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* Department of Animal Sciences, Washington State University, Puyallup 98371
Agro Pacific Industries, Inc., Chiliwack, BC
Pioneer Hi-Bred International, Des Moines, IA 50131
Department of Biological System Engineering, University of Wisconsin, Madison 53706
Corresponding author:
J. Harrison; e-mail:
harrison{at}puyallup.wsu.edu.
| ABSTRACT |
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Key Words: corn silage mechanical processing maturity digestibility
Abbreviation key: BL = blackline, DE = digestible energy, ME = metabolizable energy, ML = milkline, TLC = theoretical length of cut
| INTRODUCTION |
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Since the mid-1990s, forage harvesters with onboard mechanical processors have gained widespread acceptance throughout the United States. Increasing the surface area exposed can potentially increase nutrient digestibility of the corn silage in the rumen and may lead to improvements in animal performance. Five studies have reported increased starch digestibility due to processing with an onboard mechanical processor attached to a forage harvester (Doggett, 1998; Harrison et al., 1998; Young et al., 1998; Bal et al., 2000a; Dhiman et al., 2000). Another study (Weiss and Wyatt, 2000) reported that total tract digestibilities of starch and nonfiber carbohydrates were significantly greater for lactating cows fed mechanically processed conventional corn silage harvested at one-half ML compared with unprocessed corn silage. Mechanically processed corn silage increased TDN of the conventional corn silage diet by 5.3% (Weiss and Wyatt, 2000).
The rapid adoption of onboard mechanical processing units has provided the need for research to determine the benefits of mechanically processing corn silage over a wide range of maturities. Two different hybrids of corn silage were chosen that differed in corn grain characteristics (Hybrid 3845, dent variety; Hybrid Quanta, flint variety) to determine if mechanical processing affected one type of hybrid to a greater extent. The objective of these experiments was to evaluate the effects of maturity and mechanical processing of two corn silage hybrids on the energy content of the diets and ruminal and total tract digestion of starch, fiber, and fat. The energy requirements for maintenance and milk production were evaluated also.
| MATERIALS AND METHODS |
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All cows used in these experiments were multiparous. Experimental periods were 14 d; the first 10 d were for adjustment, and the last 4 d were for collection of samples and data. Cows were individually fed with Calan headgates (American Calan, Inc., Northwood, NH) in a free-stall barn during the adaptation periods. Cows were fed enough TMR twice daily (1000 and 1600 h) to allow 10% orts. In all experiments, cows were fed diets balanced to meet NRC specifications (National Research Council, 1989) and containing a similar proportion of corn silage (26.8% of diet DM), alfalfa hay (13.2% of diet DM), whole cottonseed (13.6% of diet DM), and grain mix (46.4% of diet DM; Table 1
).
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Experiment 1.
Cows averaged 126 DIM at the beginning of the experiment. Pioneer hybrid 3845 corn silage was harvested during the 1996 growing season. Corn silage was harvested at hard dough (25.3 DM%), one-third ML (28.5 DM%), and two-thirds ML (27.9 DM% with two light frosts and one killing frost) stages of maturity. The theoretical length of cut (TLC) for the corn silage was 6.4 mm. Corn silage was stored in Ag Bags (Ag Bag International, Ltd., Warrenton, OR).
Experiment 2.
Pioneer hybrid 3845 corn silage was harvested during the 1997 growing season at one-third ML (27.1 DM%), two-thirds ML (33.3 DM%), and BL (38.2 DM%) stages of maturity. The TLC for the corn silage was 12.7 mm. Corn silage was stored in bunker silos. Cows fed hybrid 3845 corn silage averaged 140 DIM at the beginning of the experiment. Hybrid Quanta corn silage was harvested during the 1997 growing season at one-third ML (34.1 DM%), two-thirds ML (41.5 DM%), and BL (47.5 DM%) stages of maturity. The TLC for the corn silage was 12.7 mm. Cows fed hybrid Quanta corn silage averaged 128 DIM at the beginning of the experiment.
