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A series of experiments was conducted to determine muscle fiber type, area, and distribution, and muscle total collagen, color, proximate composition, total fatty acid profile, calories, and cholesterol content for Pekin duckling and broiler chicken Pectoralis muscle. Duckling Pectoralis contained approximately 16% white fibers and 84% red fibers compared with 100% white fibers in the chicken Pectoralis. Duckling white fibers were significantly (P

The effects of beak trimming at day old on performance and behavioral activities of male and female Large White turkeys were evaluated. One hundred and twenty poults of each sex were evenly assigned to 20 treatment pens and evaluated for body weight, feed usage, and livability characteristics to 18 wk of age. Behavioral observations were conducted for feeding, drinking, sleeping, huddling, resting, and agonistic activities. Beak trimming affected body weight and feed usage levels for the sexes differently. From 6 wk, trimmed males were significantly heavier than untrimmed males, whereas untrimmed females were heavier than trimmed females from 12 wk. Similar to body weights, feed usage levels from 13 to 18 wk were higher for trimmed males compared with untrimmed males and lower for trimmed females compared with untrimmed females. Feed conversion ratios after 12 wk and survival to 18 wk were not affected by trimming treatment. Livability rates, however, were lowest for untrimmed males and highest for untrimmed females. Effects on behavioral activities were confined primarily to the brooding and early rearing phases. Beak trimming reduced feeding activity of females and drinking activity of both males and females during the first 2 wk. Sleeping, huddling, and resting activities were increased by beak trimming for both sexes during brooding. Agonistic acts were reduced by beak trimming main effect at 3 and 6 wk. Trimmed males committed fewer agonistic acts at 6 wk than untrimmed males.

An experiment was conducted to evaluate the performance of two commercial strains of turkey poults (British United and Nicholas) subjected to two feeding programs (day or night feeding) during chronic daily heat stress (90°F for 9 hours) from 9 to 18 weeks of age. Neither day nor night feeding programs had significant effects (P>. 05) on body weight gain, feed usage, and feed conversion ratio, in the heat stress environment. Night feeding improved livability significantly (P

Individual and combined effects of electrical stimulation and polyphosphate marination on drip and other quality attributes of early-harvested, individually quick-frozen chicken breast fillets were evaluated. Broiler chickens were slaughtered, half conventionally processed and half with electrical stimulation. Fillets were harvested 1 h postmortem and marinated in either NaCl solution or NaCl plus polyphosphate solution. Marinade absorption, pH, drip, cooking loss, and shear values were observed. Electrical stimulation had no direct effect on pH, cooking loss, or shear values, whereas polyphosphate increased pH and decreased cooking loss. Polyphosphate treatment caused fillets from unstimulated carcasses to absorb more marinade and yielded more drip that those from stimulated carcasses. Fillets from stimulated carcasses marinated in NaCl solution without polyphosphate yielded less drip than those from unstimulated carcasses. Polyphosphate reduced drip of fillets from unstimulated carcasses but not of those from stimulated carcasses. Results support previous reports indicating interactions between polyphosphates and processing parameters that can affect ultimate quality of poultry meat products.

Campylobacter spp. are frequently present in the intestinal tract and internal tissues of broiler breeder and broiler chickens. Campylobacter spp. ecology in commercial Leghorn laying hens has not been extensively studied. The objectives of the current study were to determine 1) Campylobacter spp. presence in the reproductive tract, lymphoid organs, liver-gallbladder, and ceca of commercial Leghorn laying hens; 2) species of Campylobacter present; and 3) antimicrobial resistance pattern of Campylobacter isolates. In study 1, three flocks ranging from 94 to 105 wk of age were sampled from a commercial laying complex. In study 2, two flocks, 82 and 84 wk of age, were sampled from a separate complex. Hens were killed, defeathered, aseptically necropsied, and the spleen, liver-gallbladder, ovarian follicles, and upper (infundibulum, magnum, and isthmus) and lower (shell gland and vagina) reproductive tracts were aseptically removed before the ceca. Samples were packed on ice and transported to the laboratory for evaluation. For speciation, a standard BAX real-time PCR method was used while susceptibility testing was performed using US National Antimicrobial Resistance Monitoring System (NARMS) standards and recommended quality control organisms. Isolates were examined for susceptibility using a semi-automated testing system (Sensititer) to the following 9 antimicrobials: azithromycin, clindamycin, ciprofloxacin, erythromycin, florfenicol, gentamicin, nalidixic acid, telithromycin, and tetracycline. In study 1, the isolation rate was 13, 67, 53, 3, 13, and 57% from the ovarian follicles, lower reproductive tract, upper reproductive tract, spleen, liver-gallbladder, and ceca, respectively. In study 2, the isolation rate was 17, 43, 33, 20, 17, and 73% from the ovarian follicles, lower reproductive tract, upper reproductive tract, spleen, liver-gallbladder, and ceca, respectively. Overall, 50% of isolates were Campylobacter jejuni, 49% Campylobacter coli, and 1% Campylobacter lari. In study 1, all of the isolates were pan-susceptible. In study 2, thirty-seven percent of the isolates were resistant to tetracycline. Commercial table egg laying hens housed in colony cages on wire floors had diverse Campylobacter spp. recovered from different tissues and these isolates were not resistant to a broad range of antimicrobials.

Campylobacter inoculation studies are limited without a suitable marker strain. The lurpose of this study was to screen Campylobacter strains (n=2073) obtained from poultry carcass rinses through the Centers for Disease Control and Prevention's National Antimicrobial Resistant Monitoring System for resistance to gentamicin and evaluate one strain's efficacy as a marker. A C. coli strain was found resistant to gentamicin at32 microg/ml. Gentamicin was incorporated into media (Campy-Cefex agar, Brucella agar, and blood agar) from 0 to 1000 microg/ml, and the upper level of gentamicin resistance was determined. C. coli strain's upper level of growth on Campy-Cefex plates, blood agar plates, and Brucella agar plates was 400, 300, and 200 pg/ml, respectively. Ceca and postpick carcass rinses were obtained and streaked onto Campy-Cefex agar at the above gentamicin levels to evaluate background microflora exclusion. Campy-Cefex agar containing gentamicin at 100 ag/ml prevented from the ceca, and reduced from the rinse, background microflora. The C. coli strain was orally or intracloacally inoculated into chicks. At 1, 3, and 6 weeks of age, inoculated broilers were removed and several tissue types sampled for the presence of the marker strain. At 6 weeks of age, 10 additional noninoculated penmates were sampled. The C. coli strain colonized chicks, disseminated to body tissues, colonized penmates, and persisted throughout the 6-week grow-out. The C. coli strain's unique characteristic, being resistant to high levels of gentamicin, allows for a marker that can be used in a wide range of Campylobacter research projects.

