Within poultry science, a variety of behavioral observation sampling methods have been used. Although the method for determining the acceptability of a chosen time sampling strategy should be provided, the reasoning behind the selection of a specific sampling strategy is seldom explained in publications. A previous study provided a framework for validating behavioral sampling schemes for adult laying hens. Rather than utilizing this framework, some researchers have used the results of the published time sample validation to justify their sampling scheme. However, the results may not be generalizable due to sample size limitations. Application of previously validated time sampling methods to new research contexts may be particularly problematic when a validation is completed on older birds but applied to other ages. This is due to developmentally relevant differences in activity levels and resource use. We examined the appropriateness of different interval scan sampling durations for estimating resource use by laying hen pullets reared in a single-platform aviary system. We hypothesized that younger birds would be more active, and therefore more frequent sampling would be needed to accurately capture their location within the aviary during the day. Dekalb White pullets were reared in 4 pens (55 per pen). Using continuous observations, we identified the location (floor, perch, ramp and platform) of each of 20 individually marked focal birds (5 pullets/pen) at 6 and 12 weeks of age. Observations were carried out on one of two days within each week (half of the pens observed on each day), for a total of 6 hours per day. We conducted pairwise comparisons between the actual frequencies of resource use (continuously sampled data converted into 1-s interval data) and data representing 1, 5, 10, 15, and 30 min scan intervals. Scan sampling intervals were deemed to be accurate if 3 criteria were met: the slope of the regression between the actual and estimated values did not differ from 1 (P > 0.05), the intercept did not differ from 0 (P > 0.05), and the association among the actual and estimated values was strong. The Benjamini-Hochberg adjustment was applied to account for multiple testing on the same data. The results demonstrate that different sampling intervals are appropriate for different resources and ages. The study highlights the necessity of validating behavioral sampling schemes for each age and behavior independently, as well as reporting the validation process in research publications.

Acute stress response has been linked to body condition and associated with the allocation of finite energy resources in wild, free-living birds. However, the relationship between the body condition of individuals and the acute stress response is less clear for birds kept in captive settings, where energy resources are abundant and readily available. We evaluated how individual variation in body condition, reflected as body mass, relates to the acute stress response in adult captive Wood Ducks (Aix sponsa) hatched from eggs collected in the wild and reared in captivity while birds were fed ad libitum, in and out of the breeding season. We determined plasma corticosterone (CORT) levels from blood collected within 3 min of capture and at 10, 30, and 60 min post-capture from 28 ducks during spring and fall, in and out of breeding season. Body condition measurements were recorded once for each bird in early spring. The effects of body mass, age, and time of year (in vs. out of breeding season) on total and maximum CORT secreted were analyzed in Generalized Linear Mixed Models (GLMM). No relationships between age, body mass, and total or maximum CORT were found. There was a significant difference in response in and out of the breeding season for total CORT (p < 0.01) and maximum CORT (p < 0.001), with a higher response during the breeding season. Measures of individual responses for total (p = 0.001) and maximum CORT (p < 0.01) were consistent across seasons. Baseline CORT levels were consistently low, with 53.6 % and 78.6 % of the samples below the detection limit during and outside of breeding season, respectively. These results highlight differences in baseline CORT maintenance compared to studies on wild Wood Ducks, potentially relating to environmental differences such as unlimited food supply and protection from predators in captivity. Additionally, we found that captive birds maintain seasonal variation in acute stress response, which reflects some trends found in wild birds, although more research across multiple seasons is warranted. We also found that some captive Wood Ducks continue to increase CORT secretion at the end of the 60 min handling period, indicating that longer handling times may reveal differences in total CORT secreted. Further investigation should be done to assess the costs and benefits of variation in body condition in terms of coping ability across life stages.

