Materials and Methods
Animals. 355 steers born on 4 years and weaned in
early autumm, belonging to a dialell crossbreeding experiment
involving Angus and Hereford breeds, and Limousin as terminal breed.
All possible genetic groups were generated. Number of sires within
breeds varied from 4 to 18.
Management. Fattening started on april every year.
Steers grazed cultivated pastures under two feeding regimes: R1= pasture grazing + autumn-winter supplementation with maize silage; R2= pasture grazing only. Steers were fattened until 6-8 mm ultrasound
back fat thickness was achieved, and then were slaughtered in a
commercial abbatoir.
Data collection. The following measurements were
performed: Ultrasound (Pie Medical 200 machine, 3.5 MHz) back-fat
thickness (UFT) and m.longissimus dorsi area (ULDA) over the 12th-13th
rib interval; slaughter weight (SW); hot carcass weight (HCW) and
dressing percentage (DP=HCW/SW*100); kidney fat weight (KFW) and
percentage (KFP=KFW/(HCW+KFW)*100).
The 12th-13th rib steak from the left half
carcass was removed after 24h cooling at 0-50C and was stored at
-180C. At the laboratory, actual fat thickness (AFT) and actual
m.longissimus dorsi area (ALDA) were determined on each steak, as well
as the cooking water loss proportion (WL), ultimate pH (pH), colour
readings in the L*a*b* colour space, Warner-Bratzler shear force (WB)
and the longissimus muscle ether extract percentage (EE).
Data analyses. Mixed models (PROC MIXED, SAS)
were used to estimate direct and maternal additive genetic and
individual heterosis effects. Fixed effects included breed Group (G),
birth Year (Y), feeding Regime (R) and YxR interaction. Sire within
breed or cross was included as a random effect. Age at slaughter (a)
was included as covariate. Contrasts to estimate genetic effects were
used according to Malik (1984). |