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Ruminal ammonia concentration and energy expenditure of cattle estimated by the carbon dioxide entry rate technique
- O. N. Di Marco, P. Castiñeiras, M. S. Aello
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- Journal:
- Animal Science / Volume 67 / Issue 3 / December 1998
- Published online by Cambridge University Press:
- 02 September 2010, pp. 435-443
- Print publication:
- December 1998
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Five ruminallyfistulatedAngus steers (360 (s.e. 15·4) kg) were givenfood to maintain body weight constant: maize silage (TO) at 0·6 kg dry matter (DM) per 100 kg body weight twice a day. After a 15-day adaptation period they were infused continuously (I) for 96 h, with a solution of NaH14CO3 at a rate of 7 to 8 micro Curies (μCi) per h. On the last 2 days of infusion 30 g (Tl) and 60 g (T2) urea, respectively, were placed in the rumen at the end of the morning meal. Spot samples of urine (250 ml) were taken before and 5 h after the morning meal and after at least 24 h of infusion. Thereafter, animals continued with TO for one additional week, in which they were prepared with catheters inserted in salivary ducts and infused for 48 h, as previously described. Eighteen pairs of spot samples of urine and saliva were takenfrom three of thefive steers (369 (s.e. 20·7) kg), over a period of 5 h, after at least 24 h infusion (six per animal). Rate of carbon dioxide (CO2) production was estimated as the ratio USA (specific activity of CO2)from which energy expenditure was calculated (22 kj/l CO2). Silage composition, in situ degradability and ruminal ammonia and pH were measured. In situ degradability in thefirst 6 h was 200 g/kg and ruminal ammonia was in the range of 20·6 to 39·6 mg/l. Ammonia increased rapidly to 394·2 (T1) and 673·9 mg/l (T2) 1 h after addition of urea into the rumen but in 6 h in situ degradability was unchanged. Ruminal ammonia decreased linearly at rates (mgll per h) of89·3 in Tl (R2 = 0·57, s.d. = 21·5) and 151·6 in T2 (R2 = 0·81, s.d. = 23·3). Animal energy expenditure rates were not affected (P > 0·05) by treatment (TO = 15·6, Tl = 15·6 and T2 = 15·8 kj/h per M075). There was no difference (P > 0·05) in CO2 production rate (mllh per kg M0·75) determined from the SA of CO2 from urine (604) or saliva (630) samples. It was concluded that the energy cost associated with detoxification of the excess of ruminal ammonia was of minor importance in terms of total animal energy expenditure and that estimations ofC02 ratesfromsamples ofurine or saliva are comparable.
Energy expenditure of cattle grazing on pastures of low and high availability
- O. N. di Marco, M. S. Aello, D. G. Méndez
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- Journal:
- Animal Science / Volume 63 / Issue 1 / August 1996
- Published online by Cambridge University Press:
- 02 September 2010, pp. 45-50
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- August 1996
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The energy expenditure of freely grazing cattle was investigated in the National Institute of Agricultural Technology and Agricultural Science College of Balcarce, Argentina (37° 45'S, 58° 18'W), by the CO2 entry rate technique. Two experiments were carried out in the autumn in March 1994 (experiment 1) and in April 1995 (experiment 2) with animals prepared with catheters in the parotid gland (collection of saliva) and into the peritonea for infusion of a solution of 14C. Six Angus steers (259 (s.e. 11) kg) were used in experiment 1 and seven (298 (s.e. 36) kg) in experiment 2. In experiment 1 animals grazed ryegrass pastures for 5·5 h in two periods of 1·5 h in the morning and of 4 h in the afternoon and in experiment 2 animals grazed oat pasture in one period of 1 h in the morning. Twenty hours before and during the experiments a solution ofNaH14CO3 was infused at a rate of 9·4 (experiment 1) and 8·1 (experiment 2) μiCi/h for 48 h with portable peristaltic pumps carried by each animal. Saliva samples were