Woody or wooden breast (WB) is characterized by hardening and paleness of the Pectoralis major muscle and can affect up to 85% of broilers. We hypothesized that increased locomotor activity would lead to a lower prevalence of WB and increased tibia bone quality, with a greater effect on a faster growing than a slower growing broiler strain. Ross 708 (N = 188) and Ranger Gold (N = 213) broilers were raised in 3.05x3.05 m(2) pens in groups of 23 to 24 and 26 to 27, respectively. Target ages for the Ross 708 and Ranger Gold birds were 42 and 56 d. There were 8 pens per strain: 4 assigned to an exercise treatment and 4 unexercised controls. An exercise regimen was applied for 10 min every hour for 6 h during each weekday with the goal of increasing frequency of standing and walking. A perch was placed between the feeder and drinker line in the exercise treatment pens to further promote broiler activity. WB severity was determined by palpation for all birds at the target age. Tibial bone mineral content (BMC) and bone mineral density (BMD) were measured using a dual-energy x-ray absorptiometry. The Fisher's Exact Test was used to determine treatment effects on the prevalence and severity of WB. Both prevalence (Ross 708: 77.5 vs. 90.5% control, P = 0.013; Ranger Gold: 57.9 vs. 76.4% control, P = 0.005) and severity (Ross 708: 12.9 vs. 24.2% control, P = 0.02; Ranger Gold: 4.7 vs. 0.02% control, P = 0.01) were reduced by treatment. The effects of strain, treatment and their interaction on tibial BMC and BMD were analyzed using linear mixed models. Only strain affected BMC (P = 0.003) and BMD (P = 0.03), with Ross 708 broilers having higher BMC (control: 3.246 g +/- 0.061; treatment: 3.251 g +/- 0.058) and BMD (control: 0.177 g/cm(2) +/- 0.002; treatment: 0.174 g/cm(2) +/- 0.002) values compared to Ranger Gold's BMC (control: 2.966 g +/- 0.067; treatment: 2.987 g +/- 0.064) and BMD (control: 0.168 g/cm(2) +/- 0.002; treatment: 0.168 g/cm(2) +/- 0.002) values. However, per unit of final body weight, Ranger Gold birds had a significantly higher BMC (P = 0.006) and BMD (P = 0.01) than Ross 708 broilers. Promoting broiler activity can reduce the prevalence and severity of WB prevalence in fast and slow growing broilers.

Keel bone damage, which presents as fractures and/or deviations of the keel, has been detected in laying hens housed in all types of systems. Factors leading to keel bone damage in hens housed with limited vertical space, such as those housed in furnished systems, are not well understood, and are the topic of this study. Ten focal hens from each of 12 furnished cages (4 rooms of 3 cages) were fitted with keel mounted tri-axial accelerometers. Their behavior was video recorded continuously over two 3-wk trials: the first when the hens were between 52 and 60 wk of age, and the second approximately 20 wk later. The integrity of each hen's keel was evaluated at the start and end of each 3-wk trial using digital computed tomography. We identified predominant behaviors associated with acceleration events sustained at the keel (collisions, aggressive interactions and grooming) by pairing accelerometer outputs with video data. For each recorded acceleration event we calculated the acceleration magnitudes as the maximum summed acceleration recorded during the event, and by calculating the area under the acceleration curve. A principle components analysis, which was used as a data reduction technique, resulted in the identification of 4 components that were used in a subsequent regression analysis. A key finding is that the number of collisions a hen has with structures in her environment, and the number of aggressive interactions that a hen is involved, each affect the likelihood that she will develop 1 or more fractures within a 3-wk time span. This relationship between hen behavior and keel fracture formation was independent of the magnitude of acceleration involved in the event. Observed behavior did not have an impact on the formation of keel bone deviations, further supporting reports that the mechanisms underlying the 2 types of keel bone damage are different.

