AbstractKeywords
Introduction
Materials and
Methods
Results
Discussion
Conclusions/
Implications
References
Project
Background
|
Discussion
In terms of cattle performance,
these data suggest that pea and hull-less oat are
suitable substitutes for barley and SBM when
concentrate replacement is on an equivalent
protein basis and fed in backgrounding type
diets. Average daily gains were not affected by
the inclusion of either of the test grains. Other
studies have also reported similar ADG when
hull-less oat replaced barley in growing calf
diets (Johnson et al., 1995; Anderson et al.,
1997). Poland and Faller (1997) and Schimek et
al. (1997) reported linear decreases in ADG when
hull-less oat was included in lamb (barley
control) and steer (corn control) finishing
diets, respectively. Johnson et al. (1995) and
Anderson et al. (1997) reported increases in ADG
when hull-less oat replaced barley in cattle
diets. Many of these differences between control
and hull-less oat containing diets in ADG seem to
be related to changes in DMI, type of grain
processing and/or base grain in the control diet.Johnson et al. (1995) reported no
differences in DMI when hull-less oat was
included in backgrounding calf diets and compared
to coarsely ground barley. An increase in ADG was
only observed in one experiment where oat was
also coarsely ground. When whole hull-less oat
was fed, no differences in DMI or ADG were
observed. Other studies have reported decreases
in DMI when diets contained various levels of
hull-less oat (Poland and Faller, 1997; Schimek
et al., 1997). Intake and ADG were closely
correlated when whole hull-less oat was compared
to whole barley in growing lambs (Poland and
Faller, 1997) and when ground hull-less oat was
compared to ground corn in finishing cattle
(Schimek et al., 1997). Only one study (Anderson
et al., 1997) documented a decrease in DMI with a
corresponding increase in ADG. In this study,
dry-rolled hull-less oat was compared to
dry-rolled barley. The disparity between DMI and
gain occurred during a fnishing phase (last 103
days of 181 days on feed). During a grower phase
(0-78 days), DMI was decreased while ADG was
unaffected by level of hull-less oat in the diet.
Dry matter intake was also decreased with the
inclusion of hull-less oat in the present
experiments with no change in ADG.
Bauer (1997) suggested that a
decrease in intake can be expected when diets
containing hull-less oat are compared with diets
containing barley or corn. Three factors were
cited as possibly contributing to this
phenomenon. These included ruminal acidosis,
dietary fat level and protein degradation or
supply. Whether any or all of these factors
contributed to the reduced intakes of hull-less
oat containing diets in these experiments is
unclear. When diets are low in roughage or where
roughages are finely ground, acidosis can occur
(Fahey and Berger, 1988). The oat hay used in
both of these experiments was ground using a 2 in
screen prior to mixing in diets. Although hay
particle size was not measured, visual
observations did not suggest that forage particle
size would create an acidotic problem. Fat
supplementation above 6% of diet dry matter can
reduce digestibility of other feed ingredients in
the rumen, which may in turn lead to a decrease
in dry matter intake (Bauer, 1997). However, the
total fat concentration of diets fed (Tables 2
and 3) in these experiments did not exceed 6%.
Deficiencies of ruminally-available protein (DIP)
and metabolizable protein supply (MP) were also
implicated as possibly producing a reduction in
dry matter intake in hull-less oat containing
diets (Bauer, 1997). An evaluation (Bauer, 1997)
of hull-less oat containing diets using a
nutrient requirment model (NRC, 1996) to assess
the adequacy of DIP and MP supply did not
indicate that either of these were consistently
related to depressions in dry matter intake in
the diets used in these experiments.
