Professional Documents
Culture Documents
Dairy Nutrition
Dairy Nutrition
supply the correct amounts and balance of nutrients required for optimal productive and
reproductive performance.
during the assimilation and processing of nutrients to meet the physiological needs of the
animal.
feeding and management strategies for dairy cattle for health and production. Dairy cattle
nutrition can be defined broadly as the use of the components of feeds for the processes
Feeds
Milk yield per cow continues to increase with a slower rate of increase in dry matter
components are key factors in improving the efficiency of feed use (Eastridge, 2006).
Cereal Grains
Most of the research with cereal grains has been with corn, barley, sorghum, and
wheat, and has been recently reviewed (Firkins et al., 2001). Reducing particle size of
cereal grains by mechanical processing (grinding or dry rolling) increases ruminal starch
digestibility but may slightly reduce ruminal NDF digestibility, and the benefit of the
processing is greater for the starch sources with lower ruminal digestibility of starch (e.g.,
1
Although diets generally have about 40 to 60% concentrates for lactating dairy
cows in early and midlactation and 30 to 40% concentrates during late lactation, research
not adequate. The forage-to-concentrate ratio does not take into consideration the quality
of the forage, particle size of the forage, the type and processing of the cereal grains, and
the concentration of nonforage fiber sources in the diet to affect dietary starch
concentration.
By-Products
Widely used cereal grain by-products include wet and dry corn gluten feed, corn
gluten meal, wet and dry brewers grains, distillers grains (with and without solubles; corn,
Oilseed by-products include the meals (high in protein) after extraction of the oil,
hulls, and whole cottonseed as a by-product from the ginning industry. Soybean meal is
Other oilseed meals such as cottonseed, canola, sunflower, and safflower are used in the
In the drying of by-products, such as with distillers grains, the heat can decrease
rumen degradability of the protein, but excessive heat can cause the Maillard reaction to
render the protein indigestible Soybean hulls are effective as a nonforage fiber source in
diluting starch from rations of high producing dairy cows, and cottonseed hulls are an
The hulls and cotton lint on whole cottonseed result in it being an effective fiber
source, with its effectiveness being similar to forages, unlike the fiber from most other by-
2
product feeds. Effects of gossypol, a toxic pigment in cottonseed, on cows and heifers is
often minimized by limiting the amount of cotton products in diets, but cotton products are
usually excluded in diets for bulls because of the negative effect of gossypol on viability
of sperm.
Molasses is produced from sugar beets, sugar cane, and citrus products. Some
by-products generated from the food industry that are used as animal feed include beet
pulp, citrus pulp, bakery wastes, vegetables, apple and tomato pomaces, nut fractions
and hulls, and whey. Dried whey is a common ingredient in milk replacers for young
animals; and to minimize the costs of drying, it is sometimes fed in liquid form to mature
animals(Eastridge, 2006).
Forages
Forages remain a vital part of the diet for dairy cattle to maintain rumen health, and
in many cases, for reduc-ing costs associated with feeding; therefore, more research has
been reported with forages than with other types of feed. Forages under primary
investigation include alfalfa, whole plant corn, whole plant sorghum, cereal grains, and
Grass, alfalfa and corn silages are among the most widely used components of
dairy cow rations due to their high nutritional value and high fiber content. In France corn
silage is consumed by about 80% of dairy cows during the year (AFSSA, 2004) and in
the US it is used extensively (Jokela and Russelle, 2003). In Denmark, output of corn
silage increased by more than 70% between 1990 and 2008 and is equal to or greater
than the output of grass silage (Storm et al., 2010). Worldwide, corn silage may constitute
3
50–75% of the diet (Driehuis et al., 2008) for a dairy cow consuming approximately 26 kg
Forage preservation is a crucial element for productive and efficient livestock farms
in most parts of the world. Forages can be preserved to feed livestock during periods of
shortage caused by limited pasture growth or inadequate pasture conditions or when fed
forage when production is faster than can be adequately utilized by animals. It prevents
abundant growth from becoming too mature. Subsequently, it also offers a more uniform
level of high quality forage for ruminant livestock throughout the year.
