INTRODUCTION
Carcass grades of finishing steers can be predicted using ultrasound technology before they are slaughtered. In beef cattle industry, real-time ultrasound measurements on live animals may aid owners to save extra labor and feed costs. Average age at slaughter of Hanwoo steers after decision making by ultrasound prediction was decreased by 1.6 months compared to the national average age at slaughter in 2012 (
Ministry of Food, Agriculture, Forestry and Fisheries, and Livestock Research Institute, NACF, 2012).
In Korea, the National Institute of Animal Science (NIAS) and the National Agriculture Cooperative Federation (NACF) adopted ultrasound technology in late 1990s. Several researches have been focused on prediction of carcass characteristics in live Hanwoo cattle (
Kim et al., 2003;
Rhee et al., 2003,
2005). Application of ultrasound technology to genetic improvement of Hanwoo cattle has been tried by scientists as well (
Lee, 2003;
Roh et al., 2010). However, there were some variations in the parameters estimated by scientist depending on the time of ultrasound scanning and population of study.
Kim et al. (2003) estimated correlation between ultrasound and carcass measures at about 0.60 when ultrasound scanning was applied at 17 months of age for BF, LMA, and MS, while those estimates were as high as 0.90 when ultrasound scanning was applied after 22 months of age.
Song et al. (2002) reported that the correlation coefficients between ultrasound and carcass measurements: between UBF and BF, ULMA and LMA, UMS and MS were 0.75, 0.57, and 0.67, respectively.
The objective of this study, therefore, was to evaluate phenotypic and genetic relationships between ultrasound measurements (UBF, ULMA, and UMS) and carcass measurement (CW, BF, LMA, and MS) in a regional Hanwoo steer population when ultrasound scanning procedures were applied three months before the animals were send to slaughter houses.
RESULTS AND DISCUSSION
The measurements of traits from ultrasound and carcass were summarized in
Table 2. The average ages at ultrasound and slaughter were 848.02 and 934.87 days, respectively. Interval between these is approximately 90 days or three months, which support the fact that ultrasound measurement was taken three months prior to slaughter. However, the intervals between these two activities were about 30 days at minimum and about 170 days at maximum. That is ultrasound measures were taken one to almost five and a half months prior to slaughter. The averages of UBF, ULMA and UMS were 10.73 mm, 88.50 cm
2 and 4.36. And the averages of CW, BF, LMA, and MS were 435.26 kg, 13.07 mm, 90.16 cm
2 and 5.68. All of the differences between corresponding measures from ultrasound and from carcass were within one SD units. Therefore, we could consider that were no extra effects on carcass traits other than animal management effects and individual animals’ genetic effects that are normally accounted in genetic analysis models. The similar age structure for ultrasound measures and carcass measures were found in the studies by
Cheong et al. (2012) or by
Kim et al. (2012). The averages of UBF, ULMA, UMS were 9.71 mm, 86.88 cm
2, 4.14, respectively in the report of
Cheong et al. (2012), and 9.41 mm, 87.38 cm
2, 5.16, respectively in the report of
Kim et al. (2012). The averages of CW, BF, LMA, and MS were 417.94 kg, 12.91 mm, 89.92 cm
2, 5.31, respectively in the report of
Cheong et al. (2012), and 393.14 kg, 10.59 mm, 89.84 cm
2, 5.93, respectively in the report of
Kim et al. (2012). The averages calculated in our study population were similar to those in the report of
Cheong et al. (2012). The averages of carcass traits reported by
Koo et al. (2011) were 415.23 kg for CW, 88.29 cm
2 for LMA, 12.71 mm for BF and 5.42 for MS.
Osawa et al. (2008) reported that the averages of CW was 445.0 kg and LMA, BF and MS (12 score scales) estimated at the section between the 6th and 7th thoracic vertebra were 56.8 cm
2, 2.3 mm and 5.5 at 29.6 months in Japanese Black steers. These differences might reflect regional differences in feeding steers in Korea or different methods of carcass evaluation between Korea and Japan (Japanese carcass evaluation is made between the 6th and 7th thoracic vertebra).
Estimates of additive genetic variance for ultrasound measurements and carcass measurements by multiple trait analysis are presented in
Table 3. In Korea, there have been several research works to estimate genetic parameters for carcass traits of Hanwoo steers (
Yoon et al., 2002;
Roh et al., 2004;
Choi et al., 2006;
Hwang et al., 2008). Most of the genetic (co)variances were estimated using records of steers on progeny tests at the Livestock Improvement Center. Also, the average age at slaughter of steers on progeny tests was 24 months. However, age at slaughter of steers in our study was older than that of those steers on progeny tests. Furthermore, feeding environments (feed intake, management and so on) were also different by operating farms.
