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South Dakota State University, Brookings 57007
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Key Words: Cattle Feed Intake Feedlots Management
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The simplistic title of this manuscript is fraught with ambiguities. Intake variation can be an issue on a pen basis or on an individual basis. It is unclear to what extent, and in what ways the two are related. The link in a cause and effect relationship to inefficiency, morbidity, or mortality exists only in extreme instances. Finally, in a feedlot setting, we are inclined to refer to feed delivered as feed intake without providing evidence that all feed offered was consumed on that day.
The overwhelming consideration of bunk management is control of clinical and subclinical metabolic disorders. In spite of our improved capabilities to weigh and mix properly proportioned diets, grain overloads do occur. Digestive disorders are a leading cause of death in feedlot cattle (USDA, 2000
). Subclinical and clinical acidosis reduce gain efficiency, cause liver abscesses, and ruminitis (Owens et al., 1996
). The question at hand is whether bunk management can reduce variability in feed intake and ameliorate these maladies. To evaluate this, we will break down bunk management into component parts and examine their influence on cattle performance.
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The second and third points in this chapter were in turn quoted from Mumfords Beef Production (1907)
. "As soon as the fattening process begins, the cattle should be fed at certain hours and in the same way. This cannot be varied 15 minutes without some detriment to the cattle. The extent of injury will depend upon the frequency and extent of irregularity...." We interpret this to mean that beef cattle, like dairy cows, are creatures of habit. If behavior can be modified favorably by cultivating and respecting good habits, the potential exists to improve performance. Hungate (1966)
likened the rumen to a continuous culture fermentor and discussed in detail how diet, eating, rumination, and digestive tract function coordinate to achieve this steady-state condition. The consistent management steps advocated by Mumford may complement this expectation.
The final point, again attributed to Mumford (1907)
, is that "Scouring, the bane of the stockfeeder, should be carefully avoided since a single days laxness may cut off a weeks gain. The trouble is generally brought on by overfeeding, by unwholesome feed, or by a faulty ration. Overfeeding comes from a desire of the attendant to push cattle to better gains or from carelessness or irregularity in measuring out the feed supply. The ideal stockman has a quick discernment... which guides the hand in dealing out feed ample for the wants of all but not a pound in excess." Here Mumford has described weaknesses in human nature that persist as a critical element of bunk management today. It also seems that Mumford advocated a clean bunk feeding strategy, where no feed should be carried over from one feeding to the next.
Feeding vs. Eating
A dichotomy exists between the motivation behind the cattle feeders bunk management decisions and motivation of cattle to eat. Feedlot management has to be concerned with the capability to manufacture and deliver sufficient quantities of feed in a timely fashion. Bunk volume allocation per animal may be limited. Combined, these constraints may force management to plan two to four feed deliveries per pen, per day. Inherent in multiple feedings are the advantages that feed delivery errors or weather interruptions are reduced to some degree for each multiple of feed deliveries per day.
Cattle eating behavior is driven by a loss of the satiety signals that suppress hunger. Cattle consume most feed near sunrise and especially around sunset (Stricklin and Kautz-Scanavy, 1984
). Short winter days in northern latitudes promote more nighttime eating, and high effective ambient temperatures can reduce mid-day and daily DMI (Hahn, 1999
). When observing eating behavior by adapted cattle in a commercial feedlot, Hicks et al. (1989)
reported that 7.5 to 20% of cattle might not be observed eating in a 24-h period. It is unclear whether this was caused by digestive disorder or is an inherent eating behavior trait. Cattle not observed to be eating were not identified as morbid.
Hickman et al. (2002)
noted fluctuations in day-to-day DMI with a new system for monitoring feed intake by individuals in a group-fed environment. The feed intake pattern variability was not compressed in faster-growing or more efficient steers. They did not report any episodes of inappetence in that research. Day-to-day fluctuations in DMI are not surprising when considering that the short term feed intake regulation mechanism in cattle was evolved to support relatively high roughage diets. This research does cloud the issue of how/when aberrations in DMI can lead to clinical or subclinical acidosis.