Forage is preserved in the form of hay, haylage or baleage, and silage. While
several techniques have been proven as efficient ways to store forages, it is important to
keep in mind that, at best, conserved forages can rarely match the nutritive value of fresh
forage, and some losses of highly digestible nutrients (sugar, protein, and fat) are
unavoidable. Focusing on minimize losses, which start immediately after cutting should
Silage techniques decrease the loss of nutrients as from harvest time until storage.
Moreover, they also improve the quality of feed (Beltzer 2003). The lactic acid bacteria
that are present on forage crops are involved in the fermentation of water-soluble
Due to the increasing use of silage around the world, it is necessary to ensure that
the silage produced is of good final quality. This review will emphasis to review up-to-date
information with a focus on silage, and possible advances techniques to limit silage
degradation.
4
Strategies to limit silage degradation and its economic and health impacts
diminishes animal performance in terms of body weight gain and increases feeding costs
for farmers who have to increase the daily silage provision or add other feedstuffs.
Currently, nothing can be done to rectify spoiled silage and it has to be thrown out.
transmitting pathogenic agents to animal and humans. Major issues in silage processing
are the use of poor quality or immature plant material, insufficiently rapid establishment
meet the economic and health risks associated with silage degradation, innovative
strategies in silage processing and respect of good manufacturing practices are required.
opening and the aerobic stage. The following section will discusses the possibilities for
prevented from entering the silage ecosystem. Pre-ensiling GMP is a matter of common
sense and includes such preventive measures as limiting crop degradation by fungi and
molds in the field and waiting some times between manure or slurry application and
harvest.
Crops should be harvested no sooner than four weeks after the last manure
spreading, to limit the presence in silage of butyric bacteria (Johansson et al., 200 5). This
5
measure also limits the introduction of other pathogens such as Listeria, Clostridium or
To limit the risk of incorporating telluric microorganisms in the silage, any mixing
of dirt or soil with the crop should be avoided by adjusting the harvester to the appropriate
height. Growth conditions and choice of harvesting period also have an important impact.
It has been shown that high dry matter concentration (>50% DM) in the raw material due
to late harvesting makes silage more susceptible to self-heating and infestation with toxin-
the nutritive value of the silage (Ashbell and Weinberg, 2006). Pathogens can also be
introduced into silage via silos and agricultural equipment. Cleaning before filling should
silos is also essential to limit contact with small animals such as rodents and birds, which
are potential vectors of many pathogens. Finally, before each feeding, any feed left over
from the previous feeding should be removed to prevent ingestion of spoiled silage and
development and acidification. Crops should be loaded into silos as fast as possible, and
firmly compacted, in order to quickly exclude air from the ensiled mass.
appropriate DM content (30–40% DM) and, with low-DM crops (mainly wet grasses and
6
Anaerobiosis can establish quickly when the silage particles are small and
therefore easily compacted in the silo. However, a too short particle size is linked to
excessive effluent (Demarquilly et al., 1998) and it has been shown that chopping length
influences the conservation and digestibility of the silage. Indeed, too many very short
particles entail a loss of the fibrous roughage properties necessary for good rumen
function and may result in acidosis (Zebeli et al., 2009). Optimal chopping length for
grasses ranges between 4 and 6 cm. Corn silage for dairy cows is recommended to
contain less than 1% of large particles (>2 cm), 8–12% of medium particles from 1 to 2
anaerobiosis (which promotes LAB fermentation) and on the buffering capacity and DM
of the crop. The incorporation of soil in silage increases its buffering capacity (Weinberg
and Ashbell, 2003). If buffering capacity is high, aerobic microorganisms found at the
beginning of ensiling, will remain active for an extended period and will reduce the quantity
of hexoses and pentoses available for further LAB fermentation. Silage acidification is
thus delayed and secondary fermentation by Clostridia occurs, during which lactic acid is
Mineral acids such as sulfuric and chlorhydric acids were used to promote silage
acidification and limit pathogenic microorganism growth. The authors have observed that
undissociated acid values in silage of pH 4.1–4.5 could be 10–100 times higher than
7
Formic acid increases the initial rate of decline of enterobacteria in grass silage
and is effective in reducing E. coli O157:H7 (O’Kiely et al., 2001). Formic acid is also
considered effective for reducing levels of biogenic amines (BA) in grass and alfalfa
(Steidlová and Kalac, 2004).BA contents in silage could be reduced by lowering plant
2007).
