Accepted Manuscript Title: Stylosanthes cv. Campo Grande silage with or without concentrates in sheep diets: Nutritional value and ruminal fermentation Author: T.C. da O.G. Pereira M.C.N. Agarussi V.P. da Silva L.D. da Silva L.L. Cardoso K.G. S.C. Valadares PII: DOI: Reference:
S0921-4488(15)00113-3 http://dx.doi.org/doi:10.1016/j.smallrumres.2015.03.011 RUMIN 4915
To appear in:
Small Ruminant Research
Received date: Revised date: Accepted date:
19-12-2014 11-3-2015 12-3-2015
Please cite this article as: da, T.C., Agarussi, M.C.N., da Silva, V.P., da Silva, L.D., Cardoso, L.L., Valadares, S.C.,Stylosanthes cv. Campo Grande silage with or without concentrates in sheep diets: nutritional value and ruminal fermentation, Small Ruminant Research (2015), http://dx.doi.org/10.1016/j.smallrumres.2015.03.011 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
1
Highlights
2 Stylosanthes silage (SS) has lower intake and digestibility than corn silage
4
Corn silage (CS) and SS are nutritionally similar in diets containing concentrate (C)
5
The microbial protein synthesis is similar between the SS and CS diets with C
6
Stylosanthes silage is recommended for use in sheep diets containing C
cr
ip t
3
Ac ce p
te
d
M
an
us
7
1
Page 1 of 19
7
Stylosanthes cv. Campo Grande silage with or without concentrates in sheep diets:
8
nutritional value and ruminal fermentation
9
T.C. da Silvaa, O.G. Pereiraa,, M.C.N. Agarussia, V.P. da Silvaa, L.D. da Silvaa, L.L.
11
Cardosoa, K.G. Ribeiroa, S.C. Valadares Filhoa
12
a
13
Brazil.
14
[email protected]
[email protected],
[email protected],
us
[email protected],
cr
Animal Science Department, Federal University of Vicosa, Vicosa 36570-000, MG,
an
15 16
ip t
10
Abstract
Intake and apparent digestibility of nutrients, ruminal ammonia concentration,
18
ruminal pH, and microbial protein synthesis were evaluated in sheep fed diets
19
containing Stylosanthes cv. Campo Grande silage (StS) or corn silage (CS) with and
20
without concentrate [C; 40% of the dry matter (DM)]. Four sheep with an average initial
21
body weight of 41 ± 2.68 kg were used and were distributed in a 4 × 4 Latin square
22
design, arranged in a 2 × 2 factorial scheme. The SS diets with C showed similar intake
23
of DM and total digestible nutrients (TDN) (P > 0.05) in comparison with CS diet with
24
C. However, in the diets without the concentrate, SS showed lower intake of TDN than
25
CS (P < 0.05). The digestibility of organic matter (OM) did not differ between the SS
26
and CS in the diets with C (P > 0.05). The efficiency of microbial protein synthesis was
27
also similar (P > 0.05) between the SS and CS diets with C (59.13 and 66.11 g CP/kg
Ac ce p
te
d
M
17
Corresponding author. Av. P.H. Rolfs, sn, Centro, Viçosa-Minas Gerais, 36570-000 Tel.: +55 31 3899 3323; fax: +55 31 3899 2275. E-mail address:
[email protected] (O.G. Pereira). 2
Page 2 of 19
28
TDN, respectively). The Stylosanthes cv. Campo Grande silage is a suitable roughage
29
source to feed sheep, in diets containing 40% concentrate in the total DM.
30
Keywords: intake, microbial protein synthesis, digestibility, tropical legumes
32
ip t
31
1. Introduction
Forage legumes have been used to feed goats and sheep in tropical regions,
34
mainly as pasture or conserved as hay (Mupangwa et al., 2000; Bamikole et al., 2009;
35
Foster et al., 2009). Recently, interest in legume silage for livestock systems has
36
increased in tropical countries, including Brazil (Heinritz et al., 2011; Souza et al.,
37
2014). Among tropical legumes, Stylosanthes spp. has been used in diets for sheep and
38
goats (Mupangwa et al., 2000; Hue et al., 2008). In Brazil, promising results have been
39
obtained with the production of Stylosanthes cv. Campo Grande silage (StS),
40
considering the fermentation profile, the intake and performance of beef cattle (Souza et
41
al., 2014). Therefore, it is important to evaluate the potential use of StS in the sheep
42
diets, given the limited amount of information available about this type of feed for
43
ruminants.
us
an
M
d
te
Ac ce p
44
cr
33
Stylosanthes silage was therefore hypothesized to have similar levels of intake,
45
digestibility and ruminal fermentation to corn silage in diets with 40% concentrate. The
46
intake and digestibility of nutrients, ammonia concentration and ruminal pH and
47
microbial protein production were evaluated in sheep fed diets containing StS or corn
48
silage (CS) with and without addition of concentrate.
