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* Department of Dairy Science
Department of Agronomy, University of Wisconsin, Madison 53706
2 Corresponding author: dkcombs{at}wisc.edu
| ABSTRACT |
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Key Words: forage utilization pasture silage milk production
| INTRODUCTION |
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Alfalfa (Medicago sativa L.) is the predominant forage legume grown and fed to lactating dairy cows in the midwestern United States because it has the highest yield potential and feeding value of the perennial forage legumes. However, alfalfa is not suitable for all soil conditions, especially soils that are poorly drained or that have low pH, and is vulnerable to winter-kill. In addition, alfalfa is not commonly used in grazing systems because cattle are at risk of bloat and the stands decline because of damage caused by grazing animals. Cool-season grasses and legumes tend to be the highest producing species in the Upper Midwest and are often planted together in pastures for dairy cattle. These mixtures offer the benefits of increased yield, improved seasonal distribution of forage, and higher nutritive quality when compared with grass monocultures. Combining legumes with grasses also reduces dependence on nitrogen fertilizer. Grass-legume mixtures reduce the possibility of bloat, decrease the risk of winter-kill, and provide greater stand longevity when compared with pure legume stands. (Zemenchik et al., 2002).
Kura clover (Trifolium ambiguum M. Bieb.) and reed canarygrass (Phalaris arundinacea L.) grown together result in a mixture that is persistent and high yielding, with the potential to be a quality forage source for lactating dairy cows. Both species are cool-season perennial forages with an extensive rhizome system, which contributes to their persistence and grazing tolerance (Brummer and Moore, 2000). The quality of kura clover is higher than that of most other forage legumes, including alfalfa (Allinson et al., 1985; Sheaffer and Marten, 1991; Sleugh et al., 2000). Reed canarygrass produces high yields of total biomass (Marten and Hovin, 1980) and has the potential to produce more summer re-growth (Balasko and Nelson, 2003), resulting in greater seasonal distribution. The mixture of reed canarygrass and kura clover produces similar biomass yields as alfalfa (K. A. Albrecht, unpublished data). In contrast to its reputation as a low-quality forage, the release of newer varieties of reed canarygrass containing low levels of alkaloids offers potential for improved animal performance, and these varieties have similar or greater nutrient digestibilities when compared with other perennial cool-season grasses (Buxton and Marten, 1989; Buxton, 1990).
This mixture, grown in permanent pastures, requires careful management. The greatest production occurs in May and June, similar to other cool-season forage crops in the midwestern environment, resulting in surplus forage in the spring. Failure to properly manage this flush of spring growth will result in overmature, low-quality forage that is not suitable for grazing or hay production. Some pastures can be taken out of the grazing system during the spring flush to mechanically harvest high-quality forage as hay or silage to be used during times when growth is not abundant.
Besides being used in grazing systems, this mixture could also be used in confinement systems where environments are not consistent for alfalfa production. Kura clover and reed canarygrass are able to tolerate drought, wet soils and short-term flooding, soils with low pH, cold open winters, and ice sheeting (Pederson, 1995; Carlson et al., 1996). Because of their winter hardiness, adaptation to diverse soil and climatic conditions, and performance under conditions that are less than optimal for alfalfa, this mixture may provide an alternative forage in environments not suitable for alfalfa.
Research has been performed in laboratories with small-scale silos or bags to evaluate silage characteristics of these forages after undergoing fermentation. Results indicated ensiled kura clover was well preserved, with minimal changes in forage quality (Seguin and Mustafa, 2003; Contreras-Govea et al., 2006). The pH and VFA profile of ensiled reed canarygrass suggest proper fermentation occurred (Cherney et al., 2006), and mixtures of kura clover and reed canarygrass also fermented well in laboratory silos (K. A. Albrecht, unpublished data). However, the intake and lactation performance of dairy cows fed this mixture as fermented silage are not known.
The objective of this trial was to compare DMI and performance of lactating dairy cows fed a TMR containing equal DM from either alfalfa silage (AS) or kura clover-reed canarygrass silage (KRS) as the sole source of forage in the diet.
| MATERIALS AND METHODS |
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Animals and Diets
Twenty multiparous lactating Holstein cows were used in a crossover design with 2 experimental periods of 28 d each. The first 14 d of each period was allowed for adaptation to the diet. At the beginning of the study, cows averaged 190 ± 16 (mean ± SD) DIM, 33.2 ± 5.5 kg/d of milk, and 667 ± 81 kg of BW. Cows were housed at the University of Wisconsin-Madison Arlington Agricultural Research Station in individual tie stalls or stanchions and had free-choice access to water throughout the trial. Cows were milked twice daily in a milking parlor and turned outside in a concrete lot for 3 h daily after the morning milking, with access to water but no feed. The Animal Care Committee of the College of Agricultural and Life Sciences of the University of Wisconsin-Madison approved all procedures involving animals.