The skeletal health of laying hens improves when birds are given opportunities to perform load-bearing movements with elevated structures, such as perches. We investigated how early access to elevated structures varying in complexity and height would affect bone quality and subsequent keel bone fractures in a layer multitiered aviary. Female Dekalb White pullets were reared in floor pens furnished with floor perches (FL), single-tiered aviaries (ST), or 2-tiered aviaries (TT; n = 5 pens/treatment) through 16 wk of age. At 17 wks, all structures were replaced with identical multitiered layer aviaries. The keel, both tibiae, and both humeri were collected from 60 euthanized birds from each rearing treatment at 8, 16 and 30 wk of age, and analyzed with dual X-ray absorptiometry (DEXA) for bone mineral density and length. At 18, 26, 28, and 30 wk of age, 10 focal hens/pen were radiographed repeatedly and the presence, severity of keel bone fractures were assessed with a tagged visual analogue scale. The number of fractures was also recorded. At 16 wk of age, FL pullets had lower BMD of the tibia (P = 0.003), keel (P = 0.013), and humerus (P = 0.004) compared to ST and TT pullets. Most of the observed treatment differences disappeared after pullets were transferred to the aviary. BMD continued to increase for all hens through 30 wk of age. Pullet rearing did not affect the presence or severity of keel bone fractures, or number of new fractures incurred between ages (P > 0.05). The prevalence and severity of keel bone fractures increased between 26 to 28 wk and remained high to 30 wk of age (P < 0.0001). Hens experienced more new fractures between 26 to 30 wk than between 18 to 26 wk of age (P = 0.0046). The effects of pullet housing on bone quality were short-term when hens had access to adult housing with multiple opportunities for load-bearing movements. Keel fractures with minor severity were high in prevalence reflecting the use of radiography to assess this injury.

Spatial abilities of hens are particularly sensitive to development during early life. Experiences in pullet housing may have lasting consequences on adult hens' movements in cage-free environments. We tested whether opportunities to access elevated spaces during rearing improved hens' use of a multitiered aviary. Female Dekalb White pullets were reared in either floor pens (FL), single-tiered aviaries (ST), or 2-tiered aviaries (TT; n = 5 pens/environment) through 16 wk of age. Rearing structures were replaced with identical multitiered aviaries at 17 wk. The distribution of the flock within the aviary and the vertical transitions of 10 focal hens/pen across the aviary were determined from videos recorded during their first (D1) and seventh (D7) day of aviary access, as well as at 19, 23, and 27 wk of age. Prevalence of floor eggs was recorded weekly from 17 to 28 wk of age. On D1, more ST and TT hens utilized the aviary during the daytime (P = 0.0077), made more vertical transitions when searching for a roosting spot in the evening (P = 0.0021), and maintained a consistent distance traveled during transitions compared to FL hens (P = 0.02). These differences disappeared by D7, except that ST and TT hens continued to roost on the highest perches of the aviary more (P < 0.0001) than FL hens through 27 wk of age. FL hens laid more floor eggs than ST and TT hens for the first 2 wk of lay (P < 0.0001). The majority (97.9%) of vertical transitions was controlled. Uncontrolled transitions were highest at D1 and decreased by D7 (P = 0.0009) and were not affected by rearing (P = 0.33). The results suggest that hens reared with minimal height are hesitant to use the laying hen aviaries when they are first transferred. They acclimate within 1 to 2 wk, but continue to roost less in the highest accessible level.