Five, fat-soluble dyes and one, metachromatic tissue dye were administered to White Leghorn hens and broilers to determine how these compounds would color parathyroid tissue for subsequent gland localization. Sudan black, sudan red, canthaxanthin, oil red O, beta-apo-8'-carotenal, and toluidine blue O were administered orally in gelatin capsules once a day for 1, 2, or 3 days before slaughter. The dyes were administered at approximately 100 mg/dose. The carotenoid pigments were given at 200 mg/dose. Two administrations were required to develop sufficient visible staining. All dyes except the toluidine blue O were visibly deposited in the parathyroid glands. Sudan black resulted in the greatest contrast with surrounding adipose tissue. Male broilers 3 wk of age that were given one dose of sudan black showed gland definition comparable to that seen in the hens after two doses. Male broilers 5 wk of age showed less gland definition when given sudan black or sudan red for 1 or 2 days. A histological examination indicated that the fat-soluble dyes were located extracellularly. These results indicate that sudan black can be used to visually identify the parathyroid glands of chickens.

During processing, fecal material may contact broiler carcasses externally or internally. A study was conducted to determine the effect of external vs. internal fecal contamination on numbers of bacteria on broiler carcasses. In each of 3 trials, 12 carcasses just prior to evisceration were obtained from a commercial processing plant, placed on a shackle line, and eviscerated with commercial equipment in a pilot scale processing plant. Also, approximately 20 intestinal tracts were collected from the processing plant; then cecal contents were collected and pooled. One gram of cecal content was placed on the exterior breast skin (external), inside the carcass cavity (internal), or not applied (control). All carcasses were held 10 min, then placed on the shackle line and passed through a commercial inside-outside bird washer set at 552 kPa, 5 s dwell time, using approximately 189 L per min of tap water at ambient temperature. After a 1-min drip, whole carcass rinses were conducted on each carcass, and coliforms, Escherichia coli, and Campylobacter counts were determined and reported as log cfu/mL of rinse. External carcass contamination resulted in significantly higher (P0.05) coliform, E. coli, and Campylobacter numbers than internal contamination (5.0 vs. 4.5, 4.9 vs. 4.2, and 3.6 vs. 2.6, respectively). Control carcass counts were significantly lower than external or internal carcass contamination counts for coliforms (3.7), E. coli (3.6), and Campylobacter (2.2). External contamination resulted in higher numbers of bacteria after carcass washing, but carcasses with internal contamination still have higher numbers of bacteria after washing than carcasses without applied contamination.

Experiments were conducted to compare litter sampling methods for the detection of Salmonella. In experiment 1, chicks were challenged orally with a suspension of naladixic acid-resistant Salmonella and wing banded, and additional nonchallenged chicks were placed into each of 2 challenge pens. Nonchallenged chicks were placed into each nonchallenge pen located adjacent to the challenge pens. At 7, 8, 10, and 11 wk of age the litter was sampled using 4 methods: fecal droppings, litter grab, drag swab, and sock. For the challenge pens, Salmonella-positive samples were detected in 3 of 16 fecal samples, 6 of 16 litter grab samples, 7 of 16 drag swabs samples, and 7 of 16 sock samples. Samples from the nonchallenge pens were Salmonella positive in 2 of 16 litter grab samples, 9 of 16 drag swab samples, and 9 of 16 sock samples. In experiment 2, chicks were challenged with Salmonella, and the litter in the challenge and adjacent nonchallenge pens were sampled at 4, 6, and 8 wk of age with broilers remaining in all pens. For the challenge pens, Salmonella was detected in 10 of 36 fecal samples, 20 of 36 litter grab samples, 14 of 36 drag swab samples, and 26 of 36 sock samples. Samples from the adjacent nonchallenge pens were positive for Salmonella in 6 of 36 fecal droppings samples, 4 of 36 litter grab samples, 7 of 36 drag swab samples, and 19 of 36 sock samples. Sock samples had the highest rates of Salmonella detection. In experiment 3, the litter from a Salmonella-challenged flock was sampled at 7, 8, and 9 wk by socks and drag swabs. In addition, comparisons with drag swabs that were stepped on during sampling were made. Both socks (24 of 36, 67%) and drag swabs that were stepped on (25 of 36, 69%) showed significantly more Salmonella-positive samples than the traditional drag swab method (16 of 36, 44%). Drag swabs that were stepped on had comparable Salmonella detection level to that for socks. Litter sampling methods that incorporate stepping on the sample material while in contact with the litter appear to detect Salmonella in greater incidence than traditional sampling methods of dragging swabs over the litter surface.

Day-old male broiler breeder chicks were obtained from a commercial hatchery and raised as broilers. For Experiment 1, at 5 wk of age, the broilers were orally inoculated with a 10(6) cfu/ml of a characterized strain of Campylobacter jejuni and a cocktail (three naladixic acid-resistant strains) of Salmonella serovars. One week after inoculation, the birds were euthanatized and defeathered. The abdominal cavity was examined and any unabsorbed yolk material (and remaining yolk stalk) and ceca were aseptically removed for microbiological analyses. For each pooled sample (two birds per pool), an aerobic plate count (APC), an Enterobacteriaceae (ENT) count, and a test for the presence of Campylobacter and Salmonella was performed. For Experiment 2, at 5 wk of age, the broilers were orally inoculated with 10(5) cfu/ml of a characterized strain of Campylobacter jejuni. One week after inoculation, the birds (n = 20) were killed, defeathered, and the yolk stalk, attached yolk, or free-floating yolk and ceca were individually analyzed for presence of Campylobacter. For Experiment 1, the Salmonella-inoculated birds had 2/12 ceca and 0/12 unabsorbed yolk samples positive for Salmonella. The average yolk APC was log10 3.4 cfu/g and the average ENT was log10 1.9 cfu/g. For the Campylobacter-inoculated birds, 12/12 ceca and 9/12 unabsorbed yolk samples were positive for Campylobacter. The average yolk APC was log10 3.5 cfu/g and the average ENT was log10 3.1 cfu/g. For Experiment 2, the inoculated Campylobacter birds had 19/20 ceca, 5/20 free floating yolks, and 19/20 yolk stalks positive. In Experiment 1, the inoculated Campylobacter colonized the ceca in every instance and were present in 75% of the unabsorbed yolks. Alternatively, the inoculated Salmonella were not found in any of the unabsorbed yolks and only rarely in the ceca. In Experiment 2, the inoculated Campylobacter was found in very high numbers in the yolk and internal body samples. Determining to what extent these internal bodies and unabsorbed yolks play in bacterial colonization and contamination of the birds at processing has not been determined. The next step will be to determine the incidence of unabsorbed yolks and presence of Campylobacter and Salmonella in these bodies of commercial broilers at processing.

Campylobacter are known to cause acute bacterial gastroenteritis in humans. Poultry products have been implicated as a significant source of these infections. Six experiments were performed to determine whether Campylobacter could be isolated naturally from the primary and secondary lymphoid organs, liver/gallbladder, and ceca of commercial broiler breeder hens. Broiler breeder hens were acquired from different commercial sources during the early, middle, and late lay cycles. The birds were euthanatized, defeathered, and aseptically opened. To reduce the possibility of cross-contamination between samples, the thymus, spleen, and liver/gallbladder were aseptically removed prior to removal of the ceca. Individual samples were placed in sterile bags, packed on ice, and transported to the laboratory for evaluation. In this study Campylobacter were found in 11 of 43 thymii, eight of 43 spleens, four of 43 liver/gallbladders, and 30 of 43 ceca. Overall, 28 of 53 isolates from the above samples were Campylobacter coli and 25 of 53 isolates were found to be Campylobacter jejuni.