Cattle eating behavior is also driven by nonbiological signals. Like Pavlovs dogs, cattle may learn to come to the feed truck. They acquire aversions to feeds (Provenza, 1996
), and they respond to changes in the weather. These intuitive and learned responses may interact with signals provided by bunk management in favorable or unfavorable ways. Ample feed, available on a consistent schedule may indeed reduce aggression at feeding time, and that may improve production. Unfortunately, data are limited on this subject.
Feed Delivery Management Approaches
Limit-fed high-concentrate diets involve a substantial restriction of feed allocation relative to expected DMI. Cattle performance can be predictable. When bias occurs, it is likely that cattle are more efficient than modeled predictions (Loerch and Fluharty, 1998
). When cattle are fed at 75 to 80% of expected DMI, prehension is rapid, and cattle do not sort through feed. Amounts fed are constant from day to day, and this system would accommodate a consistent feed delivery schedule.
Programmed or restricted feeding systems involve lesser restrictions of feed deliveries, perhaps at 5 to 10% less than expected DMI. As in limit feeding, cattle can be expected to remove all feed from bunks relatively quickly, leaving bunks empty much of the day. Growth rate is predictable and gain efficiency is sometimes improved over full-fed cattle (Plegge, 1986
). Feeding at this level likely meets the criteria of ample feed for all, but with no excess. This method eliminates the human factor of the inclination to overfeed the cattle. When improved gain efficiency is observed, it is not possible to discern whether it is brought about by affecting digestibility of the diet, ruminal methane production, or reduced variability in feed deliveries (Zinn, 1995
).
Clean-bunk management systems attempt to allow cattle to achieve long-term average DMI that will meet or exceed that of cattle fed ad libitum. The caveat that distinguishes clean bunk from ad libitum management is that in clean-bunk systems, it is expected that the bunks will contain no carryover feed at a specified time each day. This approach, with its many possible variations, has become a common practice in the major cattle feeding regions of the United States. This system, however, is susceptible to errors of judgment regarding feeding quantities. It may be more susceptible to time variations. By virtue of the high intake level, the effects of errors in quality or quantity of feed delivered may be more acute.
True ad libitum feeding can be achieved using feed bunks or self-feeders. The intent is to allow unrestricted access to feed at all times. Self-feeders cannot accommodate high-moisture feeds and usually can accommodate only low levels of small-particle-size roughages. Feeding schedules and variable feed deliveries presumably are not components of these systems. The animal has absolute control of daily feed consumption. It has not been proven that ad libitum access to high-grain diets results in higher DMI than that which occurs with clean-bunk management systems.
We can evaluate the bunk management systems for their application with the constraints set forth earlier. Limit feeding and restricted/programmed feeding allow management to be consistent in quantities of feed delivered and to not overfeed cattle. The cyclic feed delivery patterns described by Fulton et al. (1979)
are avoided. Finite feed deliveries and competition for this feed among contemporaries dictates the upper limits of daily DMI by individuals. There is a compressed window of feed availability. Sorting is not likely under these conditions. Excess feed is not available to allow binge eating, if indeed this is the root of acidosis problems in feedlot cattle. Variability in DMI must occur at less than a critical level since growth rates are predictable and gain is efficient (Sip and Pritchard, 1991
; Loerch and Fluharty, 1998
). Furthermore, the literature does not make reference to an inordinate frequency of digestive disorders associated with these prescriptive feeding programs. By definition, restricted feeding has a bias that may not allow cattle to demonstrate maximal growth rates. Restricted feeding may cause reductions in carcass quality (Pritchard, 1995
). By virtue of their systematic approach, these programs may cultivate favorable learned eating responses in cattle.
