Compensatory growth in crossbred Aberdeen Angus and Belgian Blue steers: Effects on the colour, shear force and sensory characteristics of longissimus muscle.

The effect of feed restriction (99days) followed by compensatory growth during a 200day re-alimentation period on the colour and sensory characteristics of meat from Aberdeen Angus×Holstein-Friesian (AN) and Belgian Blue×Holstein-Friesian (BB) steers was examined. Compensatory growth had no effect on muscle pH and temperature decline, chemical composition, drip loss, fat colour, or juiciness, but increased (P=0.009) Warner-Bratzler shear force and decreased tenderness (P=0.08) and overall liking (P=0.09). Compared to meat from BB steers, meat from AN steers had a higher intramuscular fat concentration and was rated similarly for tenderness, but higher for many of the flavour characteristics examined. While adjustment for intramuscular fat concentration removed some of these differences, genotype-specific flavour differences remained. It is concluded that genotype had greater effects on meat quality than the compensatory growth feeding regime imposed in this study.

Effects of genetic merit for carcass weight, breed type and slaughter weight on performance and carcass traits of beef × dairy steers.

Crossbreeding of Holstein-Friesian dairy cows with both early maturing (e.g. Aberdeen Angus (AA)) and late maturing (e.g. Belgian Blue (BB)) beef breeds is commonly practised. In Ireland, genetic merit for growth rate of beef sires is expressed as expected progeny difference for carcass weight (EPD(CWT)). The objective of this study was to compare the progeny of Holstein-Friesian cows, sired by AA and BB bulls of low (L) and high (H) EPD(CWT) for performance and carcass traits. A total of 118 spring-born male progeny from 20 (9 AA and 11 BB) sires (8 L and 12 H) were managed together from shortly after birth to about 19 months of age. They were then assigned to one of two mean slaughter weights (560 kg (light) or 620 kg (heavy)). Following slaughter, carcasses were graded for conformation class and fat class, the 6th to 10th ribs joint was dissected as an indicator of carcass composition, and samples of subcutaneous fat and musculus longissimus were subjected to Hunterlab colour measurements. A sample of m. longissimus was also chemically analysed. Slaughter and carcass weights per day of age for AAL, AAH, BBL and BBH were 747, 789, 790 and 805 (s.e. 10.5) g, and 385, 411, 427 and 443 (s.e. 4.4) g, respectively. Corresponding carcass weight, kill-out proportion, carcass conformation class (scale 1 to 5) and carcass fat class (scale 1 to 5) values were 289, 312, 320 and 333 (s.e. 4.0) kg, 516, 522, 542 and 553 (s.e. 3.5) g/kg, 2.5, 2.4, 3.0 and 3.1 (s.e. 0.10), and 3.4, 3.5, 2.9 and 2.8 (s.e. 0.11). There were few breed type × genetic merit interactions. Delaying slaughter date increased slaughter weight, carcass weight and all measures of fatness. It also reduced the proportion of carcass weight in the hind quarter and the proportions of bone and muscle in the ribs joint. None of these effects accompanied the increase in carcass weight due to higher EPD(CWT). It is concluded that BB have superior production traits to AA. Selection of sires for higher EPD(CWT) increases growth rate, kill-out proportion and carcass weight of progeny with little effect on carcass or muscle traits. The extra carcass weight due to higher EPD(CWT) is more valuable commercially than a comparable carcass weight increment from a delay in slaughter date because it comprises a higher proportion of muscle.

Colour of bovine subcutaneous adipose tissue: A review of contributory factors, associations with carcass and meat quality and its potential utility in authentication of dietary history.

The colour of bovine subcutaneous (sc) adipose tissue (carcass fat) depends on the age, gender and breed of cattle. Diet is the most important extrinsic factor but its influence depends on the duration of feeding. Cattle produced under extensive grass-based production systems generally have carcass fat which is more yellow than their intensively-reared, concentrate-fed counterparts and this is caused by carotenoids from green forage. Although yellow carcass fat is negatively regarded in many countries, evidence suggests it may be associated with a healthier fatty acid profile and antioxidant content in beef, synonymous with grass feeding. Nonetheless, management strategies to reduce fat colour of grass-fed cattle are sought after. Current research suggests that yellow colour of this tissue is reduced if pasture-fed cattle are converted to a grain-based diet, which results in accretion of adipose tissue and dilution of carotenoids. Colour changes may depend on the initial yellow colour, the carotene and utilisable energy in the finishing diet, the duration of finishing, the amount of fat accumulated during finishing and the rate of utilisation of carotene from body fat. Differences in nutritional strategies which cause differences in fatty acid composition may be reflected by differences in fat colour and carotenoid concentration. Fat colour and carotenoids are prominent among a panoply of measurements which can aid the authentication of the dietary history and thus to some extent, the origin of beef, although this potential utility is complicated by the simultaneous rather than discrete use of forages and concentrates in real production systems.

