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The increased nitrogen (N) use efficiency in cattle farming is proposed as a key action to improve N management and reduce the environmental impact of cattle farming systems. Most attention has been given to lactating cow nutrition, excluding the elements of fertility, disease, and the non-lactating animals within the herd. Therefore, the aim of the current study was to develop a herd-level simulation model incorporating these elements to assess dairy farm N use efficiency. We developed a cattle N use efficiency (CNE) model with six primary compartments: (i) heifer growth, (ii) heifer removal, (iii) pregnancy, (iv) cow removal, (v) disease and fertility, and (vi) milk production. The CNE model calculates N loss or gain for each compartment, and then calculates the lifetime N loss or gain taking into account the replacement rate (rep) and/or the corresponding number of lactations in a herd (Lact = 1/rep). Finally, three N use efficiencies were estimated: (i) ReplNE: replacement cattle N use efficiency, (ii) LactNE: lifetime N use efficiency for lactation, and (iii) LNE: lifetime N use efficiency. The sensitivity of the model to variation in farm- and animal-related input values was evaluated using Monte Carlo simulation. Values for a model dairy farm were used based on published data reflecting typical dairy farming practices in the United Kingdom. To assist reporting net values of main N outputs, a dairy herd of 100 lactating cows was modelled. Productive N outputs (1000s of kg) over the course of an animal's lifetime, partitioned into milk and meat, were dominated by milk production (89% of total N output). We estimated a mean ReplNE of 23.7%, affected most by the last stage of heifer growth. The Monte Carlo sensitivity analysis suggested that variation in time to first calving (T1stCal) might cause larger changes on ReplNE than variation in feed. The sensitivity analysis revealed a strong positive correlation between dietary oriented milk N use efficiency (MNE) and LactNE and LNE (r = 0.99 and 0.97 for LactNE and LNE, respectively). However, our study highlighted two other model variables that affected LNE. Variation in calving interval (CI; r = -0.15) and T1stCal (r = -0.15) may cause measurable reductions of overall LNE. The first is an indicator of lactating cattle fertility, and the second an indicator of replacement cattle growth and fertility efficiency. In conclusion, with the current study we provided a dairy cattle herd model that is sensitive in elements of diet, fertility and health. Lifetime N use efficiency of dairy cattle is dominated by MNE, but we detected specific non-diet related variables that affect ReplNE, LactNE and LNE., Competing Interests: The authors have declared that no competing interests exist.

Two experiments were carried out to determine the effects of feeding grass silages differing in their water-soluble carbohydrate content, with or without red clover silage, on the efficiency of nutrient use. High-sugar grass, control grass, and red clover were ensiled in laboratory silos for use in an in vitro experiment (Exp. 1). For an in vivo experiment (Exp. 2), the same forage types were baled and ensiled. All silages were well preserved; within experiments the grass silages had similar composition, except for greater (P < 0.05) water-soluble carbohydrate concentrations in the high-sugar than the control grass silage. In Exp. 1, high-sugar grass, control grass, and red clover silages were fed alone or as mixtures (30:70, 50:50, or 70:30 on a DM basis, respectively) of each grass with the red clover silage to a simulated rumen culture system. There were no significant differences in microbial N flow or efficiency of microbial protein synthesis between individual forages. However, the corresponding values for the 70:30 ratio of high-sugar grass:red clover silage were greater (P < 0.05) than for the red clover silage. The value for the efficiency of N use (g of microbial N/g of feed N) was greater (0.86; P < 0.05) for high-sugar grass silage than the control grass silage. In addition, the high-sugar grass:red clover silage mixtures all gave greater (P < 0.05) values for the efficiency of N use than red clover silage alone; this difference was not achieved with the control grass mixture. Experiment 2 was an incomplete Latin square design conducted with 6 Here-ford x Friesian steers (163 +/- 5.9 kg of BW) with rumen and duodenal cannulas fed the following 5 silage diets: high-sugar grass silage; control grass silage; high-sugar grass and red clover silage (50:50 DM basis); control grass and red clover silage (50:50 DM basis); and red clover silage. Rumen NH3-N concentration was lowest (P < 0.05) with the high-sugar grass silage. Microbial N flows to the duodenum and efficiency of microbial protein synthesis were greater (P < 0.05) for steers fed the high-sugar grass silage than for control grass and red clover silages, and mixing red clover with grass silages increased (P < 0.05) these values compared with red clover silage alone. In both experiments, the efficiency of incorporation of silage N into microbial N was more than 20% greater (P < 0.05) for high-sugar grass than for control grass silage. These data suggest that grass silage with high-sugar content provides a forage-based strategy for balancing N and energy supply and improving the efficiency of use of grass silage N in the rumen.

