Keyword(s):  
Growth Performance ◽  
Experimental Period ◽  
Feed Additives ◽  
Control Treatment ◽  
Experimental Unit ◽  
Gut Health ◽  
Wide Range ◽  
Feeding Program ◽  
Feed Costs ◽  
Combined Feed

Abstract The response to probiotics and enzymes is often documented in research facilities with a high degree of control and via pigs with no insults to health or feed intake. However, in commercial conditions, the response to feed additives promoting advanced gut health and improved digestion must be consistent and defined over a wide range of health statuses, stocking densities, feed intakes, environments, and diet formulations. The objective of this experiment was to determine if a combined feed protease and probiotic system (Syncra® SWI 201, DuPont, Wilmington, DE) would improve growth performance and mortality under commercial conditions. A total of 127,092 pigs (6.0 ± 0.1 kg; PIC 337 sired, Hendersonville, TN) from a sow farm producing porcine reproductive and respiratory virus and rotavirus positive weaned pigs were placed in 53 2,400-head commercial wean-to-finish barns that were alternated to 1 of 2 treatments (a control treatment without Syncra® SWI (SSWI) or with SSWI included at 72.6 g/ton of finished feed from 22.7 kg of BW to harvest) in a rolling allotment over a 12-month period. Pigs were on the experiment for an average of 162 ± 1.0 days (until harvest). Throughout the 12-month experimental period, diets (outside of the SSWI inclusion) could change in order to maximize return over feed costs. Data were analyzed using Proc MIXED (SAS 9.4; Cary, NC) with treatment as the main effect and barn as the experimental unit. Compared to the control, adding SSWI improved mortality by 1.9% and percent grade 1 marketed pigs by 2.2% (P ≤ 0.025). Compared to the control, SSWI did not improve ADG (control = 0.75 vs. SSWI = 0.78 kg) or gain:feed (control = 0.401 vs. SSWI = 0.396). In conclusion, the inclusion of the SSWI combined feed protease and probiotic system can improve mortality and grade 1 marketed pigs, but not growth performance under commercial conditions.

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