49
2. Materials and Methods
50
2.1. Experimental location and climatic conditions
3
Page 3 of 19
The experiment was conducted at the Laboratory of Animals, and the chemical
52
analysis were performed at the Forage Crops Laboratory from the Animal Science
53
Department of Federal University of Vicosa [Universidade Federal de Viçosa (UFV)],
54
located in Vicosa, Minas Gerais, Brazil. The city of Vicosa has a mean altitude of 648
55
m, latitude 20°45'14" south and longitude 42°52'55" west. According to the Köppen
56
classification, the climate is Cwa, a humid subtropical climate with coldest monthly
57
temperatures above 18 ◦C; annual average rainfall between 1400 and 1600 mm and with
58
rainy summers and dry winters.
59
2.2. Experimental diets and silages
us
cr
ip t
51
The Stylosanthes cv. Campo Grande (Stylosanthes capitata plus Stylosanthes
61
macrocephala) and the corn (Zea mays) were harvested at the pre-blooming stage and
62
one -third milk-line respectively. The crops were chopped using a stationary chopper (2
63
mm theoretical chop length). and packed in laboratory-scale silos with capacity of 550
64
kg and packing density of 550 kg/m3. The treatments consisted of diets containing
65
Stylosanthes cv. Campo Grande silage (StS) and corn silage (CS) with or without
66
concentrate (C), which was included at a proportion of 40% of the dry matter (DM) of
67
the diets. Diets were formulated according to the NRC (2007) (Table 1).
68
2.3. Animals, handling, measurement and sample collection
70 71
M
d
te
Ac ce p
69
an
60
The animal handling and treatment were performed in accordance with the
guidelines and recommendations of the Animal Ethics Committee from UFV. Four crossbred sheep (predominantly Santa Ines breed) rumen-cannulated were
72
used with an average initial weight of 41 ± 2.68 kg. The animals were housed in a
73
covered barn in individual cages equipped with feeders and drinking water systems.
4
Page 4 of 19
Each experimental period lasted 15 days, with 10 days for adaptation and five
75
days for collect samples and data. The animals were weighed at the beginning and at the
76
end of each experimental period. The total collections of orts, feces and urine for four
77
days of each period were used to estimate the digestibility of the nutrients.
ip t
74
Urine collection was performed using collector funnels that were attached to the
79
cages and drained into a bucket on the ground containing 100 mL of 20% (v./v.) sulfuric
80
acid to prevent the loss of nitrogen. After 24 hours of collection, the weight and the total
81
volume of urine were recorded, and an aliquot of 5% of the daily volume was removed
82
and stored in a freezer. A composite sample was made for each animal after four days of
83
collection. This composite sample was then homogenized, and a 10-mL sample was
84
collected, which was then mixed with 40 mL of 0.036 N sulfuric acid (H2SO4) to
85
prevent bacterial destruction of urinary purine derivatives and precipitation of uric acid.
86
The samples were stored at -15ºC for subsequent laboratory analysis.
d
M
an
us
cr
78
To determine the pH and ammonia concentration in the ruminal fluid, samples
88
were taken on the last day of each period, just prior to feeding and 2, 4 and 6 hours after
89
feeding. Approximately 50 mL of rumen fluid was collected through the rumen cannula,
90
and the pH of the fluid was immediately determined using a digital pH meter. After
91
measuring the pH, 1 mL of a 50% H2SO4 (v./v.) solution was added to each sample to
92
determine the concentration of ammonia in the sample.
93
2.5. Chemical analyses
95
Ac ce p
94
te
87
At the end of each experimental period, samples of the feed, orts and feces were
thawed, dried at 55°C for 72 h and ground in a Wiley mill with a 1-mm sieve.