A study was conducted to investigate the bacteriological impact of using different volumes of water during immersion chilling of broiler carcasses. Market-aged broilers were processed, and carcasses were cut into left and right halves along the keel bone immediately after the final bird wash. One half of each carcass pair was individually chilled at 4 degrees C in a separate bag containing either 2.1 L/kg (low) or 16.8 L/kg (high) of distilled water. Carcass halves were submersed in a secondary chill tank containing approximately 150 L of an ice-water mix (0.6 degrees C). After chilling for 45 min, carcass halves were rinsed with 100 mL of sterile water for 1 min. Rinses and chill water were analyzed for total aerobic bacteria (APC), Escherichia coli, Enterobacteriaceae, and Campylobacter. After chilling with a low volume of water, counts were 3.7, 2.5, 2.6, and 2.1 log(10) cfu/mL of rinse for APC, E. coli, Enterobacteriaceae, and Campylobacter, respectively. When a high volume of chill water was used, counts were 3.2, 1.7, 1.6, and 1.8 log(10) cfu/mL of rinse for APC, E. coli, Enterobacteriaceae, and Campylobacter, respectively. There was no difference in bacterial counts per milliliter of chill water among treatments. These results show that using additional water during immersion chilling of inoculated broilers will remove more bacteria from the carcass surfaces, but numbers of bacteria per milliliter in the chiller water will remain constant. The bacteriological impact of using more water during commercial immersion chilling may not be enough to offset economic costs.

It has been demonstrated that horizontal and vertical transmission of Salmonella and Campylobacter can occur in broiler breeder flocks. The mechanism of this transmission is still unclear. Previously negative broiler breeder flocks have been reported to become positive with Salmonella, Campylobacter, or both after the introduction of “spike” roosters at 45 wk of age. To determine whether the rooster semen is a possible source of transmission to hens for colonization, we evaluated the association of both Salmonella and Campylobacter spp. to segments (head, midpiece, and tail) of individual spermatozoa after artificial inoculation. Salmonella typhimurium, Salmonella heidelberg, and Salmonella montevideo, or Campylobacter jejuni (in 0.85% saline) was added to a freshly collected (by abdominal massage) aliquot of pooled semen from roosters housed in individual cages. The semen and bacteria solutions were incubated 1 h at room temperature. Samples were fixed using Karnosvsky and Zamboni fixatives for 24 h prior to centrifuging and rinsing in 0.1 M cacodylate × HCl buffer. Individual aliquot samples were then subjected to both scanning (JSM-5800) and transmission (JEM-1210) electron microscopy. The scanning electron microscopy showed that Salmonella was associated with all 3 segments (head, midpiece, and tail) of the spermatozoa and apparently equally distributed. Campylobacter was mainly associated with the midpiece and tail segments; few isolates were located on the head segment. The transmission electron microscopy showed apparent attachment of Salmonella and Campylobacter to the spermatozoa.

Eggs collected from hens of different ages and that differed in infection status with Salmonella enteritidis were evaluated for the ability to resist cracking following application of maximum compression load from an Instron materials testing machine. Orally infected 24-wk-old hens that were prepeak produced eggs with significantly lower hardness units (HU) of shells compared with a paired control group (Por = 0.01). However, 1 of 3 additional infection trials in hens at peak (29 wk) and older hens postpeak (58 wk) showed an increase in HU in one trial and no difference in the other 2 trials. Thus, Salmonella enteritidis may be able to alter HU in a manner that is influenced by multiple factors, which include the age of the hen and the strain used for infection. Hardness was overall a sensitive physiological barometer of age, because readings correlated positively (all R0.50) with hens entering peak production, regardless of infection status. Detection of a very low HU reading (1.0) was indicative of a hairline crack in the egg, which increased in incidence from 0.01% preinfection to 0.08% postinfection. Two other clinical signs noted postinfection in hens were that i) daily egg production significantly increased in older hens, and ii) emaciation was evident in a few hens that were infected by contact. These results suggest that there may be supportive approaches to achieve reduction of S. enteritidis in table eggs that do not rely on culturing.

Occlusion of the trachea and decapitation were compared with a conventional unilateral neck cut for effects on bacteria entering into the respiratory tract of broiler carcasses during scalding. In experiment 1, the trachea was occluded prior to the carcass entering the scalder to determine if bacterial recovery from the respiratory tract could be diminished. The first carcass was removed at the end of bleeding, and a plastic cable tie was placed around the neck of a second carcass and tightened to occlude the trachea. After proceeding through the triple-tank immersion scalder, the second carcass (trachea occluded) was removed, and a third carcass (without the trachea occluded during scalding) was removed. In experiment 2, after being stunned, carcasses were unilaterally bled or decapitated. Unilaterally bled and decapitated carcasses were removed at the end of bleeding and after scalding. In both experiments, trachea were cannulated, and respiratory tract rinses were collected. For experiment 1, the numbers of bacteria recovered (log10 cfu/mL of rinse) from prescald nonoccluded carcass respiratory tract rinses were 2.5 Escherichia coli, 2.6 coliforms, and 3.2 total aerobes. Respiratory tract rinses from carcasses sampled postscald (without occluding the trachea) had higher bacteria numbers at 4.6 E. coli, 5.0 coliforms, and 5.4 total aerobes. Respiratory tract rinses from carcasses with the trachea occluded prior to scalding had the lowest number of bacteria at 1.9 E. coli, 2.3 coliforms, and 2.7 total aerobes. In experiment 2, the numbers of bacteria recovered from respiratory tract rinses of unilaterally bled or decapitated carcasses did not differ prescald or postscald, although all postscald values were higher (P < 0.05). Results confirmed that bacteria numbers increased within the respiratory tract during immersion scalding, the increase could have been prevented by occluding the trachea prior to scalding, and decapitation did not alter the number of bacteria recovered from respiratory tract rinses prior to or following immersion scalding.

Campylobacter and Salmonella are known to cause acute bacterial gastroenteritis in humans. Raw poultry products have been implicated as a significant source of these infections. Five trials were conducted to determine whether Campylobacter and Salmonella spp. exist naturally in the mature and immature ovarian follicles of late-life broiler breeder hens. Broiler breeder hens ranging from 60 to 66 wk of age were obtained from four different commercial breeder operations. For each trial, the hens were removed from the commercial operation and held overnight at the University of Georgia processing facility. The hens were euthanized, defeathered, and aseptically opened. To reduce the possibility of cross-contamination between samples, first the mature and immature ovarian follicles, then the ceca, were aseptically removed. Individual samples were placed in sterile bags, packed on ice, and transported to the laboratory for evaluation. Overall, Campylobacter was found in 7 of 55 immature follicles, 12 of 47 mature follicles, and 41 of 55 ceca. Campylobacter was found in at least one of each sample of mature follicles and in ceca in each of the five trials. Salmonella was found in 0 of 55 immature follicles, 1 of 47 mature follicles, and 8 of 55 ceca. In this study, the recovery rate of Salmonella from late-life broiler breeder hen ovarian follicles was relatively low. However, the recovery rate of Campylobacter from the hen ovarian follicles was reasonably high, suggesting that these breeder hens could be infecting fertile hatching eggs. Determining how Campylobacter contaminated these ovarian follicles and how many chicks could be colonized from this source are the next steps in helping to elucidate a better understanding of this ecology and the control of Campylobacter in poultry production.