Sample Collection
Cows were housed in a metabolism barn during the collection period (d 11 through 14). Bodyweights were recorded at the beginning (prior to entering the metabolism barn) and end (prior to entering the free-stall barn) of the collection period. Milk yield was measured twice daily at 0700 and 1900 h. Total mixed rations were provided individually to cows twice daily at 1000 and 1600 h. Weights were recorded, and samples were collected once daily for the corn silage, TMR, and orts. Samples were frozen until further analysis (–20°C). Urine was collected via urine cups (Fellner et al., 1988) and flowed through polyvinyl tubing into a collection jug located beneath the floor. Hydrochloric acid (36.5%) was added to the urine to maintain the pH < 4 to minimize loss of ammonia. Urine was weighed once daily, and 1% of the total weight was subsampled and frozen for further analysis (–20°C). Feces passed through grates in the floor and were collected in tubs located beneath the floor. Feces were weighed once daily, and 1% of the total weight was subsampled and frozen for further analysis (–20°C). Corn silage, TMR, orts, urine, and fecal samples were composited across the 4 d of collection for each period by cow.
Grass silage labeled with Yb was prepared prior to the beginning of each experiment and used as a particulate flow marker. Silage was prepared by spraying YbCl36H2O dissolved in water to reach a final concentration of 2.5% Yb in silage DM (Hartnell and Satter, 1979). Once silage was sprayed with YbCl36H2O, the silage was dried at 55°C in a forced-air oven for 48 h. On d 7 through 9 of each period, 20-g aliquots of silage labeled with Yb were added via the ruminal cannula once daily. On d 10 through 13, silage labeled with Yb was dosed twice daily (12 h apart) in 10-g aliquots. Duodenal and ileal samples were taken four times daily at 6-h intervals from d 11 to 13. On d 12 and 13, sampling time was moved forward 2 h/d to allow for samples to be obtained every even h of a 24-h d. The initial sample was taken at 0600 h on d 11. During the collection of duodenal samples, the initial flow of duodenal contents (approximately 200 ml) from the cannula was discarded, and the next 200 ml were collected and frozen at –20°C.
Sample Preparation and Analysis
At the end of each collection period, samples of corn silage, TMR, orts, and feces were dried at 55°C in a forced-air oven. Duodenal samples were thawed and blended at high speed for 3 min with a Waring blender and dried at 55°C in a forced-air oven. Dried corn silage, TMR (Tables 2
and 3
), orts, duodenal, and fecal samples were ground through a 1-mm screen using a Wiley mill (Arthur H. Thomas, Philadelphia, PA) and analyzed for DM and ash (AOAC, 1990). Corn silage, TMR (Tables 2
and 3
), orts, duodenal contents, and feces were analyzed for NDF with sulfite (Van Soest et al., 1991), ADF (Goering and Van Soest, 1970), and starch (modified version of Holm et al., 1986; described in Johnson et al., 2002). Total mixed rations (Tables 2
and 3
), orts, and feces were analyzed for ether extract (AOAC, 1990). Total mixed rations were analyzed for CP (AOAC, 1990), lignin (Goering and Van Soest, 1970), acid detergent insoluble CP (Goering and Van Soest, 1970), and neutral detergent insoluble CP (Goering and Van Soest, 1970; Tables 2
and 3
). Hemicellulose concentration of the TMR and orts was calculated by subtracting ADF concentration from NDF concentration (not corrected for neutral detergent insoluble CP), and cellulose concentration of the TMR and orts was calculated by subtracting lignin concentration from ADF concentration. Nonfiber carbohydrate concentration for the TMR was calculated using the formula: nonfiber carbohydrate = 100 – (NDF + CP + ether extract + ash). The NDF concentration in the nonfiber carbohydrate calculation was not corrected for neutral detergent insoluble CP.
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Statistical Analysis
The model to test for treatment differences in experiment 1 and Experiment 2 was:
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where µ = overall mean, Ci = cow effect (i = 1 to 6), Pj = period effect (j = 1 to 6), Tk = treatment effect (k = 1 to 6), and Eijk = error term.
