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Department of Animal Health, Welfare and Nutrition, Danish Institute of Agricultural Sciences, Research Centre Foulum, 8830 Tjele, Denmark
1 Corresponding author: MargitBak.Jensen{at}agrsci.dk
| ABSTRACT |
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Key Words: calf cross-sucking group size milk feeding method
| INTRODUCTION |
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When calves are housed in groups they compete for the milk. Competition is increased among teat-fed calves when access to teats is reduced, but the calves compete even when there is one teat per calf (Keyserlingk et al., 2004). Calves take longer to ingest milk via a teat than to drink it from the open surface in a bucket (Jung and Lidfors, 2001), and the rate of ingestion may be reduced considerably when teat feeding is used (Haley et al., 1998a). Furthermore, teat-fed calves tend to suck on the empty teat after milk ingestion. However, it is unknown if the slower rate of ingestion and the tendency to suck the empty teat after milk ingesting will reduce competition for milk in teat-fed calves compared with bucket-fed calves. Therefore, the second objective of the present study was to investigate if teat feeding reduces competition for milk in group-housed calves.
| MATERIALS AND METHODS |
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Calves were assigned to blocks according to date of birth; within blocks, the calves were allocated to milk feeding method (bucket or teat) balanced for date of birth and sex. Before the calves of a block were moved to the experimental pens they were assigned to either pair housing or group housing balanced for milk feeding method and age. Thus, the treatments were 1) pair housing and bucket feeding; 2) pair housing and teat feeding; 3) group housing and bucket feeding; and 4) group housing and teat feeding. When the calves were moved to the experimental pens and the experimental period began, the calves were on average 17 (±7) d old and weighed 54 (±6.3) kg. The experimental period lasted for 6 wk and at the end of the experimental period the calves weighed 92 (±13) kg. One teat-fed calf from a group of 6 calves was removed from the pen due to arthritis, and data for this calf were not included in the analyses.
The experimental pens for pair-housed calves measured 1.94 m x 2.15 m (2.1 m2/calf) and the experimental pens for calves in groups of 6 calves measured 2.49 m x 4.15 m (1.7 m2/calf).
For bucket feeding, open steel buckets were used. For teat feeding of pair-housed calves, plastic buckets fitted with one teat (Peach Teat, Skellerup Industries, Ltd., Christchurch, New Zealand) were used. In both cases there was one bucket per calf. For teat feeding of group-housed calves, so-called teat bars (Power Feeder for 6 calves, Skellerup Industries, Ltd.) were used. The teat bars were compartmented and each compartment had one teat.
When the calves were offered the milk it was ensured that all calves in a pair or a group had access to the milk simultaneously. For pair-housed calves, 3 L of milk was poured into each of the 2 buckets simultaneously. For bucket-fed calves in groups of 6, a cover made from wire mesh was placed over the 6 buckets while 3 L of milk was poured into each of them. Once all the milk had been poured, this cover was removed and all calves in a group could start drinking simultaneously. For teat-fed calves in groups of 6, the 18 L of milk was poured so that the 6 compartments of the feeder were filled at the same time and it was ensured that all calves accessed a teat immediately after the milk was poured. For all treatments the buckets or feeders were placed in the pens just before the milk was poured and they were not removed until 30 min after.
The behavior of the calves was recorded at milk feeding in the morning by direct observations using instantaneous recording at 45-s intervals (blocks 1, 2, and 3; observer 1), or 60-s intervals (blocks 4, 5, and 6; observer 2). The recordings of calves in a group began the minute the calves in the group had access to the milk and continued for 30 min. The behaviors recorded are defined in Table 1
. The calves in each block were observed by direct observations once during wk 2, 4, and 6 of the experiment.
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Calves were weighed twice on 1 d in wk 4 of experiment to get an estimate of the milk intake of individual calves within the groups. All calves within each group were weighed immediately before and immediately after milk feeding of the calves in that group.
The behavioral data collected by direct observations were analyzed as follows. The continuous behavioral variables (ingesting milk, sucking empty bucket or teat, cross-sucking head or neck, licking fixtures, self-grooming, inactive, and other activity) were analyzed using a mixed model including the fixed effects of feeding method (bucket or teat), group size (2 or 6), feeding method x group size and week of experiment. As random effects the model included block x feeding method x group size (equal to pen) and block x feeding method x group size x week, and the covariance structure of repeated measures on the same calf was modeled as compound symmetric. The behavioral variables, which included many zero observations (cross-sucking under belly, licking calf, bunting calf, and bunting bucket or teat) were transformed into binary variables and analyzed by
2 test, or Fishers exact test (Siegel and Castellan, 1988), for each observation week.
From the behavioral data collected from the videotapes, the number of switches between buckets or teats was calculated for each calf. First, the number of switches from a bucket or a teat that still contained milk to another bucket or teat was calculated. Second, the number of switches from a bucket or teat to another while at least one bucket or teat in the pen still contained milk, was calculated. These variables included many zero observations and were therefore transformed into binary variables and analyzed by
2 test.