Heritability estimates of the ultrasound measures were 0.43 for UBF, 0.16 for ULMA and 0.33 for UMS (
Table 3). Compared to the genetic parameters estimated from this study, other reports showed some different estimates of additive genetic (co)variances ratios. Our heritability estimate for UBF was between the estimates of
Roh et al. (2010). Their estimate was 0.41 when ultrasound scanning was made at 12 months of age and 0.60 when ultrasound scanning was made at 24 months of age.
Stelzleni et al. (2002) reported that the heritability estimate of ultrasound fat thickness was 0.26 in yearling Brangus bulls and heifers.
Kim et al. (2012) and
Park et al. (2012) with repeated measures animal models reported that the heritability estimates for UBF in Hanwoo cows were 0.43 and 0.38, respectively. In Angus steers, the heritability estimates of UBF, measured at yearling stage, was 0.39 in the report by
Kemp et al. (2002), and was 0.26 in the report by
MacNeil and Northcutt (2008). For ULMA, our heritability estimate was lower than those in the literature.
Roh et al. (2010) reported that the estimates for ULMA were 0.57 when ultrasound images of Hanwoo steers were taken at 12 months of age and 0.57 when taken at 24 months of age. In cows,
Park et al. (2012) and
Kim et al. (2012) estimated heritability in Hanwoo cows with repeated measures animal models and their estimates were 0.23 and 0.31. In the other breeds,
Kemp et al. (2002) reported that the heritability estimate of ULMA in yearling Angus steers was 0.29. And
Stelzleni et al. (2002) reported that the heritability estimate of ULMA was 0.31 in yearling Brangus bulls and heifers.
Our heritability estimate for UMS was similar to the estimate (0.27) of
Park et al. (2012) with repeated measures animal models or the estimate (0.32) of
Kim et al. (2012), both for Hanwoo cows.
Our heritability estimates for carcass traits were moderate to high: 0.50, 0.39, 0.40, and 0.56 for CW, BF, LMA, and MS, respectively (
Table 4).
For CW, the estimate in this study was higher than the estimates of
Yoon et al. (2002),
Hwang et al. (2008), or
Roh et al. (2010) that ranged from 0.28 to 0.41 in Hanwoo steers slaughtered at 24 months of age after the end of progeny testing or in Japanese Black steers (
Osawa et al., 2008) that were slaughtered at 25 to 37 months of age. However, the heritability estimate of CW (0.61) in Japanese Black steers and heifers slaughtered at 27 to 31 months of ages was much higher (
Nogi et al., 2011) than our estimate.
The heritability estimate for LMA in this study was similar to that of
Yoon et al. (2002) or that of
Roh et al. (2010). However this estimate was lower than that of
Hwang et al. (2008), the estimate of which was on Hanwoo steers raised in a test station and slaughtered at 24 months of age, earlier in life compared to steers observed in this study.
Crew and Kemp (2001),
Devitt and Wilton (2001),
Kemp et al. (2002),
Osawa et al. (2008), and
Nogi et al. (2011) reported that the heritability estimates for LMA in their study populations were 0.54, 0.45, 0.44, 0.43, and 0.49, respectively.
For BF, our estimate was similar to the estimates reported by
Yoon et al (2002), or by several other researchers (
Roh et al., 2004;
Hwang et al., 2008) ranging from 0.39 to 0.44 in Hanwoo steers. Compared to this study,
Osawa et al. (2008) estimated a lower heritability (0.22) for BF in Japanese Black steers.
Crews and Kemp (2001) and
Nogi et al. (2011) estimated a higher heritability, 0.55 in beef steers slaughtered at around 15 months of age and 0.51 in Japanese Black steers and heifers slaughtered at around 29 months of age.
Kemp et al. (2002)’s estimate for BF in Angus steers and
Devitt and Wilton (2001)’s age constant estimate in composite breed steers, both populations of which were slaughtered at about 15 months of age were 0.35 and 0.41, respectively.