96
The analyses were performed according to AOAC standards (1990) for
97
determining the DM (method 934.01), organic matter (OM; method 930.05), CP 5
Page 5 of 19
(method 981.10) and ether extract (EE; method 920.39). The neutral detergent fiber
99
(NDF) was determined by thermostable amylase and was corrected for ash using the
100
techniques described by Mertens (2002). The NDF correction for nitrogenous
101
compounds and estimates of neutral detergent insoluble nitrogen (NDIN) were based on
102
the method of Licitra et al. (1996). Lignin analyses were only performed on the samples
103
from the ingredients of the diets, using the method of cellulose solubilization in sulfuric
104
acid (Van Soest and Robertson, 1985) and the acid detergent fiber (ADF) method based
105
on the work of Goering and Van Soest (1967). The ammonia concentration in the
106
ruminal fluid samples was determined to according Chaney and Marbach (1962). The
107
concentration of non-fibrous carbohydrates (NFC) in the diet containing urea was
108
calculated based on Detmann and Valadares Filho (2010).
M
an
us
cr
ip t
98
The analyses of allantoin, uric acid, xanthine and hypoxanthine in urine were
110
performed using the colorimetric methods described by Chen and Gomes (1992). The
111
absorbed purines (mmol/day) were calculated based on the excretion of purine
112
derivatives, and the ruminal synthesis of nitrogenous compounds (g N/day) was
113
calculated as a function of the absorbed purines, both using the equations reported by
114
Chen and Gomes (1992).
115
2.6. Statistical analysis
te
Ac ce p
116
d
109
Data from intake, digestibility, purine derivatives and microbial efficiency were
117
analyzed using the MIXED procedure on SAS (version 9.3), based on a 4 × 4 Latin
118
square design in a 2 × 2 factorial design, and the effects of the model were the type of
119
silage (S), concentrate (C) and the S × C interaction (fixed effects), and animal and time
120
(random effects). Data were submitted to the analysis of variance and t-test was used for
121
comparisons of the means. A matrix of compound-symmetry covariance was used, 6
Page 6 of 19
which was selected based on the corrected Akaike information criterion (AICC).
123
Homogeneity of variance among treatments was assumed, and degrees of freedom were
124
estimated using the Kenward-Roger method (Kenward and Roger, 2009). All statistical
125
procedures were performed using 0.05 as the critical probability level for type I error.
126
3. Results and discussion
127
3.1. Nutrient intake and digestibility
cr
ip t
122
There was S × C interaction (P < 0.05) on the intake of nutrients, except for the
129
intake of NDF (Table 2). The addition of concentrate to the diets increased the intake of
130
DM, OM, NFC and TDN (P < 0.05) for both corn and Stylosanthes silages. The diet
131
containing SS with C had similar values of DM, OM and TDN intake (P > 0.05)
132
compared to the diet with CS and C, whereas in diets without C, lower levels of nutrient
133
intakes were observed for the SS diets compared to the CS diets (P < 0.05). The lower
134
intake of DM, OM, NFC and TDN in the diet containing only SS compared to the CS
135
diet is probably due to the filling effect caused by SS, which has a higher concentration
136
of lignin and indigestible NDF (iNDF), as reported by Silva et al. (2012). The values of
137
the DM intake for the diets with C (31.5 and 33.8 g/kg BW for CS and SS, respectively)
138
observed in this study were similar to those observed by Moreno et al. (2010) in sheep
139
fed diets with 40% C (31.3 g/kg kg BW). Cardoso et al. (2006) observed DM intake of
140
3.19 kg/100 kg of BW in Île-de-France lambs fed diets containing approximately 40%
141
C.
