Can UV light induce movement in cage-free laying hens?

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SUMMARY

In recent years, more farms have been transitioning to cage-free systems as multiple states passed regulations banning use of conventional cages, and several large food service companies pledged to exclusively source cage-free eggs by 2025–2026. However, transition and management of hens within new cage-free systems has been problematic. Additionally, catching hens prior to mass depopulation or carcass removal after depopulation becomes a challenging task for workers in these systems. The goal of this study was to explore 10-sec flashes (2 pulse/d, 1 pulse in AM and 1 pulse in PM) of UV light and darkness as management tools to stimulate a movement response from laying hens, with the aim of moving hens from within the aviary system to floor area. Approximately 1,800 Lohmann Brown hens were divided into 4 rooms equipped with Big Dutchman Natura 60 aviary; 150 hens were placed into 3 sections of aviary, totaling 450 hens per room. Six UV-light bars in the 395 to 400 nm wavelength were used. Four lighting treatments were as followed: 1) Control, 2) UV light flashed for 10-sec (UV), 3) floor area was darkened (DF), and 4) UV flashed for 10-sec plus floor area darkened (DF + UV). Each treatment was applied once in the AM and once in the PM. Videos were recorded to assess hens’ spatial distribution (difference in number of hen pre- and post-treatment application) and behavior (preening, dust bathing, wing flapping, perching, and standing alert), before and after treatments were applied. Results demonstrated that when UV flash was combined with darkened floors in AM application, a greater difference in number of hens was observed in this treatment compared to other lighting treatments; whereas in PM application this difference was only observed when comparing DF + UV to control. UV light flashes influenced hens’ behavior, with more stress related behaviors apparent in treatments where UV lights were used, whereas more hens exhibited normal behaviors in non-UV light treatments. Based on these observations, a flash of UV light was successful in moving laying hens out of aviary and onto floor area, but this was only effective for a short period and may not be effective for long-term movement.

    DESCRIPTION OF PROBLEM

    Through legal and market channels, United States consumers, food retailers, and restaurants have mandated changes to laying hen housing systems, moving away from conventional cages to alternative systems (Ochs et al., 2019). The additional resources provided in alternative non cage systems are known to improve hen welfare by promoting hens’ ability to express natural behaviors (Mellor and Webster, 2014; Campbell et al., 2016; Hartcher and Jones, 2017). The World Organization for Animal Health’s (OIE) definition of animal welfare refers to how well an animal can cope within its living conditions and is comprised of both physical and mental health (World Organization for Animal Health OIE, 2022). Furthermore, pledges by small and large egg buyers such as fast-food chains and large grocery store chains, have committed to discontinue purchasing eggs from cage raised hens and replace them with cage-free eggs; however, certain company pledges may fail to meet deadlines (Trejo-Pech and White, 2021). According to United Egg Producers, as of March 2021, organic and cage free shell egg production accounted for 29.3% of the table egg layer flock, whereas most of the United States layer population was in conventional cages (70.7%). To meet projected demand, approximately 66% of U.S. hens must be in cage free production by 2026 (United Egg Producers, n.d.).

    Over the last few decades, the poultry industry has advanced remarkably due to improvements in bird genetics, nutritional advancements, and increased labor efficiency (Brannan and Anderson, 2021). Moving away from intensive (cage) towards extensive (cage-free) production systems requires a substantial increase in labor hours, particularly when transitioning from conventional cage to cage-free production, with an estimated 45% increase in human labor hours (Anderson, 2014). Increased labor is needed for transitioning pullets to layer housing because they must be trained to find feed and water, improving litter quality within the system towards the end of the laying cycle, and frequent inspections to minimize floor eggs, feather pecking, piling, and equipment assessment (Brannan and Anderson, 2021; de Haas et al., n.d).

    Laying hens, like other poultry species, possess 4 cone photoreceptors to detect blue, green, red, and ultraviolet (UV) light that provides tetrachromatic vision (Burkhardt, 1982; Wilby et al., 2015; Seifert et al., 2020). When studying individual cone sensitivity in chickens, Wilby et al., (2015) found violet and blue cones had greater sensitivity compared to red and green cones.