An estimate of milk intake was calculated as the difference between the weight before and the weight after milk feeding. Within each group the difference between the minimum and maximum weight increase was calculated. This difference, which indicate the difference between the highest and the lowest milk intake within each group, was subjected to analysis using a mixed model including the fixed effects of feeding method (bucket or teat), group size (2 or 6), and feeding method x group size, while block was included as a random effect.
| RESULTS |
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The time spent sucking the empty bucket or teat decreased over the weeks of the experiment [2.06 (±0.33), 1.86 (±0.31), and 1.41 (±0.27) min/feeding for wk 2, 4, and 6, respectively; F2, 45 = 4.31; P < 0.05].
Teat-fed calves changed to another teat more often than bucket-fed calves changed to another bucket while there was still milk available in the teat or bucket that they left, and while there was still milk available in at least one teat or bucket in the pen (Table 5
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| DISCUSSION |
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Teat-fed calves switched between the teats. More switching was seen between the teats than switching between the buckets, both while there was milk available in the teat or bucket that the calf left, and while there was still milk available in at least one teat or bucket in the pen. To push and butt (Haley et al., 1998a,b) and to change to another teat (de Passillé and Gaboury, 2000) are natural responses to low milk flow rate from a teat, and a stop in milk flow. The function of this behavior is to maintain a desired (high) speed of milk ingestion. However, this natural response may cause fast-drinking calves to change to a neighboring teat and thus to steal milk from slower drinking calves. Calves started the teat switching while there was still milk in the teat they were on. It may have been difficult to get the last milk out through the teat and the resulting lower flow might explain why teat-fed calves switched more than bucket-fed calves while milk was still available. However, it cannot be ruled out that the calves were able to assess that there would be a fair chance of getting sole access to a larger quantity of milk the sooner they switched to another teat. When bucket-fed calves switched they were rarely able to get sole access to the milk in the bucket to which they switched. The higher frequency of switching while there was still milk in at least one of the teats in the pen may be explained by uncertainty of where the remaining milk was. To maximize milk intake the calf should switch to one of the other teats as soon as the teat that the calf is on is empty. One explanation for less switching among bucket-fed calves could be that the calves could see which buckets were empty. Chua et al. (2002) found a low frequency of teat displacements in pair-housed calves fed ad libitum and the teat switching may be a problem only if low milk allowances are used and calves are still hungry when they have ingested their own milk ration. Competition for milk clearly depends on milk allowance. Holstein-Friesian calves with ad libitum access to milk consume approximately 9 L/d of milk (Jasper and Weary, 2002), which is 50% more than the amount offered in the present experiment.
Bucket-fed calves were more often observed licking the fixtures of the pen and more bucket-fed calves were observed performing social grooming compared with teat-fed calves. More oral activity directed toward fixtures of bucket-fed compared with teat-fed calves have been reported earlier (Veissier et al., 2002), and the more social grooming is possibly a side effect of the more cross-sucking of bucket-fed calves.
The results suggest that competition for milk was higher among calves in groups compared with calves in pairs. First, the rate of ingesting milk was higher in group-housed calves than in pair-housed calves. Second, calves in groups changed more often to another teat or bucket than calves in pairs while there was still milk available in at least one teat or bucket in the pen. A higher rate of ingestion, which may be taken as indicative of social constraint (Nielsen, 1999), has also been found in group-housed compared with individually housed calves when the milk was offered in a trough (Babu et al., 2004). Also, among calves fed from a computer-controlled milk feeder (in which the calves could not steal milk from each other but competed for access to the feeder), the rate of ingestion was higher in groups of 24 compared with groups of 12 (Jensen, 2004). The finding that the difference between minimum and maximum milk intake was larger in group-housed than in pair-housed calves has to be interpreted with caution, because range may increase with sample size. It was hypothesized that the teat feeding would reduce competition for milk among the group-housed calves in the present study. However, this was not found. The competition for milk in group-housed calves is intensified on low milk allowances. Therefore, when milk is fed restrictively it is essential that milk stealing is limited to ensure minimal variation in milk intake within the group. Future studies should focus on improving milk feeding methods for group-housed calves so that competition, as well as variation in milk intake, within groups of calves is minimized.
| ACKNOWLEDGEMENTS |
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Received for publication March 17, 2006. Accepted for publication June 29, 2006.
| REFERENCES |
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This article has been cited by other articles:
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M. B. Jensen, A. M. de Passille, M. A. G. von Keyserlingk, and J. Rushen A Barrier Can Reduce Competition over Teats in Pair-Housed Milk-Fed Calves J Dairy Sci, April 1, 2008; 91(4): 1607 - 1613. [Abstract] [Full Text] [PDF] |
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