Chondrodysplasia in Australian Dexter cattle

Objective To describe the occurrence of chondrodysplasia in Australian Dexter cattle.
Design A pathological and genetic case report.
Procedure Congenital lethal chondrodysplasia was studied in two female Dexter foetuses aborted mid to late gestation. Clinicopathological findings including histological changes in limb bones, and analysis of pedigree information were evaluated.
Results Characteristic features of congenital lethal chon-drodysplasia (Dexter bulldog) include abortion, disproportionate dwarfism, a short vertebral column, marked micromelia, a relatively large head with retruded muzzle, cleft palate and protruding tongue and a large abdominal hernia. Histological changes in limb bones are consistent with failure of endochondral ossification. Dexter chondrodysplasia is considered to be inherited in an incompletely dominant manner with the homozygous form producing the congenital lethal condition. A preliminary minimum estimate of heterozy-gote frequency is 19% within the registered Australian Dexter herd, based on analysis of the contribution of three obligate heterozygotes whose semen has been widely used by artificial insemination in Australia.
Conclusion Dexter chondrodysplasia is present in Australian cattle and further cases of the homozygous form, congenital lethal chondrodysplasia, are likely to occur.
Recommendation It is requested that spleen and liver tissue from bulldog foetuses and blood from their parents be collected to assist research into Dexter chondrodysplasia.     

Genetic diversity of Afrikaner cattle in southern Africa

The Afrikaner is an indigenous South African breed of “Sanga” type beef cattle along with breeds such as the Drakensberger and Nguni. Six composite breeds have been developed from crosses with the Afrikaner. Additionally, Afrikaner has been the base from which exotic breeds were established in South Africa through backcrossing. The study examined genetic diversity of Afrikaner cattle by genotyping 1257 animals from 27 herds in different geographic areas of South Africa and Namibia using 11 microsatellite markers. Multiple-locus assignment, performed using the Bayesian clustering algorithm of STRUCTURE, revealed three underlying genotypic groups. These groups were not geographically localized. Across herds and markers, the proportion of unbiased heterozygosity ranged from 0.49 to 0.72 averaging 0.57; mean number of alleles per locus ranged from 3.18 to 7.09, averaging 4.81; and allelic richness ranged from 2.35 to 3.38, averaging 2.67. It is concluded that a low inbreeding level of 2.7% and a moderate to high degree of variation still persists within the Afrikaner cattle breed, despite the recent decline in numbers of animals.     

Estimates of genetic parameters for Boran, Friesian, and crosses of Friesian and Jersey with the Boran cattle in the tropical highlands of Ethiopia: milk production traits and cow weight

Breed additive and non‐additive effects plus heritabilities and repeatabilities for milk yield per lactation (LMY), milk yield per day (DMY), lactation length (LL), annual milk yield (AMY), annual milk yield per metabolic body weight (AMYBW) and cow weight at calving (BW) were estimated for 5464 lactation records collected from purebred Boran (B), Friesian (F), and crosses of Friesian and Jersey (J) breeds with the Boran breed raised in the tropical highlands of Ethiopia. Single trait analysis was carried out by using two equivalent repeatability animal models. In the first model the genotype was fitted as a fixed group effect, while in the second model the genotype was substituted by breed additive, heterotic and recombination effects fitted as fixed covariates. Both the F and J breed additive effects, measured as a deviation from the B breed were significant (p < 0.01) for all traits, except for BW of the J. The F and J additive contributions were 2774 ± 81 and 1473 ± 362 kg for LMY, 7.1 ± 0.2 and 4.8 ± 0.8 kg for DMY, 152 ± 7 and 146 ± 31 days for LL, 2345 ± 71 and 1238 ± 319 kg for AMY, 20.6 ± 0.9 and 18.9 ± 4.3 kg for AMYBW, and 140 ± 4 and ?21 ± 22 kg (p > 0.05) for BW. The heterotic contributions to the crossbred performance were also positive and significant (p < 0.01) for all traits. The F₁ heterosis expressed as a deviation from the mid‐parent values were 22 and 66% for LMY, 11 and 20% for DMY, 29 and 29% for LL, 21 and 64% for AMY, 42 and 42% for AMYBW, and 2% (p < 0.05) and 11% for BW for the F × B and J × B crosses, respectively. The recombination effect estimated for the F × B crosses was negative and significant for LMY (?526 ± 192 kg, p < 0.01), DMY (?3.0 ± 0.4 kg, p < 0.001), AMY (?349 ± 174 kg, p < 0.05) and BW (?68 ± 11 kg, p < 0.001). For the J × B crosses the recombination loss was significant and negative only for DMY (?2.2 ± 0.7 kg, p < 0.05) and BW (?33 ± 17 kg, p < 0.05). The direct heritabilities (h²) estimated for LMY, DMY, LL, AMY and AMYBW were 0.24 ± 0.04, 0.19 ± 0.03, 0.13 ± 0.03, 0.23 ± 0.04 and 0.17 ± 0.05, respectively. Based on the genetic parameters estimated, the best breeding strategy to increased milk production under highland Ethiopian conditions is to apply selection on purebred base populations (Boran and Friesian) and then crossing them to produce F₁ dairy cows. However, for breeding decision based on total dairy merit, further investigations are needed for traits such as milk quality, reproduction, longevity and survival.     