The model to test for main effects and interactions in experiment 1 was:
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where µ = overall mean, Ci = cow effect (i = 1 to 6), Pj = period effect (j = 1 to 6), Mk = maturity effect (k = 1 to 3), Kl = processing effect (l = 1 to 2), (M x K)kl = interaction effect of Mk and Kl, and Eijkl = error term.
The model to test for main effects and interactions in experiment 2 was:
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where µ = overall mean, Ci(H)k = cow effect nested within hybrid (i = 1 to 12), Pj = period effect (j = 1 to 6), Hk = hybrid effect (k = 1 to 2), Ml = maturity effect (l = 1 to 3), Km = processing effect (m = 1 to 2), (H x M)kl = interaction effect of Hk and Ml, (H x K)km = interaction effect of Hk and Km, (M x K)lm = interaction effect of Ml and Km, (H x P)kj = interaction effect of Hk and Pj, and Eijklm = error term. Significance was declared at P < 0.05, and trends were observed at P < 0.10 (SAS, 1988).
| RESULTS AND DISCUSSION |
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There was a hybrid by processing interaction and a maturity by processing interaction for starch intake in experiment 2 (Table 4
). Starch intake tended to be greater (P < 0.06) for cows fed hybrid Quanta unprocessed corn silage based diets compared with the other treatments, and cows fed processed corn silage harvested at one-third ML maturity had significantly lower (P < 0.009) starch intake than the other treatments (Table 4
). The greater intake of starch for cows fed diets containing hybrid Quanta unprocessed corn silage was due to the greater concentration of starch in the TMR (29% starch) compared with other treatments (27% starch; Table 3
). The lower intake of starch for cows fed processed corn silage harvested at one-third ML maturity was due to a lower concentration of starch in the TMR (~26% starch) compared with other treatments (~28% starch; Table 3
).
Starch flow to the duodenum was not affected by treatment in experiment 1 and was influenced by maturity of corn silage and processing method in experiment 2 (Table 4
). As maturity advanced from one-third ML to two-thirds ML, for hybrid 3845 in experiment 2, starch flow significantly increased (P < 0.05; Table 4
). Starch flow to the duodenum was significantly lower for cows fed diets containing processed corn silage (P < 0.0004; Table 4
). The greatest decrease (P < 0.01) in starch flow to the duodenum between processed and unprocessed corn silage treatments was achieved when corn silage was processed at two-thirds ML compared to processing corn silage at the other maturities (experiment 2; Table 4
).
Two hybrids of corn silage differing in corn grain characteristics (hybrid 3845, dent characteristics; hybrid Quanta, flint characteristics) were selected in experiment 2 to evaluate the effects of maturity and mechanical processing on ruminal digestibility. In experiment 2, ruminal starch digestibility tended to be greater for the hybrid that was supposed to have a larger percentage of vitreous endosperm (70.2%; hybrid Quanta) than the hybrid that was supposed to have a larger percentage of floury endosperm (67.1%; hybrid 3845; P < 0.07; Table 4
). This differed from data reported in the literature which suggest that flint corn grains typically have a greater percentage of the endosperm that contains vitreous starch, whereas dent corn grains typically has a greater percentage of the endosperm that contains floury starch. The hybrids that contain a greater percentage of floury endosperm tend to have greater ruminal starch digestibility (Philippeau and Michalet-Doreau, 1997).
