The effects of pelleted dried distillers grains and solubles fed with different forage concentrations on rumen fermentation, feeding behavior, and milk production of lactating dairy cows.

The physical form of feeds can influence dairy cow chewing behavior, rumen characteristics, and ruminal passage rate. Changing particle size of feeds is usually done through grinding or chopping forages, but pelleting feed ingredients also changes particle size. Our objective was to determine if pelleted dried distillers grains and solubles (DDGS) affected the feeding value for lactating dairy cattle. Seven lactating Jersey cows that were each fitted with a ruminal cannula averaging (± standard deviation) 56 ± 10.3 d in milk and 462 ± 75.3 kg were used in a crossover design. The treatments contained 15% DDGS in either meal or pelleted form with 45% or 55% forage on a dry matter basis. The forages were alfalfa hay, corn silage, and wheat straw. The factorial treatment arrangement was meal DDGS and low forage (mDDGS-LF), pelleted DDGS and low forage (pDDGS-LF), meal DDGS and high forage (mDDGS-HF), and pelleted DDGS and high forage (pDDGS-HF). Dry matter intake and energy-corrected milk were both unaffected by treatment averaging 19.8 ± 2.10 kg/d and 33.9 ± 1.02 kg/d, respectively. Fat yield was unaffected averaging 1.7 ± 0.13 kg/d, but protein yield was affected by the interaction of forage and DDGS. Protein yield was similar for both low forage treatments but was increased by when pDDGS was fed in the high forage treatment (1.05 vs. 0.99 ± 0.035 kg/d). When forage concentration was increased, starch digestibility increased by 1.9 percentage units, crude protein digestibility tended to increase 1.1 percentage units, and residual organic matter digestibility decreased 3.4 percentage units. Pelleting DDGS increased digestibility of neutral detergent fiber (NDF) digestibility (49.2 vs. 47.5 ± 1.85%) and gross energy (68.2 vs. 67.1 ± 1.18%). Increasing forage increased ruminal pH (5.85 to 5.94 ± 0.052). Passage rate slowed from 2.84 to 2.65 ± 0.205 %/h when feeding HF compared with LF. Rumination time increased from 417 to 454 ± 49.4 min with increasing forage concentration but was unaffected by the form of DDGS or the interaction of forage and DDGS. Eating time increased with pDDGS (235 vs. 209 ± 19.8 min), which may be a result of increased feed sorting behavior. Pelleting DDGS increased preference for particles retained on the 8-mm sieve and decreased preference for particles on the 1.18-mm sieve and in the pan (<1.18 mm). Results confirm that increasing forage concentration increases ruminal pH, rumination time, and slows passage rate, but contrary to our hypothesis increasing forage concentration did not increase NDF digestibility. Results also suggest that pelleted DDGS do not appear to affect milk production, ruminal characteristics, or passage rate, but pelleted DDGS may increase sorting behavior of lactating Jersey cows and increase NDF and gross energy digestibility.

The effects of 2 genetic lines on spatial distribution and use and preference of perch and nest area in an aviary system.

The objective of this trial was to evaluate spatial distribution, nest and perch usage, and preference of Lohmann Brown (BH) and Bovan White (WH) Leghorn hens raised in an aviary system. At 5 wk, 400 floor raised pullets, BH and WH strains, in equal numbers, were placed into 8 modified Big Dutchman Natura aviary units. Each aviary unit had 3 tiers with perches and an indoor litter area. At 25 wk, the number of birds was recorded by scan sampling every 4 h. The number of birds perching in each aviary unit was recorded every 4 h at 15, 25, and 35 wk. The number of eggs laid was recorded daily from 22 to 53 wk. A split-plot factorial design with Poisson distribution was used for analysis of spatial distribution and perch preference. Nest and perch usage was analyzed using a split-plot factorial design with binomial distribution. There was an interaction (P < 0.0001) indicating that during late afternoon and night, a higher number of WH were observed in the middle and top tier while a higher number of BH were observed in the litter area and bottom tier at 25 wk. The odds of observing WH perching were higher than the odds of observing BH perching during late morning, late afternoon, and night at 15 wk, from early afternoon to night at 25 wk, and during all afternoon at 35 wk. WH had higher nest usage than BH expressed by the higher odds of observing eggs from the nest area (P = 0.071). There was a strain and egg location interaction (P < 0.0001) for number of eggs laid indicating that WH were laying more eggs in the nest area and litter floor area compared to BH, whereas BH were laying more eggs in the metal aviary wire tiers in comparison with WH. In conclusion, WH showed greater degree of adaptation to aviary systems than BH expressed by greater usage of perches and nest areas and elevated tiers.