Similar ADG and decreased DMI
resulted in improved FE when hull-less oat
replaced barley. Improvements in FE with the
inclusion of hull-less oat in barley-based diets
have been previous reported (Johnson et al.,
1995; Anderson et al., 1997). Feed efficiency did
not differ when barley was replaced by whole
(unprocessed) hull-less oat (Johnson et al.,
1995; Poland and Faller, 1997) or when corn was
replaced by ground hull-less oat (Schimek et al.,
1997). Improved FE associated with diets
containing processed hull-less oat suggest their
net energy concentrations exceed those containing
barley and SBM (NRC, 1984).
A separate explanation for the
improved feed efficiencies of hull-less oat
containing diets relates to a negative
relationship between level of intake and
digestibility (Merchen, 1988) or efficiency of
nutrient use (Merchen and Bourquin, 1994). Intake
effects on diet digestibility are much more
pronounced with mixed diets than with diets
consisting of single feedstuffs (Merchen, 1988).
In mixed diets, decreases of approximately 4% for
each unit increase in DMI have been reported. A
unit of intake (MM) equals level of DMI necessary
to achieve zero energy balance or maintenace.
Depressions in digestibility due to increasing
DMI are thought to result from increased rate of
passage of digesta through the digestive tract
(Merchen, 1988). However, the depression in
digestibility due to increased intake may not be
of major importance in a growing-finishing animal
in which DMI rarely exceeds 3 MM, but can become
quite meaningful in a lactating dairy cow where
DMI may exceed 5 MM (Ferrell, 1988). Generally,
in diets of sufficient quality and consumed at
approximately 3 MM, a correction of metabolizable
energy concentratioin due to feeding level is not
necessary (Ferrell, 1988). Dry matter intake of
calves consuming control diets (Tables 4 and 5)
equated to 2.75 and 3.09 MM for experiments 1 and
2, respectively. Average depressions in DMI
between the hull-less oat and control diets were
1.7 (.27 MM) and 3.9 (.48 MM) lb for experiments
1 and 2, respectively. Although an effect of DMI
on diet digestibility was not determined in these
experiments, the changes in DMI were not seen to
be large enough to account for the observed
improvements in FE for diets containing hull-less
oat.
Average NEm and NEg values for
hull-less oat grain were 1.17 and .84 Mcal/lb,
respectively (see Table 6). If these values are
adjusted for experimental bias and fat
concentration (Table 7), the net energy
concentration of hull-less oat is similar to oat
groat and numerically greater than corn (NRC,
1984). Until additional data is collected,
assuming that the net energy concentration of
hull-less oat equals that of oat groat seems
reasonable. Thus, conservative estimates of the
NEm and NEg value of hull-less oat in growing
calf diets are 1.07 and .75, respectively. When
NE concentration of test grains in Exp 2 were
assumed, the NE concentration of COMB2 (.78 and
.51 Mcal/lb for NEm and NEg, respectively) was
calculated to be similar to the dietary NE of
FPEA2 (.78 and .50) and HOAT2 (.78 and .51). This
similarity was expected given the relative
similarity of the estimated NE concentration of
FPEA2, HOAT2 and COMB2 (Table 6).
| Table
7. Net energy (NE) concentrations
(Mcal/lb) of Paul
oat, oat groat and corn and barley grain. |
|
| |
NEm |
NEg |
|
| Paul oat |
|
|
| --Average NE |
1.17 |
.84 |
| --Experimental biasa |
-.059 |
-.045 |
| --Fat concentration
adjustmentb |
-.059 |
-.041 |
| -- Conservative
estimate |
1.06 |
.76 |
| |
|
|
| Oat groat |
1.07 |
.75 |
| |
|
|
| Corn |
1.02 |
.70 |
| Barley |
.93 |
.64 |
|
aExperimental bias is
the average difference between calculated
and estimated net energy values for the
control diets.
bFat concentration adjustment
calculated assuming fat concentrations of
Paul oat and oat groat as 9.6 and 6.9%,
respectively, and the NEm and NEg of pure
fat are 2.15 and 1.59 Mcal/lb,
respectively. Fat adjustments are
calculated as the difference in fat
concentration multiplied by the NE
concentration of fat. |
The differential response of pea containing diets
between these two experiments warrants further
work aimed at understanding the nutritional
benefits of pea as a feed grain for growing
calves. It is difficult to compare results across
experiments. Experiments differed in calf sex,
initial age/weight, and base diet offered.