The difference in trends in ruminal starch digestibility between data reported in this paper and in the literature may be partially explained by the proportion of vitreous endosperm present in each hybrid as maturity of corn silage advanced. The proportion of vitreous starch present in the corn kernels for hybrid Quanta did not change drastically as maturity advanced (range of approximately 36 to 45%; Johnson et al., 2002), and ruminal starch digestibility also did not change much as maturity advanced (range of approximately 69 to 72%; Table 4
). However, the proportion of vitreous starch present in the corn kernels for hybrid 3845 increased as the maturity of corn silage advanced from one-third ML (28.2%) to BL (73.3%; Johnson et al., 2002), and ruminal starch digestibility declined (P < 0.01) as maturity of corn silage advanced from one-third ML to two-thirds ML and BL (Table 4
). Therefore, the hybrid that was chosen for its dent characteristic (hybrid 3845) of increased proportion of floury endosperm (highly digestible) actually had a greater proportion of vitreous endosperm (less digestible) at the advanced maturities (two-thirds ML and BL) than hybrid Quanta (Johnson et al., 2002). This may partially explain the reduction in ruminal starch digestibility for cows fed diets containing hybrid 3845 corn silage (dent characteristics) instead of diets containing hybrid Quanta corn silage (flint characteristics) (Table 4
).
Mechanically processing corn silage had an effect on apparent digestion of starch in the rumen and lower tract (Table 4
; experiment 2). Starch apparently digested in the rumen (experiment 2; P < 0.003) and lower tract (experiment 2; P < 0.05) was significantly greater for cows fed processed corn silage (Table 4
). There was a hybrid by processing interaction, and starch apparently digested in the rumen was greater (P < 0.01) for cows fed hybrid 3845 processed corn silage compared with hybrid 3845 unprocessed corn silage (Table 4
). There was also a maturity by processing interaction, and starch apparently digested in the rumen was greater (P < 0.0004) for cows fed diets containing processed corn silage compared with unprocessed corn silage harvested at two-thirds ML stage of maturity (experiment 2; Table 4
). Apparent postruminal starch digestibility (approximately 90%) was greater than ruminal starch digestibility (approximately 68%). However, a greater amount of the starch in the diet was digested in the rumen (~70%) versus postruminally (~30%). Other studies (Doggett, 1998; Harrison et al., 1998; Bal et al., 2000b), using the macro in situ technique, reported an increase in ruminal starch digestibility due to mechanical processing of corn silage. An in vivo study (Rojas-Bourrillon et al., 1987) demonstrated that mechanical processing of corn silage increased ruminal (P < 0.01) and postruminal digestion of total
-glucosides (starch) compared with control silage.
Starch apparently digested in the total tract was not affected by maturity or mechanical processing of corn silage in experiment 1, and was affected by maturity and mechanically processing of corn silage in experiment 2 (Table 4
). Processing corn silage enhanced digestion of starch in the total tract compared to unprocessed corn silage diets (experiment 2; P < 0.0001; Table 4
). There was a hybrid-by-maturity interaction for total tract starch digestibility (Table 4
; experiment 2). For hybrid 3845 in experiment 2, starch apparently digested in the total tract declined (P < 0.003) as maturity advanced from one-third ML to two-thirds ML and BL (Table 4
). There was a maturity by processing interaction, and at advanced stages of maturity, processing enhanced starch digestion to a greater extent than with less mature silages [experiment 2, two-thirds ML and BL (P < 0.008)].
The difference in total tract starch digestibility between experiments can be partially explained by particle size of the corn silage. In experiment 1, the TLC was 6.4 mm, and in experiment 2, the TLC was 12.7 mm. The short particle size in experiment 1 tended to minimize differences between processed and unprocessed corn silages which may have led to no difference being detected in total tract starch digestibility. In experiment 2, the particle size of the corn silage was longer; therefore, mechanical processing had a greater potential to alter the physical characteristics of the corn silage that may have led to the increase in total tract starch digestibility. Others reported a significant decline in total tract starch digestibility as maturity advanced (Harrison et al., 1996; Bal et al., 1997), or when medium to physiologically mature corn silage was not mechanically processed (Rojas-Bourrillon et al., 1987; Young et al., 1998, Dhiman et al., 2000, and Weiss and Wyatt, 2000; Bal et al., 2000a).
Fiber intake and digestion.
