Genetic parameters for liveweight (LWT), greasy fleece weight (GFW), mean fibre diameter (MFD), standard deviation of MFD (MFD-s.d.), mean fibre curvature (CURVE) percentage of medullated (%MED) and kemp (%KEMP) fibres, faecal worm egg count (WEC), packed cell volume (PCV), mean corpuscular volume (MCV) mean corpuscular haemoglobin content (MCHC), circulating anti-nematode IgG (IgG) and counts of circulating eosinophils (EOS), lymphocytes (LYM), neutrophils (NEU), basophils (BASO) and monocytes (MONO) up to 18 months of age were estimated in Australian Angora goats (608 animals, 14 sires 3 years of birth). Measurements were made during a period of natural parasite challenge up to 5 months of age, or following artificial challenge with 10 000 infective larvae of Trichostrongylus colubriformis at 5.25 months of age. Year of birth had a significant impact on production and parasite-associated traits at all ages studied. Sex had a marked effect on production and erythrocyte traits. Birth type had no effect on any traits in animals older than 6 months. Maternal effects were not significant except for LWT at 3, 5 and 6 months and for IgG at 3 months. Most production traits were highly (LWT, GFW, MFD, %MED) or moderately (CURVE, MFD-s.d.) heritable (range 0.17–0.59) with only %KEMP having a low heritability (0.02–0.14). The heritability estimates (±s.e.) for CURVE are novel for goats and ranged from 0.18 ± 0.09 at first shearing to 0.44 ± 0.14 at third shearing. Heritability estimates were low for WEC (0.02–0.16) and for specific IgG during natural infection (0.14–0.15) but higher for IgG following artificial challenge with T. colubriformis (0.42 ± 0.13). Of the haematological variables NEU and all red cell traits were highly heritable (0.45–0.71), LYM and MONO were moderately to highly heritable (0.31–0.55), and EOS was weakly to moderately heritable (0.06–0.28). Strong phenotypic correlations existed between production traits. MFD was positively correlated with GFW and negatively correlated with CURVE, indicating that finer fibres have a higher crimp or wave count. WEC had consistent negative phenotypic correlations with PCV, LYM and EOS, and positive correlations with NEU. Correlations with IgG were positive up to 5 months and negative thereafter. Phenotypic correlations between WEC and LWT as well as with GFW and MFD were negative. Heritability estimates for production traits were generally consistent with other studies. Haematological and fibre curvature findings are completely novel for Angora goats. Estimates of heritability for WEC fell in mid range of published findings for other goat breeds, and these results suggest that there is some scope for breeding for worm resistance in Angoras but the response is likely to be slow.
The present study was designed to estimate genetic parameters of 17 production, parasite-associated and haematological traits in Australian cashmere goats. It comprised 796 records of female progeny of 532 dams sired by 29 bucks over a 4-year period. Measurement of haematological and parasite-associated traits was carried out on female kids during low-level natural gastrointestinal nematode challenge at 3 and 5 months of age and at 28 and/or 35 days after artificial challenge with 10 000 infective larvae of Trichostrongylus colubriformis administered 1 week after the 5-month measurement. Production traits were measured up to 18 months of age. Year of birth significantly affected all traits apart from cashmere diameter (CSD). Twin kids had significantly lower liveweight (up to 10 months), packed cell volume and mean corpuscular volume (at 3 and 5 months) but higher specific IgG levels and mean corpuscular haemoglobin content at 3 months. Paddock of birth and early rearing and its interaction with year of birth had significant effects on worm egg count (WEC) during natural challenge, on IgG at both natural and post-artificial challenge measurements and on liveweight at early ages. The level of gastrointestinal nematode challenge in the nine different paddocks clearly influenced both WEC and IgG during natural and subsequent artificial challenge. Maternal permanent environmental effects were important only for liveweights at 3 month of age and for IgG at 5 months of age. For other traits, a simple animal model without maternal permanent environmental effects gave the best fit. Estimates of heritability (h2) of WEC and IgG were low (0.06–0.22) with the highest h2 estimates occurring after 5 months of natural infection or 35 days after artificial challenge. The majority of fleece traits were moderately to highly heritable, ranging from 0.38 to 0.78. The h2 estimates for mean fibre curvature are novel for cashmere goats and were moderate, varying from 0.32 to 0.48. Heritability estimates for erythrocyte traits were uniformly high (0.49–0.98) while those for leukocyte traits varied from low to moderate (0.09–0.43). Strong genetic and phenotypic correlations existed between major production traits. Due to the comparatively small dataset, the standard errors of genetic correlations were relatively high. CSD was positively correlated with cashmere weight and yield, an unfavourable direction. CSD was negatively correlated with fibre curvature, indicating that animals producing finer fibres produce cashmere with a higher crimp count. No phenotypic relationships were observed between WEC and fleece traits. Liveweight was weakly but negatively correlated with WEC and circulating neutrophils, while it was positively associated with eosinophils, lymphocytes and packed cell volume. This study has shown that selection for increased resistance to gastrointestinal nematode infection cashmere goats is possible but progress will be slow. WEC should remain the phenotypic marker of choice and the additional cost of alternative measures of resistance is not justified. Many of the parasite-associated traits appear to under independent genetic control.
When live-export sheep from Australia arrive in the Middle East during the northern summer months, they may be offered drinking water at temperatures exceeding 40°C. There is little published research to indicate whether drinking water temperature is important in managing heat stress in sheep or its effect on their health and welfare. Three studies were conducted with Merino wethers in climate-controlled rooms to investigate: (i) responses to drinking water temperatures of 20°C, 30°C and 40°C in a cool (20°C) and hot (40°C) environment, (ii) preferences for drinking water temperature at 20°C or 30°C when in a hot or cool environment and (iii) effects of water restriction when offered hot water (40°C) in a hot environment. Sheep assigned to the hot room had significantly higher respiration rates than those assigned to the cool room. In the cool environment, water intakes were the same when water temperatures were 20°C, 30°C or 40°C; however, when the sheep were given a choice between drinking water at 20°C and 30°C, they preferred (P < 0.05) to drink water at 20°C. In the hot environment, water intake increased as drinking water temperature increased, and sheep preferred to drink water at 30°C rather than 20°C. When the availability of 40°C drinking water was restricted (to ~10% of liveweight) in the hot environment, sheep had higher respiration rates than those offered unlimited water.
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