supplementation. With crops such as alfalfa which contain few WSC (3–7% DM), it may
to ensure the fermentation process. Added molasses represents 0.5 kg and whey 0.75
enzymes such as cellulase can convert the cellulose and hemicellulose of plant cells into
Bacterial inoculants are also commonly used for silage preservation. The purpose
of adding bacterial inoculants is to ensure faster accumulation of organic acids during the
ensiling period . The main organic acid produced by epiphytic LAB or silage additives is
lactic acid, responsible for the rapid pH decrease. Homofermentative lactic acid bacteria
are used in most commercially available inoculants, as they are efficient producers of
considered that 1×106 viable inoculant cells per gram is a sufficient for the bacterial
additives to overwhelm the epiphytic LAB and become the predominant population in the
8
silage (Gollop et al., 2005). Other Lactobacillus or Pediococcus species may be employed
and Enterococcus faecium is also frequently used (Li and Nishino, 2011)
A healthy crop at ensiling should remain so from silo filling through the storage
air into the silage should be avoided. To seal bunker and stack silos for extended periods,
plastic sheeting, usually polyethylene, is generally used (Weinberg et al., 2011). A new
black-on-white (125-m) coextruded oxygen barrier (OB) film have been shown to
constrain spoilage and dry matter losses under critical farm conditions and to improve the
stability of corn silage in the peripheral areas of the silos even when a proper harvest-
tofeedout management was implemented (Borreani et al., 2007). Dolci et al. (2001) have
observed a delay in yeast and mold growth during aerobic exposure of silages previously
physical damage by birds and rodents and to UV. Ensiling is a competition between
aerobic and anaerobic processes. At silo opening, air can enter the forage mass and
trigger silage degradation (McEniry et al., 2010). Silo capacity should be determined
according to feeding needs (herd size and rations), and the dimensions should be
calculated so that a sufficient depth of silage is removed each day from the silo face to
minimize silage exposure to air. A clean cut at the silage front limits air penetration and
Aerobic stability can be achieved by the use of various silage additives. Among chemical
additives, formic acid has been shownto enhance the aerobic stability of whole-crop
9
wheat, sorghumand cornsilages by causingmore extensiveheterolactic fermentation with
high levels of acetic and propionic acids in the silage (Kung and Ranjit, 2001).
storage, several authors have shown that lactic acid could be used as substrate by
(Filya et al., 2004). Heterolactic fermentation is therefore preferred in order to improve the
been shown to increase aerobic stability and reduce fermentation losses in numerous
commonly added to the ensiled mass. Sodium nitrite in combination with hexamine
effectively prevented clostridia growth, while sodium benzoate restricted yeast growth
(Knicky and Lingvall, 2001). The use of calcium formiate, sodium benzoate and sodium
nitrite have also resulted in high hygienic quality corn silage and significantly reduced
et al., 2009).
The silage quality affects the intake and digestibility of ruminants. The dry matter
populations present in the forage are the main factors that can interfere with the
fermentation of the silage. Forage with low DM and WSC concentrations may indicate
10
unfavorable fermentation and forage with excessive WSC content may create acidic
The intake and digestibility of silage determines the feeding value of silage
(Huhtanen et al., 2002). Intake of dried forages is generally closely related to digestibility
and cell wall contents (Mertens, n.d.), but this relationship is weaker for ensiled forages,
process.
(Mizubuti et al., 2002) . The intake of silage is mostly lower than the intake of fresh forage
(Mauro et al., 2013) because of the occurrence of toxic substances produced during the
fermentation as amines; also because of the high concentration of organic acids and
decline in the water soluble carbohydrate content which lower availability of energy for
………………………….x………………………………..x…………………………………….