Intake of NDF (kg/d) was affected by hybrid of corn silage in the diet (experiment 2; Table 6
). Cows fed diets containing hybrid 3845 consumed approximately 0.43 kg more NDF/d than cows fed hybrid Quanta (P < 0.02; Table 6
). The increase in NDF intake was mainly associated with a greater NDF concentration (P < 0.01; Johnson et al., 2002; Table 3
) for the diet containing hybrid 3845 because DMI (Table 5
) was similar between hybrids. The greater NDF concentration for the diet containing hybrid 3845 corn silage was related to the greater (P < 0.0001) NDF concentration in hybrid 3845 corn silage (44.3%) compared with hybrid Quanta corn silage (41.2%; Johnson et al., 2002).
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Neutral detergent fiber digestion postruminally was not different from zero in experiment 1 and for hybrid 3845 in experiment 2 (Table 6
). The negative NDF digestion postruminally is possible; however, it is probably an artifact of the assay. Crocker et al. (1998) demonstrated that neutral detergent insoluble ash differed greatly among different digestion sites, and this accounted for negative NDF digestibilities. Apparent ruminal NDF digestibility was significantly lower (P < 0.007), and apparent postruminal NDF digestibility was significantly greater (P < 0.0004) for cows fed diets containing hybrid Quanta compared to cows fed diets containing hybrid 3845 in experiment 2 (Table 6
).
Cows fed diets containing hybrid Quanta corn silage (45.4%) had significantly greater (P < 0.001) total tract NDF digestibility than cows fed hybrid 3845 corn silage diets (40.1%). Total tract NDF digestibility significantly increased (P < 0.001) as maturity advanced (hard dough, 49.4% and one-third ML, 49.4% to two-thirds ML, 53.2%) in experiment 1, and total tract NDF digestibility tended to increase (P < 0.09) as maturity advanced from one-third ML to two-thirds ML and BL in experiment 2 (Table 6
). This is contradictory to published data that reported a decrease in total tract NDF digestibility as maturity advanced (Bal et al., 1997). Total tract NDF digestibility tended to be greater (P < 0.09) for cows fed diets containing unprocessed (51.4%) corn silage compared to processed (50.0%) corn silage diets in experiment 1 (Table 6
). However, in experiment 2, cows fed diets containing processed corn silage had greater total tract NDF digestibility (P < 0.04; Table 6
). Others (Rojas-Bourrillon et al., 1987; Young et al., 1998; and Weiss and Wyatt, 2000; Bal et al., 2000a) have reported no difference or a decline (Dhiman et al., 2000) in total tract NDF digestibility between processed or unprocessed corn silage-based diets.
Ether extract intake and digestion.
Hybrid, maturity, and processing all affected ether extract intake (Table 7
). The differences in intake were usually influenced by the concentration of ether extract (crude fat) in the respective TMR (Tables 2
and 3
). Total tract ether extract digestibility was affected by maturity of corn silage in experiments 1 and 2 (hybrid by maturity interaction; Table 7
). Total tract ether extract digestibility was lower for cows fed diets containing corn silage harvested at the middle maturity compared to the other maturities in experiment 1 (P < 0.03) and lower at the middle maturity compared to the early maturity for hybrid 3845 in experiment 2 (P < 0.02; Table 7
). The opposite trend was observed for cows fed diets containing hybrid Quanta corn silage in experiment 2 (P < 0.02; Table 7
). The differences in total tract ether extract (crude fat) digestibility are most likely related to the concentration of ether extract in the TMR (Tables 2
and 3
) and orts because ether extract excreted in the feces was not affected by maturity of corn silage. Others (Huber et al., 1965) reported no significant difference in total tract ether extract digestibility due to maturity. However, in the second year of one study (Huber et al., 1965), there was onea fairly substantial decline (8.2 percentage units) in total tract ether extract digestibility as the corn matured from soft dough (25.4% DM) to medium dough (30.3% DM).
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Energy Estimates of TMR and Energy Requirements
Methane and urinary energy output.