    UV light is composed of the shorter wavelengths (100–400 nm) of electromagnetic radiation spectrum and is divided into 3 parts: UVA (315–400 nm), UVB (280–315 nm), and UVC (100–280 nm) (Rana and Campbell, 2021). UV light (UVA and UVB) may be used as a management tool to improve the welfare and health of poultry species, whereas UVC wavelengths may be utilized to protect poultry species against airborne viral infections, although continuous exposure can cause eye damage (Lewis and Gous, 2009; Rana and Campbell, 2021). However, more research must be conducted to find “optimal timing of exposure commercially, particularly UVB wavelengths which can cause damage with high exposure and thus may limit practical application” (Rana and Campbell, 2021). During a preference test, laying hens that were 16 to 24 wk of age preferred daylight (combination of UVA and LED white light) and forest light (combination of UVA and red, green, and blue LED light) compared to conventional light (LED white) used in poultry housing and had higher frequencies of locomotion, standing and foraging behaviors (Wichman et al., 2021). Additionally, researchers assured light intensity was similar across treatments by taking measurements with a light meter at 5 different locations in study pens at bird level (Wichman et al., 2021).

    An essential management practice for producers is implementing the right lighting programs throughout the production cycle of poultry species (Patel et al., 2016). For this reason, this area is of particular interest to researchers as there is an economic benefit to producers because feed consumption and growth rate can be influenced by light. Researchers have attempted to improve feed efficiency and growth rate by the addition of light flashes throughout the production cycle of broilers and dual-purpose breeds found in Egypt (Farghly, 2014; Fargly and Makled 2015). Fargly et al., (2017), investigated the effect of applying light flashes (20 pulses/min) during rearing of 360 naked neck (Sharkasi) birds (growing and laying periods). Concluding points from the study were that birds subjected to 10, 20, or 30-min of light flashes per hour had an overall better growth performance, egg production, shell thickness, and livability as opposed to birds reared under common light (12-h during growing and 16-h during laying), 40-min and 50-min of light flashes per min (Farghly et al., 2017).

    Mass depopulation of livestock and poultry is implemented under urgent circumstances, such as immediate disease control, and response to natural or human-made disasters (AVMA, 2019). The depopulation methods widely used for depopulation of poultry species include water-based foam generators or nozzles; whole house, partial house, or containerized gassing; and under constrained circumstances, ventilation shutdown plus (VSD+) (AVMA, 2019; AAAP, 2021). The use of water-based foam or gas may not be feasible at times due to the amount of area that must be treated because cost and logistics are directly proportional to the area (AVMA, 2019). Moreover, logistical problems for cage-free systems, particularly aviary systems, arise during the catching process of depopulation. Because aviary systems encourage hens to freely move through the system, hens may be scattered throughout and require human labor for individual hens to be chased and caught (Knowles and Wilkins 1998; Gerpe et al., 2021). Another problem personnel may face is access to the hens inside of aviary systems, because catching can cause unintended injury to the hens that attempt to escape and crash into housing equipment (Knowles and Wilkins 1998; Gerpe et al., 2021).

    While research has investigated effects of UV light supplementation on avian health and welfare, no research has been conducted using flashes of UV light as a management tool to move birds (Maddocks et al., 2001; Schutkowski et al., 2013; Rana and Campbell, 2021). Being able to concentrate all birds in one area may provide an appropriate method to improve flock inspections and catching hens prior to depopulation. Therefore, the objective of this study was to determine if flashing UV light for 10-sec (2 pulse/d, 1 pulse in AM and 1 pulse in PM), combined with darkening of floor area, could elicit a movement response from laying hens reared in a cage free system. We hypothesized that when UV lights were flashed for 10-sec, hens would leave the aviary and move to the floor area, having a greater number of hens on the floor area compared to the aviary system.

    MATERIALS AND METHODS

    This study was conducted at Michigan State University’s Poultry Teaching and Research Center (East Lansing, MI). All procedures involving live birds were approved by Michigan State University Institutional Animal Care and Use Committee (IACUC-202100026).

