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Microbial fermentation of carbohy- drates in the hindgut of dairy cattle is responsible for 5 to 10% of total-tract carbohydrate digestion. When dietary, animal, or environmental factors contribute to abnormal, excessive flow of fermentable carbohydrates from the small intestine, hindgut acidosis can occur. Hindgut acidosis is characterized by increased rates of production of short-chain fatty acids including lactic acid, decreased digesta pH, and damage to gut epithe- lium as evidenced by the appearance of mucin casts in feces. Hindgut acidosis is more likely to occur in high-producing animals fed diets with relatively greater proportions of grains and lesser proportions of forage. In these animals, ruminal acidosis and poor selective retention of fermentable carbohydrates by the rumen will increase carbohydrate flow to the hindgut. In more severe situations, hindgut acidosis is characterized by an inflammatory response; the resulting breach of the barrier between animal and digesta may contribute to laminitis and other disorders. In a research setting, effects of increased hindgut fermentation have been evaluated using pulse-dose or continuous abomasal infusions of varying amounts of fermentable carbohy- drates. Continuous small-dose abomasal infusions of 1 kg/d of pectin or fructans into lactating cows resulted in decreased diet digestibility and decreased milk fat percentage without affecting fecal pH or VFA concen- trations. The decreased diet digestibility likely resulted from increased bulk in the digestive tract or from in- creased digesta passage rate, reducing exposure of the digesta to intestinal enzymes and epithelial absorptive surfaces. The same mechanism is proposed to explain the decreased milk fat percentage because only milk concentrations of long-chain fatty acids were decreased. Pulse-dose abomasal fructan infusions (1 g/kg of BW) into steers resulted in watery feces, decreased fecal pH, and increased fecal VFA concentrations, without caus- ing an inflammatory response. Daily 12-h abomasal in- fusions of a large dose of starch (~4 kg/d) have also induced hindgut acidosis as indicated by decreased fe- cal pH and watery feces. On the farm, watery or foamy feces or presence of mucin casts in feces may indicate hindgut acidosis. In summary, hindgut acidosis occurs because of relatively high rates of large intestinal fer- mentation, likely due to digestive dysfunction in other parts of the gut. A better understanding of the relation- ship of this disorder to other animal health disorders is needed.

The concept of improving animal performance by going beyond simply meeting requirements and synchronizing ruminal availability of protein and energy has been with us for at least 3 decades. Although theoretically appealing, research and field results have not supported this approach to diet formulation. Why? Essential to successful ruminal synchrony is the ability to predict available amounts and fates of diverse substrates. The substrates come from varied sources; their efficiencies of use and yields of products are affected by inherent properties, interactions, transformations, and passage. However, substrate quality and availability in the rumen are affected only in part by diet. For example, NPN, true protein, and peptides are contributed by diet and intraruminal recycling, with additional endogenous NPN contributions by the cow. Changes in factors that alter the rate or extent of substrate fermentation, such as the rate of passage or ruminal pH, can alter nutrient yield from the rumen and must be accounted for in order for synchrony to work. Our ability to estimate ruminally available substrate is also challenged by normal variation in feed composition and imprecision in component and digestibility analyses. Current in vitro assays may not be adequate to accurately describe the digestibility of feed components in vivo in mixed diets. There are some indications that the amount or pattern of supply of fermentable carbohydrate has a greater impact on microbial production and efficiency than does the pattern of protein supply. Animal responses to modifications in the supply of true protein from the rumen may be masked if additional protein is oxidized by tissues or if AA from endogenous sources cover deficiencies. Animal factors, such as response to immune challenge and sustained damage to tissues, will also affect partitioning of nutrients for production and may alter an animal's response to changes in nutrient supply. With the array of factors internal and external to the diet that must be considered, "synchrony" implies a greater deliberate precision in diet manipulation than may be currently possible to effect. Perhaps we should consider balance. Within the rumen and cow, can we generate conditions so that needed substrates or nutrients are available from the diet or accessible from endogenous resources to meet requirements and enhance productivity and efficiency? This approach involves the whole animal, rather than only the rumen and feed we offer to the cow.

Effects of sucrose (Suc) concentration on fermentation kinetics and products were evaluated using 3 concentrations of Suc, with 1 concentration of isolated NDF from Bermudagrass fermented together in batch culture in vitro with rumen inoculum. Fixed amounts of medium and inoculum were the protein sources, so protein:Suc decreased with increasing Suc. Kinetics were calculated from gas production over 48 h in a randomized complete block design (n = 28), and product yield was evaluated with sampling every 4 h for 24 h in a split-split plot in time design (n = 84). Fermentation vial was the experimental unit. Increasing Suc increased the lag time of rapidly (P 1 indicate incorporation of C from the medium, likely from AA and peptides. The results support the premises that direct effects of Suc concentration and perhaps protein:Suc alter yields of fermentation products. That substrate concentration altered fermentation products and kinetics, possibly due to interactions with the run conditions, advises the clear definition of substrates and fermentation conditions to determine how the results integrate into our knowledge of ruminant nutrition.