Experiments were conducted to determine the effect of prechill trisodium phosphate (TSP) treatment on reducing salmonellae recovery from broiler carcasses immediately after chilling or following 7 d of storage. Carcasses were sampled for salmonellae using whole carcass enrichment for 24 h at 37 degrees C. In each of 7 trials, 40 carcasses were obtained from a commercial processing plant. Batches of 4 carcasses were subjected to a 5-s dip in 10% TSP (treatment) or not dipped (control). Two carcasses from each batch were sampled immediately after chilling (d 0) and 2 carcasses were sampled after 7 d of storage. For trials 1 and 2, TSP treatment and control groups were chilled in separate chill tanks for 45 min. For trials 3 through 7, carcasses were rinsed with water and individually bagged with ice and water before chilling. For trials 1 and 2, 85% (17/20) of control carcasses were salmonellae-positive on d 0 compared with 45% (9/ 20) of the TSP-treated carcasses; after 7 d, 75% (15/20) of control carcasses were positive compared with 35% (7/ 20) for the TSP-treated carcasses. For trials 3 through 7, 46% (23/50) of control carcasses were salmonellae-positive on d 0 compared with 26% (13/50) of the TSP-treated carcasses; after 7 d, 20% (10/50) of control carcasses were positive compared with 4% (2/50) of the TSP-treated carcasses. TSP treatment resulted in significantly higher pH values for rinses. Salmonella recovery was decreased by refrigerated storage and treatment with TSP before immersion chilling.

Paired carcass halves were used to test whether fecal contamination of skin during processing of broiler chickens can be detected by increased bacterial counts in samples taken before and after immersion chilling. In each of three trials, six freshly defeathered and eviscerated carcasses were cut in half, and a rectangle (3 by 5 cm) was marked with dots of ink on the breast skin of each half. One half of each pair was chosen randomly, and 0.1 g of freshly collected feces was spread over the rectangle with a spatula. After 10 min, both halves were sprayed with tap water for 10 to 15 s until feces could no longer be seen in the marked area. Both halves were sampled with a 1-min carcass rinse and were then put in a paddle chiller with other eviscerated carcasses for 45 min to simulate industrial immersion chilling. Immediately after chilling, each carcass half was subjected to another 1-min rinse, after which the skin within the rectangle was aseptically removed from the carcass halves and stomached. Rinses of fecally contaminated halves had significantly higher Enterobacteriaceae immediately before chilling, but there were no differences in coliform and Escherichia coli counts. After chilling, there were no differences in Enterobacteriaceae, coliform, and E. coli counts in rinse or skin samples from the paired carcass halves. Correlations were generally poor between counts in rinse and skin samples but were significant between prechill and postchill rinses for both control and fecally contaminated halves. Correlations were also significant between counts in rinses of control and contaminated halves of the same carcass after chilling. Bacterial counts in postchill carcass rinses did not indicate that fecal contamination occurred before chilling.

For evaluation of the filling and emptying of the alimentary tract, broiler breeder hens were cooped and processed over a 2-d period. Hens were fed at 0600 h on d 1 and after access to feed for 0, 2, 4, and 6 h were placed into coops. Half of the hens from each pen were either immediately processed or were held in coops over-night and processed the following morning, d 2. The alimentary tract was excised from the carcass and then separated and weighed in three segments: the crop, proventriculus and gizzard, and intestines. Hens processed on d 1, after access to feed for only 2 h, had attained maximum intestine weight (176 g), but not until after access to feed for 6 h were peak crop weight (95 g) and peak weight for the proventriculus and gizzard (78 g) attained. Hens processed on d 2 did not differ in crop (12 to 14 g) or intestine (140 to 162 g) weight, but proventriculus and gizzard weights were significantly lower for hens not fed on d 1 prior to cooping (54 g) compared with hens fed on d 1 and cooped after 2, 4, or 6 h (62 to 63 g). However, hens processed on d 2 had proventriculus and gizzard weights that were the same as for those hens processed on d 1 and cooped at 0 h (63 g). Clearance of ingesta from the crop, proventriculus and gizzard, and intestines readily occurred while hens were held overnight without access to water.

Four experiments were conducted to determine the effects of electrical stunning and decapitation on bird activity as well as carcass and meat quality. In Experiment 1, broilers were subjected to one of four stunning and killing methods: no stun and neck cut, stun and neck cut, no stun and decapitation, and stun and decapitation. Birds were scored for severity of physical activity on a scale of 1 to 4 with 1 being no activity and 4 being severe wing flapping and muscular contractions. Carcasses were also scored for red wing tips and broken bones. In Experiments 2 to 4, all birds were stunned prior to neck cut or decapitation. Carcasses were scored as described in Experiment 1 as well as measurements of blood loss, feather removal, and breast meat pH, color, cook loss, and tenderness. Based on carcass activity in Experiment 1, decapitation following stunning was similar to a conventional stun and unilateral neck cut, except there was almost no late activity (after 60 s) observed in the decapitated birds. Decapitation following stunning did not result in any consistent carcass quality defects compared to conventional killing in the four experiments. No differences were found in 24-h lightness values, yellowness, cook yield, tenderness, and ultimate pH between conventionally killed and decapitated birds. Blood loss and breast meat redness were inconsistent. These results indicate that high frequency stunning and decapitation may be an acceptable alternative to conventional slaughter based on carcass and meat quality and by ensuring an irreversible loss of consciousness.

Zero tolerance of feces on the surfaces of meat and poultry carcasses during slaughter was established as a standard to minimize the likelihood of microbial pathogens. Microbial pathogens can be transmitted to humans by consumption of contaminated meat and poultry. Compliance with zero tolerance of feces in meat processing establishments is currently verified by visual observation. The objective of this study was to investigate the use of visible, near–infrared reflectance spectroscopy as a method to discriminate between uncontaminated poultry breast skin and feces, and to select key wavelengths for use in a hyperpspectral system. Feces (n = 102), uncontaminated poultry breast skin, and skin contaminated with fecal spots were analyzed from 400 to 950 nm. The spectra were reduced by principal component (PC) analysis. The first four PCs explained 99.8% of the spectral variation. PC 1 was primarily responsible for the separation of uncontaminated skin from feces and for the separation of uncontaminated skin from contaminated skin. A classification model was developed and evaluated to classify fecal–contaminated skin from the spectral data with a success rate of 95%. Key wavelengths were identified by intensity of loading weights at 628 nm for PC 1, 565 nm for PC 2, and 434 and 517 nm for PC 4. Discrimination was dependent on the spectral variation related to fecal color and myoglobin and/or hemoglobin content of the uncontaminated breast skin.

