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Optimizing Starch Nutrition for Rhythmic Dairy Cattle: The Sustaining Economic and Environmental Challenges of Today's Industry | ||
Iranian Journal of Applied Animal Science | ||
دوره 11، شماره 2، شهریور 2021، صفحه 207-215 اصل مقاله (437.57 K) | ||
نوع مقاله: Review Article | ||
نویسنده | ||
A. Nikkhah* 1، 2 | ||
1Ferdows Pars Agriculture and Livestock Holding Co., Mostazafan Foundation, Tehran, Iran | ||
2Department of Animal Science, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran | ||
چکیده | ||
Starch makes up a considerable portion of dairy diets (up to >30%). Thus, starch utilization efficiency immensely affects rumen function, animal performance and health, farm economics, and environmental quality. It is crucial to take into account the ruminal digestion rhythms of different cereals when formulating diets for optimal dry matter intake (DMI), milk production, and animal health. Optimizing the physical processing of cereal grains is required for maximal microbial protein yield and minimal sub-acute rumen acidosis (SARA). Physical processing of barley and corn grains, as the two most popular cereals in dairy diets, needs more contemplation towards synchronizing rhythms of starch and protein fermentation in the rumen. Optimizing the dietary inclusion rates of cereal grains and starch has been a key missing part in improving nutrient efficiency and gastrointestinal health and integrity. Global guidelines need to be developed to precisely address optimal dietary inclusion rates of different cereal grains. Setting such guidelines becomes more important when high-starch corn silage is major forage in the diet. Monitoring circadian rhythms of rumen fermentation when differently processed cereal grains are fed will allow developing feeding strategies that minimize the occurrence of SARA. The minimized SARA will enable decreasing nutrient loss across portal drained viscera (PDV) and splanchnic tissues. An innovative global philosophy is being developed to rely more on oil seeds and less on starchy grains in feeding dairy cows. To practically prevent SARA, physical processing can be partly effective, but essentially the dietary inclusion rate of differently processed cereal grains needs to be optimized. Lessons are to be learnt from human nutrition. Although metabolism differs between ruminants and non-ruminants, carbohydrates especially sugars and starch are under scrutiny and need to be limited in human diets to minimize risks from obesity and diabetes. Education, education and education is the final frontier for success in improving rumen and animal health as far as starch nutrition is concerned. For now, it is recommended to feed dairy cows no more than 25-28% starch (DM based). Future research will focus on establishing optimal dietary inclusion rates of differently processed barley and corn/sorghum grains for cows of different production levels and lactation stages. Rumen fermentation circadian rhythmicity and environmental considerations including decreased methane production and urinary and fecal nitrogen excretion will be discussed. | ||
کلیدواژهها | ||
cereal؛ dairy cow؛ economics؛ environment؛ rhythm؛ starch | ||
اصل مقاله | ||
INTRODUCTION Starch is a significant portion of dairy diets (up to >30% of diet dry matter) and immensely affects rumen health and function and cow performance (NRC, 2001). Dietary starch is mainly supplied from cereals including corn, barley, wheat, oats, and sorghum grains as well as cereal forages namely corn silage and other cereal silages. What makes starch nutrition challenging is differential rumen fermentation dynamics amongst differently processed grains and forages (Van Soest, 1994). Controversy exists as to the optimum site and rhythms of starch digestion (rumen vs. small intestine). Nonetheless, two facts are known. First, starchy grains must be optimally processed to maximize rumen microbial mass production while not increasing the risk of sub-acute rumen acidosis (SARA). Second, due to limited small intestinal capacity for starch assimilation and glucose transport, excessive escape of undigested or partially digested starch from the rumen fermentation must be avoided (Orskov, 1986; Huntington, 1997; Nikkhah, 2010). Notably, however, the key reason for starch malnutrition has been the suboptimal dietary inclusion rates of cereal grains in relation to dietary forage. Optimizing the dietary inclusion rate of cereal grains requires special attention in rhythmic starch nutrition management for dairy cows (Oba and Allen, 2003). The use of oil seeds and decreased dietary starch should allow mitigating methane production and decreased risk from SARA (Beauchemin et al. 2009). These dietary changes will result in improved production, health and profitability and decreased nutrient excretion via urine and feces that can potentially benefit the environment. Therefore, the main objective of this review was to describe how to optimize starch nutrition for rhythmic dairy cows to help overcome the sustaining economical and environmental challenges of today's industry. To meet this objective, rumen rhythms of differently processed grains and optimal dietary inclusion rates of cereal grains in relation to forage type will be discussed. In addition, circadian rhythms of rumen fermentation and hypothetically of portal-drained visceral and splanchnic tissues will be addressed. Moreover, lessons from human nutrition that are to be learned will be delineated to discuss how to reduce risks from SARA and other health disorders.