Estimated methane energy was not significantly affected by maturity, processing, or maturity by processing interactions in experiment 1 (Table 8
). There was an effect of treatment on estimated methane energy production in experiment 2 (P < 0.06); however, there were no significant effects of hybrid, maturity, or processing on estimated methane energy production (Table 8
).
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Digestible energy of TMR.
The concentration and intake of DE was affected by maturity in experiment 1. The DE concentration (Mcal/kg) was significantly lower (P < 0.004) for diets containing corn silage harvested at two-thirds ML (2.92 Mcal/kg) compared to one-third ML (3.07 Mcal/kg) and hard dough (3.07 Mcal/kg; experiment 1; Table 8
). The amount of DE consumed (Mcal/d) was greater (P < 0.09) for cows fed diets containing corn silage harvested at hard dough compared to two-thirds ML (experiment 1; Table 8
). In experiment 1, the greater amount of DE consumed (Mcal/d) at hard dough maturity was related to the greater intake of gross energy [Mcal/d; data not shown] compared to two-thirds ML.
Other studies have evaluated the effect of maturity of corn silage on energy concentration and digestibility of the diet (Huber et al., 1965; Buck et al., 1969; Goering et al., 1969; St. Pierre et al., 1987). In these studies, corn silage was typically the only forage provided and usually made up a large portion of the diet DM (70 to 90%). Varying results were observed, and statistical significance was achieved only in Trial 1 of the study conducted by Goering et al. (1969). A summary of the four research studies indicates that decreases in energy digestibility were very gradual with increasing maturity estimated by DM concentration of the corn silage. However, there was a trend of decreasing energy digestibility with increasing maturity that followed trends observed in experiment 1 and for hybrid 3845 in experiment 2.
Mechanical processing of corn silage affected energy digestibility (Table 8
). Digestible energy, as a percent of gross energy, was significantly lower (P < 0.03) for cows fed processed corn silage diets in experiment 1. The decrease in total tract NDF (P < 0.09; Table 6
), ether extract (P < 0.003; Table 7
), and CP (P < 0.03; data not shown) digestibilities for cows fed processed corn silage diets mainly contributed to the decline in DE (% of gross energy) in experiment 1.
Two older studies have evaluated the effect of processing corn silage on energy content (Buck et al., 1969 and Rojas-Bourrillon et al., 1987) in animal digestion studies. In both trials of Buck et al. (1969), recutting corn silage had no beneficial effect on energy digestibility. No significant difference was observed between regular cut and recut silages because the difference in indigestibility of available carbohydrates was not large enough to result in a significant change in energy digestibility (Buck et al., 1969). Rojas-Bourrillon et al. (1987) reported no significant difference in gross energy digestibility at the rumen, small intestine, large intestine, or in the total tract. The authors (Rojas-Bourrillon et al., 1987) concluded that no difference in gross energy digestibility was observed because of the opposing effect of increased
-glucoside digestibility and decreased digestibility of fiber when cows were fed processed corn silage diets vs. unprocessed corn silage diets.
Metabolizable energy of TMR.
Estimated metabolizable energy (ME) of the diets followed similar trends as DE measurements because they were estimated from DE. The amount of ME in the diet was significantly affected by maturity in experiment 1. Metabolizable energy intake (Mcal/d) was greater (P < 0.05) at early maturities (hard dough and one-third ML) compared with the advanced maturity (two-thirds ML; Table 8
). Also, in experiment 1, diets containing corn silage harvested at two-thirds ML had the lowest concentration [Mcal/kg; P < 0.002] and digestibility of ME [% of DE; P < 0.0002], compared with one-third ML and hard dough stages of maturity (Table 8
).
Converting fibrous carbohydrates to energy is less efficient than converting nonfibrous sources of carbohydrates to energy in the rumen due to the metabolic pathways that each carbohydrate source uses. Greater amounts of methane are produced when fiber is digested. In experiment 1, there were greater levels of fiber and lower levels of nonfiber carbohydrate sources fed compared to experiment 2 (Tables 2
and 3
). Therefore, the assumption could be made that the diets fed in experiment 1 would produce a greater amount of methane than diets fed in experiment 2.