The efficacy of various carbohydrate-based cocktails in reducing the number of enteropathogens in the crops of broilers subjected to feed withdrawal was examined. Market-aged broilers that had been orally challenged with Salmonella typhimurium were provided the cocktails during a 12-h feed withdrawal. After feed withdrawal, the broilers were processed, and their crops were aseptically removed and weighed. Crops were then blended in distilled water, and the pH of the suspensions was measured electronically. Populations of S. typhimurium, Campylobacter, and lactic acid bacteria in the crop suspensions were enumerated. Findings indicated that significantly fewer S. typhimurium and Campylobacter were recovered from the crops of broilers that had been provided cocktails supplemented with sucrose than from the (Key words: crop, carbohydrate, feed crops of broilers provided cocktails supplemented with equal concentrations (wt/vol) of glucose. Furthermore, significantly fewer S. typhimurium were recovered from the crops of broilers provided cocktails supplemented with 2 to 10% sucrose than from the crops of broilers provided water or cocktails that were not supplemented with carbohydrates. The pH of the crop contents of broilers provided carbohydrate cocktails were lower than the pH of the crops of broilers provided water or cocktails that were not supplemented with carbohydrates. Consumption of the cocktails did not produce significant changes in the crop weights. Findings indicate that altering the composition of carbohydrate-based cocktails provided to broilers during feed withdrawal may affect the efficacy of cocktails in reducing the number of enteropathogens recovered from the crops of broilers.

The objective of this project was to determine if removal of skin prior to evisceration lowers the number of bacteria that can be recovered by whole carcass rinse or sponge sampling. Four experiments were conducted, two with each type of sampling (rinse or sponge). New York dressed carcasses obtained from a commercial broiler processing plant were aseptically skinned or left with skin intact. The carcasses were then aseptically eviscerated by hand. Carcasses were rinsed in 100 mL sterile water or sampled by moist sponge. When sampled by rinse, significantly fewer Campylobacter and total aerobic bacteria were recovered from carcasses that had been skinned prior to evisceration. When sampled by sponge, significantly fewer Campylobacter, Escherichia coli, coliform and total aerobic bacteria were recovered from the outer surface of carcasses without skin. No differences were noted for bacterial counts recovered from internal surfaces by sponge sampling. Similar trends were observed when carcasses were subjected to an inside and outside washing step after evisceration. Removal of skin and washing the carcass led to significantly less Campylobacter being recovered by whole carcass rinse compared to carcasses that were washed with the skin on. When sampled by sponge, incidence of Campylobacter and level of total aerobic bacterial counts were lower on the outer surface of skinned and washed carcasses than on washed carcasses with intact skin. Like the unwashed carcasses, no differences were noted for bacterial counts recovered from internal surfaces by sponge sampling. Although not commercially practical, it is possible to lower the level of Campylobacter on the outside of broiler carcasses by removal of the skin prior to evisceration.

Electrostatic charging of particles in enclosed spaces has been shown to be an effective means of reducing airborne dust. Dust generated during the hatching process has been strongly implicated in Salmonella transmission, which complicates the cleaning and disinfecting processes for hatchers. Following two preliminary trials in which dust reduction was measured, four trials were conducted to evaluate the effectiveness of an electrostatic space charge system (ESCS) on the levels of total aerobic bacteria (TPC), enterobacteriaceae (ENT), and Salmonella within an experimental hatching cabinet. The ESCS was placed in a hatching cabinet that was approximately 50% full of 18-d-old broiler hatching eggs. The ESCS operated continuously to generate a strong negative electrostatic charge throughout the cabinet through hatching, and dust was collected in grounded trays containing water and a degreaser. An adjacent hatching cabinet served as an untreated control. Air samples from hatchers were collected daily, and sample chicks from each hatcher were grown out to 7 d of age for cecal analysis in three of the trials. The ESCS significantly (P < 0.05) reduced TPC and ENT by 85 to 93%. Dust concentration was significantly reduced (P < 0.0001) during the preliminary trials with an average reduction of 93.6%. The number of Salmonella per gram of cecal contents in birds grown to 7 d of age was significantly (P < 0.001) reduced by an average log10 3.4 cfu/g. This ionization technology is relatively inexpensive and could be used to reduce airborne bacteria and dust within the hatching cabinet.

A hyperspectral imaging system including a camera with prism-grating-prism spectrograph, fiber optic line lighting, motorized lens control, and hyperspectral image-processing software was developed for poultry safety inspection, particularly identification of fecal and ingesta contamination on poultry carcasses. Both spectral and spatial image data between 400 and 900 nm with 512 spectral bands were acquired from fecal and ingesta contaminated poultry carcasses. Four dominant wavelengths (434, 517, 565, and 628 nm) were selected by principal component analysis from visible/near-infrared spectroscopy for wavelength selection of hyperspectral images. A calibration model for the hyperspectral imaging system was developed from calibration lighting sources (HgAr, Kr, and lasers) for accurate band selection from the hyperspectral images to identify spatial and spectral characterization of fecal and ingesta contaminants. Hyperspectral image processing algorithms, specifically band ratio of dual-wavelength (565/517) images and histogram stretching, were effective in the identification of fecal and ingesta contamination of poultry carcasses. Test results indicated that the detection accuracy was 97.3% for linear and 100% for non-linear histogram stretching. This article presents the research results that hyperspectral imaging can be used effectively for detecting feces (from the duodenum, ceca, and colon) and ingesta on poultry carcasses and demonstrates the potential application for on-line safety inspection of poultry.

This study was conducted to evaluate the influence of a vancomycin pretreatment on the ability of marker (nalidixic-acid resistant) Salmonella Enteritidis (SE(M)), field Salmonella Enteritidis (SE(E)), and marker Salmonella Typhimurium (ST(M)) strains to colonize within the intestinal and reproductive tracts and translocate to other organs of leghorn laying hens. In each of three trials, caged laying hens (76, 26, and 33 wk ofage) were divided into six groups designated to receive SE(M), SE(F), or ST(M), and half were pretreated with vancomycin (n = 11-12 hens). Vancomycin-treated hens received 10 mg vancomycin in saline/kilogram body weight orally for 5 days to inhibit Gram-positive bacteria within the intestines. On Day 6, all hens were concurrently challenged by oral, intravaginal, and intracolonal routes with Salmonella and placed into separate floor chambers by Salmonella strain. Two weeks postinoculation, all hens were euthanatized and the ceca, spleen, liver/gall bladder (LGB), upper (URT), and lower (LRT) reproductive tracts, and ovarian follicles were aseptically collected, and analyzed for Salmonella. Results did not differ for the three hen's ages and were therefore combined. The vancomycin pretreatment also had no significant effect on the colonization ability of SE(M), SE(F) or ST(M), and therefore results were combined within Salmonella strain. The marker strain of Salmonella Enteritidis was recovered from 21% of ceca, 4% of LGB, 9% of LRT, and 17% of the fecal samples. The field strain of Salmonella Enteritidis was recovered from 88% of ceca, 96% of spleen, 92% of LGB, 30% of LRT, 4% of URT, 13% of follicle, and 42% of the fecal samples. The marker strain of Salmonella Typhimurium was recovered from 100% of ceca, 74% of spleen, 91% of LGB, 30% of LRT, 9% of URT, 9% of follicle, and 100% of the fecal samples. Among ceca, spleen, LGB, and fecal samples, SE(F) and ST(M) colonization was significantly greater than SE(M) colonization. Overall prevalence of Salmonella in the reproductive tracts of challenged hens was relatively low, ranging from 4% to 30%.

