Utilizing the accuracy of estimated breeding values to improve selection response

SUMMARY: Stochastic simulation was used to evaluate the increase in selection response by incorporating accuracies of estimated breeding values (ebvs) in an index to form indexed breeding values (ibvs). Simulations were made using a standard population with a selected proportion of 5%, with 10 000 selection candidates and an average accuracy of breeding value determination, r? = 0.4 with variance, σ(r) (2) = 0.075(2) . In the standard population, candidates selected on ibvs showed an 8.4 % increase in average true breeding values (tbvs) compared to selection using ebvs. Using the same standard population, but changing the proportion selected to 1.0 % and 10 %, the relative increase in the average tbvs from ibv selection was 13.5 % and 5.5 % respectively. Similarly, changing r? to 0.22, 0.32 and 0.55, the relative increase from ibv selection was 48 %, 19 % and 1.3 % respectively. As σ(r) was changed to 0.025 and 0.125, the relative increase from ibv selection was 0.6 % and 24 % respectively. In general, the average accuracy in candidates chosen for selection using ibvs was lower than that from selection using ebvs. In the standard population the accuracy was 0.38 from ibv selection and 0.43 from ebv selection. As a result the increase in inbreeding will be lower with ibv than with ebv selection. ZUSAMMENFASSUNG: Verwendung von Genauigkeiten gesch?tzter Zuchtwerte zur Verbesserung des Selektionserfolges Durch stochastische Simulation wurde Steigerung des Selektionserfolges durch Einschlu? von Genauigkeiten gesch?tzter Zuchtwerte (ebvs) in einen Index indizierter Zuchtwerte (ibvs) untersucht. Simulationen wurden mit einer Standardpopulation 5% selektierter von 10 000 Kandidaten und einer durchschnittlichen Genauigkeit der Zuchtwertsch?tzung r = 0.4; σ(r) (2) = 0.075(2) durchgeführt. In der Standardpopulation hatten Kandidaten, mit ibvs selektiert, eine Steigerung des durchschnittlichen wahren Zuchtwertes (tbvs) von 8.4 % verglichen mit Selektion auf ebvs-Basis. Bei Verwendung derselben Standardpopulation, aber Remontierung von 1 % bzw. 10 %, war der relative Zuwachs im durchschnittlichen tbvs bei ibvs-Selektion 13.5 und 5.5%. Die relative Zunahme von der ibvs-Selektion, mit r von 0.22, 0.32 oder 0.55, war 48 %, 19 % und 1.3 %. Bei Ver?nderungen von σ(r) auf 0.25 und 0.125 betrug die relative Zunahme 0.6 und 24 %. Im allgemeinen waren die durchschnittlichen Genauigkeiten bei Selektionskandidaten auf der Basis von ibvs geringer als bei Verwendung von ebvs. In der Standardpopulation waren diese Genauigkeiten 0.38 bei ibvs und 0.43 bei ebvs. Daher sollte die Zunahme der Inzucht mit ibvs geringer sein als mit ebvs.     

Associations between body weight and rectal temperature in turkey poults

1. Associations between body weight and rectal temperature were observed in female turkeys.

2. Turkeys with lower weights between 13 and 30 d of age tended to have higher temperatures.

3. Turkeys with lower weights at 7 d exhibited depressed body temperatures.

4. Higher or lower body temperatures may be associated with poorer performance depending on the time of appearance.     

Changes in liveweight and behaviour of alpaca dams and offspring following weaning

The effects of offspring sex, weight, age, and level of interaction with the dam on responses to weaning were examined to assist in the development of a weaning protocol for alpacas. In the first study, preand post-weaning activities, and weight change over Days -12-0,0-7 and 7-16 with respect to weaning, were recorded for 20 dam-offspring (hembra-cria) pairs aged 81-200 days. Pre-weaning changes in dam and offspring weights were positively related (P<0.05). Although heavier crias tended to be found closer to their dams than lighter crias (P<0.05) no additional effect of age on the dam-offspring relationship was found. Following weaning, cria growth rates were low over Days 0-7 but improved over Days 7-16, and hembra weight change followed the same pattern. Over Days 0-2, grazing and sitting activities of hembras and crias were replaced by standing and walking along paddock fencelines, although by Day 2 fenceline activities had decreased (P<0.05). Crias which were more frequently observed at fencelines had lower post-weaning growth rates (P<0.05). In the second study, pre-weaning sucking behaviour, and weight change over Days -30-0, 0-8 and 8-16 with respect to weaning, were recorded for 19 hembra-cria pairs aged 124-160 days. During 10 hours of observation on Days -5 and -4, the total duration of sucking by individual crias varied from 0-18 minutes, and the mean +/- SEM duration of sucking was 1.94 +/- 0.113 minutes. Cria sucking behaviour was positively related to growth rate prior to and weight at weaning (P<0.05). As in the first study, pre-weaning changes in dam and offspring weights were positively related (P<0.05). Following weaning, growth rates of the crias were depressed and the hembras lost weight over Days 0-8 and 8-16. The changes in growth rate and behaviour in Studies 1 and 2 indicated that weaning can be stressful for hembras and crias. However, there was no evidence from either study that pre-weaning behavioural or physical characteristics were related to the changes.     

Malignant catarrhal fever in a swamp buffalo (Bubalus bubalis) calf in New Zealand

Malignant catarrhal fever was diagnosed in a newly imported swamp buffalo calf. This disease is prevalent in deer and cattle in New Zealand and causes sporadic losses in these species. The disease is recognised as a problem in buffaloes overseas and this paper records the first case in a swamp buffalo in New Zealand.