We offered 43 Holstein-Freisian dairy heifers that calved for the first time at either 2 or 3 yr of age ad libitum access to ryegrass silage and a standard concentrate allowance of either 2 or 7 kg/d from the middle to the end of their first lactation. All animals were given the same relatively poor quality dry period diet of a mixture of ryegrass silage and barley straw (63:37 dry matter basis) from 6 wk before their predicted second-calving date. Following their second calving, all animals received access to the same ration of ad libitum grass silage and concentrates at a rate of 8 kg/d to 120 d of lactation and 5 kg/d thereafter until the end of the experimental recording at about 150 d of lactation. Nitrogen balance was significantly higher at the end of the first lactation for animals that were given the higher concentrate allowance and tended to be higher for older animals. There was no effect of age or residual effect of concentrate allowance on N balance during the dry period or during the second lactation. Labile body protein reserves, as estimated by the depth of the muscle Longissimus dorsi (which was significantly correlated with body condition score), were similar for all animals during the dry period, but younger animals previously offered the lower concentrate allowance did not lose L. dorsi depth early in the second lactation as did other animals. Arterial plasma concentrations of amino acids Phe, Trp, and Leu were significantly higher in younger animals at wk 8 of the second lactation, and Gly was significantly lower, although mammary blood flow, arteriovenous differences, and rates of uptake of the AA measured were unaffected by treatment. It is concluded that differences in second-lactation milk yield were not mediated through the availability of labile body protein or the supply of nutrients to the mammary gland.

We offered 48 multiparous Holstein-Friesian cows one of three different dry-period diets for 6 wk before predicted calving: A) a grass silage and barley straw mix (60:40 on a dry-matter basis), with a low protein content; B) grass silage only (medium protein); or C) grass silage plus 0.5 kg of high protein corn gluten meal (high protein)/d. A standard grass silage-based diet was offered to all cows following calving. All animals were blood sampled at weekly intervals during the dry period, and at wk 1, 3, 5, 7, 13, 17, and 21 of lactation. Nitrogen balance was measured in a subset of 12 cows (four per treatment) at 3 wk before calving, and at wk 8 and 18 of lactation. Nitrogen balance in the dry period increased significantly as dietary protein supply increased [9, 34, and 50 g of N/d (SED 8.8) for the three diets, respectively]. We measured no residual effects of dry-period treatment on N balance during lactation. Plasma concentrations of growth hormone became significantly higher in the late dry period in cows offered the silage and straw diet, although treatment differences disappeared after calving. Insulin concentrations were significantly affected by treatment throughout the dry period and indicated inadequate nutrient supplies from the low protein diet, leading to losses in body reserves of energy and protein. The results indicate that animals offered the low protein diet accumulated less N per day than is required for fetal development, suggesting that protein must have been repartitioned from maternal tissues.

We hypothesized that an increased uptake of ammonia from the gut of dairy cows would increase the use of amino acids for urea synthesis and decrease the availability of amino acids for milk protein production, leading to a reduction in milk protein output. To test this hypothesis, four multiparous Holstein-Friesian dairy cows offered a constant diet based on grass silage were continuously infused with ammonium acetate (ammonia) or acetic acid (control) into the duodenum for 5 d in each period of a changeover design experiment. Silage intake, rumen ammonia, pH and volatile fatty acid concentrations, and feces N excretion and whole body N balance were all unaffected by treatment, although urinary N excretion increased. Similarly, there was no effect of treatment on milk yields or on milk constituent yields. We concluded that ammonia absorption represents a loss of protein to the animal, but that it is unlikely to result in reduced amino acid availability for productive purposes such as lactation.