The effects of heat, water, acid, and alkali treatment of tomato cannery wastes on growth, metabolizable energy value, and nitrogen utilization of broiler chicks.

Two experiments were conducted to determine the effects of heat, water, acid, and alkali treatment of tomato pomace on gain, feed to gain ratio, nitrogen utilization, and ME of diets for broiler chicks. In Experiment 1, both treated and untreated tomato pomace was included in broiler diets at a 10 or 20% level. Results indicated that the level or antinutritional factors present in untreated tomato cannery waste did not appreciably depress any measured production parameter. Hence, it appeared that untreated tomato cannery wastes might be used as a feed ingredient in low-energy poultry diets (broiler breeder and laying hen recycling rations), ruminant diets, and as a protein source in regions of the world where such feed ingredients are scarce. The second experiment was designed to test the effect of alkali concentration and treatment time of tomato pomace on the performance of broiler chicks. Alkali treatment of tomato cannery wastes increased gain and decreased feed to gain ratios of broiler chicks over those of untreated tomato waste controls. Results indicated that the increased gain and decreased feed to gain ratios of the chicks were due in part to the acid neutralization phase of the alkali treatment. Alkali treatment apparently affects the tomato cannery wastes almost instantaneously, as differences among actual treatment times and concentrations were small. However, only the highest alkali treatment increased the pH of the tomato cannery waste above 7, suggesting that a true alkali treatment might cause additional improvements in gain and feed to gain ratio when fed to broiler chicks.

Genetic and phenotypic relationships in Japanese quail. 1. Body weight, carcass, and organ measurements.

Live BW, carcass data, and organ data taken at 34 days of age on approximately 1,000 quail of both sexes from 110 sires and 290 dams were utilized to estimate genetic parameters from the initial generation of a selection study. The birds represented a sample of a line selected for high 4-wk BW. Data were analyzed using Henderson's Method 3 (MM3) and restricted maximum likelihood (REML) with and without a relationship matrix. The paternal half-sib heritabilities for body, carcass, and organ weights in Japanese quail were moderate to high for most traits studied, suggesting that selection to increase or decrease these traits should be successful. With the exception of BW, abdominal fat (AF), and heart weights, maternal half-sib heritability estimates were smaller than paternal half-sib estimates. Heritability estimates of traits adjusted for BW tended to be lower than counterparts not adjusted for BW. The genetic correlations of BW with the other carcass measurements were positive, and tended to be moderate to high. The correlation of BW with AF was .34, suggesting that selection for increased BW alone will lead to a bird with more abdominal fat. The correlations of AF with the other traits tended to be low to moderate in magnitude, with three of the correlations being negative, suggesting correlated responses with other traits when selecting for increased or decreased AF would be small. Genetic correlations among various muscle measurements were all positive and most were high in magnitude, indicating that traits easiest to measure and collect can be used in a selection process. The genetic correlations among the organ measurements were positive and moderate as were the correlations of organ weights with muscle weights. Negative genetic correlation estimates between AF and muscle measures were obtained from analysis when BW was a covariate. The REML heritability estimates were higher than MM3 estimates and REML genetic correlation estimates were less extreme than MM3.

Estimates of genetic parameters in turkeys. 3. Sexual dimorphism and its implications in selection procedures.

Live, carcass, and skeletal data taken at 16 wk of age on 504 female and 584 male turkeys from 34 sires and 168 dams were utilized to evaluate sex differences in genetic parameter estimates. Data were transformed to common mean and variance to evaluate possible scaling effects. Genetic parameters were estimated from transformed and untransformed data. Further analyses were conducted with a model that included sire by sex and dams within sire by sex interactions, and the variance estimates were used to calculate genetic correlations between the sexes and genetic regression parameters. Heritability estimates from transformed and untransformed data were similar, indicating that sex differences were present in the genetic parameters, but scaling effects were not an important factor. Genetic correlation estimates from paternal (PHS) and maternal (MHS) half-sib estimates were close to unity for BW (1.14, PHS; 1.09, MHS), shank width (.99, PHS; .93, MHS), breast muscle weight (1.23, PHS; 1.04, MHS), and shank length (1.09, PHS; .97, MHS). However, abdominal fat (.79, PHS; .59 MHS), total drumstick muscle weight (.75, PHS; 1.14, MHS), rough cleaned shank weight (.78, PHS; not estimatable, MHS), and shank bone density (1.00, PHS; .53, MHS) estimates were somewhat lower. The estimates suggest that the measurement of these latter "traits" at the same age in the two sexes may, in fact, be measuring different genetic effects and that selection procedures in turkeys need to take these correlations into account in order to make optimum progress. The genetic regression parameters indicated that more intense selection in the sex that has the smaller genetic variation could be practiced to make greater gains in the opposite sex.

