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Effects of forage source, concentration of metabolizable protein (MP), and type of carbohydrate on manure excretion by dairy cows and production of ammonia from that manure were evaluated using a central composite experimental design. All diets (dry basis) contained 50% forage that ranged from 25:75 to 75:25 alfalfa silage:corn silage. Diets contained 10.7% rumen-degradable protein with variable concentrations of undegradable protein so that dietary MP ranged from 8.8 to 12%. Starch concentration ranged from 22 to 30% with a concomitant decrease in neutral detergent fiber. A total of 15 diets were fed to 36 Holstein cows grouped in 6 blocks. Each block was a replicated 3 x 3 Latin square resulting in 108 observations. Manure output (urine and feces) was measured using total collection, and fresh feces and urine were combined into slurries and incubated for 48 h to measure NH3-N production. Feces, urine, and manure output averaged 50.5, 29.5, and 80.1 kg/d, respectively. Manure output increased with increasing dry matter intake (approximately 3.5 kg of manure/kg of dry matter intake), increased concentrations of alfalfa (mostly via changes in urine output), and decreased concentrations of starch (mostly via changes in fecal output). The amount of NH3-N produced per gram of manure decreased with increasing alfalfa because excreted N shifted from urine to feces. Increasing MP increased NH3-N produced per gram of manure mainly because of increased urinary N, but increased fecal N also contributed to the manure NH3. Manure NH3-N production per cow (accounts for effects on manure production and NH3-N produced per unit of manure) was least and milk protein yields were maximal for diets with high alfalfa (75% of the forage), moderate MP (11% of diet dry matter), and high starch (30% of diet dry matter).

The dynamics of 25 blood constituents in newborn calves were monitored. Eight calves were immediately removed from dams following birth. Jugular blood samples for carbohydrate determinations were taken at birth (within 2 min), 1, 3, 6, 8, 12, 18, and 24 h and every 12 h until 144 h of age. Samples for blood chemistries were taken at birth, 1, 3, 6, 12, 24, 48, 72, 120, and 144 h. Colostrum was first fed at either 1 h (group 1) or 12 h (group 2) of age. At birth, plasma glucose concentrations were lower than the plasma fructose in both groups. Plasma glucose increased substantially from birth to 24 h, whereas fructose decreased to nondetectable concentrations by 18 h. Increases in insulin were associated with time of first feeding. Serum cortisol decreased rapidly from birth to 3 h for group 1 and at 15 h for group 2. Colostrum intake resulted in increased activities of serum alkaline phosphatase, gamma-glutamyl transpeptidase, and glutamic oxaloacetic transaminase at 6 h for group 1 and at 15 h for group 2. Activities of these enzymes decreased to "normal" values after 24-h samplings for group 1. Serum glutamic pyruvic transaminase and lactate dehydrogenase increased gradually in activity over the first 24 h in both groups and decreased after 24 h for group 1. Triglycerides and cholesterol increased from birth to 24 h in both groups and continued to increase in group 1 until 144 h. Creatinine decreased and bilirubin increased from birth to 24 h in both groups. These changes indicated that the newborn calves were undergoing many adaptive changes in relation to either maintenance of homeostasis or nutrient intake.

The effects of forage source, concentration of metabolizable protein (MP), type of carbohydrate, and their interactions on nutrient digestibility and production were evaluated using a central composite treatment design. All diets (dry basis) contained 50% forage that ranged from 25:75 to 75:25 alfalfa silage:corn silage. Rumen-degradable protein comprised 10.7% of the dry matter (DM) in all diets, but undegradable protein ranged from 4.1 to 7.1%, resulting in dietary MP concentrations of 8.8 to 12.0% of the DM. Dietary starch ranged from 22 to 30% of the DM with a concomitant decrease in neutral detergent fiber concentrations. A total of 15 diets were fed to 36 Holstein cows grouped in 6 blocks. Each block consisted of three 21-d periods, and each cow was assigned a unique sequence of 3 diets, resulting in 108 observations. Milk production and composition, feed intake, and digestibility of major nutrients (via total collection of feces and urine) were measured. Few significant interactions between main effects were observed. Starch concentration had only minor effects on digestibility and production. Replacing corn silage with alfalfa decreased digestibility of N but increased digestibility of neutral detergent fiber. Increasing the concentration of MP increased N digestibility. The concentration (Mcal/kg) of dietary digestible energy (DE) increased linearly as starch concentration increased (very small effect) and was affected by a forage by MP interaction. At low MP, high alfalfa reduced DE concentration, but at high MP, increasing alfalfa increased DE concentration. Increasing alfalfa increased DM and DE intakes, which increased yields of energy-corrected milk, protein, and fat. Increasing MP increased yields of energy-corrected milk and protein. The response in milk protein to changes in MP was much less than predicted using the National Research Council (2001) model.