Starch sources for dairy cattle: A global outlook Cereal grains (Figure 1) are the main dynamic starch sources for dairy cattle. They vary in amylose and amylopectin content as well as in starch, protein, fiber, and fat percentage and vitamins and minerals (Figure 2). Starch comprises 55 (oats) to almost 75% (corn) of whole grains on a dry matter basis. Maize or corn is broadly grown across the world. Corn has the highest world production among all cereals with approximately 817 million tons per year (FAOSTAT, 2017). Corn is a vital principal food in many countries with wide usage in animal feed and other industries. The corn crop has remarkable genetic variability, enabling it to flourish in tropical, subtropical, and temperate climates. Wheat grain is the second most prevalent cereal in the world with an annual production of 755 million tons.
Figure 1 Specified cereal grain structure (Bernstein et al. 2013)
Figure 2 Starch, fiber, fat and protein fractions of cereal grains (McKevith, 2004)
The largest producers of wheat are China, India, Russia and United States. Because of its fast and extensive rumen fermentation, wheat grain may be used in dairy rations only in limited or moderate rates. Rice is a staple food for humankind throughout the world and a feed for animals. Rice as a staple food for more than half the human population of the world is the third largest produced cereal after maize with over 685 million tons production per year (FAOSTAT, 2017). The largest rice producers are China, India, Indonesia and Pakistan. The rice produced in Iran possesses unique taste that is distinct from the rice produced in other countries. Rice cultivation requires more water than other cereals and is more labor intensive. Where produced, rice can be considered as a dietary cereal choice in ruminant diets, but not in major amounts. Barley grain ranks fourth in the global cereal production, with an approximate world yield of 136 million tons per year (FAOSTAT, 2017). The barley crop requires a temperate climate with the major growing areas including Europe and Russia. However, barley is also a valuable and resilient crop in arid and semi-arid areas of Asia, the Middle East, and North Africa. It is primarily used as flour for human consumption, in animal feed, and as malt for beverage production. Due to its unique nature, barley grain is profoundly viewed as a treasure or tragedy in ruminant nutrition (Nikkhah, 2010). Sorghum is the fifth most significant cereal with an annual world production of over 55 million tons (FAOSTAT, 2017). Sorghum varieties are usually more heat and drought tolerant than other cereal crops. Thus, sorghum is an important crop in arid areas. Sorghum is a valuable food for humans as well in Africa, Central America, and South Asia. It is also used to produce beverages and biofuel. Millet is a communal word referring to various small-seeded annual grasses grown as grain crops, mainly on marginal lands in dry areas of temperate, sub-tropical and tropical regions. Millet is considered a subsistence grain cultivated for food and animal fodder. The largest producers of millet are India and Nigeria with a total world production of 31 million tons per year (FAOSTAT, 2017). Traditionally, cereal grains have been compared in terms of major nutrients such as energy and protein. Less attention has been paid to their differences in minerals and vitamins while they vary considerably in this regard.