Ad libitum feeding provides feeds in excess. As a consequence, binge feeding cannot be curbed. In dairy systems that allow continuous access to feed, feed tossing is a common problem (Albright, 1993
). This behavior is also observed in feedlots and strongly suggests that sorting is a concern since feed tossing causes diet separation. Atwood et al. (2001)
showed that cattle vary in their feed preferences and that an individuals preferences may change over time. Selective eating could alter diets of individuals doing the sorting/selection, as well as those left with access to their refusals. The potential for sorted diets to affect gain efficiency is obvious when considering the large disparity of nutrients and energy density of individual ingredients included in a diet.
The short-term intake regulation mechanisms employed by cattle are not conducive to concentrate feeding (Preston, 1995a
). The mechanism by which cattle learn to regulate grain intake on low/no roughage diets provided in self-feeders is unclear. A better understanding of this situation may aid other types of feed-delivery management. These self-fed cattle may indeed learn to reduce intake or meal sizes to avoid the discomfort of indigestion. Alternatively, they may develop an aversion to the diet. In spite of this aversion, hunger is a force strong enough to cause them to eat. Having no substitute feeds available, intake may reflect the balance of hunger and aversion. Perhaps it is a combination of these concepts that allows cattle to avoid a lethal meal size.
Fluctuating Feed Deliveries
We had occasion to feed a common set of steers either ad libitum or in a clean bunk system. Feed deliveries for a 56 d period for two representative pens are depicted in Figure 1
. These two feeding programs ran concurrently, but were managed by different individuals in separate facilities. In such a comparison, the gambit of factors contributing to bunk management occur (timing, batching, etc.) and there could be facility influences on performance. For the pooled replicates of pens (n = 5), there was no effect on DMI (9.18 vs. 8.95 kg; P > 0.10), but ADG was reduced (0.94 vs. 1.71 kg; P < 0.05) and feed:gain ratio was increased (9.58 vs. 5.35; P < 0.05) by ad libitum feeding. It should be noted that DMI in this study was DM delivered to the pens. Feed wastage becomes a part of the problem of lost efficiency in these data, just as it occurs in commercial feeding operations.
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In a similarly designed experiment, Zinn (1994)
found no difference in cattle performance attributable to fluctuating deliveries. Holstein steers were on feed for 138 d and controls were program-fed to gain 1.1 kg/d. The lack of an effect of daily 20% feed fluctuations may have been because the extended time on feed could dilute out early effects (interim data were not reported). Also, the control cattle were fed to achieve a relatively low growth rate. Applying fluctuations at this level of production may not have constituted a metabolic challenge to the rumen or to the steers.
Cooper et al. (1998)
applied feed delivery fluctuations of ± 0.91 kg daily from control steers. Unlike the two previous examples of restricted feed deliveries, control steers in these two experiments were provided feed to appetite. During the initial 140-d trial, fluctuating deliveries caused a 1.7% increase in DMI (P < 0.05), with no influence on other production variables. In the second similar experiment lasting 147 d, performance was not influenced by feed deliveries.
The feed-delivery patterns depicted in graphs included by Cooper et al. (1998)
bring to light how we look at variation. In those trials, the feed deliveries for the control cattle appeared to deviate as much as 20% above and below the overall mean daily DMI. The patterns for the controls may be typical, but we have yet to establish whether those deviations constitute variability that affects performance. If the typical fluctuations for controls represent sufficient variability to affect performance, the deviations imposed from the control may not cause further compromises of production efficiencies. This may be especially true in that the imposed deviations are consistent and symmetrical, unlike a cyclic intake pattern.