Nonetheless, an interesting observation is that
pea seemed to perform better in a higher forage
diet (Exp 2) .
The protein in pea is highly
degradable in the rumen (DIP, 78% of CP;
Hickling, 1994). Thus, pea protein may be an
excellent supplemental source of DIP at times
when a base diet is determined to be deficient in
ruminally-available nitrogen. In South Dakota (C.
Birkelo, personal communication), pea improved FE
in finishing cattle consuming a high-concentrate,
corn grain based diet. Corn grain is relatively
high in energy, low in CP (relative to energy)
and low in DIP (NRC, 1996). Pea may have
alleviated an inherent DIP deficiency in the base
diet, allowing for an overall improvement in diet
digestibility. Personal observations using a
nutrient requirement for beef cattle (NRC, 1996)
suggests that forage-based diets are typically
first-limiting in DIP. Whether DIP supply from
pea containing diets can explain the enhancement
in FE seen in Exp 2 is speculative. Nonetheless,
given the abundance of forage produced in
northern Great Plains, this possibility needs
further study.
Conclusion/Implications of
this research
Pea and hull-less oat are
suitable substitutes for barley and SBM when
replacement is on an equivalent protein basis in
growing calf diets. The improved feed
efficiencies associated with those diets
containing hull-less oat suggest the net energy
concentrations for this particular feed grain
exceeds those of barley. Conservative estimates
of NEm and NEg in Paul oat are 1.07 and
.75, respectively.
Additional/future research
needs resulting from this project
The differential response of pea
containing diets between these two experiments
warrants further work aimed at understanding the
nutritional benefits of pea as a feedstuff for
cattle. Effects of processing on the feeding
value of these feed grains was not evaluated in
these studies and as yet needs to be determined.
References
Anderson, V.L, M.L. Bauer,
J.S. Caton, P. Berg and D.H. Dhuyvetter. 1997. An
evaluation of reciprocal levels of hull-less oats
and barley in diets for growing and finishing
steers. Carrington Res. Ext. Center Field Day
Beef and Bison Res. Report. pp20-23. (http://www.ag.ndsu.nodak.edu/carringt/97beef/art5.htm).
AOAC. 1990. Official
methods of Analysis. Vol. I (15th
Ed.). Association of Official Analytical
Chemists, Arlington, VA.
Bandyk, C., D. Simms and
G. Kuhl. 1994. Grower, ration balancing software
for growing beef cattle - Version 2.nd. Kansas
State University, Manhatten.
Ensminger, M.E. and C.G.
Olentine. 1978. Feeds and nutrition - complete.
The Ensminger Publishing Company. Clovis, CA.
Fahey, G.C. and L.L.
Berger. Carbohydrate nutrition of ruminants. In:
D.C. Church (ed.) The Ruminant Animal: Digestive
Physiology and Nutrition. Prentice Hall,
Englewood Cliffs, NJ. pp294.
Ferrell, C.L. 1988. Energy
metabolism. In: D.C. Church (ed.) The Ruminant
Animal: Digestive Physiology and Nutrition.
Prentice Hall, Englewood Cliffs, NJ. pp257.
Freund, R. J., R. C.
Littell, and P. C. Spector. 1986. SAS system for
linear models. SAS Institute Inc., Cary, NC.
Hickling, D. 1994.
Canadian peas: Feed industry guide. Canadian
Special Crops Association (Winnipeg, MB) and
Western Canada Pulse Growers Association (Regina,
SK). pp21.
Johnson, J., D.
Dhuyvetter, B. Kreft, and K. Ringwall. 1995. A
comparison of naked oats to barley when fed in a
grower diet to beef calves. North Dakota cow/calf
conference and beef cattle and range research
report. December 1 and 2, Bismarck.