Limestone particle size fed to pullets influences subsequent bone integrity of hens.

This study was conducted to evaluate limestone particle size (LPS) in 2 strains of laying hens housed in conventional cages or aviaries on bone integrity. Lohmann Brown and Bovan White pullet chicks were started in equal numbers on the floor or in battery brooders and were intermingled throughout all subsequent housing systems. At 5 wk of age, 432 floor-raised pullets were moved to 8 aviary cages. At 10 wk, 256 battery-raised pullets were transferred to 64 conventional layer cages. Pullets were given diets containing fine (LPS-FINE, 0.431 mm) or a blend of fine and coarse (LPS-BLEND, 0.879 mm) LPS from 7 to 17 weeks. Data were analyzed as a split plot factorial design with strain as subplot and with 4 replicates for each treatment combination. Body weight, feed intake, egg production, and eggshell breaking strength and percentage were measured. Tibia bone mineral density (BMD) was determined using a dual energy x-ray absorptiometry. Presence of keel indentations, curvatures, or fractures was recorded. LPS-BLEND increased BMD (0.215 vs. 0.208, P = 0.03) at 18 weeks. During the pullet phase, the odds of pullets fed LPS-FINE displaying keel curvatures were 2.8 times the odds of those fed LPS-BLEND (P = 0.04). At 54 wk, hens fed LPS-BLEND as pullets had lower odds of keel indentations (P = 0.02). Brown aviary hens fed LPS-BLEND as pullets had the lowest egg production compared to the rest of the treatment combinations (P = 0.004). Taken together, feeding LPS-BLEND to pullets improved bone mineralization at the onset of sexual maturity and reduced keel damage during the pullet and layer phases, regardless of strain; however, LPS-BLEND was associated with lower egg production in Brown hens housed in aviaries compared to all others.

Energy content of reduced-fat dried distillers grains with solubles for lactating dairy cows.

Eight Holstein and 8 Jersey multiparous, lactating cows were used to complete 56 energy balances to determine the energy content of reduced-fat dried distillers grains with solubles (RFDDGS). A repeated switchback design was used to compare treatments with and without RFDDGS. Diets consisted of 24.2% corn silage, 18.4% alfalfa hay, 6.94% brome hay with either 22.9% rolled corn or 14.8% soybean meal (control), or 8.95% rolled corn, 28.8% RFDDGS, and 0% soybean meal [Co-P; dry-matter (DM) basis]. The inclusion of RFDDGS did not affect DM intake, averaging 21.4 ± 0.53 kg of DM for all cows, but milk production tended to increase from 29.8 to 30.9 ± 1.46 kg/d for control and Co-P treatments, respectively. Milk fat percentage and energy-corrected milk did not differ between treatments, averaging 4.33 ± 0.14% and 34.1 kg/d, respectively. Milk protein was significantly decreased by the Co-P treatment (3.56 and 3.41 ± 0.08% for control and Co-P treatments), but protein yield was not affected. Milk energies were 1.40 Mcal/d greater with Co-P. Energy lost as methane was reduced by 0.31 Mcal/d with the addition of RFDDGS to the diet. Heat loss averaged 29.9 ± 0.55 Mcal/d and was not different between diets. Average energy retained as tissue energy was -2.99 ± 0.93 Mcal/d and did not differ between treatments. Intake of digestible and metabolizable energy were not different between the control and Co-P treatments, averaging 2.68 and 2.31 Mcal/kg of DM, respectively. The net energy of lactation values of control and Co-P diets were calculated to be 1.43 and 1.47 Mcal/kg of DM, respectively. These energy estimates suggest greater energy content of diets containing RFDDGS than diets containing a mixture of corn and soybean meal in lactating dairy cows.