Multi-tiered aviary systems provide laying hens with opportunities for species-specific behaviors, including vertical and horizontal movement. However, collisions and failed landings that occur during vertical movement can be associated with injuries. Previous studies suggest that floor rearing of pullets with minimal access to elevated structures may negatively impact adult laying hens' ability to navigate vertical space. However, it is not clear whether this is due to deficits in physical ability or differences in depth perception. This was investigated in pullets and egg-laying hens using a modified Y-maze task and a visual cliff task at 7-8, 15-16, and 29-30 weeks of age. Dekalb White pullets (N = 450) were reared in three different environments until 16 weeks of age: floor, single-tier aviary, and two-tier aviary. From 16 weeks of age, all birds were housed in a multi-tier aviary. The Y -maze task consisted of two arms that were either a ratio of 1:3 or 1:1 in length. Each bird's ability to discriminate the different arm lengths was evaluated based on latency to exit and arm choice. The illusion of depth over a plexiglass floor was tested in the visual cliff task at 15, 30, and 90 cm. Birds were given 1.5 min to either leave the start perch by jumping to a platform suspended over the visual cliff, or step down off the perch to the shallow side. Latency to jump to the platform and frequency of looking down over the visual cliff were recorded. There were no main effects of age or rearing treatment on behavior in the Y-maze, with all birds choosing the shorter arm more than chance (p < 0.001). Regardless of cliff height, birds reared on the floor were less likely to cross the visual cliff at 8 and 16 weeks of age than single and two-tier treatment birds (p = 0.01). However, these dif-ferences were not observed after they were given experience with elevated structures in the adult aviary. The results of the present study suggest that the lack of exposure to vertical complexity during rearing do not cause long-term detriments to depth perception, but could impact successful engagement with elevated heights (i.e., hesitancy to access vertical structures). Further research is needed to determine the timing, quality, and quantity of elevated height exposure that is needed in the rearing environment to encourage sufficient use of vertical space in the adult aviary for cage-free laying hens.

Commercially housed Pekin ducks (Anas platyrhynchos) are typically reared in same sex groups to facilitate separate diet provisioning. Several female ducklings are sometimes mixed into the otherwise all-male pens. This practice is thought to increase flock reproductive success. To evaluate this hypothesis, we reared ducklings in alternating same-sex groups (150 hens or 30 drakes/pen; 8 groups/sex) and evaluated the impacts of rearing on drake mounting behavior, testosterone levels, and flock fertility. At 12 days, three females were placed into four of the male duckling pens. At 20–22 weeks of age, adjacent male and female pens were moved into pens within a breeder barn, and combined to form mixed-sex pens. The number of correctly aligned mounts performed by 10 focal drakes per pen was evaluated over 3 days (12 h/day) at 26, 32, and 45 weeks of age. Circulating testosterone concentrations were analyzed from blood plasma samples collected from the focal drakes at 15 (baseline), 22, 28, 34 and 45 weeks of age. Pen-level fertility was determined at 33–34 and 45–46 weeks of age. Mount and testosterone data were analyzed using a Generalized Linear Mixed Model and a Linear Mixed Model in R 4.0.5, with duck in pen as a random effect. A Linear Mixed Model was used to analyze fertility data, with pen as a random effect. None of the measured variables were impacted by rearing treatment, but all varied with flock age. Physical access to female ducklings during rearing did not enhance flock reproductive success.

Pullets reared with diverse behavioral experiences are faster to learn spatial cognition tasks and acclimate more successfully to laying environments with elevated structures. However, the neural underpinnings of the improved spatial abilities are unclear. The objective of this study was to determine whether providing structural height in the rearing environment affected the development of the hippocampus and whether hippocampal neural metrics correlated with individual behavior on spatial cognition tasks. Female Dekalb White pullets were reared in a floor pen (FL), single-tiered aviary (ST), or two-tiered aviary (TT; 5 pens/treatment). Pullets completed floor-based Y-maze and elevated visual cliff tasks to evaluate depth perception at 15 and 16 wk, respectively. At 16 wk, brains were removed for Golgi-Cox staining (n = 12 for FL, 13 for ST, 13 total pullets for TT; 2 to 3 pullets/pen) and qPCR to measure gene expression of brain-derived neurotrophic factor (BDNF;n = 10 for FL, 11 for ST, and 9 pullets for TT). Rearing environment did not affect various morphometric outcomes of dendritic arborization, including Sholl profiles; mean dendritic length; sum dendritic length; number of dendrites, terminal tips, or nodes; soma size; or BDNF mRNA expression (P > 0.05). Hippocampal subregion did affect dendritic morphology, with multipolar neurons from the ventral subregion differing in several characteristics from multipolar neurons in the dorsomedial or dorsolateral subregions (P < 0.05). Neural metrics did not correlate with individual differences in behavior during the spatial cognition tasks. Overall, providing height during rearing did not affect dendritic morphology or BDNF at 16 wk of age, but other metrics in the hippocampus or other brain regions warrant further investigation. Additionally, other structural or social components or the role of animal personality are areas of future interest for how rearing environments influence pullet behavior.