The study was conducted from July 29 to September 25, 2005. Treatments were TMR formulated with either 57% of total DM from 1) AS or 2) KRS. The TMR consisted of silage, ground high-moisture corn, and supplement containing soybean meal (48% CP), corn gluten meal, minerals, and vitamins. Both diets had the same feed ingredients except for the forage, which the sole source was either AS or KRS, and chemical composition of the diets was mathematically calculated from individual feedstuffs. The TMR was mixed once daily and fed ad libitum twice daily with 67 and 33% of TMR offered at 1000 and 1700 h, respectively. The amount of feed offered was adjusted daily to obtain approximately 5 to 10% orts. Dry matter (48 h at 60°C) of forages was determined weekly, and diets were adjusted to account for changes in DM content to maintain a constant forage-to-concentrate ratio.
Sampling and Analysis
Samples of AS and KRS were collected weekly during feed-out throughout the trial and stored at –20°C pending analysis. Forage samples were composited by period and analyzed by Dairyland Laboratories Inc. (Arcadia, WI) for nutrient composition and fermentation profile by using AOAC (2006) methods for DM (method 930.15), ash (method 942.15), CP (method 954.01), and ammonia-nitrogen (method 920.03). Lignin, NDF, and ADF were determined by using methods described by Goering and Van Soest (1970). Organic acids and ethanol were measured by using a modification of the HPLC method of Siegfried et al. (1984). Neutral detergent fiber digestibility was determined by a 48-h in vitro procedure (Goering and Van Soest, 1970) at the University of Wisconsin Soil and Forage Analysis Laboratory (Marshfield, WI).
Dry matter intake and milk production were recorded daily throughout the experiment; however, only d 15 through 28 of each period were used in analysis. Efficiency of conversion of feed DM was computed for each cow by dividing mean milk yield by mean DMI for d 15 through 28 of each period. Milk samples were collected at 4 consecutive milkings from d 25 (p.m.) through 27 (a.m.) of each period and analyzed for fat, protein, lactose, SNF, and MUN by the AgSource Milk Analysis Laboratory (Menomonie, WI) with a Foss FT6000 near-infrared analyzer (Foss Electric, Hillerød, Denmark).
Ort samples were collected once daily before the morning feeding on d 24 through 28 of each period. Orts were dried at 60°C for 48 h, composited by cow and period, ground to pass through a 1-mm screen (Wiley mill, Arthur H. Thomas, Philadelphia, PA), and analyzed for DM, CP, NDF, ADF, and ash. The analytical DM was determined by oven-drying at 100°C for 24 h, and ash content was determined by ashing at 550°C for 12 h. Samples were analyzed for CP (method 2001.11; AOAC, 2006) with the following modifications: 0.3 g of sample was analyzed; 15 mL of H2SO4, 2.87 g of Na2SO4, and 0.13 g of CuSO4 were added to each tube for digestion; digestion time was 90 min; 40 mL of water was added to the tubes after digestion; samples underwent steam distillation into a boric acid solution (4% wt/ vol) containing 0.20% methyl red indicator solution and 0.98% bromocresol green solution; and 0.1 N H2SO4 was used to titrate the distillate. Ash-corrected NDF was determined according to Van Soest et al. (1991) adapted for an Ankom200 Fiber Analyzer (Ankom Technology, Fairport, NY) by using
-amylase and sodium sulfite, and ADF was determined as described by Goering and Van Soest (1970) adapted for an Ankom200 Fiber Analyzer (Ankom Technology).
Apparent total tract nutrient digestibilities were measured by using lanthanum as an external marker. A gelatin capsule (Torpac Inc., Fairfield, NJ) containing La2O3 dissolved in HCl and carried on wheat middlings was administered twice daily at 0700 and 1900 h orally via a balling gun on d 18 through 28 to provide approximately 0.87 g of lanthanum/d. Fecal grab samples were collected twice daily at 0700 and 1900 h on d 24 through 28 of each period. Fecal samples were composited by cow and period, freeze-dried (period 1) or oven-dried at 60°C (period 2) to a constant weight, ground to pass through a 1-mm Wiley mill screen, and analyzed for DM, CP, NDF, ADF, and ash as described previously. Duplicate 1-g fecal samples were weighed into 30-mL beakers and ashed in a muffle furnace (Thermolyne 62700, Barnstead/Thermolyne Corp., Dubuque, IA) at 500°C for 16 h. After ashing, 15 mL of HCl was added to each beaker and allowed to stand for 1 h. Beaker contents were then diluted to 50 g in a standard 100-mL class A volumetric flask with deionized water. The fecal concentration of lanthanum was measured by inductively coupled plasma-optical emission spectroscopy (Vista-MPX Simultaneous ICP-OES, Varian, Palo Alto, CA) at Analab Inc. (Fulton, IL) by using wavelengths 333.749, 379.082, 379.477, 399.852, and 408.671 nm to produce a median value. Total tract nutrient digestibilities were calculated from lanthanum and nutrient concentrations in orts-adjusted diet and feces.