Optimizing dietary starch inclusion rate: The missing key Much attention has long been paid to physical processing of cereal grains for optimal rumen and post-rumen starch utilization (Orskov, 1986; Huntington, 1997). However, optimizing the dietary inclusion rate of starch has received very inadequate thoughts. Optimizing the dietary inclusion rate of starch is the key missing part of the whole starch story. Many dairy farmers feed more starch than recommended to their high-producing and to even low-producing lactating cows (farm observations). It is usually considered very risky to feed more than 25-28% starch (on a DM basis) to high-merit cows (Table 1). Assuming a minimum of 4-5% of total dietary starch coming from corn silage (presuming that 20% of diet DM is corn silage), about 20-25% starch is allowed to be supplied from grains. This calculation implies a maximum allowance of 26-34% corn in diet. Such a starch equivalent amount would be lower for barley grain since barley is fermented in the rumen with greater extent and rate than is corn grain. Nevertheless, it is often observed that farmers feed diets with 60-65% concentrate (DM basis), 60% of which is cereal grain that means feeding 36-42% cereal grain to dairy cows. Such high dietary cereal grain levels would be considered very risky (explosive in the rumen) given that an additional 5-10% starch is supplied from forages. At these starch inclusion rates, it is not surprising to observe high rates of SARA on many dairy farms (Humer et al. 2018). Public and farmer education must be enhanced to assist farmers to lower the risk of SARA occurrence. When we can prevent a problem or challenge from happening by practicing wisdom, why should we make it happen and then look for ways to overcome it?! Thus, the current concept and practice of excessive starch inclusion in the diet of dairy cows must be fundamentally challenged and refined for further improvement in dairy cow health and profitability.
Optimizing the physical processing of rhythmic starchy grains Physical processing and damage to the whole cereal kernel is mandatory to make its endosperm accessible to microbial adherence and fermentation in the rumen. Different processing methods and technologies for starchy grains for dairy cows have previously been discussed (Ørskov, 1986; Huntington, 1997). An innovative philosophy with regards to choosing optimal grain processing methods is based on the nature of endosperm in different cereals. For instance, barley grain is fermented in the rumen more rapidly and extensively than is corn grain. As a result, the entire philosophy of using steam-processing is different for barley vs. corn grain. Barley grain is already highly degradable and, hence, steam-processing is conducted to slow down its fermentation rate to better synchronize starch and protein degradation rates (Hall and Huntington, 2008). Steam-rolling vs. grinding or dry-rolling produces larger barley particles that are more slowly degradable in the rumen, thereby minimizing SARA risks. In contrast, corn grain is slowly degradable in the rumen. Thus, steam-processing of corn grain aims to increase its degradation rate and extent in the rumen for increased nutrient synchrony and improved microbial mass production. In addition, the duration of steam exposure is shorter for rapidly fermentable grains (i.e., 5-10 minutes for barley and wheat) and longer for slowly degradable grains (i.e., 20-30 minutes for corn and sorghum grains). In addition to decreasing barley and wheat rumen degradation rate, steam-rolling decreases feed dusts and makes feed more palatable. These benefits hold especially true for early lactation cows when DMI is relatively low. However, fundamentally, when dietary inclusion rates of barley and wheat grains are kept low to moderate (e.g., <10-20% of diet DM), steam-rolling would be expected to offer less advantage over grinding (Sadri et al. 2007; Soltani et al. 2009).
Table 1 Carbohydrate recommendations for high-merit lactating dairy cows (Sniffen, 2004)
Thus, the dietary inclusion rate is more important than processing method in optimizing barley starch use, whereas, for corn grain, processing method would seem more important than dietary inclusion rate.
Optimizng rhythms of cereal silage and forage feeding in relation to grain choice Forage type chosen for ensilage affects how efficiently dietary starch is utilized in the rumen and post-rumen. When corn silage (and thus corn starch) is fed to dairy cows, it would be more efficient to include barley grain in the diet to improve nutrient synchrony (Figure 3; Kowsar et al. 2008).