Some of the N consumed by the cow is excreted in urine and not used as an energy source. When the level of N in the diet exceeds the N requirements of the cow a greater amount will be excreted in the urine. The dietary CP concentration was greater in experiment 1 than experiment 2 (Tables 2
and 3
). Therefore, the assumption could be made that a greater amount of urinary energy would be excreted in experiment 1 than experiment 2 (Table 8
). In experiment 2, the dietary CP concentration (P < 0.0001; Table 3
) and urinary N output (P < 0.0001) were greater for hybrid Quanta than hybrid 3845.
Based on the above assumptions, ME as a % of DE should be lower in experiment 1 than experiment 2, and ME as a % of DE should be lower for hybrid Quanta than hybrid 3845 in experiment 2. In experiment 1, ME as a percent of DE averaged 84.8%, and in experiment 2, ME as a percent of DE averaged 87.3% (Table 8
). The lower ME as a % of DE was mainly attributed to greater urinary energy output in experiment 1 because methane output was actually greater in experiment 2 than in experiment 1 (Table 8
). In experiment 2, ME as a percent of DE was significantly lower (P < 0.02) for cows fed diets containing hybrid Quanta corn silage (86.9%) than hybrid 3845 (87.7%; Table 8
).
Total digestible nutrients and NEL concentration of TMR.
Total digestible nutrients (TDN) were calculated two ways in this paper. An equation was used that converts measured DE into TDN [TDN = DE (Mcal/kg)/0.04409; NRC, 1989]. Total digestible nutrients (TDN) were also measured using the digestion coefficients and nutrient concentration in TMR [measured TDN = digestible CP + digestible nonfiber carbohydrates + digestible NDF + (digestible ether extract x 2.25)]. Total digestible nutrients (TDN) measured from nutrient digestibilities (68.0, 69.9, and 68.2%, respectively) were similar to TDN calculated from DE (measured via bomb calorimetry; 68.5, 68.5, and 68.7%, respectively) in experiment 1 and for hybrids 3845 and Quanta in experiment 2, respectively.
Measured TDN (measured from nutrient digestibilities) and NEL concentrations were affected by maturity of corn silage in experiment 2 (Table 8
). There was a hybrid by maturity interaction, and diets containing hybrid Quanta corn silage harvested at two-thirds ML had significantly greater TDN (P < 0.02) and NEL concentrations (P < 0.02) than diets containing hybrid Quanta corn silage harvested at other maturities in experiment 2 (Table 8
). For hybrid Quanta in experiment 2, the increase in TDN and NEL concentrations for diets containing corn silage harvested at two-thirds ML was partially related to increased total tract ether extract digestibility (P < 0.02; Table 6
).
Mechanical processing had a significant effect on measured TDN and NEL concentrations in experiments 1 and 2 (Table 8
). The measured TDN (P < 0.01) and NEL concentrations (P < 0.02) were greater for diets containing unprocessed corn silage in experiment 1 and lower (TDN, P < 0.04; NEL, P < 0.03) for diets containing unprocessed corn silage in experiment 2 (Table 8
). The greater TDN and NEL concentrations for diets containing unprocessed corn silage in experiment 1 can be explained by the increased total tract NDF (P < 0.09; Table 6
), ether extract (P < 0.003; Table 7
), and CP (P < 0.03) digestibilities for cows fed unprocessed corn-silage diets. The lower TDN and NEL concentrations for diets containing unprocessed corn silage in experiment 2 can be attributed to lower total tract starch (P < 0.0001; Table 4
) and NDF (P < 0.04; Table 6
) digestibilities for cows fed unprocessed corn silage diets.