an
M
d
te
Ac ce p
142
us
128
The intake of CP in the diets without C was not different between the SS and CS
143
(P > 0.05), but with the addition of C to the diets, the SS showed higher intake levels
144
than CS (P <0.05). The diet with SS and C with diet had higher NFC intake compared to
145
the diet with CS and C, but the opposite behavior was observed for the diets containing 7
Page 7 of 19
146
only silage. The similar CP intake between the diets without C and the higher intake for
147
the diet with SS and C is because animals fed the SS diets selected more leaves, which
148
have higher concentrations of CP, compared to the CS diet. The apparent digestibility of the nutrients was not affected by the interaction S ×
150
C (P > 0.05), with an exception for the OM digestibility (P < 0.05; Table 3). There were
151
effects of S and C (P < 0.05) on the digestibility of DM, EE and NFC (P < 0.05). The
152
SS diets showed lower digestibility of these nutrients than the CS diets. In the diets
153
containing only forage, the CS had a higher OM digestibility compared to the SS diet (P
154
< 0.05). However, the OM digestibility did not differ between the SS and CS diets, both
155
containing C (P > 0.05). Sheep fed the diet SS and C probably had a sorting behavior to
156
achieve the same energy requirement, by selecting a diet with a higher energy content,
157
despite the nutritional characteristics of the SS, like the high iNDF content and lower
158
DM digestibility. Furthermore, the addition of concentrate to the SS diet minimized the
159
effects of the lower DM intake of the diet containing only SS, resulting in OM
160
digestibility to those of the CS diet with the concentrate. The similar CP intake between
161
the diets without C and the higher intake for the diet with SS and C is because animals
162
fed the SS diets selected more leaves, which have higher concentrations of CP
163
compared to the CS diet. This sorting behavior was evidenced by the high proportion of
164
stems in the orts of animals fed the SS diet.
cr
us
an
M
d
te
Ac ce p
165
ip t
149
The lack of an effect on the digestibility of NDF for different silages can be
166
explained by the increase in the ruminal retention time of the particles in the diets with
167
higher forage proportion, as previously observed in other studies with sheep
168
(Mupangwa et al., 2000; Silva et al., 2012).
169 8
Page 8 of 19
170
3.2. Ammonia concentration and ruminal pH The ruminal pH was affected by the S × C interaction and by the sampling time
172
(P < 0.05, Table 4). Considering the diets without C, the pH of SS was higher than CS.
173
However, in the diets with C, the pH values were similar for both SS and CS diets. The
174
higher ruminal pH in the animals fed the SS diet without concentrate compared to those
175
fed the CS diet (6.74 vs. 6.08) was probably due to the high concentrations of anionic
176
salts and CP in the legumes, which increase the buffering capacity of these plants
177
(Playne and McDonald, 1966; Heinritz et al., 2012). In addition, the higher starch
178
content in CS decreases the pH because of the higher fermentation. Ladeira et al. (2002)
179
observed an average ruminal pH of 7.0 in sheep fed Stylosanthes guianensis hay.
an
us
cr
ip t
171
The SS diet showed higher ruminal ammonia concentration than the CS diet
181
(11.75 vs. 9 mg/dL). The higher ruminal ammonia concentration in the animals fed the
182
SS diets (with or without concentrate) was most likely due to the higher nitrogen levels
183
in the rumen resulting from the increased consumption of CP, as explained previously.
184
The ruminal ammonia concentration observed in the present study was similar to that
185
observed by Ladeira et al. (2002).
186
3.3. Microbial protein synthesis
d
te
Ac ce p
187
M
180
The efficiency of microbial protein synthesis (EfMic) was affected by the S × C
188
interaction (P < 0.05). In diets without C, the EfMic was higher for the SS than CS.
189
However, the EfMic values were similar for both the SS and CS diets with concentrate.
190
The addition of concentrate to the SS diet decreased the EfMic, whereas no changes
191
were observed with the addition of C to the CS diet. The increase in microbial protein
192
production when the concentrate was added to the diet is due to the increased
193
availability of energy for the development of rumen microorganisms, resulting from the 9
Page 9 of 19
increased TDN intake. The lack of an effect based on the type of silage indicates that SS
195
can replace CS without compromising the development of ruminal microorganisms. The
196
increase in the EfMic in the SS diet can be explained by the decrease in TDN intake,
197
because this parameter is a ratio between CPmic production and TDN intake.
198
Furthermore, the animals fed the SS diet without concentrate had an increase in nitrogen
199
recycling because of the low intake of DM and TDN.
200
5. Conclusions
cr
ip t
194
Feeding exclusive Stylosanthes cv. Campo Grande silage results in lower intake
202
and digestibility compared to corn silage. However, Stylosanthes silage has a high
203
potential for sheep feeding in the diets containing 40% concentrate in the total DM,
204
because it has similar effects on nutritional value and ruminal fermentation as corn
205
silage. Thus, Stylosanthes silage is recommended for use in sheep diets.