Scalding with unheated water in the first tank of a simulated three-tank scalder was tested to determine whether carcass bacteria, efficiency of feather removal, and cooked breast meat tenderness are affected as compared with carcasses scalded at the same temperature (57 C) in all tanks. This experiment was performed on 3 d using 6-wk-old broilers. On each day, eight birds per treatment were processed. During the first 40-s scalding period, one carcass was placed in approximately 24 C water. The other carcass was placed simultaneously in a scalder unit containing approximately 2,050 L of water at 57 C. Carcasses were then held out of the water for 15 s, after which both were placed for 40 s in opposite ends of the scalder containing water at 57 C. After the second scalding period, both carcasses were again removed from the water for 15 s, followed by another 40 s in the 57 C water. Total scald time was 2 min for each treatment. After picking, carcasses were rinsed with 200 mL of sterile 0.1% peptone water for 1 min. Aerobic bacteria and Escherichia coli were enumerated and incidence of salmonella was determined by standard methods. After rinsing, carcasses were eviscerated by hand and chilled for 30 min in ice slush. All carcasses were scored for the presence of feathers, and the appearance and condition of the skin were noted. Four hours postmortem, breast fillets were removed from carcasses and chilled overnight at 2 C. The next morning, breast fillets were cooked to an internal endpoint temperature of 75 to 80 C. Warner-Bratzler shear values were measured to determine tenderness. No differences were found in numbers of aerobic bacteria and E. coli, incidence of salmonellae, tenderness of cooked breast meat, or number of feathers left on carcasses.

This study was undertaken to determine if broiler chicken parts without skin are less contaminated with Campylobacter than those with skin. Samples were taken in a commercial plant from defeathered carcasses before evisceration. Bacterial counts from rinse of aseptically removed meat samples were lower than those from stomached skin samples. No Campylobacter were recovered from meat collected from the breasts or thighs, and only 2 of 10 drumstick meat samples had detectable levels of Campylobacter However, 9 of 10 breast skin, 10 of 10 thigh skin, and 8 of 10 drumstick skin samples were positive for Campylobacter, with between 2 and 3 log 10 CFU/g of Campylobacter. Breasts, thighs, and drumsticks were removed from broiler carcasses following evisceration before entering the chill tank. There was a significant difference (50 to 90%) in the levels of Campylobacter on breasts, thighs, and drumsticks with and without skin. Similar trends were noted for coliform, Escherichia coli, and total aerobic bacterial counts from samples collected in the plant. Broiler part samples were also collected at retail outlets. These samples were either skin on and skinned in the laboratory or skin off at purchase. Aseptic removal of skin from broiler breasts, thighs, and drumsticks did not cause change in Campylobacter, coliform, E. coli, or total aerobic counts recovered from the skinned part. Likewise, parts purchased without skin did not have different bacterial counts than paired parts purchased with the skin on. Consumers should not expect to significantly lower the number of bacteria present on a chicken breast, thigh, or drumstick by removing the skin.

Egg weight, specific gravity, conductance, and ability of Salmonella to penetrate the shell and membranes were determined for hatching eggs from a commercial broiler breeder flock. Thirty unsanitized eggs were sampled on Weeks 29, 34, 39, 42, 48, 52, and 56 of flock age for specific gravity and conductance. An additional 10 intact eggs were inoculated with Salmonella by a temperature differential immersion method for 1 min. Eggs were then emptied of contents and filled with a selective medium that allowed visualization of Salmonella growth on the inside of the shell and membrane complex. Over the 27-wk sampling period, egg weight increased from 56 to 66 g and was positively correlated with hen age (r = 0.96, P0.05). However, neither specific gravity (ranging from 1.077 to 1.082) nor eggshell conductance (ranging from 14.7 to 17.9 mg weight loss/d per torr) showed any clear trend throughout the life of the flock despite the increase in egg weight. Conductance values were not correlated with specific gravity. The number of eggs positive for Salmonella penetration after 24 h incubation showed a general upward trend with flock age; however, penetration frequency and hen age were not found to be significantly correlated (P0.05). No relationship was found between egg specific gravity, conductance, or egg weight and the likelihood of Salmonella to penetrate the eggshell. Because shell characteristics did not change over time and the penetration patterns did vary, it is likely that factors other than specific gravity and conductance were involved in the penetration of eggshells by Salmonella.

Stunning and slaughter trials were conducted to evaluate the influence of carcass orientation (inverted or supine), angle of feather extraction (parallel or perpendicular to the carcass surface), and slaughter method (exsanguination without or with spinal cord transection) on feather retention force (FRF) in commercial broilers sampled ante-, peri-, and post-mortem. The pectoral, sternal, and femoral feather tracts were sampled before and after stunning contralaterally, with a maximum indicating force gauge, from broilers suspended on a shackle (inverted) or laying on a table (supine). For all trials and sample periods FRF was consistently greater in the femoral area (547 to 679 g) than in the pectoral area (273 to 391 g), with the sternal feather tract requiring the least force at 246 to 343 g. Feathers extracted parallel to the carcass resulted in consistently greater FRF (9 to 29%) than feathers extracted at a perpendicular angle, at all sample periods. Broilers suspended on shackles ante- and peri-mortem had higher FRF values (5 to 30%) than those restrained in shackles in a supine position on a table. Other parameters resulted in minor and inconsistent alterations in FRF. Electrical stunning, when not followed by bleeding, resulted in small reductions in FRF (up to 7%). Bleeding after stunning without or with spinal cord transection resulted in variable peri-mortem FRF changes (+7 to -11% and +11 to -11%, respectively). Only in the pectoral feather tract was there a significant increase (5 to 6%) in FRF as broilers went from the ante- to peri-mortem state. At 2 and 6 min after stunning and initiation of exsanguination, post-mortem FRF was unaffected by carcass orientation for the pectoral and femoral tracts.

Stunning and slaughter trials were conducted to evaluate the influence of stunning method (electrical 50 V alternating current, CO2 gas: 0 to 40% for 90 s or 40 to 60% for 30 s) on feather retention force (FRF) in commercial broilers. Feathers from the pectoral, sternal, and femoral feather tracts were sampled with a force gauge before stunning (ante-mortem) and contralaterally either after stunning (peri-mortem from 0.5 to 4 min) or after stunning and bleeding (post-mortem from 2 to 6 min). Prior to stunning, ante-mortem FRF values varied among assigned stunning methods only for the pectoral (7%) feather tract. After stunning, peri-mortem FRF values were higher only for the sternal tract (11% for 40 to 60% CO2 for 30 s); whereas after stunning and bleeding, post-mortem FRF values were lower than ante- or peri-mortem only for the sternal tract (10% lower for 40 to 60% CO2 for 30 s). Peri- and post-mortem FRF values did not differ among stunning methods for the pectoral and femoral feather tracts. Small changes in FRF values occurred from ante-mortem to peri-mortem (-1 to +12%), and from ante-mortem to post-mortem (-2 to +8%) across stunning methods. A significant increase was determined for only the pectoral tract (7%) from ante- to peri-mortem across stunning methods. Electrically stunned broilers that were not bled gained weight in excess of the 36 feathers removed (0.16%), apparently due to body surface water pickup during the brine-stunning process, whereas CO2-stunned broilers lost weight due to excretion of cloacal contents (-0.31 to -0.98%). The change in body weight among stunning methods was significant (P0.0233). Peri- and post-mortem FRF, in addition to bleed-out body weight loss, were not substantially influenced by electrical or CO2 stunning methods, and, therefore, carcass defeathering efficiency may not differ after scalding.