Bierman and Pritchard (1996)
attempted to answer part of that question by allowing control treatment feed deliveries to fluctuate as we fed cattle to appetite. The managed treatment was intended to allow cattle to achieve expected maximal feed intake, but to not allow periods of higher than expected DMI. Variation in feed deliveries to control pens (Figure 2
) was quite similar to that depicted in the first trial of Cooper et al. (1998)
. Feed delivery highs and lows were eliminated in the managed bunk treatment (Figure 2
), but it appears that restricted feeding may have been imposed. Intake was reduced 12% (P < 0.01) by the managed bunk approach (Table 1
) even though there was carryover feed present in the bunks at 0700 on 40% of the pen days. Feed carryover occurred in 69% of the pen days for cattle fed to appetite. Growth rate was not affected by bunk management. However, ADG became more variable before d 30 (P < 0.05) and after d 85 (P < 0.10) when steers were fed to appetite. Feed efficiency and marbling scores tended (P < 0.10) to be improved by the more restrictive bunk management. Gain efficiency was numerically higher early and late in the feeding period (Figure 3
), which corresponds with periods of heterogeneity of ADG between treatments. The variable ADG was caused by a disproportionate increase in steers with very low ADG (<0.5 kg) when fed to appetite. This may reflect individuals experiencing acidosis and would be consistent with responses observed for gain:feed and marbling.
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If the advantages of restricted or programmed feeding are that they prevent unacceptably high feed intakes, there may be a simpler approach. Preston (1995b)
described the use of maximal intake limits on cattle during step-up and finishing phases. The principle would accommodate most classes of cattle and diets in that limits are set as multiples of maintenance energy intake. Feed deliveries are allowed to deviate as needed for the circumstances at hand, but overfeeding is avoided by the limits. The limits proposed were 2.1, 2.3, and 2.5 times maintenance DMI for step-up and 2.7 times maintenance DMI for finishing. We have calculated the 2.7 times maintenance value for the latter periods of the experiment reported by Bierman and Pritchard (1996)
and imposed those levels on the daily feed delivery graph (Figure 4
). Managed deliveries were coincidentally similar to the 2.7 times maintenance threshold. In contrast, when cattle were fed to appetite, feed deliveries frequently spiked well above the maximal intake limit, but did not increase ADG.
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Hanke et al. (1981)
saw no advantage to multiple daily feed deliveries. We (Pritchard and Knutsen, 1995
) have observed that in some, but not all, instances, feeding twice daily results in better gain efficiency than feeding once daily in the morning. The reason behind the inconsistent response is unclear. As mentioned previously, multiple feedings may reduce the magnitude of feeding errors, and the opportunity for binge feeding may be reduced as well.
It may be that multiple feeding may better accommodate the inherent variability in an individual steers access to feed or the accuracy of its short-term intake regulation. Soto-Navarro et al. (2000)
studied the influence of once vs. twice daily feeding, with or without imposed fluctuations in feed delivery on ruminal conditions. Interactions occurred where feeding twice daily caused numerical increases in the amount of time ruminal pH was below 6.2 (P < 0.10) and in the rate of acetate production (P < 0.05). Both responses would be considered liabilities in growing-finishing cattle. However, when feed deliveries were fluctuated, ruminal conditions became more favorable for steers fed twice daily than those fed once daily. In group-feeding situations, variability in feed availability to an individual is inevitable. Consequently, multiple feed deliveries may be beneficial to the ruminal environment although that has not been specifically tested.
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1 Correspondence: Box 2170 SDSU (phone: 605-688-5165; fax: 605-688-6170; E-mail: robbi_pritchard{at}sdstate.edu).
Received for publication August 8, 2002. Accepted for publication December 17, 2002.
| Literature Cited |
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M. S. Brown, C. H. Ponce, and R. Pulikanti Adaptation of beef cattle to high-concentrate diets: Performance and ruminal metabolism J Anim Sci, April 1, 2006; 84(13_suppl): E25 - E. [Abstract] [Full Text] [PDF] |
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G. E. Erickson, C. T. Milton, K. C. Fanning, R. J. Cooper, R. S. Swingle, J. C. Parrott, G. Vogel, and T. J. Klopfenstein Interaction between bunk management and monensin concentration on finishing performance, feeding behavior, and ruminal metabolism during an acidosis challenge with feedlot cattle J Anim Sci, November 1, 2003; 81(11): 2869 - 2879. [Abstract] [Full Text] [PDF] |
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