In recent years, welfare certification companies have encouraged the use of scatter feeding as enrichment material, though there is little scientific evidence to support a scatter feeding program. This study aimed to understand the impact of scatter feeding on the foraging behavior of broilers. One hundred eighty Ross 308 chicks were allocated into six treatment groups (six replicates/treatment). Broilers were scatter fed dried mealworms, whole wheat, shredded cabbage, alfalfa pellets, wood shavings, or no scatter feeding, respectively. Enrichment was provided on the first three days of each week. Total foraging, active foraging, and feeding were observed for one-hour periods immediately after scattering, 2 h later, and 6 h later. In all groups, broilers increased both total (p = 0.001) and active (p = 0.001) foraging, though this was most pronounced in the dried mealworm group. Across all groups, active foraging decreased with age (p = 0.001). The mealworm group also showed a corresponding decrease in feeding during hour one compared to the later hours (p = 0.001). These results did not provide evidence that scatter feeding encourages foraging behavior, except for a short-term effect of a high value feed item. This finding suggests that the item scattered and the delivery method should be studied further.

prohibited us from conducting a meta-analysis. We begin by detailing our literature review search, screening, and inclusion criteria. We highlight global publication trends on the topic before discussing our key findings in the context of KBF assessment methodology, bird age and strain considerations, the role of adult and rearing housing systems, and other management practices. We conclude this review by summarizing and providing several recommendations for how to address the existing knowledge gaps.

Factors contributing to the development of keel bone damage are not well understood. This study aimed to identify behaviors and cage structures associated with acceleration events experienced by individual hens at their keels as the birds navigated their enriched colony cage environments. Additionally, we aimed to characterize the accelerations associated with these behaviors, as we postulated that behaviors associated with higher accelerations may be more likely to lead to keel bone damage. Sixty five 19 week old Hyline W36 hens were placed in each of 12 enriched colony cages. Ten focal hens per cage were selected for observation. Each hen was fitted with a jacket which contained a tri-axial accelerometer with an external sensor that was fitted into a small pocked over the hen's keel. The logger recorded any time that the hen sustained an acceleration event at the keel ( > 12 G-units). Logger output was matched with video data, allowing us to describe the behavior of the affected bird at the time of the acceleration event recorded at the keel. Data on each bird were collected continuously over two 3-week periods, when the hens were between 52-60 and 74-83 weeks of age. Collisions accounted for nearly 81% of observed acceleration events with acceleration peaks of at least 20 G-units. The majority of collisions were with the perch and were sustained mainly as the hen attempted to ascend onto it. It has previously been reported that the prevalence of keel bone fractures is higher among hens housed in cages that do versus do not contain perches. This study lends support to the growing body of evidence indicating that interactions with perch contribute to the keel bone damage sustained by laying hens housed in enriched colony cage systems, however, the relationship between acceleration events and occurrence of keel bone damage has yet to be directly assessed.