Dried distillers grains with solubles in laying hen diets.

A study was conducted to test the inclusion rate of corn dried distillers grains with solubles (DDGS) in laying hen diets on egg production (EP) responses for a full production cycle. A total of 288 Bovan Single Comb White Leghorn laying hens were fed diets containing 0, 5, 10, 15, 20, or 25% DDGS from 24 to 46 wk (phase 1) and 47 to 76 wk (phase 2) of age. The diets were formulated to be isocaloric at 2,775 and 2,816 kcal/kg of ME and isonitrogenous at 16.5 and 16.0% CP for phases 1 and 2, respectively. Nutrient retention of both N and P were determined by the indicator methods during phase 2. Diets were replicated with 8 pens/treatment and 6 hens/pen in an unbalanced randomized complete block design. Average daily feed intake, EP, and overall weight gain were similar (P = 0.08 to 0.1) among treatments during the study. Egg weight was affected (P = 0.064) by DDGS treatment during phase 1. Hens fed 0, 5, 10, 15, 20, or 25% DDGS had an average egg weight of 60.6, 60.4, 60.8, 60.0, 59.0, and 59.0 g, respectively; however, no differences were detected in egg weight during phase 2. During phase 1, diets were formulated based on TSAA, allowing Met to decrease as DDGS increased, but during phase 2, diets were formulated to keep Met equal across DDGS treatments, allowing TSAA to increase as a result of high Cys in DDGS. Yolk color increased with increasing DDGS level; the highest Roche score (P = 0.001) was 7.2 for hens fed 25% DDGS. Nitrogen and P retention was greater (P = 0.003) in hens fed 25% DDGS. Also, N and P excretion decreased (P = 0.007) linearly as DDGS increased. In summary, feeding DDGS up to 25% during EP cycles had no negative effects on feed intake, EP, Haugh units, or specific gravity, and improved yolk color at the highest levels. Increasing DDGS level beyond 15% caused a reduction in egg weight during phase 1 of egg production, though no differences were observed in egg weight during phase 2. Nitrogen and P excretion were lower at higher inclusion rate of DDGS. Hens fed 25% DDGS had the highest N and P retention.

Effect of corn processing method and corn wet distillers grains plus solubles inclusion level in finishing steers.

Two experiments were conducted to determine the effect of corn processing method and corn wet distillers grains plus solubles (WDGS) level on steer performance and metabolism. In Exp. 1, 480 crossbred steer calves (314 +/- 18 kg of BW) were used in a finishing experiment with a randomized complete block design and a 3 x 4 treatment structure. Diets were based on dry-rolled (DRC), high-moisture (HMC), or steam-flaked corn (SFC) with increasing levels of WDGS (0, 15, 27.5, or 40%; DM basis). A corn processing x WDGS level interaction (P < 0.01) was observed for ADG and G:F. Average daily gain and G:F increased linearly (P < 0.01) in steers fed DRC; ADG increased quadratically (P = 0.04) and G:F increased linearly (P = 0.02) in steers fed HMC; and ADG decreased quadratically (P = 0.02) with no change in G:F (P = 0.52) in steers fed SFC as WDGS increased. In Exp. 2, 7 ruminally fistulated steers (440 +/- 41 kg of BW) were used in a 6-period crossover design with 3 x 2 factorial treatment structure. Diets were the same as those fed in Exp. 1, except they contained only 2 levels of WDGS (0 or 40% of diet DM). Total tract starch digestibility was greater (P < 0.01) for steers fed SFC than for steers fed DRC or HMC. Minimum ruminal pH was less (P < 0.01) for steers fed SFC than for steers fed HMC or DRC. Variance of ruminal pH was different among all 3 processing methods with DRC < HMC < SFC (P < 0.10). In situ 22-h DM digestibility of DRC and HMC and starch digestibility of DRC were greater (P < 0.10) in steers fed DRC compared with steers fed HMC or SFC. Steers fed 0% WDGS had less (P < or = 0.02) intake of DM, OM, NDF, and ether extract compared with steers fed 40% WDGS. Total tract digestibility of DM and OM was greater (P < or = 0.08) and digestibility of ether extract tended (P = 0.11) to be less for steers fed 0% WDGS compared with steers fed 40% WDGS. Maximum ruminal pH and pH variance were greater (P < or = 0.08) in steers fed 0% WDGS. A corn processing x WDGS level interaction (P = 0.09) was observed for ruminal acetate to propionate ratio (A:P). Within diets containing 0% WDGS, A:P in steers fed SFC was less (P < or = 0.08). In diets containing 40% WDGS, A:P was similar between processing methods and not different from the SFC with 0% WDGS. The corn processing x WDGS level interaction observed in the finishing experiment may be due to the decreased ruminal A:P in DRC and HMC diets with 40% WDGS.