Figure 3Ruminal rhythms and dynamics of rapidly (A and X), moderately (B and Y) and slowly (C and Z) fermentable starch and protein (Hall and Huntington, 2008) For optimal rumen microbial yield and health, it is recommended to have various types of differently processed cereal grains that can supply all three portions of starch and protein for a fruitful rhythmic metabolism
Since small intestinal capacity to assimilate starch and glucose is limited in ruminants (Huntington, 1997), includeing much corn grain in rations based on corn silage may not lead to optimal starch utilization. However, when low-grain and high-fiber corn silage or barley silage are fed, diets may accommodate higher inclusion rates of corn grain, but this should rather be fed alongside barley grain to be optimally utilized in the rumen and post-rumen. When alfalfa hay or silage is fed as main dietary forage, there would be ample opportunities for corn starch (either as grain or silage) to be effectively utilized by the dairy cow. Specifically and globally, it would be advisable to include combined legume and cereal forages alongside corn (or sorghum) and barley (or wheat and oats) grains to provide healthier nutrient synchrony. In terms of ration particle size, when total mixed rations (TMR) are offered, forage hay or silage are mixed with the concentrate in chopped and smaller particles, and as a result, adequately long physically effective fiber may not be provided to fresh and high-producing cows. Hence, it would be recommendable to supply top-dress long forages to these cows. This trend would follow the ruminant nature and holds true particularly when barley grain is fed, since barley grain based diets would require greater physically effective fiber than would corn grain based diets (Beauchemin and Rode, 1997). Basically, when feeding ensiled forages, adequate rapidly fermentable starch (e.g., ground and steam-rolled barley, and steam-flaked corn or sorghum) should be provided to enable capturing fast-release non-protein nitrogen of silage into microbial proteins (Figure 3). This would avoid substantial nitrogen losses in urine. The interactive effects of grain and forage sources on periparturient cow performance and health require future studies. Sadri et al. (2009) found that grain source (barley vs. corn) affects periparturient cow response to chromium-methionine supplementation, such that cows on barley, but not corn, based diets increased peripartal DMI.
Circadian rhythmicity of rumen fermentation and starch nutrition Rumen fermentation possesses circadian rhythmicity (Nikkhah, 2013). This rhythmicity stems partly from diurnal patterns of feed intake (Nikkhah et al. 2008; Nikkhah et al. 2010). Ruminants in nature have developed a specialized grazing behavior to eat/graze mostly during sunrise and sunset and ruminate mostly overnight. As a result, the rumen experiences increased fermentation overnight (Robinson et al. 1997). Recent studies suggested that dairy cows fed once daily in the evening vs. morning had more extensive rumen fermentation shortly post-feeding and increased total tract nutrient and fiber digestibility (Nikkhah et al. 2008; Nikkhah et al. 2010). Accordingly, the evening-fed cows consumed more feed during 3-h after feeding than did the morning-fed cows. As a result, rumen fluid from the evening-fed cows exhibited lower pH and greater concentrations of acetate and total volatile fatty acids (VFAs) shortly post-feeding than that from the morning-fed cows (Figure 5). Consequently, the evening-fed cows experienced higher concentrations of blood beta-hydroxy butyric acid (BHBA) and lactate after feeding. Finally, the evening-fed cows produced milk with greater percentage and yield of fat and energy, compared to the morning-fed cows (Nikkhah et al. 2008; Nikkhah et al. 2010). These data challenge the traditional thought and conventional wisdom that greater diurnal fluctuations in the rumen fermentation may necessarily be undesirable. The evening-fed cows had more fluctuations in their circadian rhythms of rumen acidity and fermentation products, but were still healthy and were able to produce greater daily milk fat, when compared to the morning-fed cows. Importantly, despite greater diurnal fluctuations, the nadir in rumen pH was above 5.5 that means only none or modestly (if any) compromised rumen fiber digestion. This finding was supported by the increased total tract apparent fiber digestibility by evening vs. morning feeding (Nikkhah et al. 2010). Ruminant and non-ruminant chronophysiology is a rising science. Chronophysiology relates to how internal metabolism is altered by altering external cues such as feeding timing and photoperiod. The increased rumen volume overnight (by evening instead of morning feeding) suggests increased VFA absorption capacity. This would imply decreased exposure to acidotic conditions overnight. The chrono-provision of various starch sources has recently been postulated to ease transition from pregnancy to lactation in dairy cows. Offering more fermentable ration components (e.g., barley-based concentrate) during afternoon and evening hours may provide healthier rumen conditions overnight when rumination prevails. The increased rumen buffering capacity overnight may reduce duration of SARA and prevent milk fat depression. This "school of thought" will need to be substantiated in future studies.