Effects of genetic strain, slow versus rapid-feathering maternal genotype, and cage density on the performance of Single Comb White Leghorns.

Two hatches involving 11,158 pullets from 22 Single Comb White Leghorn strain crosses were used in these experiments: 13 from rapid-feathering (k+/-) and 9 from slow-feathering (K/-) dams, some of which shared common genetic backgrounds; and all from 5 homozygous k+ sire types. Birds were grown intermingled within hatch, and were subsequently caged in two laying houses, one with 30.5 cm x 40.6-cm cages and the other with 40.6 cm x 30.5-cm cages, at densities of three or four birds/cage. Data were collected by cage on hen-day rate of lay from 50% production to 52 wk of age; (HD%), number of eggs produced per hen housed (EHH), percentage mortality (%M) to 52 wk of age; 35-wk BW (BW35); egg weight (EW34), specific gravity (SG34), and percentage bloodspots (BS%34) at 34 wk of age. The effects of hatches or house (H), density (D), maternal feathering type (MFT), genetic strain within MFT (GS/MFT), bank level within house (BL/H), and all possible interactions were included in the analysis model. Hatch, house, and cage type were completely confounded, so no general conclusion can be made concerning the effects of the reverse and standard cages on performance. The H effects were significant for all traits except HD%. Cage D significantly affected all traits except SG34 and BS%34. Pullets housed at three/cage weighed 26 g less, produced 5.5 more eggs that were .3 g/egg lighter, laid at a 1.7% higher hen-day rate, and had 3.6 less %M from 20 to 52 wk of age than those housed at four/cage. The MFT significantly affected all traits except %M, SG34, and BS%34. The k+/- daughters from K/- dams weighed 34 g less, produced at a 2.8% lower HD%, laid 6.9 fewer eggs, which eggs averaged .6 g/egg less than the eggs from the k+/- daughters of the k+/- dams. Interactions were in general small and nonsignificant. However, the H x GS/MFT interactions were significant for HD%, EHH, BW35, %M, and EW34 (P less than .05); their significance is suggestive of the presence of genotype x environment interactions.

Estimates of genetic parameters in turkeys. 1. Body weight and skeletal characteristics.

Heritabilities (h2) of and genetic (rG) correlations among body weight and a number of skeletal characteristics were estimated from data on 1,088 pedigree turkeys (504 females and 584 males) of a randombred control line. All measurements were made at 16 wk of age. The h2 estimates (sire component) obtained from females (F) and males (M), respectively, were: BW .23, .60; shank width (SW) .54, .47; shank length (SL) .43, .54; drum length .66, .60; rough-cleaned weights of the thigh (nonestimable, .60), drum .09, .57, and shank .28, .69; cleaned weights of the drum .37, .71, and shank .30, .40; fat-free weights of the drum .44, .93, and shank, .45, .82; bone density measured at 40 and 60% of the length from the proximal end of the drum .68, .80 and .34, .92, respectively, and shank .28, .69 and .31, .55. Genetic correlations (rG) among the various bone weights were all above .66, with most above .85. The rG between BW and SW were .33 from M and .47 from F. These correlations suggest there is a relatively weak relationship, indicating that selection for BW alone might not cause a large enough increase in SW to support the increase brought about in BW. Shank width also had relatively low correlations with bone weight measurements, ranging from .27 to .53 from M and .17 to .56 from F. The h2 of walking ability score (WA) was .06 and the rG of WA with BW was -.73, which indicated that the low body weight families tended to have poor WA (i.e., higher scores). This may be a spurious rG, because poor walking ability scores tended to be grouped in families. Birds with poor walking ability would have difficulty eating, and would, therefore, tend to have low BW. The rG between SW:WA (-.09) and SL:WA (.03) indicated little relationship between those traits. The WA and the bone density readings had high negative rG (range -.75 to -1.47), indicating that families with poor WA ratings also had low bone density scores.

Estimates of genetic parameters in turkeys. 2. Body weight and carcass characteristics.