Technical note: estimating statistical power of mixed models used in dairy nutrition experiments.

Statistical power is defined as the probability of correctly rejecting the null hypothesis. Power calculations may be useful in planning experiments. The objective of this technical note is to outline an applied method that estimates statistical power of a dairy nutrition experiment that employs a Latin square as the experimental design. Because the SAS MIXED procedure (PROC MIXED) is commonly used to analyze data sets, this note outlines basic programming procedures that may be used to estimate statistical power of a mixed model using this procedure.

Lack of evidence for cytoplasmic effects for four traits of Polypay sheep.

Analyses of birth and weaning weights, fleece weights of ewes, and number born per litter of Polypay sheep collected at the U.S. Sheep Experimental Station from 1978 through 1998, confirmed previous analyses of three other dual-purpose breeds that cytoplasmic effects do not contribute to variation in these four traits. In general, estimates of genetic parameters that would be needed for national genetic evaluation were similar to previous estimates for Columbia, Rambouillet, and Targhee sheep, although estimates of direct heritability for Polypay were somewhat less for birth weight, slightly greater for weaning weight, significantly greater for fleece weight, and the same for number born as for those three breeds. For birth weight only, evidence was found for important dam x year or dam x number born interactions, which are essentially litter effects, as was found for the other dual-purpose breeds. There were 11,896, 11,104, 7,748, and 7,831 records for birth and weaning weights, fleece weight, and number born per litter, with 255 to 316 sires of animals with records. There were 260 and 261 cytoplasmic lines for fleece weight and number born, and 861 and 882 for weaning and birth weights.

Models with nuclear, cytoplasmic, and environmental effects for production traits of Columbia sheep.

Statistical models (16) were compared for birth weight of 24,741 Columbia lambs recorded at the U.S. Sheep Experiment Station (USSES; 1950 to 1998). The goal was to estimate fractions of variance due to cytoplasmic line (c2; n = 590) and sire x cytoplasmic line interaction (sc2; n = 12,831) with other nuclear and environmental effects included in the model. The basic model included direct genetic (fractional variance, a2; n = 26,623), maternal genetic (m2, with direct-maternal correlation ram), and maternal permanent environmental (p2m; n = 6,385) effects. The model with sc2 was significantly (P < 0.05) better than the basic model with c2, but with other random effects added, sc2 became zero. Significant (P < 0.05) variance components were associated with random dam x year (dy2) and dam x number born (dn2) interaction effects. Estimates with all effects in the model were: a2, 0.26; m2, 0.24; ram, -0.05; p2m, 0.02; c2, 0.00; dn2, 0.04; dy2, 0.08; sd2, 0.04; sc2, 0.00. Estimates for a2, m2, and ram were the same for all models. Estimate of p2 changed when other effects were added to the model. The largest estimates for nongenetic effects were: p2m, 0.06; c2, 0.00; dy2, 0.14; sd2, 0.13; and sc2, 0.04. Parameter estimates were similar regardless of whether fixed genetic groups (n = 84) were in the model. For weaning weight (120 d, n = 23,903), estimates of variances of effects added to the basic model were all near zero (a2, 0.14; m2, 0.09; ram, 0.23; p2m, 0.04). For fleece weight (FW, n = 29,024) and number born (NB, n = 29,688), animal permanent environmental effects were added to the model (p2a; n = 7,741 and 7,840) and ram was dropped. For these traits, effects not in the basic model had small variances. For FW, estimates with the full model were: a2, 0.52; m2, 0.01; p2m, 0.00; p2a, 0.06; c2, 0.00; dy2, 0.00; sd2, 0.02; and sc2, 0.06, and for NB they were: a2, 0.08; m2, 0.00; p2m, 0.00; p2a, 0.02; c2, 0.00; dy2, 0.00; sd2, 0.00; and sc2, 0.01. Cytoplasmic effects were not important. Unusual random effects in the model did not change estimates for basic parameters. Although some effects were significant, especially for BW, effects on genetic evaluations are likely to be small.

