Gregarious nesting in relation to floor eggs in broiler breeders.

Gregarious nesting has often been observed in laying hens, where hens prefer to visit a nest already occupied by other hens over empty nests. This may result in overcrowding of the nests which is considered a welfare issue and, moreover, can increase the economic issue of floor eggs. This study aimed to describe gregarious nesting and spatial behavior in broiler breeders and how this relates to genetic background, fearfulness and mating behavior. Five commercially available genetic lines of broiler breeders were housed in 21 pens of 550 females and 50 males (six pens for lines 1 and 2, five pens for line 3 and two pens for lines 4 and 5) during the ages 20-60 weeks. Every 10 weeks, the plumage condition and wounds were assessed of 50 random hens per pen. Avoidance distance and novel object tests were performed to assess fearfulness at four time points. Distribution of eggs over nests was observed for 6 weeks at the onset of egg production at 26 weeks of age, and use of space was recorded at four time points, while (floor) egg production was noted daily per pen. We found differences between genetic lines over time in plumage condition and prevalence of wounds. Fear of humans was highest at the earliest age tested and did not correlate with general fearfulness as assessed by the novel object test. The distribution of eggs over nests was related to genetic background and was more uneven at the earliest age compared to later ages, and a more uneven distribution was correlated with an increased percentage of floor eggs. Distribution of birds over the litter area differed between the genetic lines, and less use of the litter area was correlated with an increased fear of humans and presence of wounds, suggesting an association with aggressive mating behavior. This difference in distribution of the birds could also explain the correlation between increased presence of wounds and decreased percentage of floor eggs. It is concluded that broiler breeders do show gregarious nesting, which is affected by genetic background. Both increased gregarious nesting and wounds are related to increased floor egg percentage, which should be studied further in broiler breeder research. Genetic selection for even use of the available nests and of the litter and slatted area would therefore support both broiler breeder welfare and performance.

Influence of a raised slatted area in front of the nest on leg health, mating behaviour and floor eggs in broiler breeders.

European farms for broiler breeders often have raised slatted areas in front of the nests, but in other regions of the world no raised slatted areas are provided. This study aimed to investigate the effects of a raised slatted area on leg health, mating behaviour and floor laying behaviour. Ten groups of 33 broiler breeder hens and three males were housed in two pen types: with or without a raised slatted area in front of the nests. Each pen had one plastic and one wooden nest. Between 25 and 31 weeks of age, ten marked hens per pen were weighed and assessed weekly on foot pad dermatitis, hock burn and wounds. At the end of week 31, animals were euthanized and bone strength of the tibia and humerus of these individuals was assessed. At 24, 27 and 30 weeks of age, mating behaviour was observed for an hour per pen, noting both numbers of successful and unsuccessful copulations. The number of eggs laid in the nests and on the floor was recorded daily between 20 and 31 weeks of age. Foot pad dermatitis scores were affected by age, but not by pen type. Generally, there were only minor issues with foot pad dermatitis (scores <11 on a 0-100 scale), probably due to the young age of the hens. Body weight was not affected by pen type, while the prevalence of hock burns was too low to analyse and no difference in bone strength was found for the tibia and the humerus. Overall, mating behaviour was less frequent in pens with raised slats than in pens without raised slats (29 ±â€¯2 vs 35 ±â€¯3 times/h) and more frequent at 27 weeks of age than at 24 and 30 weeks of age (38 ±â€¯1 vs 31 ±â€¯4 and 27 ±â€¯2 times/h). The pens with raised slats had a lower percentage of floor eggs than pens without raised slats (11.2 ±â€¯0.4 vs 19.3 ±â€¯0.5%). The wooden nest was preferred over the plastic nest as on average 63% of the eggs were laid in the wooden nest. This study shows that providing raised slats decreases mating behaviour and percentage of floor eggs, although its effects on leg health remain inconclusive.

Predicting hairline fractures in eggs of mature hens.

Eggshell damage poses a serious problem for the consumption egg industry. Increasing the maximum age of laying hens will increase eggshell damage due to loss of shell strength. This poses a serious problem for automatic collection, packing, and transport. We performed a model based study focused on hairline fractures in eggs of 88-week-old hens, and simulated side collisions on 1,235 eggs using a specially designed pendulum. The kinetic energy at the moment of impact was related to the accelerations measured by an electronic egg going through the transport chain. Further, several egg mechanical properties were measured.For collisions with a realistic impact, fracture occurrence correlated negatively with dynamic stiffness (14%), mass (15%), shape index (9%), and damping ratio (12%). We manipulated the data set to investigate the influence of improving egg properties. Removing the least favorable 50% of the eggs based on stiffness and mass resulted in a moderate reduction of fracture occurrence, from 7.7% down to 4.4%.The peak acceleration of an egg running through the transport chain lies typically in the range of 15 to 45 g. Our model predicts that a moderate decrease from 30 g down to 20 g will result in a drastic reduction of fracture occurrence from 7.7% down to 0.3 to 1% (95% confidence region), whereas an increase to 40 g will increase fracture occurrence to 42 to 55%.The model predicts that severe collisions pose a relatively high risk for eggshell damage, which suggests that a reduction of collision severity is of first priority when increasing the age of laying hens.