Feeding systems and strategies: Different cereal processing choices Feeding management for dairy cows is a highly dynamic phenomenon that is in close relation with dietary properties such as dietary starch inclusion rate and cereal grain processing method (Robinson, 1989; Shabi et al. 1999). Feeding management includes feeding systems and feeding strategies. Feeding system is concerned with how rations are prepared (i.e., totally mixed ration (TMR), partially mixed ration (PMR), or component feeding (CF)). Feeding strategies are attributed to feeding frequency (FF), feeding sequence (FS), and feeding timing (FT). Altering feeding systems and strategies would alter starch digestion site and nutrient efficiency (Nocek and Tamminga, 1991). Although it is believed that more frequent feeding may decrease diurnal variations in nutrient intake and rumen fermentation, and thus, may improve milk solids yield. Under uncompetitive environments, feeding less frequently (1 vs. 4 times daily) increased DMI and altered feeding behavior of lactating dairy cows. This finding would place FF at the interface of tradition and modernity in dairy production. Principally, when feeding rapidly fermentable starch sources (e.g., barley, wheat, and oats), it would be recommended to feed TMR instead of PMR or CF. In contrast, when the main dietary grains are corn and sorghum, PMR and CF systems may also lead to desirable health and production outcomes. Accordingly, barley-based rations need to be fed more frequently than corn-based rations just to ensure that rumen fermentation would not face dramatic alterations unfavorable for fiber digestion. As for FS, the data are scarce and inconclusive.
Starch nutrition and sub-acute rumen acidosis: Practical and immune revelations Sub-acute rumen acidosis is one of the main challenges of today's dairy industry with increased research interests (Figure 6; Plaizier et al. 2009; Humer et al. 2018). Sub-acute rumen acidosis may occur when rumen pH decrease below 5.8 for more than 5-6 h per day (Zebeli et al. 2012). Humer et al. (2018) suggested that when dietary starch concentration increases to 22-26%, physically effective NDF > 8 requirements increase to above 18% that may limit DMI. This warns against feeding excessive amount of starch to dairy cows. Realistically, often dairy farmers feed more than 22-26% starch to their high-producing lactating cows. There are many farmers that feed up to 35% starch that along with dietary (unavoidable) sugars would seriously threaten rumen and cow health.
Figure 4 Rumen fermentation rates of differently processed cereal grains (Nikkhah, 2010)
Education must receive adequate attention at least as does the interest for higher milk production. Farmers need to realize that they ought to strive for maximal nutrient efficiency and minimal SARA incidence. Increased starch intake above 25% may increase milk production during certain periods of time, but it may eventually compromise cow health and longevity and may result in major economic losses to the whole enterprise.
Lessons from human chrono-nutrition and chrono-physiology Bridging human physiology and nutrition to animal agriculture could help overcome both sides' challenges more effectively. There is an ongoing debate among human nutritionists on optimal dietary regimens for healthier lifestyle. It has been suggested to rely on low-carbohydrate (i.e., low sugar and starch) high-fat high-fiber ketogenic diets (Aude et al. 2004; Ludwig and Ebbeling, 2018). Feeding low-sugar, low-starch diets is recommended to decrease risks from diabetes because of obesity and insulin resistance (Ludwig and Ebbeling, 2018).