Estimates of genetic parameters and genetic change for reproduction, weight, and wool characteristics of Targhee sheep.

Genetic parameters from both single-trait and bivariate analyses for prolificacy, weight, and wool traits were estimated using REML with animal models for Targhee sheep from data collected from 1950 to 1998 at the U.S. Sheep Experiment Station, Dubois, ID. Breeding values from both single-trait and seven-trait analyses calculated with the parameters estimated from the single-trait and bivariate analyses were compared across years of birth with respect to genetic trends. The numbers of observations were 38,625 for litter size at birth and litter size at weaning, 33,994 for birth weight, 32,715 for weaning weight, 36,807 for fleece weight and fleece grade, and 3,341 for staple length. Direct heritability estimates from single-trait analyses were 0.10 for litter size at birth, 0.07 for litter size at weaning, 0.25 for birth weight, 0.22 for weaning weight, 0.54 for fleece weight, 0.41 for fleece grade, and 0.65 for staple length. Estimate of direct genetic correlation between litter size at birth and weaning was 0.77 and between birth and weaning weights was 0.52. The estimate of genetic correlation between fleece weight and staple length was positive (0.54), but was negative between fleece weight and fleece grade (-0.47) and between staple length and fleece grade (-0.69). Estimates of genetic correlations were near zero between birth weight and litter size traits and small and positive between weaning weight and litter size traits. Fleece weight was slightly and negatively correlated with both litter size traits. Fleece grade was slightly and positively correlated with both litter size traits. Estimates of correlations between staple length and litter size at birth (-0.14) and litter size at weaning (0.05) were small. Estimates of correlations between weight traits and fleece weight were positive and low to moderate. Estimates of correlations between weight traits and fleece grade were negative and small, whereas estimates between weight traits and staple length were positive and small. Estimated breeding values averaged by year of birth from both the single- and seven-trait analyses for the prolificacy and weight traits increased over time, whereas those for fleece weight decreased slightly and those for the other wool traits were unchanged. Estimated changes in breeding values over time did not differ substantially for the single-trait and seven-trait analyses, except for traits highly correlated with another trait that was responding to selection.

Models with cytoplasmic effects for birth, weaning, and fleece weights, and litter size at birth for a population of Targhee sheep.

Fifteen models were compared for the birth weight of 33,994 lambs recorded at the U.S. Sheep Experimental Station (1950 to 1998). The initial intent was to estimate fractions of variance due to cytoplasmic line (c2; n = 892) and sire by cytoplasmic line interaction (sc2; n = 17,557). The basic model included direct genetic (fractional variance, a2; n = 35,684), maternal genetic (m2, with correlation r-am), and maternal permanent environmental (p2; n = 8,418) effects. The model with sc2 was significantly better than the basic model with and without c2. When other random effects were added, sc2 became zero. Significant effects were associated with random dam x year (dy2; n = 24,801), sire x dam (sd2; n = 23,924), and dam x number born (dn2; n = 12,944) interaction effects. Estimates with all effects in the model were a2, 0.24; m2, 0.19; r-am, 0.11; p2, 0.05; c2, 0.00; dn2, 0.04; dy2, 0.06; sd2, 0.05; sc2, 0.00. Estimates for a2, m2, and r-am were the same for all models. Estimate of p2 changed when other effects were added to the model. Largest estimates for nongenetic effects were: p2, 0.08; c2, 0.00; dy2, 0.13; sd2, 0.11; and sc2, 0.04. Regardless of whether Westell groups (n = 91) were in the model, estimates were similar. For weaning weight (120-d, n = 32,715), estimates of variances of effects added to the basic model were all near zero (a2, 0.18; m2, 0.12; r-am, -0.01; p2, 0.06). For number born (NB, n = 37,020) and fleece weight (FW, n = 36,197), animal permanent environmental effects were added to the model (ap2; n = 9,871 and 9,760) and r-am was dropped. For these traits, effects not in the basic model had small variances. Nonzero estimates with full model were a2, 0.10; ap2, 0.01; dy2, 0.02; and sc2, 0.01 for NB, and a2, 0.54; m2, 0.02; ap2, 0.02; dy2, 0.04; and sc2, 0.02 for FW. Cytoplasmic effects were not important. The addition of unusual random effects to the model did not change estimates for the basic parameters. Although some of these effects were significant, especially for BW, the effects on genetic evaluations are likely to be small.