Data were taken from 1,088 individuals--504 females (F) and 584 males (M)--produced by 34 sires and 168 dams from a randombred control line (RBC2) of turkeys maintained at the Ohio Agricultural Research and Development Center, Wooster, OH. Turkeys were used to estimate genetic and phenotypic parameters among 16-wk body weight and a number of body composition characteristics. Heritabilities (h2) were estimated from sire components of variance for 16-wk weights of muscles of breast (BM: F = .08, M = .35); thigh (TM: F = .12, M = .17); and drum (DM: F = .30, M = .44); weights of leaf fat (LF: F = .13, M = .51) and total abdominal fat (AF: F = .21, M = .55); and total percentage carcass fat (%F:F = .06, M = .24), percentage protein (F = .07, M = .20), and percent moisture (F = nonestimable, M = .11). The h2 of percentage carcass ash was nonestimable from both data sets due to negative estimates of the sire variance components. Due to the non-normal distributions of some of the fat measures, the fat measure data were converted to natural logarithms. Genetic estimates from the transformed data were similar to those from the nontransformed data. Genetic correlation (rG) estimates indicated a positive genetic association between body weight (BW) and all the fat characteristics measured. The BW was highly correlated with BM (F = .48, M = .86), TM (F = .81, M = 1.01), and DM (F = 1.04, M = .70). However, BW was correlated to a lesser degree with LF (F = .02, M = .27), AF (F = .25, M = .32), and %F (F = .93, M = .50). The BM was only moderately correlated with TM (F = .43, M = .28) and DM (F = .73, M = .27). The TM and DM were highly correlated (F = 1.02, M = .84). The existence of these correlations, which are less than unity, indicate that selection for BW alone will lead to increasing levels of fat in commercial turkeys, and to disproportionate increases in breast vs. leg muscles.

Breed differences in uterine and ovarian measurements in gestating swine.

Ovulation rate, ovary weight, corpora lutea weight and uterine length were measured at 10 or 35 d of gestation in Duroc (199) and Yorkshire gilts (114). Embryos were counted at d 35. Yorkshires had significantly more corpora lutea than Durocs (13.6 vs 12.3 at d 10; 13.9 vs 12.4 at d 35). At d 10 breeds did not differ in uterine length, but by d 35 Duroc uteri were longer (P less than .01) than Yorkshire uteri (411 vs 375 cm) despite having fewer (P greater than .05) embryos (9.9 vs 10.5). Ovary weight did not differ between breeds at 10 or 35 d. Homogeneity analyses showed that the correlation matrices were significantly different between breeds at d 35 but not at d 10. In Durocs, high positive correlations existed between total embryo number and corpora lutea number (.57), ovary weight (.53) and corpora lutea weight (.25), whereas corresponding correlations were small in Yorkshires (.21, -.02 and -.03, respectively). In Yorkshires, strong negative correlations existed between total embryo survival and corpora lutea number (-.55), ovary weight (-.30) and corpora lutea weight (-.55), but in Durocs corresponding correlations were small (-.12, .14 and -.10, respectively). These results suggest that animal scientists should consider breed differences in levels of performance and its relationships among traits when designing or interpreting experiments.

Body condition of sows across parities and relationship to reproductive performance.

Weight, heartgirth, backfat and body condition of sows was monitored in a commercial, farrow-to-finish unit during 1 yr. Measurements were obtained during the third, ninth and fifteenth week of gestation and the day after weaning. Litter performance and rebreeding rate also were recorded. Body weight and heartgirth increased (P less than .01) over parities because gestational gains were larger than lactational losses. Backfat tended to be lower in later parities. Body weight, heartgirth and backfat, but not condition score, declined from weaning to the third week of the subsequent gestation in both first and second litter sows. Correlations among measures of body condition were low (less than .45), except the overall correlation between body weight and heartgirth. Number of pigs born alive increased and interval to estrus decreased in later parities. There were no significant relationships between changes in body condition and rebreeding performance of sows. These results suggest that changes in body condition typically observed in sows housed in commercial production units may be too subtle to have an effect on reproductive performance.

Estimates of genetic correlations between testicular measurements and female reproductive traits in cattle.