Perinatal broiler physiology between hatching and chick collection in 2 hatching systems.

Little is known about physiological responses of early- versus late-hatching chicks to early posthatch conditions in broiler practice. We investigated effects of hatching time on perinatal broiler physiology in 2 hatching systems, differing in conditions: a conventional hatcher, where chicks are deprived of feed and water between hatching and the moment of chick pulling (d E21.5), and a patio system, in which the hatching and brooding phase are combined, and chicks have immediate posthatch feed and water access. Climate conditions in patio also differ with about 3°C lower temperature and 20% lower RH compared with conventional hatchers. At E18, fertile eggs were transferred to either a hatcher or the patio until the end of incubation. From each system, 50 newly hatched chicks were collected at 3 hatching times: at 468 h (early), 483 h (midterm), and 498 h (late) of incubation, of which 25 chicks were decapitated for analyses of physiological parameters. The other 25 chicks were returned to the hatching system for analyses after 515 h of incubation (E21.5). At hatch, weights of the heart, lungs, stomach, and intestine increased with hatching time, concurrent with a decrease in residual yolk weight, regardless of hatching system, and indicating that later hatching chicks are more matured. Weights of the heart, liver, stomach, and intestines were lower in hatcher than in patio chicks. Between hatch and E21.5, residual yolk weight decreased, whereas organ weights increased in both fasted hatcher and fed patio chicks, but at a higher rate in the latter. At E21.5, plasma glucose and triiodothyronine had increased with time after hatch in patio chicks, whereas levels were similar among hatching times and lower in hatcher chicks. Early feed and water access seems to enable early hatching chicks to compensate for their apparent disadvantage in development at hatching, whereas chicks subjected to fasting show metabolic adaptations to preserve nutrients. Chick physiology at chick pulling time was shown to vary with time after hatching and posthatch conditions, especially feed access.

Significance of chick quality score in broiler production.

The quality of day old chicks is crucial for profitable broiler production, but a difficult trait to define. In research, both qualitative and quantitative measures are used with variable predictive value for subsequent performance. In hatchery practice, chick quality is judged on a binomial scale, as chicks are divided into first grade (Q1-saleable) and second grade (Q2) chicks right after hatch. Incidences and reasons for classifying chicks as Q2, and potential of these chicks for survival and post-hatch performance have hardly been investigated, but may provide information for flock performance. We conducted an experiment to investigate (1) the quality of a broiler flock and the relation with post-hatch flock performance based on a qualitative score (Pasgar©score) of Q1 chicks and based on the incidence of Q2 chicks and (2) the reasons for classifying chicks as Q2, and the potential of these chicks for survival and post-hatch growth. The performance was followed of Q1 and Q2 chicks obtained from two breeder flocks that hatched in two different hatching systems (a traditional hatcher or a combined hatching and brooding system, named Patio). Eggs were incubated until embryo day 18, when they were transferred to one of the two hatching systems. At embryo day 21/post-hatch day 0, all chicks from the hatcher (including Q2 chicks) were brought to Patio, where the hatchery manager marked the Q2 chicks from both flocks and hatching systems and registered apparent reasons for classifying these chicks as Q2. Chick quality was assessed of 100 Q1 chicks from each flock and hatching system. Weights of all chicks were determined at days 0, 7, 21 and 42. There were no correlations between mean Pasgar©score and post-hatch growth or mortality, and suboptimal navel quality was the only quality trait associated with lower post-hatch growth. Growth was clearly affected by breeder flock and hatching system, which could not be linked to mean Pasgar©score or incidence of Q2 chicks. Q2 chicks showed lower post-hatch growth compared to Q1 chicks but effects on flock performance at slaughter weight were limited because early mortality in Q2 chicks was high (62.50% at 7 days). We concluded that chick qualitative scores and the incidence of Q2 chicks may be informative for the quality of incubation, but are not predictive for post-hatch flock performance. Culling Q2 chicks after hatch is well-founded in terms of both animal welfare and profitability.

Effects of egg position during late incubation on hatching parameters and chick quality.