Although a number of welfare assessment methods have been developed for poultry, none have been evaluated for use in commercial duck farms. The primary objective of the study was to evaluate the inter-rater reliability and relative accuracy of 4 duck welfare assessment strategies. Over 2 experiments, 12 flocks of commercial meat ducks (5,850 to 6,300 ducks/flock) aged 30 to 34 D were evaluated. During experiment 1, six flocks were evaluated using 2 welfare assessment methods: transect walks (TW) and catch-and-inspect (CAI). During TW, 2 observers walked predetermined transects along the length of the house and recorded the number of ducks per transect that were featherless, were dirty, were lethargic, had bloody feathers, had infected eyes, and/or had plugged nostrils or were found dead. During CAI, a total of 150 ducks per flock were corralled and individually evaluated. The same welfare indicators were assessed using both methods. During experiment 2, six flocks were initially evaluated using CAI, TW, and a distance evaluation (DE; a total of 50 ducks per flock evaluated from a walking distance) and then reassessed within 24 h during the loadout (LO) process. Data were analyzed in SAS (version 9.4) to determine the observer and method effects on the incidence of welfare indicators. Interobserver reliability was high (P > 0.05) across methods for most welfare indicators. The assessment method affected the measured outcome variables in both experiments (P < 0.05). CAI resulted in higher estimated incidences of most welfare indicators than TW (experiment 1 and 2) and LO (experiment 2). DE yielded intermediate results compared with other methods (experiment 2). Results obtained using TW and LO were most similar, the only difference being the number of dead birds observed using each method (P < 0.0001). The average time required for CAI, TW, DE, and LO was 2.40 ± 0.004, 1.12 ± 0.02, 1.54 ± 0.001, 3.56 ± 0.006 h, respectively. Bootstrapping analyses showed that the observed welfare indicator prevalence estimates were affected by the number of transects (TW) and number of birds (CAI) sampled.

Hens reared in aviaries (AVI) as pullets have improved spatial abilities compared to hens reared in non-enriched cages (CON). However, this effect on behavior has been shown only to 23 weeks of age. Lohmann LSL-Lite hens were reared in either CON or AVI until 19 weeks of age and then moved into enriched colony cages (ECC) containing two elevated perches of different heights (n = 6 ECC/treatment). Focal hens (3 per ECC) were fitted with tri-axial accelerometers to record acceleration events at 21, 35, and 49 weeks of age. Video recordings from each age were used to identify behaviors associated with acceleration events as well as the proportion of hens utilizing perches. CON hens experienced more acceleration events (p = 0.008) and more collisions (p = 0.04) than AVI hens during the day at 21 and 35 weeks of age. The total proportion of hens perching at night was similar between treatments across most time points, but fewer CON hens used the high perch compared to AVI hens throughout the study (p = < 0.001). Rearing in aviaries influences hen behavior out to peak lay for collisions and out to mid-lay for perch height preference in ECC.

Although a number of welfare assessment methods have been developed for poultry, none have been evaluated for use in commercial duck farms. The primary objective of the study was to evaluate the inter-rater reliability and relative accuracy of 4 duck welfare assessment strategies. Over 2 experiments, 12 flocks of commercial meat ducks (5,850 to 6,300 ducks/ flock) aged 30 to 34 D were evaluated. During experiment 1, six flocks were evaluated using 2 welfare assessment methods: transect walks (TW) and catch-and-inspect (CAI). During TW, 2 observers walked predetermined transects along the length of the house and recorded the number of ducks per transect that were featherless, were dirty, were lethargic, had bloody feathers, had infected eyes, and/or had plugged nostrils or were found dead. During CAI, a total of 150 ducks per flock were corralled and individually evaluated. The same welfare indicators were assessed using both methods. During experiment 2, six flocks were initially evaluated using CAI, TW, and a distance evaluation (DE; a total of 50 ducks per flock evaluated from a walking distance) and then reassessed within 24 h during the loadout (LO) process. Data were analyzed in SAS (version 9.4) to determine the observer and method effects on the incidence of welfare indicators. Interobserver reliability was high (P > 0.05) across methods for most welfare indicators. The assessment method affected the measured outcome variables in both experiments (P < 0.05). CAI resulted in higher estimated incidences of most welfare indicators than TW (experiment 1 and 2) and LO (experiment 2). DE yielded intermediate results compared with other methods (experiment 2). Results obtained using TW and LO were most similar, the only difference being the number of dead birds observed using each method (P < 0.0001). The average time required for CAI, TW, DE, and LO was 2.40 +/- 0.004, 1.12 +/- 0.02, 1.54 +/- 0.001, 3.56 +/- 0.006 h, respectively. Bootstrapping analyses showed that the observed welfare indicator prevalence estimates were affected by the number of transects (TW) and number of birds (CAI) sampled.