The spread of weeds into sensitive areas by seeds in horse faeces

The possible spread by horse faeces of plants that may become weeds in sensitive areas was investigated. It was found that the period 24-48 hours after ingestion of seeds included in rations was the retention time for seeds passing through the digestive system of the horse. The ability of seeds to germinate was not influenced by exposure to digestive fluids or sea-water. A feeding regime of compound feeds is suggested.     

Estimates of genetic parameters for Boran, Friesian and crosses of Friesian and Jersey with the Boran cattle in the tropical highlands of Ethiopia: reproduction traits

A study with the objectives of estimating breed differences, heterosis and recombination effects as well as heritabilities (h²) and repeatabilities (r²) for age at first calving (AFC), calving interval (CI), days open (DO) and number of services per conception (SPC) was conducted using reproduction records collected from 1496 cows comprising purebred Boran (B), Friesian (F), crosses of Friesian and Jersey (J) with Boran breeds. The crossbred cow groups included four F × B crosses [1/2F:1/2B(F₁), 1/2F:1/2B(F₂), 5/8F:3/8B and 3/4F:1/4B], three J × B crosses [1/2J:1/2B(F₁), 1/2J:1/2B(F₂) and 3/4J:1/4B] and one three‐breed cross (1/4F:1/4J:1/2B). The crossbreeding parameters were estimated using a repeatability animal model for CI, DO and SPC, and a unitrait animal model for AFC. The overall least‐squares means estimated were: 38.3 ± 0.26 months, 435 ± 4 days, 145 ± 10 days and 1.58 ± 0.03 (number) for AFC, CI, DO and SPC, respectively. The breed additive effects of F and J were only significant (p < 0.01) for AFC. Relative to B, both F and J additive contributions for AFC were ?5.4 ± 0.5 and ?5.5 ± 1.9 months, respectively. Crossing the B with F and J breeds also resulted in significant heterosis (p < 0.05) ranging from 10 to 21% in all traits. The estimated recombination loss was only significant for AFC (2.8 ± 1.0 months) for F × B crosses. Heritability estimates were high for AFC (0.44 ± 0.05) and low for CI (0.08 ± 0.03), DO (0.04 ± 0.03) and SPC (0.08 ± 0.02). The corresponding estimates for the repeatability (r²) were 0.14 ± 0.02 and 0.14 ± 0.02 for CI and DO, respectively. The permanent environmental effect for SPC was zero. These findings show that breed differences between F or J and B, and the individual cow variations are low for reproductive traits studied, except for AFC. Heterotic effects seem to be the major genetic causes for the improved reproductive performances in both the F × B and J × B crossbred cows.