Figure 5 Circadian rhythms of rumen pH and volatile fatty acids concentrations in evening (9 pm) and morning (9 am) fed lactating dairy cows (Nikkhah, 2010) * (P<0.05)
Despite the vast differences in gastrointestinal physiology and intermediary metabolism between ruminants and humans, feeding lower-starch diets should be contemplated in light of the production and health challenges of SARA in dairy cows. Oil seeds should be well utilized in high-yielding and fresh dairy cow diets to mitigate methane production, improve milk quality for human health, and indeed to decrease requirements for dietary starch. Adding one unit of fat from oil seeds will replace almost 2 units of starch and sugars in the diet to supply the same level of energy. In addition, oil seeds supply essential long chain fatty acids and fat-soluble vitamins that can improve fertility and milk quality. Cottonseed, canola seed, flax seed, linseed, sunflower, and soybean are the distinct oil seeds that can be fed to dairy cows (Arieli, 1998; Beauchemin et al. 2009). What make whole cottonseed unique are the physically effective fibers that along with fat, protein and vitamins-minerals provide a complete nutritional package to lactating cows (Arieli, 1998).
Figure 6 A diagram of gram-negative bacteria cell wall structure (Alexander and Rietschel, 2001) The LPS considered as endotoxins can elicit immune response in the host dairy cows when they experience sub-acute rumen acidosis
Nutritional lessons are, hence, to be learned from human studies that are applicable to animal agriculture. Also to note, glucose tolerance in human decreases as day ends and evening begins (La Fleur et al. 1999; La Fleur et al. 2001). The evening insulin resistance would suggest avoiding large evening meals to decrease obesity and diabetes. Accordingly, to improve insulin action and glucose tolerance, morning eating and evening exercise have been recommended. Such evening glucose intolerance has not yet been reported in ruminants. However, ruminants ruminate mostly overnight when they eat no or little feed. As a result, they are expected to encounter increased rumen volume and fermentation capacity during night. Feeding lactating cows at 2100 h instead of 0900 h has altered periprandial rhythms of blood glucose, such that the evening-fed cows experienced decreased blood glucose shortly pre-feeding that rose to normal concentrations shortly post-feeding (Nikkhah, 2013). This information suggests that circadian rhythms of nutrient intake and metabolism are orchestrated by feeding timing in ruminants as well. Future studies are required to enlighten how dairy cow circadian glucose and insulin dynamics are mediated and entrained by external factors such as feeding timing and photoperiod.
Industrial and environmental obligations: Future research The foremost obligation for the global dairy industry is "education" and "science edification". Without thorough education of our science philosophies to the public (e.g., dairy farmers), limited progress towards profitable production and clean environment may be realized. Maximal adaptation to healthy starch assimilation is a life-time process that should start from younger ages as calves and heifers. Heifers need to be carefully managed to be able to develop efficient microbial (rumen and hindgut) and endocrinological (small intestine) mechanisms to digest and assimilate starch and transfer glucose across portal-drained viscera. This physiological development in the gastrointestinal capacity to bioprocess starch is prerequisite for minimized nutrient losses across splanchnic tissues (Reynolds, 2002). Targeting for healthy rumen should be a priority in constructing future strategies to optimize starch utilization in dairy cows. Limit milk program is another strategy that decreases starch requirement in the diet to meet nutrient demands for increased milk production during the peak of lactation curve. Planning for smoother lactation curve with lower peak can practically decrease the need to feed too much starch and can considerably reduce SARA risks. However, lowering the peak may result in reduced milk yield per lactation. These areas warrant future studies. Exploring the optimal inclusion rates and processing methods of different cereal grains would be another promising field of research (Karam-Babaei et al. 2018). Finally, clear-cut guidelines as to optimal dietary inclusion rates of differently processed cereal grains will need to be developed for on-farm practice. Until then, it is mandatory to keep the dietary starch at logically moderate levels (<25-28%) and do not raise it to lower the risk of SARA incidence and milk fat depression amongst many other environmental and economical challenges.