Effect of concentrate feeding pattern in a grass silage/concentrate beef finishing system on performance, selected carcass and meat quality characteristics.

Steers were offered grass silage ad libitum and 6.4 kg concentrates daily for 126 days or silage ad libitum for 35 days, followed by concentrates ad libitum (Experiment 1). Steers were offered grass silage ad libitum and 6 kg concentrates daily for 154 days, concentrates ad libitum or grass silage ad libitum for 112 days followed by concentrates ad libitum (Experiment 2). All treatments received the same total concentrate allowance. In Experiment 1, there was no difference in any measurement of meat quality. In Experiment 2, ad libitum concentrate feeding per se, decreased redness and increased shear force of muscle at 2 days post-mortem. Delaying concentrate feeding decreased fat yellowness, decreased shear force at 7 and 14 days post-mortem and increased muscle redness at 14 days post-mortem. Modifications of the beef production system examined had minor effects on beef quality which are unlikely to be of commercial significance.

Colour, composition and quality of M. longissimus dorsi and M. extensor carpi radialis of steers housed on straw or concrete slats or accommodated outdoors on wood-chips.

Forty-five Charolais crossbred steers were offered a common diet and accommodated either outside on wood-chips (OWP, 18m(2)/head) or in a naturally-ventilated building in slatted-floor pens (SLA, 2.5m(2)/500kg bodyweight) or in straw-bedded pens (STR, 4m(2)/head) for 132 days. Carcass weight averaged 351, 362, and 372 (sed 6.63)kg (P<0.05), for SLA, STR and OWP, respectively. Accommodation system did not affect the colour, drip loss, shear force or composition of Musculus longissimus dorsi (LD) or Musculus extensor carpi radialis (ECR) muscles or the sensory characteristics of LD. The ultimate pH of ECR was highest (P<0.05) for OWP steers, while their LD was darker at 2 days post-mortem than LD from STR steers. It is concluded that accommodating cattle on OWP had a minor transient effect on beef colour and no impact on beef composition or eating quality.

Changes in colour characteristics and pigmentation of subcutaneous adipose tissue and M. longissimus dorsi of heifers fed grass, grass silage or concentrate-based diets.

The objective of this experiment was to determine the effect of dietary composition and duration of feeding on subcutaneous (s.c.) adipose tissue and M. longissimus dorsi (LD) colour and pigment concentrations of heifers. Fifteen heifers were permanently housed and fed a concentrate diet (PH-CON). Fifty-four heifers were grazed on pasture (PAS) for 90d, housed and offered concentrates (PAS-CON), 200g grass silage (GS)/kg dry matter (DM) (PAS-GS20), 500g GS/kgDM (PAS-GS50) or zero-grazed grass (PAS-GRA). To facilitate assessment of the temporal pattern of tissue colour, 3 heifers/treatment were slaughtered at housing (following 7d adjustment to diets) and 28, 56, 91 and 120 days thereafter. Yellowness ('b' value) of s.c. adipose tissue and lightness ('L' value) and redness ('a' value) of LD were recorded 48h post-mortem. ß-Carotene and lutein contents of s.c. adipose tissue and total LD haem pigments were determined. At housing, s.c. adipose tissue 'b' values of the PAS group (mean=13.47) were higher (P<0.01) than those of the PH-CON group (mean=10.35) but there was no difference in ß-carotene or lutein concentrations. The change in s.c. adipose tissue 'b' for each diet following housing was best described by the following equations: PH-CON: y=-0.087 (SE 0.0347) X+0.0005 (SE 0.00029) X(2)+10.06 (SE 0.600), MSE 1.94, R(2) 0.57, P<0.01. PAS-CON: y=-0.102 (SE 0.0286) X+0.0006 (SE 0.00024) X(2)+13.32 (SE 0.598), MSE 2.30, R(2) 0.62, P<0.001. PAS-GS20: y=-0.106 (SE 0.0296) X+0.0008 (SE 0.00025) X(2)+13.10 (SE 0.618), MSE 2.46, R(2) 0.47, P<0.01. PAS-GS50: y=-0.077 (SE 0.0269) X+0.0006 (SE 0.00023) X(2)+13.29 (SE 0.552) MSE 1.95, R(2) 0.38, P<0.05. PAS-GRA: y=-0.018 (SE 0.0079) X+13.77 (SE 0.528), MSE 2.28, R(2) 0.24, P<0.05, where y='b' value, x=days post-housing (d96-d216) and MSE=mean square error. Treatment had a significant effect on s.c. adipose tissue ß-carotene and lutein (both P<0.001) with PAS-GRA and PH-CON tending to have the highest and lowest concentrations, respectively. PH-CON heifers tended (P=0.058) to have lower LD haem pigments and lighter LD than other heifers. It is concluded that, while concentrate feeding led to the greatest decrease in s.c. adipose tissue yellowness relative to PAS-GRA, choice of dietary ingredients and duration of feeding will depend on the stringency of the colour criteria in particular markets.