A sensitive indicator of biotin status for lactating dairy cows is necessary to understand factors that affect milk yield responses to biotin supplementation. 3-Hydroxyisovaleric acid (3HIA) is an alternative metabolite in the pathway of Leu catabolism when the biotin-dependent enzyme methylcrotonyl-coenzyme A carboxylase is limiting. We evaluated urinary excretion of 3HIA as a determinant of biotin status in lactating dairy cows. We hypothesized that high-producing cows would have a greater biotin requirement and excrete more 3HIA than low-producing cows and that biotin supplementation would decrease 3HIA excretion. Twenty high-producing and 20 low-producing Holstein cows (43 +/- 5 and 23 +/- 4 kg/d of milk, respectively) were fed diets that contained either 0 or 0.96 mg/kg of supplemental biotin. On d 16 cows were given an intraruminal infusion of 1.4 mol of isovaleric acid and urine was sampled. Biotin supplementation did not affect basal urinary excretion of 3HIA. The infusion of isovaleric acid increased urinary excretion of 3HIA (maximum at 8 h after infusion), but biotin supplementation did not attenuate this increase. The increase in urinary 3HIA excretion was less for low-producing cows than for high-producing cows. Biotin increased yields of milk and milk components in high-producing cows but had no effect in low-producing cows. However, potential measures of biotin status (concentrations of avidin-binding substances in the plasma, milk, and urine, and urinary 3HIA excretion) responded similarly to biotin supplementation for both high- and low-producing cows. A sensitive indicator of biotin status for lactating dairy cows is still needed.

When cattle were allowed to graze land previously used as orchards, residues of DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene] were detectable in milk fat and adipose tissues. Concentrations of DDE exceeded .3 micrograms/g at times. Concentrations of DDE in adipose tissue were similar to those in milk fat at the beginning of lactation; residues in first lactation cows were approximately three times higher than in multiparous cows that were grazing similarly. Based on the equation [DDE, micrograms/g]milk fat = .28 (daily dose, mg).82, consumption of soil was likely not the sole source of residue when soil concentrations of DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane], DDE, and DDD [1,1-dichloro-2,2-bis(p-chlorophenyl)ethane] ranged from non-detected to 3.6, 2.1, and .655 micrograms/g, respectively. Grass appeared to be the likely source. Four plots were located on three orchard locations and one control location. Grasses in subplots were harvested at 2-, 4-, or 6-wk intervals during the 18-wk study. Grasses were extracted differentially to determine DDT and DDE residues adhering to the plant surface and those associated with plant tissue. Surface residue was not significant. The DDE averaged between .01 and .11 micrograms/g in dry grass tissues. Differences between residues in grasses among plots were associated with soil residue concentrations. Concentrations of DDE were not associated with air or soil temperature, relative humidity, solar radiation, or dry biomass harvested. Precipitation increased the volatilization of residues from soil and deposition in 2- and 4-wk grass samples.(ABSTRACT TRUNCATED AT 400 WORDS)

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A rapid method was developed for the extraction, isolation, and detection of polybrominated biphenyls (PBBs) from plasma, feces, milk, and bile, using disposable glassware. Use of disposable equipment greatly reduced the amount of laboratory background and cross-contamination of samples. The procedure employed a multiple extraction with a mixture of diethyl and petroleum ethers, followed by cleanup on miniature Florisil, silica gel, and sodium sulfate columns. Detection was accomplished by gas chromatography. Recoveries were determined for the six major components of a commercial PBB mixture and were approximately 96% for plasma, 59% for feces, and 98% for milk. The background levels for plasma, feces, and milk were 0.0005, 0.0007, and 0.0007 ppm, respectively, bringing the minimum detectable limits of the major hexabromobiphenyl peak to 0.0010, 0.0014, and 0.0014 ppm on a whole tissue basis.