11
References
Adesogan, A., Salawu, M., Ross, A., Davies, D., Brooks, A., 2003. Effect of Lactobacillus
buchneri, Lactobacillus fermentum, Leuconostoc mesenteroides inoculants, or a
chemical additive on the fermentation, aerobic stability, and nutritive value of
crimped wheat grains. J. Dairy Sci. 86, 1789–1796.
Adler, A., Lew, H., 1995. Seasonal-changes of epiphytic microorganisms on manured,
NPK-fertilized and not fertilized forage. Bodenkultur
AFSSA, 2004. Bonnes pratiques de fabrication de l’ensilage pour une meilleure maîtrise
des risques sanitaires. Agence Franc¸ aise de Sécurité Sanitaire des Aliments
AFSSA.
AFSSA, 2009. Avis sur l’augmentation des cas de listériose et le lien éventuel avec
l’évolution des modes de production, de préparation et de consummation des
aliments (no, MIC-RA-ListerioseAlim). Agence Franc¸ aise de Sécurité Sanitaire
des Aliments AFSSA, France.
Ashbell, G., Weinberg, Z., 2006. Silage Production and Utilization. Food and Agriculture
Organization, FAO Electronic Library.
Biro, D., Juracek, M., Kacaniova, M., Simko, M., Galik, B., Michalkova, J., Gyongyova,
E., 2009. Occurrence of microscopic fungi and mycotoxins in conserved high
moisture corn from Slovakia. Ann. Agric. Environ. Med. 16, 227–232.
Borreani, G., Tabacco, E., Cavallarin, L., 2007. A new oxygen barrier film reduces aerobic
deterioration in farm-scale corn silage. J. Dairy Sci. 90, 4701–4706.
Demarquilly, C., Dulphy, J.-P., Andrieu, J.-P., 1998. Valeurs nutritive et alimentaire des
fourrages selon les techniques de conservation: foin, ensilage, enrubannage.
Fourr. 155, 349–369.
Devendra, C., 1995. Nutritional ecology of the ruminant. 1994: Peter J. van Soest,
Cornstock Publishing Associates, Cornell University Press, Eage House, 512 East
State Street, Ithaca, NY 14850, USA. HB US $71.50. ISBN 0-8014-2772-X. 476
pp. Elsevier.
12
Dolci, P., Tabacco, E., Cocolin, L., Borreani, G., 2001. Microbial dynamics during aerobic
exposure of corn silage stored under oxygen barrier or polyethylene films. Appl.
Environ. Microbiol. 77 (21), 7499–7507.
Drackley, J.K., Donkin, S.S., Reynolds, C.K., 2006. Major advances in fundamental dairy
cattle nutrition. J. Dairy Sci. 89, 1324–1336.
Eastridge, M.L., 2006. Major Advances in Applied Dairy Cattle Nutrition 89, 13.
Girardin, H., Morris, C.E., Albagnac, C., Dreux, N., Glaux, C., Nguyen-The, C., 2005.
Behaviour of the pathogen surrogates Listeria innocua and Clostridium
sporogenes during production of parsley in fields fertilized with contaminated
amendments. FEMS Microbiol. Ecol. 54, 287–295.
Gollop, N., Zakin, V., Weinberg, Z.G., 2005. Antibacterial activity of lactic acid bacteria
included in inoculants for silage and in silages treated with these inoculants. J.
Appl. Microbiol. 98, 662–666.
J. Appl. Microbiol. 109, 1017–1026 Driehuis, F., Spanjer, M., Scholten, J., Giffel, M., 2008.
Occurrence of mycotoxins in maize, grass and wheat silage for dairy cattle in The
Netherlands. Food Addit. Contam. 1, 41–50.
Johansson, M., Emmoth, E., Salomonsson, A., Albihn, A., 2005. Potential risks when
spreading anaerobic digestion residues on grass silage crops – survival of
bacteria, moulds and viruses. Grass For. Sci. 60, 175–185.
Jokela, B., Russelle, M., 2003. Perennial Forages Benefit Soils, Other Crops, and Water
Quality in Important Ways. US Dairy Forest Research Center.