The exact reason for these results in experiment 1 is unknown. However, the authors speculate that it was partially related to the short particle size of the corn silages fed in experiment 1 (Johnson et al., 2002), which could have increased the rate of passage, and, therefore, decreased the extent of digestibility. This would be true especially for diets containing processed corn silage because the particle size was slightly shorter than the unprocessed corn silage (experiment 1; Johnson et al., 2002). Total digestible nutrients (TDN) and NEL concentrations (Mcal/kg) were, on average, 2.2 and 2.6% greater for TMR containing processed corn silage in experiment 2. Weiss and Wyatt (2000) reported that measured TDN (%) and NEL concentrations (Mcal/kg; calculated from TDN) were approximately 5% greater (P < 0.07) for TMR containing processed corn silage.
Energy requirements of lactating cows.
Digestible energy and NEL required for milk production and maintenance were estimated from actual production data (Table 9
). In experiment 1, the amount of DE and NEL (Mcal/d) required for milk production and maintenance were not significantly affected by maturity, processing, or maturity by processing interactions (Table 9
). Digestible energy (P < 0.04) and NEL (P < 0.06) required for milk production and maintenance were lower for cows fed diets containing corn silage harvested at physiological maturity (BL) compared to the earlier maturities in experiment 2 (Table 9
). The reason for this is unknown because milk production was not significantly different among cows fed diets differing in maturity of corn silage (Table 5
). In experiment 2, the amounts (Mcal/d) of DE (P < 0.0001) and NEL (P < 0.0001) required for milk production and maintenance were significantly greater for cows consuming diets containing hybrid 3845 corn silage compared with hybrid Quanta corn silage (Table 9
). The significant increase in energy required for milk production and maintenance can be attributed to the greater (P < 0.0004) milk production of cows consuming diets containing hybrid 3845 corn silage (Tables 5
and 9
).
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| CONCLUSIONS |
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Maturity of corn silage also affected digestibility and energy content of the TMR fed to lactating dairy cows. For hybrid Quanta in experiment 2, the TDN and NEL concentrations of TMR containing corn silage harvested at two-thirds ML was greater than at other maturities. This agrees with published data that suggests that the energy value of corn silage tends to be maximized between one-half and two-thirds ML (Harrison et al., 1996; Bal et al., 1997). However, experiment 1 had some contradictory results. Digestible energy and metabolizable energy, measured via bomb calorimetry, tended to be lower for cows fed TMR containing corn silage harvested at two-thirds ML compared to the less mature silages.
Hybrid of corn silage influenced intake and digestibility of nutrients. The NDF intake was greater for cows consuming diets that contained hybrid 3845 corn silage compared with diets containing hybrid Quanta corn silage. Estimated urinary energy output was lower for diets containing hybrid 3845 corn silage due to the lower concentration of CP in the diet compared with diets containing hybrid Quanta corn silage. Cows consuming diets that contained hybrid 3845 corn silage had greater DE and NEL requirements for milk production and BW maintenance. This was due to the higher level of milk production for cows consuming diets containing hybrid 3845 corn silage than for those fed hybrid Quanta corn silage diets.
Received for publication January 2, 2001. Accepted for publication April 16, 2002.
| REFERENCES |
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J.-S. Eun, K. A. Beauchemin, S.-H. Hong, and W. Z. Yang Effects of Mechanical Processing on the Nutritive Value of Barley Silage for Lactating Dairy Cows J Dairy Sci, December 1, 2004; 87(12): 4170 - 4177. [Abstract] [Full Text] [PDF] |
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D. R. Ouellet, H. Lapierre, and J. Chiquette Effects of Corn Silage Processing and Amino Acid Supplementation on the Performance of Lactating Dairy Cows J Dairy Sci, November 1, 2003; 86(11): 3675 - 3684. [Abstract] [Full Text] [PDF] |
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L. M. Johnson, J. H. Harrison, D. Davidson, W. C. Mahanna, and K. Shinners Corn Silage Management: Effects of Hybrid, Chop Length, and Mechanical Processing on Digestion and Energy Content J Dairy Sci, January 1, 2003; 86(1): 208 - 231. [Abstract] [Full Text] [PDF] |
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