1978
DOI: 10.1080/00071667808416448
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Effects of regular handling and blood sampling by wing vein puncture on the performance of broilers and pullets

Abstract: 1. Broilers and pullets were regularly handled or bled by wing vein puncture over periods of 5 and 31 weeks respectively. 2. Neither procedure had any effect on body weight, food consumption nor on egg production, egg weight, shell quality or the percentage of non-marketable eggs.

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Cited by 20 publications
(8 citation statements)
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References 3 publications
(5 reference statements)
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“…of the pullets are associated with such experiments. Some effects of handling, with and without blood sampling, on growth have been reported by McPherson et al (1961), Reichmann et al (1978), and Gross and Siegel (1979). In preliminary studies, Zaalmink (1979) measured metabolic rate in pullets 3 to 5 days after immunization; however, the immediate response of injection or immunization on metabolic rate was not measured.…”
Section: Introductionmentioning
confidence: 95%
“…of the pullets are associated with such experiments. Some effects of handling, with and without blood sampling, on growth have been reported by McPherson et al (1961), Reichmann et al (1978), and Gross and Siegel (1979). In preliminary studies, Zaalmink (1979) measured metabolic rate in pullets 3 to 5 days after immunization; however, the immediate response of injection or immunization on metabolic rate was not measured.…”
Section: Introductionmentioning
confidence: 95%
“…The enhanced disease resistance and immune response in those studies could be associated with the stress modulating effect of human contact. However, others demonstrated that positive tactile interaction either had negligible [47] or negative effect [48] on growth performance. Nature of the physical contact, breed and age differences may have accounted for the discrepancies.…”
Section: Introductionmentioning
confidence: 99%
“…A total of 370 serum samples were collected via venipuncture of the wing vein from the farms under study ( Supplementary Table). Sera were separated as previously described [30]. The collected sera were heat inactivated at 56°C for 30 min then stored at -20°C.…”
Section: Serum Samplesmentioning
confidence: 99%