CONCLUSION Practical and rhythmic feeding of starch has received very inadequate research and education. This missing key part is a main reason for the high incidence of SARA in large dairy farms across the world. Farmer education and science edification are the final frontiers in improving rhythmic rumen and dairy cow health and longevity. It is recommended to feed rations with no more than 25-28% starch (DM based) under any circumstances. Relying relatively more on oil seeds and less on starchy grains is a philosophy that should be taken into consideration in planning for improved environmental quality and economical viability of future dairy enterprises. However, attention must be paid to not over-feed oil seeds too to avoid challenges such as milk fat depression. Future research should establish a rhythmic approach for optimizing daily and postprandial patterns of rumen fermentation and post-rumen host metabolism.
ACKNOWLEDGEMENT The supports of Ferdows Pars Agri-Livestock Holding Co. are gratefully acknowledged. Special thanks to Dr. Donald Beitz (Department of Animal Science, Iowa State University) for the constructive comments on an earlier version of the manuscript. | ||
مراجع | ||
Alexander C. and Rietschel E.T. (2001). Invited review: Bacterial lipopolysaccharides and innate immunity. J. Endotoxin Res. 7, 167-202.
Arieli A. (1998). Whole cottonseed in dairy cattle feeding: A review. Anim. Feed Sci. Technol. 72, 97-110.
Aude Y.W., Agatston A.S., Lopez-Jimenez F., Lieberman E.H., Almon M., Hansen M., Rojas G., Gervasio A. Lamas L. and Hennekens C.H. (2004). The national cholesterol education program diet vs. a diet lower in carbohydrates and higher in protein and monounsaturated Fat: A randomized trial. Arch. Intern. Med. 164, 2141-2146.
Beauchemin K.A. and Rode L.M. (1997). Minimum versus optimum concentrations of fiber in dairy cow diets based on barley silage and concentrates of barley or corn. J. Dairy Sci. 80, 1629-1639.
Beauchemin K.A., McGinn S.M., Benchaar C. and Holtshausen L. (2009). Crushed sunflower, flax or canola seeds in lactating dairy cow diets: Effects on methane production, rumen fermentation and milk production. J. Dairy Sci. 92, 2118-2127.
Bernstein A.M., Titgemeier B., Jirkpatrick K., Golublic M. and Roizen M.F. (2013). Major cereal grain fibers and psyllium in relation to cardiovascular health. Nutrition. 15, 1471-1487.
FAOSTAT. (2017). Database of the Food and Agricultural Organization (FAO) of the United Nations. Availabe at: http://www.fao.org/faostat/en/#home.
Hall M.B. and Huntington G.B. (2008). Nutrient synchrony: Sound in theory, elusive in practice. J. Anim. Sci. 86, 287-292.
Humer E., Petri R.M., Aschenbach J.R., Bradford B.J., Penner G.B., Tafaj M., Südekum K.H. and Zebeli Q. (2018). Invited review: Practical feeding management recommendations to mitigate the risk of subacute ruminal acidosis in dairy cattle. J. Dairy Sci. 101, 1-17.
Huntington G.B. (1997). Starch utilization by ruminants: From basics to the bunk. J. Anim. Sci. 75, 852-867.
Karam-Babaei M., Mirzaei H. and Nikkhah A. (2018). Cereal level and source effects on rumen fermentation, colostrum and milk properties, and blood metabolites in periparturient ewes. Anim. 13(6), 1165-1172.
Kowsar R., Ghorbani G.R., Alikhani M., Khorvash M. and Nikkhah A. (2008). Corn silage partially replacing short-length alfalfa hay to optimize forage use in total mixed rations for lactating cows. J. Dairy Sci. 91, 4755-4764.
La Fleur S.E., Kalsbeek A., Wortel J. and Buijs R.M. (1999). Suprachiasmatic nucleus generated rhythm in basal glucose concentrations. J. Neuroendocrinol. 11, 643-652.
La Fleur S.E., Kalsbeek A., Wortel J., Fekkes M.I. andBuijs R.M. (2001). A daily rhythm in glucose tolerance: a role for the suprachiasmatic nucleus. Diabetes. 50, 1237-1243.
Ludwig D.S. and Ebbeling C.B. (2018). The Carbohydrate-Insulin Model of Obesity: Beyond “Calories In, Calories Out”. JAMA Intern. Med. 178, 1098-1103.
