S. A. Barwick

Genetics of steer daily and residual feed intake in two tropical beef genotypes, and relationships among intake, body composition, growth and other post-weaning measures

Genetic parameters for Brahman (BRAH) and Tropical Composite (TCOMP) cattle were estimated for steer production traits recorded at weaning (WEAN), 80 days post-weaning (POSTW), feedlot entry (ENTRY) and after ∼120 days feedlot finishing (EXIT). The TCOMP was 50% Bos indicus, African Sanga or other tropically adapted Bos taurus, and 50% non-tropically adapted Bos taurus. Data involved 2216 steers, comprising 1007 BRAH by 53 sires and 1209 TCOMP by 50 sires. Individual daily feed intake (DFI) and residual feed intake (RFI) were assessed on 680 BRAH and 783 TCOMP steers over an ~70-day feedlot test. Other traits were liveweight (LWT), average daily gain (ADG), ultrasonically scanned rump (SP8) fat depth, rib (SRIB) fat depth, M. longissimus area (SEMA) and intra-muscular fat % (SIMF), body condition score (CS), hip height (HH), flight time (FT) and serum insulin-like growth factor-I concentration (IGF-I). BRAH were significantly (P < 0.05) lighter at ENTRY and EXIT, and had lower DFI (10.8 v. 13.2 kg/day) and RFI (–0.30 v. 0.17 kg/day), greater SP8 (5.8 v. 5.1 mm) but similar SRIB at ENTRY, lower SRIB (8.2 v. 8.9 mm) but similar SP8 at EXIT, and greater HH than TCOMP. Heritabilities for DFI, RFI, LWT, ADG, scanned body composition, HH and IGF-I measures, across measurement times, were generally in the 20 to 60% range for both genotypes. Genetic variance for RFI was 0.19 (kg/day)2 in BRAH and 0.41 (kg/day)2 in TCOMP, suggesting a clear potential to genetically change RFI in both genotypes. Trait variances and genetic correlations often differed between the genotypes, supporting the use of genotype-specific parameters in genetic evaluation. The genotype differences may be associated with evolutionary changes that have occurred in B. indicus as a part of their adaptation to tropical environments. Measures with potential to be used as genetic indicators of DFI were LWT measures in BRAH and TCOMP, ADG at ENTRY in TCOMP, and SP8 and SIMF at ENTRY in BRAH. Measures with potential to be genetic indicators of RFI were HH and ADG at ENTRY in BRAH, and IGF-I in both genotypes. Taller and faster-growing BRAH steers at ENTRY had genetically lower RFI. IGF-I was negatively genetically correlated with RFI whether IGF-I was measured at POSTW, ENTRY or EXIT. SRIB fatness at EXIT was strongly positively genetically correlated with RFI in TCOMP but only lowly correlated in BRAH. Fatness at ENTRY was lowly and negatively genetically correlated with RFI. The results emphasise the need for a population-specific understanding of trait relationships and of trait differences between measurement times if genetic indicator traits are to be utilised in genetic evaluation of RFI.

Genetics of meat quality and carcass traits and the impact of tenderstretching in two tropical beef genotypes.