Data from 528 male and 645 female progeny of 63 sires were used to estimate genetic correlations between female and male reproductive traits. Data were from two Hereford herds involved in a long-term selection program of the North Carolina Agricultural Experiment Service. Testicular measurements of circumference, diameter, length and volume were obtained on bulls at 205 and 365 d. Testicular growth measures were defined as differences between 205-and 365-d measurements. Heifers were placed in the breeding herd as yearlings and given two breeding seasons to produce a calf. Traits utilized from females were three age-at-first-breeding traits, two age-at-first-calving traits, two pregnancy rate traits, rebreeding interval and calving interval. Genetic correlations were estimated from half-sib and from sire-daughter analyses. Seventy-five percent or more of the correlations of testicular measurements with pregnancy rats, age at first breeding and age at first calving were in the favorable direction. Average correlations were .62, -.55 and -.66, respectively. For each of the remaining female traits, approximately 50% of the correlations were favorable and the average correlations were small. Correlations were summarized by testicular measurement with favorable correlations given a negative sign. Testicular diameter had more favorable correlations (80%) than length, volume or circumference (70%). However, average correlations were similar (-.31, -.30, -.34 and -.26, respectively). Testicular measurements taken at either 205 or 365 d had the same percentage of favorable correlations (72%), while testicular growth measurements had a slightly higher percentage of favorable correlations (78%). Average correlations of 365-d measures were higher (-.38) than either 205-d or growth measures (-.25 and -.28, respectively). Heritabilities for testicular measurements tended to be moderate to high, while those for female reproduction tended to be low to moderate. These results suggest that selection for increased testicular size would lead to improvement in female reproduction, particularly an increase in calving rate and a decrease in age at first breeding.

Genetic parameters for testes traits in swine.

Data were collected from 1,245 Duroc boars and 527 Yorkshire boars. This represents 128 Duroc and 57 Yorkshire sires. Body weights, testis length and combined testes width at 140 and 168 d were obtained. Of these boars, 432 were castrated at a later age to evaluate relationships between in situ measures and excised testis traits. Heritabilities for testis length, width and volume at 140 d ranged from .16 to .25 in both Duroc and Yorkshire data. Heritabilities for testis measurements at 168 d ranged from .16 to .36 in both data sets. Favorable negative genetic relationships were found between in situ testis measures and age to 104 kg and backfat adjusted to 104 kg. Correlations among in situ measurements were high and positive. All excised testicular traits were highly heritable except for right epididymis weight and excised testis width. Correlation estimates among excised testis traits were generally positive. Phenotypic and genetic correlation estimates between live (in situ testis and growth performance traits) measurements and excised testis traits were generally favorable. This study suggests that in situ testis measurements should be good predictors of sperm production. It also suggests that selection for testis size should not be antagonistic to selection for growth performance traits.

Variation in testosterone production among boards and its relationship to sexual interest and breeding performance.

Variation in ability to produce testosterone in response to both GnRH and ACTH administration and quatitative relationships between GnRH-stimulated testosterone levels, ACTH-stimulated testosterone levels, sexual interest and breeding performance were assessed in a group of 31 Duroc boars (115.4 +/- 2.5 kg body weight and 212.2 +/- 3.0 days of age). Mean area beneath the testosterone response curve increased (P<0.01) after GnRH and ACTH but the magnitude of response was variable among boars. Post-GnRH testosterone area varied from 7.44 to 50.86 ng/ml X h with a CV = 52.41% while post-ACTH testosterone area varied from 4.99 to 28.78 ng/ml X h with a CV = 45.46%. Mean sexual interest and mean breeding performance scores were correlated (r = 0.67, P<0.01); however, correlations of either variable with testosterone areas were low and nonsignificant. These results indicate that the testosterone-producing ability of boars of similar age and breeding is highly variable and suggest that peripheral testosterone concentrations may not be good indicators of either libido or breeding performance.

Breed prenatal, breed postnatal and heterosis effects for postweaning traits in swine.

Crossfostering techniques were used to evaluate breed prenatal, breed postnatal and heterosis effects in Duroc and Yorkshire swine. Traits analyzed for these effects were: age adjusted to 104 kg (DAYS), backfat adjusted to 104 kg (AJBF), average daily gain (ADG), weight/day of age (WDA), unadjusted backfat (BF) and weight at 154 d (WT154). Breed prenatal (genetics and prenatal maternal) effects were important for BF and WT154 (P less than .10). Pigs gestated by Duroc dams tended to be fatter and weigh more at 154 d than pigs from Yorkshire dams. Breed postnatal effects were important only for AJBF (P less than .05). Pigs reared by Duroc nurses were fatter than pigs reared by Yorkshire nurses. Prenatal dam x postnatal nurse interaction effects were important for BF (P less than .10) and AJBF (P less than .05). Heterosis values were -10.2, 8.0, 13.7, 13.6, 14.1 and 7.7% for DAYS, AJBF, ADG, WDA, WT154 and BF, respectively. Differences between purebred and crossbred pigs were larger when purebred and crossbred pigs were reared in the same litter than when reared separately. These data suggest that intra-litter competition between purebred and crossbred pigs may have a detrimental effect on postweaning growth for purebred pigs.