ABSTRACT:The aim of the experiment was to examine the effect of group size and stocking density on productive, carcass and meat quality traits. The trial was conducted using 230 Pannon white rabbits weaned at 5 weeks and reared until the age of 11 weeks. Seven groups were formed with different cage/pen sizes (group size) and stocking densities: SC16=small cage (0.12 m 2 ), 16 rabbits/m 2 (2 rabbits/cage); LC16=large cage (0.50 m 2 ), 16 rabbits/m 2 (8 rabbits/cage); LC12=large cage, 12 rabbits/m 2 (6 rabbits/cage); SP16=small pen (0.86 m 2 ), 16 rabbits/m 2 (13 rabbits/ cage); SP12=small pen, 12 rabbits/m 2 (10 rabbits/cage); LP16=large pen (1.72 m 2 ), 16 rabbits/m 2 (26 rabbits/cage); LP12=large pen, 12 rabbits/m 2 (20 rabbits/cage). Stocking density did not affect production signifi cantly, as stocking densities lower than 16 rabbits/m 2 had no effect on the growing rabbits' performance. Group size (size of the cage or pen) had an effect on certain growth, carcass and meat quality traits. Increasing group size resulted in lower values for weight gain (SC: 39.2>LC: 39.0> SP: 38.7> LP: 37.8 g/d; P=0.22) and body weight (SC: 2506>LC: 2498> SP: 2487> LP: 2446 g; P=0.35), similarly to other results in the literature, but the differences were not signifi cant. Aggressive behaviour was observed to be more frequent in the larger group sizes. At the age of 11 weeks the proportion of rabbits with ear lesions in the SC, LC, SP and LP groups were 0.0, 7.1, 8.7, and 17.4%, respectively, demonstrating that larger group size increases the risk of ear lesions. The effect of group size on the ratio of the fore part to the reference carcass (SC: 28.5, LC: 28.2, LP: 29.0%; P=0.02) and on the amount of perirenal fat (SC: 21.3, LC: 18.0, LP: 13.7 g; P<0.001) was signifi cant. Meat quality traits (dry matter, protein, fat and ash content, drip loss, pH, L*, a*, b* values) were not affected by group size (cage vs. pen), but successful discriminations were performed using the NIRS method.
Blood serum clinical biochemical parameters of fasted BUT Big 8 male turkeys were determined at the ages of 3 days, 4, 8, 12, 16 and 20 weeks, for a follow-up of the developmental changes of some serum metabolites, enzymes and ions. The serum protein content (total protein, albumin, globulin) increased with age, indicating also the moulting-associated metabolic changes in the age interval from the 8th to the 12th weeks. Creatinine was shown to have a peak at 3 days of age (role of muscle activity in thermogenesis), while urate concentration sensitively reflected the dietary protein amount. Serum triglycerides peaked at the time of yolk catabolism, while cholesterol was shown to indicate the moulting, as was serum malondialdehyde. Serum sodium content increased throughout the study. Alanine aminotransferase and aspartate aminotransferase activities increased along the ontogeny, while alkaline phosphatase activity decreased in parallel with the growth. Serum creatine kinase activity showed an over one-magnitude increase. General metabolic and enzymatic alterations were characteristic and applicable for the description of the ontogenetic development of a precocial (posthatch triglyceride peak), large bodied, meat-type (lactate dehydrogenase, continuously increasing creatine kinase) bird species.
The digestibility coefficient and metabolizable energy (ME) content of the most important pigeon feeds (corn, wheat, barley, red and white millet, sorghum, canary seed, peas, lentils, sunflower, and hemp) were determined. The experiment was carried out using 10 adult male homing pigeons. All feeds were fed alone, in a whole-grain form, ad libitum. Drinking water and grit were offered to the birds on a continuous basis. Each feedstuff was fed to five pigeons in 1-wk cycles. There was no significant difference between the values determined in pigeons and those reported in the literature for chickens among the digestibilities of the CP of the various feeds. For pigeons, the digestibility of carbohydrates (N-free extracts, NFE) was lower (e.g., 62.37 vs 83.00% for barley and 63.45 vs 77.00% for peas), whereas the ether extract (EE) was higher (e.g., 75.58 vs 61.00% for barley and 82.59 vs 80.00% for peas) in pigeons compared with chickens. As a result, the AMEn values determined in pigeons did not differ significantly from those reported for chickens but tended to be slightly higher. For feeds of high-oil content, that difference may be somewhat larger. The correlation between the CP, EE, crude fiber (CF), and NFE contents of the feeds and the ME values determined in this experiment were calculated by multivariate linear regression. It was concluded that it was more accurate to determine and tabulate the ME contents of other potential pigeon feeds directly by experimental methods rather than using an equation.
In Hungary almost 70% of mould-affected maize inspected since 1993 was found to be contaminated with fumonisin B1 (FB1) (mean 2.6-8.65 mg/kg; maximum 9.8-75.1 mg/kg), the degree of this contamination was found to increase from year to year (Fazekas et al., 1997b). In this experiment, in order to define tolerance limit values, the effect of exposing weaned piglets to FB1 in low doses over a 4-week period was examined. The experiment was performed with 20 weaned barrows of Danish Landrace breed. After a 5-day adaptation period cultures of the fungus Fusarium moniliforme were mixed into the animals' feed in concentrations that resulted in a daily intake of fumonisin B1 of 0, 10, 20 and 40 mg/kg feed. Feeding with the toxin was observed to exert no significant effect on body weight gain or feed consumption in the animals, no clinical signs were observed and no mortality traceable to toxic effects occurred. In computer tomography examinations performed in the second and fourth weeks mild and more severe pulmonary oedema was diagnosed in the experimental animals. The processes developing in the pulmonary parenchyma were corroborated by the mathematical and statistical evaluation procedures applied. The haematological parameters examined revealed no change attributable to toxic effects, while with respect to the biochemical parameters, an increase in aspartate aminotransferase (AST) activity dependent on dosage, indicating a pathological change in the liver, was ascertained in all three experimental groups. The free sphinganine to sphingosine ratio (SA/SO), which is regarded as the most sensitive bioindicator of fumonisin toxicosis, showed an increase proportionate to toxin concentration for all three dosages. Dissection revealed mild cases of pulmonary oedema in three of the animals given doses of 10 p.p.m. (n = 4), two mild and two severe cases in those exposed to 20 p.p.m. (n = 5), and severe cases in all five animals given 40 p.p.m. The oedema of non-inflammatory origin was confirmed by histopathological examinations. The findings of this experiment which indicate that in this study FB1 administered in substantially lower concentrations than those reported in the literature resulted in severe pathological changes, point to the importance of studies involving even lower doses.
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