Johnson, L. and S. Boyles.
1991. Oats as a feed for beef cattle. Extension
Bulletin, AS-1020. North Dakota State University.
(http://www.ext.nodak.edu/extpubs/ansci/beef/as1020w.htm).
McMullen, M.S., D.C.
Doehlert and J.D. Miller. 1997. Registration of Paul
oat. Crop Sci. 37:1016.
Merchen, N.R. 1988.
Digestion, absorption and excretion in ruminants.
In: D.C. Church (ed.) The Ruminant Animal:
Digestive Physiology and Nutrition. Prentice
Hall, Englewood Cliffs, NJ. pp190.
Merchen, N.R. and L.D.
Bourquin, 1994. Processes of digestion and
factors influencing digestion of forage-based
diets by ruminants. In: G.C. Fahey (ed.) Forage
Quality, Evaluation and Utilization. American
Society of Agronomy, Crop Science Society of
America and Soil Science Society of America,
Madison, WI. pp581.
NRC. 1984. Nutrient
requirements of beef cattle (6th Ed.).
National Academy Press.
NRC. 1996. Nutrient
requirements of beef cattle (7th Ed.).
National Academy Press.
Peel, M.D. 1997. 1997
North Dakota Barley, Oat, Rye and Flax variety
performance descriptions. Extension Bulletin,
A-1049. North Dakota State Univeristy. (http://www.ext.nodak.edu/extpubs/plantsci/smgrains/a1049w.htm).
Peel, M.D. 1998. Crop
rotations for increased productivity. Extension
Bulletin, EB-48 (revised). North Dakota State
University. (http://www.ext.nodak.edu/extpubs/plantsci/crops/eb48-1.htm).
Poland, W., and T.C.
Faller. 1997. Whole Paul oat as a
feedstuff for sheep. Sheep Day Report, Hettinger
Research/Extension Center, pp1-4.
Robertson, J.B. and P.J.
Van Soest. 1982. The detergent system of analysis
and its application to human foods. In: W.P.T.
James and O. Theander (ed.). The Analysis of
Dietary Fiber. Marcell Dekker, NY. p138.
Schimek, C., M. Bauer, J.
Caton, V. Anderson, D. Dhuyvetter and P. Berg.
1997. Influence of hull-less oats on feedlot
performance and carcass characteristics in beef
steers. An evaluation of reciprocal levels of
hull-less oats and barley in diets for growing
and finishing steers. Carrington Res. Ext. Center
Field Day Beef and Bison Res. Report. pp24-27. (http://www.ag.ndsu.nodak.edu/carringt/97beef/art6.htm).
Zinn, R. A. 1987.
Influence of lasalocid and monensin plus tylosin
on comparative feeding value of steam-flaked
versus dry-rolled corn in diets for feedlot
cattle. J. Anim. Sci. 65:256-266.
Project Background
Authors
C. Poland,
Area Livestock Specialist
Dickinson Research Extension
Center
North Dakota State University
Dickinson, North Dakota
wpoland@ndsuext.nodak.edu
www.ag.ndsu.nodak.edu/dickinso
D. Landblom,
Animal Scientist - Swine
Dickinson Research Extension Center
North Dakota State University
Dickinson, North Dakota
dlandblo@ndsuext.nodak.edu
www.ag.ndsu.nodak.edu/dickinso
Corresponding author
C. Poland
Primary location of research
Dickinson Research Extension Center, North
Dakota State University, Dickinson, North
Dakota
Funding sources
North Dakota Agricultural Products
Utilization Commission
North Dakota Dry Pea and Lentil Association
North Dakota Agricultural Experiment Station
Additional credits the authors need to
give
L. Tisor and G. Ottmar for animal care,
diet processing and data collection. J. Kolar
for manuscript preparation assistance.
|