Data were statistically analyzed by using the MIXED procedure of SAS (SAS Institute, 1999) with the following model:
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where µ is the overall mean, Ti is the fixed effect of treatment (i = 1 to 2), Pj is the fixed effect of period (j = 1 to 2), Ck is the random effect of cow (k = 1 to 20), and Eijk is the residual error term, assumed to be normally distributed.
During the second period, one cow was removed from the trial because of an injury. Consequently, data from 20 and 19 cows were analyzed for periods 1 and 2, respectively. Significance was declared at P
0.05 and a trend was declared at P
0.10.
| RESULTS AND DISCUSSION |
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According to Albrecht and Muck (1991), legumes often undergo extensive protein degradation during ensiling. This is consistent with the high concentrations of ammonia present in the 2 silages, suggesting extensive protein breakdown. Alfalfa silage had a higher concentration of ammonia-nitrogen than KRS. The extent of proteolysis is dependent on the rate of pH drop during ensiling (McKersie, 1985). Because the final pH was similar for both silages, the rate of decline for AS was likely slower than that for KRS, resulting in greater protein hydrolysis in AS. The high buffering capacity, low levels of water-soluble sugars, and lower DM content of AS could also contribute to a greater protein breakdown in AS than in KRS.
The ingredients and nutrient composition of the diets are listed in Table 2
. The diets contained approximately a 57:43 forage-to-concentrate ratio on a DM basis. Differences in forage composition were reflected in the mean nutrient composition of both treatment diets. Both diets met or exceeded the nutrient requirements for mid- to late-lactation dairy cows producing approximately 35 kg of milk/d (NRC, 2001).
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Particle breakdown and size distribution in the rumen are also different for grasses and legumes. Dewhurst et al. (2003) noted that cows consuming alfalfa had a low proportion of large particles (>2 mm) and a high proportion of intermediate particles (0.106 to 2 mm) compared with grass-fed cows. The rapid breakdown of alfalfa in the rumen results in small particles with a greater surface area, allowing for faster digestion and increased passage rates. Grass particles, which are elongated and slender, usually pass from the rumen more slowly than the cuboidal fragments of legumes (Buxton et al., 1996). The longer residence time of filamentous grass particles in the rumen may be due to entrapment in the longer fiber mat and increased buoyancy associated with a higher amount of potentially digestible NDF in cows fed grass.
These characteristics and the positive relationship between NDF and rumen fill suggest that the DMI of cows fed KRS was restricted by rumen fill. Mertens (1987) indicated that cows consume approximately 1.2% of their BW/d as NDF when intake is limited by rumen capacity. This is the level of NDF (8.03 kg of NDF/667 kg of BW x 100 = 1.2%) consumed by cows fed KRS, but the cows fed AS consumed only 1.0% of their BW as NDF in this trial.
Although intake of total NDF and digestible NDF were higher for the cows consuming KRS, the amount of ruminally undegraded NDF was similar (3.7 kg) between treatments. A higher intake of NDF and a similar intake of indigestible NDF between diets would be expected if intake were limited by the presence of indigestible fiber in the rumen (Dado and Allen, 1996). On the basis of these observations, it is also possible that intake was restricted by undegraded NDF present within the rumen for both groups.
The intake of cows fed the KRS diet was probably limited by the time required to digest fiber, reduce particle size, and move undigested residues through the digestive tract. This is consistent with the findings of Dewhurst et al. (2003), who reported that cows fed grass silage had lower voluntary intakes, higher rumen fills, and slower rumen outflow rates than cows fed AS.
Milk yield and composition are listed in Table 4
. The higher milk (P < 0.09) and FCM (P < 0.05) yields for AS are likely a result of the increased DMI for cows consuming the AS diet. Feed efficiency was similar for both forages, with approximately 1.5 kg of milk produced per kilogram of DM consumed, which suggests that digestible NDF of KRS was utilized as efficiently for milk production as were the cell wall constituents of AS. Yields of fat and protein were not affected by treatment, but lactose (P < 0.01) and SNF (P = 0.01) yields were higher for cows fed AS. Milk fat percentage tended to be higher (P = 0.09) for cows fed the AS diet. The concentrations of lactose and SNF were similar for the 2 groups, indicating that the observed increase in lactose and SNF yields for AS was a result of the higher milk yields for this group. Cows fed AS had significantly higher MUN levels (P < 0.01) than cows fed KRS. Because of the difference in dietary CP levels, it was not possible to determine whether the lower MUN concentrations on the KRS diet were due to improved N efficiency or were a reflection of the lower CP intake; however, it has been reported that protein breakdown in AS to NPN substantially reduces the efficiency of CP utilization by lactating dairy cows (Broderick, 1995).
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| CONCLUSIONS |
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| ACKNOWLEDGEMENTS |
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| FOOTNOTES |
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Received for publication November 14, 2007. Accepted for publication April 6, 2008.
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