McKevith B. (2004). Briefing paper: Nutritional aspects of cereals. Nutr. Bull. 29, 111-142.
Nikkhah A. (2013). Chronophysiology of ruminant feeding behavior and metabolism: An evolutionary review. Biol. Rhythm Res. 44, 197-218.
Nikkhah A. (2010). Barley grain for ruminants: A global treasure or tragedy. J. Anim Sci. Biotechnol. 3, 22-29.
Nikkhah A., Furedi C., Kennedy A., Crow G. and Plaizier J. (2008). Effects of feed delivery time on feed intake, rumen fermentation, blood metabolites and productivity of lactating cows. J. Dairy Sci. 91, 1-12.
Nikkhah A., Furedi C., Kennedy A., Wittenberg K. and Plaizier J.C. (2010). Feed delivery at 2100 h vs. 0900 h for lactating dairy cows. Canadian J. Anim. Sci. 91, 113-122.
Nocek J.E. and Tamminga S. (1991). Site of digestion of starch in the gastrointestinal tract of dairy cows and its effect on milk yield and composition. J. Dairy Sci. 74, 3598-3629.
NRC. (2001). Nutrient Requirements of Dairy Cattle. 7th Ed. National Academy Press, Washington, DC., USA.
Oba M. and Allen M.S. (2003). Effects of corn grain conservation method on feeding behavior and productivity of lactating dairy cows at two dietary starch concentrations. J. Dairy Sci. 86, 174-183.
Ørskov E.R. (1986). Starch digestion and utilization in ruminants. J. Anim. Sci. 63, 1624-1633.
Plaizier J.C., Krause D.O., Gozho G.N. and McBride B.W. (2009). Subacute ruminal acidosis in dairy cows: The physiological causes, incidence and consequences. Vet. J. 176, 21-31.
Reynolds C.K. (2002). Economics of visceral energy metabolism in ruminants: Toll keeping or internal revenue service? J. Anim. Sci. 80(2),74-84.
Robinson P.H. (1989). Dynamic aspects of feeding management for dairy cows. J. Dairy Sci. 72, 1179-1185.
Robinson P.H., Gill M. and Kennelly J.J. (1997). Influence of time of feeding a protein meal on ruminal fermentation and forestomach digestion in dairy cows. J. Dairy Sci. 80, 1366-1373.
Sadri H., Ghorbani G., Alikahni M. and Nikkhah A. (2007). Ground, dry-rolled, and steam-processed barley grain for midlactation Holsteins. Anim. Feed Sci. Technol. 138, 195-204.
Sadri H., Ghorbani G., Rahmani H. and Samei A. (2009). Chromium supplementation and substitution of barley grain with corn: Effects on performance and lactation of periparturientdairy cows. J. Dairy Sci. 92, 5411-5418.
Shabi Z., Bruckental I., Zamwell S., Tagari H. and Arieli A. (1999). Effects of extrusion of grain and feeding frequency on rumen fermentation, nutrient digestibility, and milk yield and composition in dairy cows. J. Dairy Sci. 82, 1252-1260.
Sniffen C.J. (2004). Optimizing carbohydrate and amino acid nutrition to maximize milk protein in dairy cows. Pp. 65-84 in Proc. Northeast Dairy Prod. Conf., Liverpool, New York.
Soltani A., Ghorbani G.R., Alikhani M., Samie A.H. and Nikkhah A. (2009). Ground versus steam-rolled barley grain for lactating cows: A clarification into conventional beliefs. J. Dairy Sci. 92, 3299-3305.
Van Soest P.J. (1994). Nutritional Ecology of the Ruminant. Cornell University Press, Ithaca, New York.
Zebeli Q., Aschenbach R.A., Tafaj M., Bogahn J., Ametaj B.N., and Drochner W. (2012). Invited review: Role of physically effective fiber and estimation of dietary fiber adequacy in high-producing dairy cattle. J. Dairy Sci. 95, 1041-1056. | ||
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