We assessed the effects of water-chilled perches as a cooling device on the physiological parameters of caged laying hens exposed to 2 cyclic heating episodes. White Leghorns, 17 wk of age, were randomly assigned to 36 cages of 6 banks placed in the same room. Each bank was randomly assigned to 1 of 3 treatments: cooled perch (CP), air perch (AP), and no perch (CTRL) resulting in 2 replicate banks and 12 cages per treatment. Chilled water (10°C) circulated through the CP during heat periods when hens were 21 wk to 35 wk and 73 wk to 80 wk of age, respectively. During the heating episodes, hens were submitted to a daily cyclic temperature regimen of 35°C (0600 h to 1800 h) and 28°C (1800 h to 0600 h). Rectal temperature, packed cell volume, heterophil to lymphocyte (H/L) ratio, and plasma levels of triiodothyronine (T3), thyroxine (T4), interleukin (IL)-6, IL-10, immunoglobulin (Ig) Y, interferon (IFN)-γ, and heat shock protein (HSP) 70 were measured on the last day of the 2 heating episodes. At the end of the first heating episode, CP hens had lower rectal temperature (P = 0.02) than both AP and CTRL hens. The CP hens also had lower HSP 70 (P = 0.04) than CTRL hens but not AP hens. At the end of the second heating episode, the CP hens had lower rectal temperature (P = 0.02) and circulating H/L ratio (P = 0.01) than both AP and CTRL hens. The CP hens also had higher levels of T3 (P = 0.002) and T3/T4 ratio (P = 0.0006) than CTRL hens but not AP hens, with a greater packed cell volume than AP hens (P = 0.02) but not CTRL hens. Cytokines and IgY levels were similar among treatments. These results indicate that CP hens were better able to cope with cyclic heat stress than CTRL and sometimes AP hens as noted by the beneficial effects on rectal temperature, thyroid activity, HSP, and H/L ratio.

Palpation is the most popular method of measuring keel bone damage on live birds, although it has been criticized for being subjective and inaccurate. The goals of this study were to examine intra- and inter-rater reliability when trained with feedback of accuracy, as well as determine the accuracy of portable radiography and sonography. Four evaluators palpated 50 103-week old Lohmann LSL-lite hens immediately following euthanasia. Of those birds, 34 were then radiographed, sonographed, and all 50 were re-palpated. Lastly, the keels were dissected and scored. The presence of deviations (DEV), fractures (FR), and tip fractures (TFR) was scored for each method. Reliability of palpation was analyzed using Cronbach's Alpha (intra) and Fleiss' Kappa (inter) tests. Radiography and Sonography scores were further compared with dissection scores to determine sensitivity and specificity. Initial inter-observer reliability was 0.39 DEV, 0.53 FR, and 0.12 TFR, with similar scores for the second round of palpation. Scores for intra-observer reliability ranged from 0.58-0.79 DEV, 0.66-0.90 FR, and 0.37-0.87 TFR. A high prevalence of TFR, but low assessor agreement, warrants the development of specialized training for the palpation of this area. Both radiography and sonography showed relatively high sensitivity for FR and TFR, but low for DEV. On the other hand, specificity was generally high across all damage types. Even with feedback, palpation reliability was poor. However, portable radiography and sonography show promise for detecting keel fractures.