Genetic and phenotypic correlations, calculated using multiple trait animal models, among ultrasound measurements and carcass measurements are shown in
Table 4. Genetic and phenotypic correlations were highly positive between UBF and BF (0.938 and 0.732), between ULMA and LMA (0.767 and 0.460) and between UMS and MS (0.925 and 0.619). A common feature in the differences in estimates between phenotypic and genetic correlation coefficients between these physiologically related traits was the fact that, in all three comparison groups, genetic correlation was always higher than phenotypic correlation. A few explanations are possible. First, lower phenotypic correlation than genetic correlation might be due to unidentified environmental effects in the models we applied in this study. Secondly, in our models, the interaction effect between individual farm’s management and the situation that the animals were raised and fattened was not included. Instead, we assumed that the animals in our study population were under same environmental conditions regardless of where they were raised because all the participant farms fed animals the same concentrate diets that Hoengseong Chukhyup provided and that the fattened steers were slaughtered after the same feeding programs. Therefore, the differences between farms were unique differences in management that might be the same over the years within each farm. High genetic correlation coefficients between ultrasound and carcass measures were also found in the works of
Kemp et al. (2002) or of
MacNeil and Northcutt (2008), the estimates of which were in the range from 0.82 to 0.90 between UBF and BF and from 0.58 to 0.90 between ULMA and LMA.
The genetic correlation between ultrasound measurements and carcass measurements were positive except between UBF and MS. Genetic correlation coefficients between UBF and CW and between BF and CW were 0.387 and 0.407, respectively. These estimates were similar to the estimates of
Roh et al. (2010); 0.354 and 0.306, respectively when ultrasound images were taken at 12 months of age; 0.456 and 0.336, respectively when ultrasound images were taken at 24 months of age. Compared to this study, several reports (
Yoon et al., 2002;
Roh et al., 2004;
Choi et al., 2006;
Hwang et al., 2008) that dealt with Hanwoo steers on progeny tests showed lower genetic correlation estimates between BF and CW, ranging from 0.08 to 0.24.
Genetic correlation coefficients between UBF and LMA and between BF and LMA were low and positive (0.139 and 0.181, respectively). Other reports on the genetic correlation between UBF and LMA or between BF and LMA were negative (
Kemp et al., 2002;
Yoon et al., 2002;
Roh et al., 2004;
Choi et al., 2006;
Hwang et al., 2008). This may be due to the different points in time of ultrasound measurement. At around yearling age, muscle growth would be the major body compositional change while in later around the age to be slaughtered, fat deposition would be active depending on individual growth curve. Therefore, at yearling faster growing animals would build heavier muscle but thinner backfat. But at the time around slaughter, faster growing animals would build thicker backfat as well as heavier muscle in their body.
Genetic correlation coefficients between UBF and MS and between BF and MS were −0.039 and −0.002, respectively, almost zero but slightly negative. Literature values of the genetic correlation between UBF at yearling and carcass MS at 24 months of age or between BF at yearling and carcass MS at 24 months of age in Hanwoo progeny tested steers were in the range from 0.18 to 0.24 (
Yoon et al., 2002;
Roh et al., 2004;
Choi et al., 2006;
Roh et al., 2010).
Kemp et al. (2002) reported the genetic correlation estimates between UBF or BF and MS in Angus steer population were 0.29 when the traits were age-adjusted and 0.45 when the traits were weight-adjusted.
Osawa et al. (2008) explained that the improvement of increasing marbling would not increase the subcutaneous fat thickness, indicating that those two traits are genetically independent.
Osawa et al. (2008) reported that genetic correlations between subcutaneous fat thickness and fat area ratio for
M. longissimusthoracis or
M. trapezius were negative (−0.21 and −0.19).
Hirooka et al. (1996) reported the negative genetic correlation (−0.12) between MS and subcutaneous fat thickness in Japanese Brown cattle from field records.
Genetic correlation coefficient between ULMA and CW (0.505) was higher than that between LMA and CW (0.378). The trends similar to this result were found by
Roh et al. (2010) at 24 months of age.
Roh et al. (2010) reported that the genetic correlation coefficients between ULMA and CW or between LMA and CW were 0.66 or 0.48, respectively.
Genetic correlation coefficients between ULMA and MS or between LMA and MS were positive (0.523 or 0.656) and higher than those of the other reports. In the other reports, genetic correlation coefficients estimated between LMA of ultrasound or carcass and MS were in the range from −0.26 to 0.30 (
Hirooka et al., 1996;
Kemp et al., 2002;
Yoon et al., 2002;
Roh et al., 2004;
Choi et al., 2006;
Roh et al., 2010). Most Hanwoo breeders in the region of our study population are interested in greater genetic potentials in LMA and MS. Therefore, our positive and rather high genetic correlation between these two traits suggests that selection of the right semen and heifers with regards to these can make favorable genetic responses on both traits of their interest.
Genetic correlation coefficients between UMS and CW or between MS and CW were 0.033 or 0.005, respectively. Genetic correlation between MS and CW was estimated to be lower than that of
Yoon et al. (2002), 0.29 and
Roh et al. (2004), 0.41 or that of
Choi et al. (2006), 0.32.
Hirooka et al. (1996) reported genetic correlation between MS and CW to be small but negative (−0.05).