Meat quality and carcass traits were measured for 2180 feedlot finished Brahman (BRAH) and Tropical Composite (TCOMP) steers to investigate genetic and non-genetic influences on shear force, and other meat quality traits. Genetic and phenotypic correlations were estimated between carcass and meat quality traits, and with live animal measurements collected in steers from weaning to feedlot exit, and their heifer half-sibs up to their first mating, which were managed in Australia’s tropical or subtropical environments. Left sides of carcasses were tenderstretched (hung by the aitch-bone) while right sides were conventionally hung (by the Achilles tendon). Tenderstretching reduced mean shear force by 1.04 kg, and phenotypic variance by 77% of that observed in conventionally hung sides. Genotype differences existed for carcass traits, with TCOMP carcasses significantly heavier, fatter, with greater eye muscle area, and lower retail beef yield than BRAH. TCOMP had lower shear force, and higher percent intramuscular fat. Meat quality and carcass traits were moderately heritable, with estimates for shear force and compression of 0.33 and 0.19 for BRAH and 0.32 and 0.20 for TCOMP respectively. In both genotypes, estimates of heritability for carcass traits (carcass weight, P8 and rib fat depths, eye muscle area and retail beef yield) were consistently moderate to high (0.21 to 0.56). Shear force and compression were genetically correlated with percent intramuscular fat (r g = –0.26 and –0.57, respectively), and meat colour (r g = –0.41 and –0.68, respectively). For TCOMP, lower shear force was genetically related to decreased carcass P8 fat depth (r g = 0.51). For BRAH steers and heifers measured at pasture, fatness traits and growth rates were genetically correlated with shear force, although the magnitude of these relationships varied with time of measurement. Net feed intake was significantly genetically correlated with carcass rib fat depth (r g = 0.49), eye muscle area (r g = –0.42) and retail beef yield (r g = –0.61). These results demonstrate that selection to improve production and carcass traits can impact meat quality traits in tropically adapted cattle, and that genotype specific evaluations will be necessary to accommodate different genetic relationships between meat quality, carcass and live animal traits.

Genetics of early and lifetime annual reproductive performance in cows of two tropical beef genotypes in northern Australia

Reproduction records from 2137 cows first mated at 2 years of age and recorded through to 8.5 years of age were used to study the genetics of early and lifetime reproductive performance from two genotypes (1020 Brahman and 1117 Tropical Composite) in tropical Australian production systems. Regular ultrasound scanning of the reproductive tract, coupled with full recording of mating, calving and weaning histories, allowed a comprehensive evaluation of a range of reproductive traits. Results showed components traits of early reproductive performance had moderate to high heritabilities, especially in Brahmans. The heritability of lactation anoestrous interval in 3-year-old cows was 0.51 +/- 0.18 and 0.26 +/- 0.11 for Brahman and Tropical Composite, respectively. Heritabilities of binary reproductive output traits (conception rate, pregnancy rate, calving rate and weaning rate) from first and second matings were generally moderate to high on the underlying scale. Estimates ranged from 0.15 to 0.69 in Brahman and 0.15 to 0.34 in Tropical Composite, but were considerably lower when expressed on the observed scale, particularly for those traits with high mean levels. Heritabilities of lifetime reproduction traits were low, with estimates of 0.11 +/- 0.06 and 0.07 +/- 0.06 for lifetime annual weaning rate in Brahman and Tropical Composite, respectively. Significant differences in mean reproductive performance were observed between the two genotypes, especially for traits associated with anoestrus in first-lactation cows. Genetic correlations between early-in-life reproductive measures and lifetime reproduction traits were moderate to high. Genetic correlations between lactation anoestrous interval and lifetime annual weaning rate were -0.62 +/- 0.24 in Brahman and -0.87 +/- 0.32 in Tropical Composite. The results emphasise the substantial opportunity that exists to genetically improve weaning rates in tropical beef cattle breeds by focusing recording and selection on early-in-life female reproduction traits, particularly in Brahman for traits associated with lactation anoestrus.

Genetic correlations of young bull reproductive traits and heifer puberty traits with female reproductive performance in two tropical beef genotypes in northern Australia