The northern fowl mite (NFM), Ornithonyssus sylviarum (Mesostigmata: Macronyssidae), is the primary blood-feeding ectoparasite found on poultry in the U.S.A. Three experiments were conducted in vitro to test the acaricidal properties of cade, garlic, lavender, lemongrass, pine and thyme essential oils against NFM, and to evaluate whether these effects are altered by adjusting oil application rates and application modality (direct vs. vapour contact). Applied at the rate of 0.21 mg/cm(2), the essential oils of cade, thyme, lemongrass and garlic resulted in higher NFM mortality at 24 h post-application than lavender and pine oils, and the untreated and ethanol-treated controls. Cade and thyme were the most consistent and fast-acting of the essential oils in terms of toxicity to NFM. Cade applied at 0.21 mg/cm(2) and 0.11 mg/cm(2) and thyme applied at 0.21 mg/cm(2) were effective in eliminating NFM within 2h through direct contact. The modality of application did not affect the efficacy of cade and thyme essential oils. The results suggest that essential oils may be utilized as alternatives to chemical pesticides and could be used as fumigants for the control of NFM.

Damage to the keel bone is a major issue in the laying hen industry. The goal of this study was to compare palpation results of live laying hens to digital computed tomography (CT) images, to assess changes in palpation reliability as training and familiarity increased, and to examine keel bone morphology over time. The longitudinal study consisted of 2 trials of 3 observation periods using 40 different (n = 120) W-36 hens housed in enriched colony cages. The first trial began when hens were 52 to 58 wk of age repeating the trial when the same birds were 74 to 81 wk of age. At 52 wk of age, each hen's keel bone was palpated by a single individual for keel bone caudal tip fractures (Tip), sagittal deviations (Evenness), and transverse deviations (Straightness). After palpation, each hen was placed in a motion limiting restraint and scanned using CT. The hens spent the next 21 d in their cages and on day 21, the hens were collected, palpated, and CT scanned again. The CT scans were imported into Mimics analysis software, 3D models of each keel bone were constructed and evaluated. Each bone and 3D model was scored (0, 1, 2) on the measurement of transverse deviation based on <0.5 cm, 0.51 to 1.0 cm, and >1.0 cm total deviation, respectively. Analysis of data using Proc Freq and Means in SAS 9.3 revealed minimal to moderate kappa values and moderate agreement percentages between palpators and digital analysis. The computer generated 3D models of individual keel bones were compared to palpation scores for Tip, Evenness, and Straightness at the beginning and end of each trial. The visual observations of the 3D models were qualitative, performed by a single individual. Overall, we found CT scanning to be a useful tool in observing changes to the keel bone, we observed changes in palpation accuracy as training/familiarity increased, and examined changes in keel morphology, specifically in the tip, after 52 wk of age.

Keel bone damage may be painful to birds and affect their production. In order to better understand the frequency, position, and timepoint of keel bone damage that occur during production, the integrity of W-36 laying hen keel bones housed in enriched colony cages at 748.4 cm(2) (116 in(2)) was evaluated. At four time points, 120 birds (10 per cage; three cages per each of four rooms) had keel bones evaluated. Each hen was placed in a motion limiting restraint, scanned using computed tomography (CT), fitted in vests containing tri-axial accelerometers, and placed back in their cages for 21 d. After 21 d, the hens were rescanned and returned to their cages. This process was repeated after 133 d. The CT scans were imported into Mimics analysis software (Materialise, Plymouth, MI, USA); 3D models were made of each keel bone at each time point and exported to 3-matic analysis software (Materialise, Plymouth, MI, USA). Each laying hen's keel bone model was superimposed onto scans from multiple time points resulting in four bone pairings representative of each 21-d period, the 133-d period, and the entire duration of the project. Next, the proximal portion of each bone pairing was edited to normalize bone shape according to a strict protocol. Additionally, each pairing was divided into three portions: distal aspect (3 cm), proximal aspect (2 cm), and middle portion (remaining). Whole bone pairing and each bone portion was analyzed using the Part Comparison tool in 3-matic. Raw data were compiled into three datasets and analyzed in SAS 9.3 using the GLIMMIX procedure using a three-level random intercept model. The model controlled for time, part, part(time), and system with random intercepts of bird(cage) and cage. Overall, results revealed that the greatest morphological changes occurred during the first 21-d period with regards to time (P = 0.03) and in the distal aspect of the keel with regards to part (P < 0.0001).