Estimates of genetic parameters and genetic change for reproduction, weight, and wool characteristics of Columbia sheep.

Genetic parameters from both single-trait and bivariate analyses for prolificacy, weight and wool traits were estimated using REML with animal models for Columbia sheep from data collected from 1950 to 1998 at the U.S. Sheep Experiment Station (USSES), Dubois, ID. Breeding values from both single-trait and seven-trait analyses calculated using the parameters estimated from the single-trait and bivariate analyses were compared with respect to genetic trends. Number of observations were 31,401 for litter size at birth and litter size at weaning, 24,741 for birth weight, 23,903 for weaning weight, 29,572 for fleece weight and fleece grade, and 2,449 for staple length. Direct heritability estimates from single-trait analyses were 0.09 for litter size at birth, 0.06 for litter size at weaning, 0.27 for birth weight, 0.16 for weaning weight, 0.53 for fleece weight, 0.41 for fleece grade, and 0.55 for staple length. Estimate of direct genetic correlation between littersize at birth and weaning was 0.84 and between birth and weaning weights was 0.56. Estimate of genetic correlation between fleece weight and staple length was positive (0.55) but negative between fleece weight and fleece grade (-0.47) and between staple length and fleece grade (-0.70). Estimates of genetic correlations were positive but small between birth weight and litter size traits and moderate and positive between weaning weight and litter size traits. Fleece weight was lowly and negatively correlated with both litter size traits. Fleece grade was lowly and positively correlated with both litter size traits, while staple length was lowly and negatively correlated with the litter size traits. Estimates of correlations between weight traits and fleece weight were positive and low to moderate. Estimates of correlations between weight traits and fleece grade were negative and small. Estimates of correlations between staple length and birth weight (0.05) and weaning weight were small (-0.04). Estimated breeding values averaged by year of birth from both the single-trait and multiple-trait analyses for the prolificacy and weight traits increased over time, but were unchanged for the wool traits. Estimated changes in breeding values over time did not differ substantially for single-trait and multiple-trait analyses, except for traits highly correlated with another trait that was responding to selection.

A 12-week clinical trial determining the efficacy of synthetic conjugated estrogens, A (SCE), in the treatment of vasomotor symptoms in menopausal women.

OBJECTIVE: To compare the clinical effects of a new oral synthetic conjugated estrogens, A (SCE), versus placebo in a clinically relevant population on the reduction in the mean number of moderate to severe vasomotor symptoms. DESIGN: A total of 120 healthy pre- and postmenopausal women (72 active, 48 placebo) were enrolled into a randomized, placebo-controlled, double-blind, multi-center clinical trial. Women of all races were enrolled, using minimal inclusion and exclusion criteria. Each subject received either orally administered SCE, in doses of 0.3 mg, 0.625 mg or 1.25 mg per day, or placebo. Analysis of variance was performed on the primary efficacy variable (change from baseline to weeks 4, 8, and 12 in the mean number of moderate to severe vasomotor symptoms). RESULTS: Changes in moderate to severe vasomotor symptoms in the intent to treat population showed statistically significant differences between the active and placebo treatments at week 4 (P < .022), week 8 (P < .010), and week 12 (P < .010). By week 12, the mean percentage reduction in moderate to severe vasomotor symptoms was 81%, from an average baseline of 96.8, to 16.5 hot flashes per week for the active treatment group. The overall incidence of expected estrogen-related adverse effects was modest. Laboratory tests and vital sign measurements did not reveal clinically significant changes or abnormalities from screening to the final visit in either treatment group. CONCLUSIONS: The results of this study confirm the efficacy and safety of SCE in the treatment of moderate to severe vasomotor symptoms in menopausal women. In addition, the study also demonstrated that the use of more liberal entry criteria did not materially affect the efficacy outcome.