206
6. Acknowledgements
an
M
d
The authors are grateful to CNPq (National Council for Science and Technology
te
207
us
201
Development), INCT-CA (National Institute of Science and Technology - Animal
209
Science) and FAPEMIG (The Minas Gerais state Research Foundation) for funding this
210
project.
211
7. References
212
AOAC, 1997. Official Methods of Analysis. Association of Officials Analytical
213
Ac ce p
208
Chemists, Vol. 1., 16th ed. Gaithersburg, Maryland, USA.
214
Bamikole, M.A., Ezenwa, I., Akinsoyinu, A.O., Arigbede, M.O., Babayemi, O.J., 2001.
215
Performance of West African dwarf goats fed Guinea grass-Verano stylo mixture,
216
N-fertilized and unfertilized Guinea grass. Small Rum. Res. 39,145–152.
10
Page 10 of 19
217
Cardoso, A.R.; Pires, C.C.; Carvalho, S., Galvani, D.B., Jochims, F., Hastenpflug, M.,
218
Wommer, T.P., 2006. Intake of nutrients and performance of lambs fed with diets
219
containing different levels of neutral detergent fiber. Cienc. Rur. 36,215–221.
221
Chaney, A.L., Marbach, E.P., 1962. Modified reagents for determination of urea and
ip t
220
ammonia. Clin. Chem. 8, 130–132.
Chen, X.B., Gomez, M.J., 1992. Estimation of microbial protein supply to sheep and
223
cattle based on urinary excretion of purine derivatives an overview of the
224
technical details. International Feed Resource Unit, Rowett Research Institute.
225
Occasional Publication, Aberdeen, pp. 2-20.
us
cr
222
Detmann, E., Valadares Filho, S.C., 2010. On the estimation of non-fibrous
227
carbohydrates in feeds and diets. Arq. Bras. Med. Vet. Zootec. 62, 980–984.
228
Foster, J.L., Adesogan, A.T., Carter, J.N., Blount, A.R., Myer, R.O., Phatak, S.C., 2009.
229
Intake, digestibility, and nitrogen retention by sheep supplemented with warm-
230
season legume hays or soybean meal. J. Anim. Sci. 87, 2891–2898.
te
d
M
an
226
Heinritz, S.N., Martens, S.D., Avila, P., Hoedtke, S., 2012. The effect of inoculant and
232
sucrose addition on the silage quality of tropical forage legumes with varying
233
Ac ce p
231
ensilability. Anim. Feed Sci. Technol. 174, 201–210.
234
Hue, K.T., Van, D.T.T., Ledin, I., 2008. Effect of supplementing urea treated rice straw
235
and molasses with different forage species on the performance of lambs. Small
236
Rum. Res. 78, 134–143.
237
Kenward, M.G. and Roger, J.H., 2009. An improved approximation to the precision of
238
fixed effects from restricted maximum likelihood. Comput. Stat. Data An. 53,
239
2583–2595.
11
Page 11 of 19
Ladeira, M.M, Rodriguez, N.M., Borges, I. Gonçalves, L.C., Saliba, E.O.S., Miranda,
241
L.F., 2002. Nitrogen balance, amino acid degradability and volatile fatty acid
242
concentration in the rumen of sheep fed Stylosanthes guianensis hay Rev. Bras.
243
Zootec. 31, 2350–2356.
245
Licitra, G., Hernandez, T.M., Van Soest, P.J., 1996. Standardization of procedures for nitrogen fractionation of ruminant feeds. Anim. Feed Sci. Technol. 57, 347–358.
cr
244
ip t
240
Mertens, D.R., 2002. Gravimetric determination of amylase-treated neutral detergent
247
fiber in feeds with refluxing in beaker or crucibles: collaborative study. J. AOAC
248
Int. 85, 1217–1240.
us
246
Moreno, G.M.B.; Sobrinho A.G.S.; Leão, A.G. Loureiro, C.M.B., Perez, H.L., Rossi,
250
R.C., 2010. Performance, digestibility and nitrogen balance of lambs fed corn
251
silage or sugar cane based diets with two levels of concentrate. Rev. Bras. Zootec.
252
39, 853–860.
d
M
an
249
Mupangwa, J., Ngongoni, N., Topps, J., Acamovic, T., Hamudikuwanda, H., Ndlovu,
254
L., 2000. Dry matter intake, apparent digestibility and excretion of purine
255
derivatives in sheep fed tropical legume hay. Small Rum. Res. 36, 261–268.