Genetic correlations of young bull and heifer puberty traits with measures of early and lifetime female reproductive performance were estimated in two tropical beef cattle genotypes. Heifer age at puberty was highly (r(g) = -0.71 +/- 0.11) and moderately (r(g) = -0.40 +/- 0.20) genetically correlated with pregnancy rate at first annual mating (mating 1) and lifetime annual calving rate, respectively in Brahman (BRAH). In Tropical Composite (TCOMP), heifer age at puberty was highly correlated with reproductive outcomes from the first re-breed (mating 2), mainly due to its association with lactation anoestrous interval (r(g) = 0.72 +/- 0.17). Scrotal circumference were correlated with heifer age at puberty (r(g) = -0.41 +/- 0.11 at 12 months in BRAH; -0.30 +/- 0.13 at 6 months in TCOMP) but correlations were lower with later female reproduction traits. Bull insulin-like growth factor-I was correlated with heifer age at puberty (r(g) = -0.56 +/- 0.11 in BRAH; -0.43 +/- 0.11 in TCOMP) and blood luteinising hormone concentration was moderately correlated with lactation anoestrous interval (r(g) = 0.59 +/- 0.23) in TCOMP. Semen quality traits, including mass activity, motility and percent normal sperm were genetically correlated with lactation anoestrus and female lifetime female reproductive traits in both genotypes, but the magnitudes of the relationships differed with bull age at measurement. Preputial eversion and sheath scores were genetically associated with lifetime calving and weaning rates in both genotypes. Several of the early-in-life male and female measures examined were moderately to highly genetically correlated with early and lifetime female reproduction traits and may be useful as indirect selection criteria for improving female reproduction in tropical breeds in northern Australia.

The genetics of cow growth and body composition at first calving in two tropical beef genotypes

The genetics of cow growth and body composition traits, measured before first calving (pre-calving: in females before calving following their first 3-month annual mating period, at an average age of 34 months) and at the start of the subsequent mating period (Mating 2: on average 109 days later), were evaluated in 1016 Brahman (BRAH) and 1094 Tropical Composite (TCOMP) cows. Measurements analysed were liveweight, ultrasound-scanned measurements of P8 and 12/13th rib fat depth and eye muscle area, body condition score and hip height. Traits describing the change in these from pre-calving to Mating 2 were also included in the analysis. The maternal genetic component of weaning weight was estimated from weaning-weight records on these cows, their steer half-sibs and their progeny generated from up to six matings (n = 12 528). Within pregnant cows at pre-calving, BRAH were significantly lighter, leaner at the P8 site and taller than their TCOMP contemporaries, and these differences were also significant at Mating 2. There was a genetic basis for variation in growth and body composition traits measured at pre-calving and Mating 2 in BRAH (h2 = 0.27–0.67) and TCOMP (h2 = 0.25–0.87). Traits describing the change from pre- calving to Mating 2 were also moderately heritable for both genotypes (h2 = 0.17–0.54), except for change in hip height (h2 = 0.00 and 0.10 for BRAH and TCOMP, respectively). Genetic correlations between measurements of the same trait at pre-calving and Mating 2 were consistently positive and strong (rg = 0.75–0.98) and similar for both genotypes. In lactating cows, genetic correlations of growth and body composition traits with their change from pre-calving to Mating 2 showed that when animals had low levels of P8 and rib fat at Mating 2, change in eye muscle area was an important descriptor of genetic body condition score (rg = 0.63). This was supported by moderate genetic relationships, which suggested that lactating cows that were genetically predisposed to lose less eye muscle area were those that ended the period with higher P8 fat (rg = 0.66), rib fat (rg = 0.72) and body condition score (rg = 0.61). Change in liveweight, body condition score and, in particular, eye muscle area was significantly related to the maternal genetic component of weaning weight (rg = from –0.40 to –0.85) in both genotypes, suggesting that cows with higher genetic milk-production potential were those with the propensity for greater loss of these traits over the period from pre-calving to Mating 2. These results showed that for tropically adapted cows, the change in eye muscle area from pre-calving to Mating 2 was a more important descriptor of body condition at Mating 2 than was change in fat depth, and that higher genetic milk-production potential, measured as maternal weaning weight, was genetically related to higher mobilisation of muscle, and therefore body condition, over this period.