Colour stability, under simulated retail display conditions, of M. longissimus dorsi and M. semimembranosus from steers given long-term daily exercise and supplemented with vitamin E.

The objective was to determine if exercise has a negative impact on the colour stability of beef and if dietary vitamin E (VE) supplementation could counteract any negative effect. Steers were not exercised or were walked 4.41km/day for 18 weeks. Within exercise treatment animals consumed, on average, either 450 or 1050IU/day of VE. Muscle α-tocopherol increased (P=0.004) from 2.35 to 3.15µg/g with VE supplementation. Following ageing M. longissimus dorsi (LD) and M. semimembranosus (SM) steaks were packaged under 80%O(2):20%CO(2) and stored at 4°C. The LD of exercised steers was more red and more saturated (both P<0.05) after 0 and 2 days of storage than LD of unexercised steers. While redness of both muscles decreased over the display period, LD retained a higher redness than SM from day 2 to 7 (P<0.05). Colour shelf-life of LD was extended by 0.75 days, to 3.25 days, due to VE supplementation.

Colour of muscle from 18-month-old steers given long-term daily exercise.

Darker beef from pasture-fed compared with grain-fed cattle may result from differences in physical activity rather than differences in nutrition. The objective was to determine if steers that were exercised produced darker meat than non-exercised steers and whether any effect was muscle-related. Exercised steers were walked 4.41 km daily in a single bout, six days per week for 18 weeks at an average speed of 5.2 kmh(-1). All steers were fed grass silage on an ad libitum basis plus 6 kg concentrates. Following slaughter, muscle colour coordinates ('L' (lightness), 'a' (redness) and 'b' (yellowness) values) of M. longissimus dorsi (LD), M. semimembranosus (SM) and M. extensor carpi radialis (ECR) were recorded at 48 h postmortem and redness and yellowness were used to calculate muscle hue ('H') and colour intensity/saturation ('C'). The pH of all muscles was measured at 1.5, 3, 6, 22 and 48 h postmortem and LD samples were recovered (90 min postmortem) for glycolytic potential (GP) assessment. Exercise did not affect muscle lightness, yellowness, hue or colour intensity. However, LD was the darkest (P<0.001) and SM the most saturated (P<0.001) muscle. Exercise affected muscle redness in a muscle-dependent manner (muscle×exercise, P=0.038) whereby ECR became more red with exercise but LD and SM were unaffected. There were muscle×time (P<0.001) and time×exercise (P=0.045) interactions for muscle pH. The ECR muscle had the highest pH at all times. The exercised steers had higher (P<0.05) LD muscle pH than control steers at 3 and 6 h postmortem. Exercise did not affect myoglobin concentration, which was muscle dependent, decreasing in the order: SM (6.72 mg/g)>ECR (6.33 mg/g)>LD (5.48 mg/g), which were all different (P<0.001). Exercise had no effect on GP in LD muscle (111 vs. 99 µmol/g for control and exercised steers, respectively; SED=6.6 µmol/g). It was concluded that although application of exercise did not affect muscle lightness and thus, did not cause 'darker' meat, it did affect muscle redness in a muscle-dependent manner.

Colour of subcutaneous adipose tissue and M. longissimus dorsi of high index dairy and beef×dairy cattle slaughtered at two liveweights as bulls and steers.

The objectives of this study were (a) to compare muscle and adipose tissue colour of male progeny of two strains of high genetic merit Friesian cows (New Zealand [NZF] and Irish [DAF]) with those of beef (Belgian Blue)×dairy (Holstein-Friesian) [BBHF] male progeny; (b) to compare bulls and steers (gender) of these genotypes and (c) to examine the effects of slaughter weight (SW) on these quality traits. Bulls (n=48) and steers (n=48) of the three genotypes were grown to nominal target liveweights of 550 kg (light) and 630 kg (heavy). Adipose tissue from the NZF genotype was more yellow (P<0.05) than from DAF or BBHF, regardless of gender or SW. For longissimus dorsi (LD) pH, bulls and heavy animals had higher pH (P<0.05) than steers or light animals, respectively, while NZF and BBHF bulls had higher pH than steers. LD muscle from the BBHF genotype had lighter colour (P<0.05) and lower haem pigments (P<0.01) than NZF or DAF progeny. There was no difference in muscle `L' value between light bulls and steers but heavy bulls had darker muscle than heavy steers. There was an interaction between genotype, gender and SW for LD redness. Thus, NZF animals were most red when slaughtered as light or heavy bulls, but there were no differences between genotypes slaughtered as light or heavy steers. These data demonstrate differences in colour of beef, especially from progeny of NZF, which produced the most yellow adipose tissue and the most red muscle tissue.