collected at least after the first 20 h of infusion. The first sample was collected in the corral just before grazing and two samples were collected in each grazing period. Also, in experiment 1 three samples were taken during resting (noon, 1 h after grazing and the next morning). In addition, bite frequency, pasture availability, plant height, in vitro digestibility and crude protein were measured. Carbon dioxide production was calculated as the ratio between the rate of infusion of 14C (μCi/h) and the specific activity of CO2 (μCi/l CO2) in saliva samples. Bite frequency was 59 and 28 bites per min on the respective pasture of ryegrass (148 g dry matter (DM) per m2 and 10·5 cm height) and oat (228 g DM per m2 and 27 cm height). Energy expenditure (EE, kJ/h per kg M0·75) in corrals was 14·9 (experiment 1) and 14·3 (experiment 2), increasing to 22·6 (proportionately 0·52) when grazing at 59 bites per min and to 16·6 (0·16) when grazing was at 28 bites per min. One hour after grazing at 59 bites per min (experiment 1) the EE was as high as during grazing, and in the next morning (after 5·5 h) of grazing remained at 19·7 kJ/h per kg M0·75 (0·32). No differences in energy expenditure were found between periods of grazing in experiment 1. It was concluded that the increase in energy expenditure of cattle due to the activity of grazing depends on the rate of biting. Grazing for 10 h at a moderate rate may boost EE proportionately by only 0·06, however grazing at the highest rates could easily add proportionately 0·20.
Energy expenditure of cattle walking on a flat terrain
- D. G. Méndez, O. N. di Marco, P. M. Corva
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- Journal:
- Animal Science / Volume 63 / Issue 1 / August 1996
- Published online by Cambridge University Press:
- 02 September 2010, pp. 39-44
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- August 1996
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A study was carried out to evaluate the effect of horizontal walking upon CO2 production rate by the carbon dioxide dilution rate technique. This was used as an indicator of animal energy expenditure. Two groups of three 18-month-old Aberdeen-Angus steers were assigned to two experiments. Average weights were 290 (s.e. 7·6) kg and 285 (s.e. 1·0) kg for experiments 1 and 2 respectively. Animals were allocated to individual pens and given 5·0 and 4·5 kg dry matter of a mixed diet for experiments 1 and 2 respectively. After a 45-day training period they were assigned to three walking treatments: 0 (T0), 3 (T3) and 6 (T2) km at 3 km/hfor 3 days in a Latin square design (3 × 3). 14C labelled sodium bicarbonate (5·4 μCi/h), diluted in carbonate-bicarbonate buffer sterile solution 0·1 mol/l, was infused for 92 h intraperitoneally with portable peristaltic pumps carried by the animals. The CO2 production rate was calculated as the ratio between the rate of infusion (μCi/h) and the specific activity of CO2 (μCi/ml CO2) in saliva samples, which were taken, in experiment 1, as an average of the day (09.00 to 16.00 h) and the night (16.00 to 09.00 h of the following day). In experiment 2 the day was divided as follows: prior to activity (09.00 to 13.00 h), activity (14.00 and 15.00 h) and post activity (16.00 h). CO2 production rate (ml CO2 per h per kg M0·75) at resting was 817 (412 kj/kg M0·75), increasing during walking to 1·46 of the resting level (T1 and T2, experiment 2) with no differences between the 1st and 2nd h of activity. One hour post activity, the CO2 production rate returned in T2 to the level of T0 but in T2 remained at 1·28 times that of T0. The average CO2 production rate during a complete day or night (experiment 1) was not affected significantly by the activity. Assuming that CO2 production rate during walking is 1·46 of resting (experiment 2) and remains at that level even at lower speeds, it can be estimated that a daily 6 km walk would increase resting energy expenditure from 1·04 when walking takes 2 h, as in this experiment (3 km/h), to 1·11 when the animal spends 6h(1 km/h).