Inexpensive fibre sources might be used as an alternative to lucerne hay in diets for finishing lambs. Thus, effects of providing fibre from lucerne hay (LH), soyhulls (SH), maize stover (MS) and Eragrostis teff hay (ET) on the nutrient digestibility of diets of finishing lambs with comparable NDF and nutrient concentration were evaluated. Thirty-six individually housed Merino ram lambs (x̄ = 43.03, SD = 3.72 kg) were randomly allocated to four diets (n = 9 lambs/treatment). A digestibility study was conducted to determine the nutrient availability of these diets. Dry matter (DM) intake of SH (1436 g) was lower than ET (1716 g). No differences were recorded between treatments for digestibility of NDF (0.32 - 0.34), acid detergent fibre (ADF) (0.41 - 0.44), and ether extract (EE) (0.67 - 0.75), except that MS (0.23) had lower NDF digestibility. Digestibility of DM, organic matter (OM) and non-structural carbohydrates (NSC) were similar for the LH (0.72; 0.75; 0.96) and SH (0.70; 0.74; 0.95) diets, whereas digestibility of crude protein (CP) (0.71 vs. 0.68), metabolizable energy (ME) (9.49 vs. 8.90 MJ/kg DM), and the available ash fraction (0.39 vs. 0.28) were altered. The SH and ET (8.70 MJ/kg DM) treatments had similar ME concentrations, but ET had lower DM digestibility (0.68). The MS treatment had the lowest ME concentration (8.25 MJ/kg DM). The LH treatment resulted in overall better nutrient availability compared with SH, MS, and ET.
The wildlife industry in South Africa has shown immense growth since the 1990s, which was brought about by the private game segment of the industry. In recent years, trophy quality Cape buffalo breeding animals have achieved extremely high prices. Much of the economic value of these animals can be attributed to horn size, which is important for breeding and hunting purposes. The main objective of the study was to estimate variance components for horn traits of economic importance as well as to develop guidelines for recording these traits. To date, no quantitative genetic analysis has been done for any traits in Cape buffalo. The total number of horn measurement records included in the evaluation was n = 945 for outer spread (BHSO), n = 470 for tip to tip (BHTSCI), n = 468 for left boss and n = 479 for right boss. For descriptive statistics, males and females were considered separately while age was divided into clusters of six months. A multi-trait animal model using Monte Carlo Markov Chains methods was used for the estimation of genetic parameters. Results suggest that it is not economically viable to measure horn spread and tip to tip of females after 48 months of age. Horns of the males continue to grow beyond 91 months of age. Boss records were unreliable owing to the applied measurement techniques for female and young animals. An inbreeding coefficient of 0.008 was calculated, suggesting adequate genetic diversity in the studied population. The heritability estimates of the horn traits were low, showing that extreme care has to be taken to develop effective selection programmes for the buffalo game industry using their horn genetic parameters. Further quantitative studies are required to support the results of the current study.
Much of the economic value of wildlife can be attributed to horn size, which is an important trait for trophy hunters. The main objective of the study was to estimate genetic parameters for the economically important horn traits of sable antelope that are currently being measured in the South African industry. To date, no quantitative genetic analysis has been done for any traits in sable antelope. The total number of records included in the evaluation were n = 1713 for horn length (SHL), n = 1503 for circumference (SHC), n = 1486 for tip to tip (SHTT), n = 1505 for tip length (SHT), and n = 1447 for rings (SHR). Males and females were considered separately in six-month age clusters. A Markov chain Monte Carlo (MCMC) multi-trait analysis was used to estimate (co)variance parameters for the horn traits. The results indicate a sex effect for all the traits and suggest that it is not economically viable to measure horn length of either sex after 54 months old. The horns of females are on average 40% shorter compared with bulls at maturity. Continuous horn growth throughout the lifetime of sable is suggested by the formation of ring posts, but is often masked by horn attrition and inadequate measuring techniques. An inbreeding coefficient of 0.0043 suggests adequate genetic diversity in the studied population. Heritability estimates of horn traits varied from 0.085 to 0.52, while genetic correlations ranged from 0.1 to 0.6 with the highest correlation being found between horn length and tip to tip. Further studies are recommended to confirm these results.
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