Four trials were conducted to evaluate the efficacy of hatcher air sanitation utilizing ultraviolet light (UV), ozone, or hydrogen peroxide on bacterial populations, the spread of Salmonella, and hatchability of broiler eggs. The UV light (254 nm, 146 mu W/s) and ozone (0.2 or 0.4 ppm) treatments were continuously applied through the last 3 d of hatch, the hydrogen peroxide treatment (2.5%) was administered 1 or 2 min of each 10 min at rates of 500 or 100 mL/h. Hatchability was not significantly reduced by sanitizing treatments when compared with the untreated control (94 vs 95.6%). As compared to controls, all sanitizing treatments reduced 75 to 99% of the total bacteria, Enterobacteriaceae, and Salmonella in the hatching cabinet air samples. The use of hydrogen peroxide resulted in greater reduction of bacteria than ozone or UV light. Only hydrogen peroxide significantly reduced Salmonella levels on eggshell fragments. Significant reductions in the number of Salmonella-positive chicks occurred using the ozone and hydrogen peroxide treatments. Hydrogen peroxide significantly reduced the magnitude of Salmonella colonization in chicken ceca. These trials demonstrated that the spread of bacteria can be effectively reduced in the hatching cabinet by air sanitization using UV light, ozone, and hydrogen peroxide. The potential to reduce bacterial cross contamination in the hatcher is achievable without depressing hatchability.

Extended posthatch holding (in the hatcher) has been reported to dehydrate chicks, reduce broiler performance, and depress immune response. Nevertheless, some commercial hatcheries are increasing incubation time in an attempt to minimize possible bacterial contamination of incompletely healed navels. The objectives of this study were to determine the effects of posthatch holding on broiler performance and the effects of bird density and additive stress on performance and immune response. Twelve hundred broiler eggs (58 to 70 g) were incubated. Chicks were removed from the hatcher after 528 h of incubation, banded, and weighed. Half of the chicks were returned to the hatcher for an additional 24 h (HELD). Both hatcher treatments were placed at two densities (.07 and .12 m2 per bird). Individual BW were taken at 21 and 43 d of placement and 43 d of age. The HELD chicks weighed significantly less than controls at time of placement. At 21 d postplacement the HELD broilers were significantly heavier than controls, but were similar by 43 d. Total feed conversion was not affected in the HELD treatment, but birds in the .07 m2 per bird density were less efficient in terms of total feed conversion. Chick holding time and density seemed to affect antibody titers at 5 wk. Although holding chicks in the hatcher for 24 h did not clinically dehydrate chicks or affect performance, it decreased immune response. In addition to less efficient growth, birds in the more crowded pens had depressed immune response.

Postmolt egg production variables were compared among hens induced into molt by feed removal, by limited daily feeding of a low-density and low-energy molt feed at 22.8 g per hen, or by limited alternate-day feeding at 45.5 g per hen, until approximate body weight loss of 15, 20, and 25% was obtained. Hens were housed two per cage (25.4 x 45.7 cm) in a house of environmental design, and photoperiod was reduced to 8 h during the 28-d molt period. When target body weight loss was obtained, packed cell volume was determined and hens were maintained on 45.5 g/d of 1.2% calcium prelay feed through the 28-d molt period. Egg production and mortality were recorded daily; egg weight, egg specific gravity, body weight, and feed intake were recorded at 4-wk intervals postmolt. Packed cell volume of hens molted by feed removal (36.4%) was higher (P.01) than that of alternate-day (34.1%) or daily limited (33.6%) hens. Hens that lost 25% of their body weight had higher packed cell volume (36.3%) than hens that had body weight loss of 20% (34.4%) or hens that lost 15% (33.4%). Postmolt mortality and egg production were not different (P.05) as a result of molt induction method or percentage body weight loss. At the 4th wk postmolt, body weights were 50 and 57 g heavier for hens that had lost 15% body weight than those that lost 25 or 20%, respectively, and egg production was negatively linearly related to body weight loss.(ABSTRACT TRUNCATED AT 250 WORDS)

Previous studies have shown that inducing a molt using feed removal exacerbated an intestinal infection by Salmonella enteritidis (SE). The current study was conducted to determine whether inducing a molt using a molt diet would still cause a pause in egg laying but not exacerbate an intestinal SE infection. In Experiments 1 and 2, hens were either provided ad libitum access to layer feed (control), fed 45 g molt diet (molt-feed) daily, or deprived of feed for 14 d (molted), and were orally infected with 1 × 107 SE on Day 4 of molt. Egg lay ceased in hens subjected to both molt treatments. The percentage of hens shedding SE did not differ among treatment groups in Experiment 1, whereas in Experiment 2 the molted hens had significantly higher shed rates than the controls on Days 10, 17, and 24 postinfection and the molt-feed hens on Days 17 and 24 postinfection. Compared with both fed groups of hens, the molted hens shed significantly more SE in Experiment 1 on Day 10 postinfection, and in Experiment 2 the molted hens shed significantly more SE on all 4 sampling days. In Experiment 3, subgroups of hens within each treatment group received serial 10-fold dilutions of SE and intestinal shedding of the organism in each subgroup was determined 7 d later. The 50% infectious dose (ID50) was calculated for each treatment group from these shedding results. The ID50 was 2.7 × 103 SE, 5.2 × 102 SE, and 1.3 SE for control, molt-feed, and molted hens, respectively, indicating that feed removal substantially increased the susceptibility of hens to an SE infection and the molt diet decreased this susceptibility. Little difference was observed in the pH of alimentary samples or of cecal contents from hens in each treatment group, indicating that increased severity of SE infection was not due to alterations of intestinal pH. Histologically, the molted hens exhibited more extensive inflammation of the intestinal tract at Day 4 postinfection compared with the unmolted group. Intestinal inflammation in the molt-feed hens was intermediate between the two. These results indicated that molt induction, using a molt diet, will not put hens at risk for the severe intestinal infection observed in birds subjected to feed removal.

Two experiments were conducted to evaluate dietary and environmental factors involved in skin tensile strength of commercial broilers. In Experiment 1 the effect of added dietary fat (4 or 7%), environmental temperature (25 or 20.5 C after 21 d), and anticoccidial drug (halofuginone or salinomycin fed continuously) were examined factorially using male and female chicks. Skin tensile strength was measured at 21, 35, and 40 d of age. Thickness of the dermal layers was measured from skin taken at Day 35. In Experiment 2, the effect of added dietary fat (0 or 7%), environmental temperature (25 or 18.5 C after 21 d), and anticoccidial drug (halofuginone or salinomycin) were examined factorially using female chicks. Skin strength and collagen content of the skin were measured at 21, 38, and 42 d of age. Skin tensile strength increased with age in both experiments, but female skin strength was subject to periodic decline. Males had significantly strong skin than females. Levels of added fat or environmental temperature did not affect skin strength in either experiment. Continuous feeding of halofuginone significantly (P < .0001) decreased skin strength compared with that of birds fed salinomycin in both experiments. Halofuginone reduced skin strength in females more than males (25 and 9%, respectively). Dermis thickness was correspondingly reduced in the birds consuming halofuginone. In Experiment 2, soluble collagen contents were reduced at all ages in birds consuming halofuginone; insoluble collagen was significantly decreased at 21 d of age. Birds with weakened skin exhibited increased incidence of skin tears during slaughter in a commercial processing plant (P < or = .0043). These results suggest that halofuginone interferes with collagen synthesis, causing decreased collagen formation and reduced skin strength. Neither added dietary fat nor ambient temperature were involved.