The frequency of caffeine withdrawal in a population-based survey and in a controlled, blinded pilot experiment.

Reports of symptoms when regular caffeine consumption is stopped have appeared in the medical literature, but the frequency and significance of this phenomenon have remained controversial. The objective of this study was to collect information on the prevalence and severity of caffeine withdrawal in the general population and determine the incidence and type of symptoms reported on blind abrupt and gradual caffeine cessation among coffee drinkers reporting past episodes of caffeine-withdrawal symptoms. A community-based telephone survey was followed by a stratified, randomized, double-blind controlled study. Participants included 11,112 persons spontaneously calling to inquire about studies not related to caffeine and 57 regular caffeine users selected from among the callers because of self-reported caffeine-withdrawal symptoms. Gradual or abrupt withdrawal from caffeine was compared to continuation of the same caffeine level. In a survey of 11,112 persons, 61% reported daily caffeine consumption, and 11% of the caffeine consumers reported symptoms upon stopping caffeine. Among the regular caffeine users, only 0.9% of males and 5.5% of females reported symptoms significant enough to interfere with normal activities when they abruptly stopped caffeine. A group of those reporting withdrawal symptoms were randomly assigned to three subsamples. In the group subjected to abrupt withdrawal (N = 18), 6 (33.3%) reported symptoms (e.g., headaches and tiredness). Including decreases in functional ratings, a total of 7 of the 18 (38.8%) could be considered to have experienced caffeine withdrawal. The gradual withdrawal group (N = 20) reported minimal if any caffeine withdrawal symptoms. A third group (N = 18) was kept on a level dose of caffeine for comparison. When participants are unaware of the caffeine-withdrawal focus of the study, these results suggest that both the frequency and severity of caffeine-withdrawal symptoms are much lower than found in some previous reports and that clinically significant symptoms may be uncommon events among the general population.

Estrus and fertility in lactating sows and piglet performance as influenced by limited nursing.

Seven trials were conducted with 126 sows and their litters to determine the influence of limited nursing (LN), starting on day 21 of lactation, on estrous activity and conception rate during lactation and on piglet performance. One-half of the sows in each of the first three trials were allowed to nurse their piglets four times daily for 30-min periods for 12 days. In the last four trials, half of the sows nursed their piglets four times daily for the first 3 days and then three times daily for 4 days (7-day limited nursing). The remaining sows in each trial were allowed to nurse their piglets in a normal manner. All piglets were weaned at the end of the LN period. Piglets were weighed at the start of the study, at weaning and at 14 days postweaning. Creep intake was measured during the LN period. In the first three trials, eight of the 26 LN sows were in estrus before weaning, whereas no control (C) sows were in estrus during lactation (P greater than .01). The average interval from weaning to breeding was 1.7 and 6.6 days for LN and C sows, respectively (P greater than .01). In the last four trials, five of 37 LN sows were in estrus before weaning, whereas no C sows were in estrus during lactation (P greater than .07). The average interval from weaning to estrus was 3.3 and 4.3 days for LN and C sows, respectively, (P greater than .05). Conception rate did not differ between trials or between treatment groups. Weight gain during the treatment period was lower and creep feed intake greater (both P greater than .01) for pigs reared by LN sows than for piglets reared by C sows. Weight gained after weaning was greater (P greater than .05) for piglets reared by LN sows than for those reared by C sows in the first three trials, but was similar for the two groups in the following four trials. Piglet death loss was similar for the two groups throughout the experiment.