Chicken eggs are commonly incubated for 17 to 18 d in setters, after which they are transferred to the hatchery for the last 3 to 4 d of incubation. Whereas eggs are positioned vertically with the air cell up during the first incubation phase, they are placed horizontally for the hatching phase. It is unknown whether egg position in the last phase of incubation is of importance to the hatching process and chick quality. An experiment was conducted to investigate effects of egg position in the last 4 d of incubation on the hatching process and chick quality. The experiment consisted of 2 identical trials, where 300 fertile eggs per trial were transferred to a hatching cabinet at embryo day 17. Eggs were placed in 1 of 3 positions: with the air cell up (ACU), with the air cell down, or horizontally (HOR). Starting at embryo day 18, the following data were collected for each egg at 3-h intervals: time of internal pipping (IP), external pipping (EP), hatching, and position of EP. Approximately 6 h after hatch, BW, chick length, and chick quality based on the Pasgar score, were determined for each chick. In addition, residual yolk weight and yolk-free body mass were determined in every fourth chick that hatched. Time of IP was not affected by egg position, but EP occurred 5 h later in ACU eggs, and thus, the IP-EP interval was increased by 3 to 4 h in this group compared with the other egg positions. Hatching occurred 1 to 2 h earlier in HOR eggs than in the other 2 positions. Body weight, yolk weight, and yolk-free body mass were not affected by egg position. Chick length was 1 to 2 mm shorter and the Pasgar score was slightly lower in air cell-down eggs compared with ACU and HOR eggs, mainly caused by a high incidence of poor navel quality, red hocks, and red beaks. Hatchability was not affected by egg position. We concluded that egg position in the last phase of incubation affects the duration of the hatching process, and has small effects on chick quality.

Hatching system and time effects on broiler physiology and posthatch growth.

A multilevel housing system for broilers was developed, named Patio (Vencomatic BV, Eersel, the Netherlands), in which the hatching and brooding phase are combined. In a Patio system, climate conditions differ from those provided in the hatchers currently in use. We compared the physiology of broilers hatched in a hatcher or in a Patio system, and included the effects of hatching time. Eggs from 1 breeder flock were incubated until embryonic d 18 in a setter and subsequently placed in a hatcher or the Patio until the end of incubation. From each hatching system, 154 chicks were collected per hatching time, at 465 h (early), 480 h (midterm), and 493 h (late) of incubation, from which 24 chicks/group were decapitated for analyses of blood plasma and organ weights. The remaining 130 chicks in each group from both systems were individually labeled and placed together in the Patio system. All chicks were given access to feed and water directly after hatch and were housed up to d 45 to monitor growth. From embryonic d 18 until the end of incubation, average ambient temperature and RH were 38.1°C and 50.8% in the hatcher and 35.2°C and 29.7% in the Patio system. Glucose and corticosterone were slightly higher in hatcher chicks, whereas organ weights were not affected by the hatching system. Although hatchling weights were lower in hatchery chicks, growth from d 0 to 45 was not affected by the hatching system. In both systems, glucose increased with hatching time, whereas lactate and triiodothyronine levels decreased. Yolk weights decreased with hatching time, whereas absolute and relative weights of the yolk-free body, intestines, stomach, lungs, and heart increased, indicating more advanced maturation of organs. Growth up to d 21 was depressed in chicks in the late group, which was possibly related to lower thyroid hormone levels at hatching. We conclude that the hatching system had minor effects on hatchling physiology and that posthatch growth and livability were not affected. Because hatching time affected broiler physiology, it seems important to take hatching time into account in future studies related to hatchling physiology.

Effects of a combined hatching and brooding system on hatchability, chick weight, and mortality in broilers.

Chicks hatch over a time window of approximately 36 to 48 h and are removed from the hatchers only when the majority of the chicks has hatched. Consequently, chicks are exposed to prolonged posthatch holding periods and delays in feed and water access, leading to dehydration and impaired posthatch performance. It is questionable whether the physiological requirements of the hatchlings can be met with current hatching systems. An alternative system that may better match the requirements of the hatchlings is a system that combines the hatching and brooding phase, so that feed and water can be provided immediately after hatch. Such a system, named Patio, was developed in the Netherlands and tested from 2006 to 2008, to evaluate effects on hatchability and early performance of broilers. This paper describes the Patio system and the results from these tests. A total of 21 broiler production trials (780,686 eggs) in the Patio system were evaluated at 3 locations and compared with control hatches of eggs of the same parental flock in the hatchery. Hatchability in the Patio was on average 1.45, 1.83, and 1.86% higher at location 1, 2, and 3, respectively. However, in the calculation of the hatchability in the Patio, possible second grade chicks were included, whereas these were excluded in the calculation of hatchability in the hatchery. Additionally, in the hatchery, the hatching process was interrupted earlier than in the Patio, meaning that possible late hatching chicks remained in the flock in the Patio, but not in the hatchery. In 3 trials, the Patio chicks were 11.6 to 16.3% heavier at d 0, when the hatchery chicks were placed in the broiler house. Mean cumulative 7-d mortality was only assessed in the Patio and was 1.27, 1.09, and 1.43% at location 1, 2, and 3, respectively. The Patio system appears to function as an alternative to current hatching and brooding systems. Further studies are required to determine to what extent the higher hatchability is due to second grade and to late hatching chicks.