Genetic relationships of female reproduction with growth, body composition, maternal weaning weight and tropical adaptation in two tropical beef genotypes

The genetic relationships of female reproduction with growth and body composition, tropical adaptation traits and maternal weaning weight (descriptive of genetic potential milk production) were estimated in 1027 Brahman (BRAH) and 1132 Tropical Composite (TCOMP) females. Female reproduction was evaluated at puberty, as outcomes of the first and second annual mating periods (Mating 1 and Mating 2, which commenced when females averaged 27 and 39 months of age, respectively), as well as annual averages over up to six matings. Traits evaluated included age at puberty, Mating 1 and 2 pregnancy rate, weaning rate and days to calving, and lifetime annual calving and weaning rate. Traits describing growth and body composition (liveweight, hip height, ultrasound-scanned P8 fat depth and eye muscle area, subjective body condition score and blood IGF-I concentration) were measured in the animals as heifers (at ~18 months of age), and again at the start of Mating 2. Traits describing tropical adaptation included coat-length scores in both genotypes and, in BRAH, buffalo fly lesion scores. Previously reported analyses of these data identified heifer IGF-I and coat and buffalo-fly-lesion scores as potential genetic indicators for age at puberty in BRAH. The results of the present study found that exploiting these relationships would have no unfavourable genetic consequences for later female reproduction and, in some cases, may be indicators of female reproduction, when evaluated as outcomes of Matings 1 or 2, or as lifetime annual calving or weaning rates. For BRAH, heifer liveweight was a genetic indicator for Mating 1 weaning rate (rg = 0.70), and, while standard errors were high, there were also positive genetic correlations of heifer hip height, eye muscle area and blood IGF-I concentration with Mating 1 weaning rate (rg = 0.61, 0.58 and 0.43, respectively). For TCOMP, significant genetic relationships of heifer growth, body composition and tropical adaptation traits with female reproduction were virtually absent, suggesting that there is less opportunity to identify earlier in life measures as genetic indicators of reproduction for this genotype. Higher maternal weaning weight was significantly genetically related to lower lifetime annual weaning rate (rg = –0.50) in BRAH, and with lower Mating 2 calving and weaning rate (rg = –0.72 and –0.59, respectively) in TCOMP, which will need to be considered when making selection decisions that affect genetic milk in these genotypes. Importantly, the results presented revealed no strong genetic antagonisms of heifer growth and body composition traits with female reproduction, suggesting that selection could be undertaken to improve these simultaneously.

Multi-trait assessment of early-in-life female, male and genomic measures for use in genetic selection to improve female reproductive performance of Brahman cattle

Early-in-life female and male measures with potential to be practical genetic indicators were chosen from earlier analyses and examined together with genomic measures for multi-trait use to improve female reproduction of Brahman cattle. Combinations of measures were evaluated on the genetic gains expected from selection of sires and dams for each of age at puberty (AGECL, i.e. first observation of a corpus luteum), lactation anoestrous interval in 3-year-old cows (LAI), and lifetime annual weaning rate (LAWR, i.e. the weaning rate of cows based on the number of annual matings they experienced over six possible matings). Selection was on an index of comparable records for each combination. Selection intensities were less than theoretically possible but assumed a concerted selection effort was able to be made across the Brahman breed. The results suggested that substantial genetic gains could be possible but need to be confirmed in other data. The estimated increase in LAWR in 10 years, for combinations without or with genomic measures, ranged from 8 to 12 calves weaned per 100 cows from selection of sires, and from 12 to 15 calves weaned per 100 cows from selection of sires and dams. Corresponding reductions in LAI were 60-103 days or 94-136 days, and those for AGECL were 95-125 or 141-176 days, respectively. Coat score (a measure of the sleekness or wooliness of the coat) and hip height in females, and preputial eversion and liveweight in males, were measures that may warrant wider recording for Brahman female reproduction genetic evaluation. Pregnancy-test outcomes from Matings 1 and 2 also should be recorded. Percentage normal sperm may be important to record for reducing LAI and scrotal size and serum insulin-like growth factor-I concentration in heifers at 18 months for reducing AGECL. Use of a genomic estimated breeding value (EBV) in combination with other measures added to genetic gains, especially at genomic EBV accuracies of 40%. Accuracies of genomic EBVs needed to approach 60% for the genomic EBV to be the most important contributor to gains in the combinations of measures studied.