257 258 259
Ac ce p
256
te
253
NRC, 2007. Nutrient Requirements of Small Ruminants: Sheep, Goats, Cervids, and New World Camelids, 1st ed. National Academy Press, Washington, DC.
Playne, M.J., McDonald. P., 1966. The buffering constituents of herbage and of silage. J. Sci. Food Agric. 17, 264–68.
260
Silva, L.D., Pereira, O.G., Ribeiro, K.G., Valadares Filho, S.C., Silva, T.C. 2012. Intake
261
and total apparent digestibility of nutrients of corn and Stylosanthes silages in
262
diets for sheep. In: Joint Annual Meeting ASAS ADSA, 2012, Phoenix. J. Anim.
263
Sci. 90, 541–541. 12
Page 12 of 19
Souza, W.; Pereira, O.G.; Ribeiro, K.G.; Santos, S.A.; and Valadares Filho, S.C. 2014.
265
Intake, digestibility, nitrogen efficiency, and animal performance of growing and
266
finishing beef cattle fed warm-season legume (Stylosanthes capitata plus
267
Stylosanthes macrocephala) silage replacing corn silage. J. Anim. Sci. 92, 4099–
268
4107.
270
Van Soest, P. J., and J. B. Robertson. 1985. Analysis of forages and fibrous foods.
cr
269
ip t
264
Cornell University, Ithaca.
Ac ce p
te
d
M
an
us
271
13
Page 13 of 19
Table 1
273
Ingredient proportions and chemical composition of the experimental diets, expressed
274
based on the dry matter (DM) Dietas a
b
StS
CSc
StS+C
ip t
271 272
CS+Cd
597.10
CS
-
-
Urea / ASe
4.83
2.90
Corn grain
-
395.10
Soybean meal
-
4.90
-
-
989.25
593.55
us
995.17
10.75
6.45
-
395.10
-
4.90
an
SS
cr
Ingredient proportions, g/kg DM
Chemical composition , g/kg DM f
286.82
Organic matter
936.15
Crude protein Ether extract
238.04
478.36
958.16
951.51
958.23
100.76
106.47
101.67
97.95
13.77
13.72
26.26
21.26
587.27
383.85
469.36
313.38
256.43
478.13
370.37
546.09
333.18
202.38
220.76
134.95
Hemicellulose
143.16
107.89
207.79
146.86
Lignin
110.93
73.58
40.82
31.57
NFCh
d
Ac ce p
Cellulose
te
NDFg
508.10
M
Dry matter, g/kg NM
275
a
Stylosanthes cv. Campo Grande silage; bStylosanthes cv. Campo Grande silage plus
276
concentrate; ccorn silage; dcorn silage plus concentrate; eurea and ammonium sulfate at a
277
9:1 ratio. fnatural matter; gneutral detergent fiber corrected for ash and protein; hnon-
278
fibrous carbohydrates; iacid detergent fiber.
279 280
14
Page 14 of 19
280
Table 2
281
Least square means for nutrient intake by sheep fed Stylosanthes cv. Campo Grande or
282
corn silage with or without concentrate.
With
Means
Dry matter (g/d)
88.79
673.54Bb
1409.41Aa
1041.47
Corn
973.56Ab
1197.67Aa
1085.61
823.55
1303.54
Means
612.43Bb
1337.61Aa
Corn
910.30Ab
1144.19Aa
761.36
1240.90
Means
8.50
0.02
<0.01
0.01
27.75
0.79
0.52
0.08
55.96
<0.01 <0.01
<0.01
73.90
0.04
<0.01
975.02 1027.24
160.36Aa
129.29
Corn
104.17Aa
115.91Ba
110.04
d
138.14
e
te
NDF (g/d)
350.5
464.8
407.68
Corn
424.9
367.4
396.14
Means
387.70
416.12
Ac ce p
Stylosanthes
NFCf (g/d)
Stylosanthes
191.04Bb
693.80Aa
442.42
Corn
392.86Ab
634.49Ba
513.67
Means
291.95
664.14
g
TDN (g/d)
Stylosanthes
395.87Bb
1025.45Aa
710.66
Corn
709.71Ab
930.13Aa
819.92
552.79
977.79
Means
0.01
0.01
98.22Ab 101.19
<0.01
<0.01
Stylosanthes Means
S × Cd
0.40
M
Crude protein (g/d)
0.50
Cc
86.72
Organic matter (g/d) Stylosanthes
Sb
an
Stylosanthes
P-value
cr
Without
SEMa
ip t
Concentrate
us
Silage
<0.01
283
Means followed by the same uppercase letter in the columns and lowercase letter in the
284
rows are not significantly different based on a t-test (P < 0.05). astandard error of the 15
Page 15 of 19
285
mean; bsilage effect; cconcentrate level effect; dsilage × concentrate level interaction
286
effect. eneutral detergent fiber corrected for ash and protein; fnon-fibrous carbohydrates;
287
g
total digestible nutrients.