Knicky, A., Lingvall, R., 2001. Possibilities to avoid growth of clostridia and/or fungi in
wilted silage by use of organic and inorganic salts. In: Proceedings of the XIX
International Grassland Congress: Grassland Ecosystems: an Outlook into the
13
21st century, Gomide, JA; Mattos, WRS; DaSilva, SC, Sao Pedro, Brazil, pp. 788–
789.
Kung Jr., L., Schmidt, R.J., Ebling, T.E., Hu, W., 2007. The effect of Lactobacillus
buchneri 40788 on the fermentation and aerobic stability of ground and whole high-
moisture corn. J. Dairy Sci. 90, 2309–2314.
McEniry, J., O’Kiely, P., Clipson, N.J.W., Forristal, P.D., Doyle, E.M., 2010. Assessing the
impact of various ensilage factors on the fermentation of grass silage using
conventional culture and bacterial community analysis techniques. J. Appl.
Microbiol. 108, 1584–1593.
Mauro, E., da Silva, T.C., Oliveira Macedo, C.H., Sena, F., 2013. Lactic Acid Bacteria in
Tropical Grass Silages, in: Kongo, J.M. (Ed.), Lactic Acid Bacteria - R & D for Food,
Health and Livestock Purposes. InTech. https://doi.org/10.5772/50703
Mizubuti, I.Y., Ribeiro, E. de A., da Rocha, M.A., Silva, L., Pinto, A.P., Fernandes, W.C.,
Rolim, M.A., 2002. Intake and apparent digestibility of corn (Zea mays L.), sorghum
(Sorghum bicolor (L.) Moench) and sunflower (Helianthus annuus L.) silages.
Nishino, N., Hattori, H., Wada, H., Touno, E., 2007. Biogenic amine production in grass,
maize and total mixed ration silages inoculated with Lactobacillus casei or
Lactobacillus buchneri. J. Appl. Microbiol. 103, 325–332.
O’Kiely, P., Byrne, C., Bolton, D., 2001. Survival of E. coli O157 H7 added to grass at
ensiling and its influence on silage fermentation. In: 19th International Grassland
Congress. Presented at the proceedings of the XIX international grassland
congress-Grassland ecosystems: an outlook into the 21st century, Gomide, JA;
Mattos, WRS; DaSilva, SC, Sao Pedro, Brazil, pp. 792–793.
Purwin, C., Laniewska-Trokenheim, L., Warminska-Radyko, I., Tywonczuk, J., 2006.
silage quality: microbial health promoting and production aspects. Med.
Steidlová, S., Kalac, P., 2004. The effects of lactic acid bacteria inoculants and formic
acid on the formation of biogenic amines in grass silages. Arch. Anim. Nutr. 58,
245–254.
Storm, I.M.L.D., Kristensen, N.B., Raun, B.M.L., Smedsgaard, J., Thrane, U., 2010.
Dynamics in the microbiology of maize silage during whole-season storage.
14
Weinberg, Z., Chen, Y., Miron, D., Raviv, Y., Nahim, E., Bloch, A., Yosef, E., Nikbahat,
M., Miron, J., 2011. Preservation of total mixed rations for dairy cows in bales
wrapped with polyethylene stretch film – a commercial scale experiment. Anim.
Feed Sci. Technol. 164, 125–129.
Weinberg, Z.G., Ashbell, G., 2003. Engineering aspects of ensiling. Biochem. Eng. J. 13,
181–188. Weter. 62, 865–869.
Wiedmann, M., 2003. ADSA Foundation Scholar Award—an integrated science-based
approach to dairy food safety: Listeria monocytogenes as a model system. J. Dairy
Sci. 86, 1865–1875.
Zebeli, Q., Ametaj, B., Junck, B., Drochner, W., 2009. Maize silage particle length
modulates feeding patterns and milk composition in loose-housed lactating
Holstein cows. Livest. Sci. 124, 33–40.
Zhang, J., Kawamoto, H., Cai, Y., 2010. Relationships between the addition rates of
cellulase or glucose and silage fermentation at different temperatures. Anim. Sci.
J. 81, 325–330.
15