White Leghorn hens were injected i.p. with fluorochromes beginning at 18, 37, and 43 wk of age. Sections of the right femur were collected in ethanol and formalin approximately 2 wk later. Dynamic and static bone variables were determined in both age groups, and the effects of fluorochrome injection on egg production was assessed in the older hens. Fluorochrome bone labeling was nontoxic. Injection of fluorochrome did not affect BW or feed consumption in either age group or egg production traits in laying hens. Fluorochrome labeling was found in the femoral cortex of sexually immature hens. The mineral apposition rate of the periosteal surface was 3.08 micrometers/day and of the osteonal surface was 2.69 micrometers/day. No uptake of fluorochrome label was observed on the periosteal or osteonal surfaces of cortical bone of laying hens. Sexually mature hens had decreased femoral cortical widths, less percentage cortical bone, and more cortical endosteal surface than sexually immature hens. The diffuse labeling of the medullary bone of laying hens indicated active medullary bone mineralization. The central area of the femur cross-section inside of the cortex was examined. Sexually mature hens had less bone area, more bone perimeter, and more bone perimeter covered by osteoclasts in the lamellar cancellous and medullary bone compared with sexually immature hens. Results indicated that the development of osteopenia in hens with the onset and progression of lay may be related to increased resorptive surface of bone and loss of structural and nonstructural bone.

The sex-linked dwarf gene (dw) was introduced into companion muscular dystrophic (am) and nondystrophic (Am+) New Hampshire chicken lines to investigate influences of the dwarf gene on breast muscle weights, muscle fiber area, and the histological expression of muscular dystrophy. Dystrophic and nondystrophic chickens within dwarf or nondwarf genotypes were similar in body and carcass weights. Pectoralis and supracoracoideus muscle weights (as a percentage of adjusted carcass weight) were similar in nondystrophic dwarf and nondwarf males and females. In addition, pectoralis weight was similar in dystrophic dwarf males and dystrophic nondwarf males and females. However, pectoralis weight was significantly smaller in dystrophic dwarf females than in dystrophic nondwarf females, whereas supracoracoideus weight was significantly larger in dystrophic dwarf males than in dystrophic nondwarf males. Supracoracoideus weight was similar in dystrophic dwarf males and females and dystrophic nondwarf females. Pectoralis muscle fiber area was influenced by sex and by dwarf and dystrophy genotype. Muscle fiber area was larger in females than in males, smaller in dwarfs than in nondwarfs, and smaller in dystrophic than in nondystrophic muscles. Muscle fiber degeneration and adipose infiltration was more extensive in dystrophic than in nondystrophic females and males, and it was more advanced in dwarfs than in nondwarfs. Excessive acetylcholinesterase staining patterns were characteristic of dystrophic muscle in both dwarf and nondwarf genotypes. Nondystrophic and dystrophic dwarf male and female chickens are comparable substitutes for nondwarfs as biomedical models with respect to pectoralis histology, acetylcholinesterase staining pattern, and pectoralis muscle hypertrophy.

A surgical method for selective denervation was developed to facilitate investigations about the postmortem characteristics of denervated pectoralis muscles in chickens, Musculus (M.) pectoralis. The M. pectoralis was denervated in anesthetized chickens unilaterally or bilaterally by excising a 1-cm section of the nervus pectoralis as it branched from the N. medianoulnaris in the brachial plexus. Denervation resulted in significant (P less than .01) and consistent depression in the relative weight of M. pectoralis from the wk 2 through 17 postoperative. The relative weight of the functionally antagonistic M. supracoracoideus was unaffected by ipsilateral denervation of the M. pectoralis. The M. coracobrachialis acts in synergism with the M. pectoralis and displayed significant muscle atrophy at 4, 6, 8 and 17 wk postoperative in treatment groups where the ipsilateral M. pectoralis was denervated. Only the M. pectoralis displayed histological signs of denervation in transverse cryostat sections. Denervated tissue was characterized by atrophic and rounded muscle-fiber profiles, an increase in the endomysial and perimysial connective-tissue spaces, and leucocytes within degenerative perimysial nerves from 2 through 17 wk postoperative. Signs of denervation were distributed throughout seven zones sampled from the M. pectoralis. This study indicated that selective denervation of the M. pectoralis was achieved and that postoperative histology was necessary to accurately assess denervation.

Six experiments were conducted to examine the feasibility of "tilting" instead of turning chicken eggs during incubation to provide a near constant air flow pattern. At hourly intervals eggs were tilted 45 degrees in opposite directions for consecutive intervals and returned to their original orientation. Eggs were oriented either vertically (large end up), at a 45 degree angle, or horizontally. Comparisons were made in terms of hatchability of fertile eggs, hatchability of transferred eggs, embryonic mortality, and malpositions. Tilting instead of turning depressed hatchability regardless of orientation. Depressions were cumulative and additive, with significant depression for all eggs tilted during the 1st wk of incubation, and diminished effects the 2nd and 3rd wk. Late incubation embryonic mortality was elevated in the tilted groups, and frequency of malpositions increased. Malposition II predominated in the tilted groups oriented 45 degree or horizontally, whereas Malposition III predominated in the controls and in the tilted groups oriented vertically. It was concluded that tilting incubating eggs is not a viable alternative to conventional turning practices.

Three experiments were conducted to examine the effects of sodium pentobarbital (SP), iodoacetate (IO), tubocurarine (TC), and surgical denervation (DN) on early rigor development in broiler breast muscle. In Experiment 1, birds were either anesthetized or not with SP before receiving an injection of IO or TC or maintained as noninjected controls. Experiment 2 was identical except that a treatment of denervation of the breast muscle was added. Experiment 3 was conducted to contrast birds at 1 day (DN1) and 3 days (DN3) denervation prior to slaughter to nonoperated controls. Measurements of muscle lactate, ATP, R value (ratio of inosine to adenine nucleotides), pH, sarcomere lengths, and shear were used to evaluate treatment effects. Results for Experiment 1 showed no significant differences among treatment and control groups for ATP and lactate contents, R values, or sarcomere lengths; however, significantly lower pH and higher shear values were observed for control birds. In Experiment 2, no significant differences were observed among the treatment groups for ATP, R values, or sarcomere lengths. However, lactate and shear values were significantly lower, and pH higher, for the DN and SP treated birds. Experiment 3 resulted in lower lactate and higher pH values for the DN3 treatment in comparison with both DN1 and control groups. Results of these studies indicate that the use of SP and DN can be used to alter the early profiles of rigor development.

This paper develops algorithms for verifying pointer values in DBTG (Data Base Task Group) type databases. To validate pointer implemented access paths and set structures, two algorithms are developed. The first procedure exploits the “typed pointer” concept employed in modern programming languages to diagnose abnormalities in directories and set instances. The second algorithm completes pointer validation by examining set instances to ensure that each DBTG set has a unique owner. Sequential processing is used by both algorithms, allowing a straightforward implementation which is efficient in both time and space. As presented, the algorithms are independent of implementation schema and physical structure.