288
Ac ce p
te
d
M
an
us
cr
ip t
289
16
Page 16 of 19
289
Table 3
290
Least square means for the apparent digestibility (AD) of nutrients for sheep fed
291
Stylosanthes cv. Campo Grande silage or corn silage with or without concentrate.
With
Mean
Dry matter (g/kg)
25.0
Stylosanthes
521.1
707.6
614.3B
Corn
636.4
748.3
692.4A
Means
578.7b
728.0a
23.9
Organic matter (g/ kg) 576.4Bb
755.9Aa
Corn
699.4Ab
786.8Aa
637.9
771.3
Means
Stylosanthes
689.8
692.6
691.2
Corn
610.5
703.8
657.1
Means
650.1
Cc
S×Cd
<0.01 <0.01
0.09
<0.01 <0.01 0.049
14.6
0.20
0.08
0.10
24.4
0.73
0.60
0.33
30.1
<0.01 <0.01
0.06
d
698.2
e
Corn
te
NDF (g/ kg)
631.5
607.5
Means
597.9
623.8
564.4
640.1
602.3 619.5
Ac ce p
Stylosanthes
Sb
7433.1
M
Crude protein (g/ kg)
666.1
an
Stylosanthes
P-value
cr
Without
SEMa
ip t
Concentrate
us
Silage
NFCf (g/ kg)
Stylosanthes
625.8
843.1
734.5B
Corn
812.6
902.5
857.5A
Means
719.2b
872.8a
292
Means followed by the same uppercase letter in the columns and lowercase letter in the
293
rows are not significantly different based on a t-test (P < 0.05). astandard error of the
294
mean; bsilage effect; cconcentrate level effect; dsilage × concentrate level interaction
17
Page 17 of 19
e
295
effect.
neutral detergent fiber corrected for ash and protein;
296
carbohydrates..
f
non-fibrous
Ac ce p
te
d
M
an
us
cr
ip t
297
18
Page 18 of 19
Table 4
298
Least square means for the pH, ruminal ammonia concentration, and the microbial
299
protein synthesis and synthesis efficiency in sheep fed of sheep fed Stylosanthes cv.
300
Campo Grande silage or corn silage with or without concentrate. Concentrate Silage
With
Mean
pH
0.06
6.74Aa
6.06Ab
6.39
Corn
6.08Ba
6.17Aa
6.12
Mean
6.41
6.11
10.21
13.29
Corn
10.04
7.97
Mean
10.12
10.63
M
Stylosanthes
0.67
0.02
0.69 0.06
0.67
6.01
0.25 0.04
0.26
5.92
0.18 0.13
0.04
9.00B
Stylosanthes
34.93
62.21
48.57
Corn
53.56
Mean
44.24b
d
58.00
te
62.32a
EfMice (g MP/ kg TDNf) Stylosanthes
89.66Aa
59.13Ab
74.39
Corn
60.74Ba
66.11Aa
63.42
Mean
75.20
62.18
Ac ce p
0.07 0.06
S×Cd
11.75A
Microbial protein synthesis (g/d) 62.43
Cc
0.049
an
Ruminal ammonia (mg/dL)
S
us
Stylosanthes
P-value
b
cr
Without
SEMa
ip t
297
301
Means followed by the same uppercase letter in the columns and lowercase letter in the
302
rows are not significantly different based on a t-test (P < 0.05). astandard error of the
303
mean; bsilage effect; cconcentrate level effect; dsilage × concentrate level interaction
304
effect; emicrobial protein synthesis efficiency; gtotal digestible nutrients.
19
Page 19 of 19