    Housing and Birds

    A total of 1,800 Lohmann Brown hens were obtained as day-old-chicks from Hy-line hatchery (Hy-line North America, LLC, GA) and transported to the Poultry Teaching and Research Center. The study began when hens were 56 wk of age and was conducted in 4 identical rooms measuring 19.81 m × 4.57 m × 3.20 m (length × width × height). All rooms had an equal number of hens and equal number of hens per aviary section. Hens were randomly divided into each room (450 hens/room) and were further divided into 3 sections (150 hens/section; 0.093 m2 per bird) of the multitier aviary system (NATURA60, Big Dutchman Inc., Holland, MI). The aviary system was internally divided into 4 sections and had approximately 120 to 130 hens/section; hen housing capacity of system per section was 144 hens/section. To mimic a commercial stocking density, hens from fourth section were divided and placed into remaining 3 sections to obtain approximately 150 hens/section (United Egg Producers, 2017).

    The aviary was located in middle of each room, with each aviary section facing the wall; each section was of equal size and equipment (i.e., each section has 3 tiers, water lines, feeders, etc.), refer to Figure 1. The first tier included a water line, feeders, outer perch, and main opening to floor area; second tier included feeders and outer perch; and third tier included one water line, nest boxes, and inner and outer perches. Within each section, there was an open litter area in front of the aviary and litter area underneath the system. Birds were able to freely move within their respective sections but could not access another section of the aviary. For a detailed description of the aviary offered to birds, please see Ali et al. (2016). Hens were provided with ad libitum access to water, fed 3 times a day (with 2 stimulations), and were under a lighting schedule of 16L:8D; room lights were turned on at 0800 (dawn). Doors on the system that restricted access to the floor area during the night (dark period) were opened prior to the start of study and kept open for the full duration of study. However, there was equipment malfunction in control room and one of the rail doors in tier 3 (nest boxes) remained closed. Although a portion remained closed, hens still had access to floor by using main opening to floor area located in tier 1.

    Figure 1

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    Figure 1. Aerial view of room layout. Room layout was identical between the treatments. Aviary system was in the middle of room and consisted of 4 sections, each with corresponding floor area; however, only 3 sections were used to house hens in present study. Bird side depicts where hens were located. Man side represents area workers used for egg collection and side where UV lights were placed. Front end of room contained entrance door and 2 air inlets, whereas 2 exhaust fans were located on backend of room. Diagram not drawn to scale.

    Lighting Treatments and Light Intensity

    Due to room setup and takedown, the experiment was conducted over the span of 4 d (1 room/d; 1 treatment/d). Each room was randomly assigned to a lighting treatment: 1) control (C), UV light flash and/or darkened floor area were not utilized, 2) UV lights flashed for one 10-sec per morning/afternoon (UV), 3) floors of the system were darkened plus UV lights flashed for one 10-sec per morning/afternoon (DF + UV), and 4) floors of the system were darkened (DF). The floor areas were darkened by turning off the floor lights on the controller, causing the floor area and tier 1 to be darker compared to the rest of the system (Figure 2). Treatments were applied once in the morning (AM) between 8 am and 9:30 am and once in the afternoon (PM) between 12 pm and 1 pm each day to observe if diurnal rhythm would influence treatment response. For the DF + UV treatment, floors were darkened 5 to 10-min prior to the UV flash. In the DF treatment, after the AM application, floor lights were turned on 60-min prior to PM application. Because in treatment C nothing was applied (i.e., no utilization of UV light flash and/or darkened floor area), bird distribution and behavior at times when other treatments were applied were used for comparison. Two rooms were equipped with 6 UV-LED purple blacklight bars (INWT504014650Dc, Barrina Lighting, Paris, France) in the UVA light spectrum (395–400 nm). UV lights were positioned on the back side of the system to encourage hens to vacate the aviary through the opened doors and onto the floor. When floor lights in UV treatment remained on, UV flash was partially observed in tier 1, whereas in tier 2 and 3 (nest box) UV flash was more noticeable. Additionally, in treatment DF + UV the UV lights illuminated all 3 tiers. The hens did not have prior exposure to UV light.

    Figure 2

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    Figure 2. Aviary system offered to hens. The levels of the aviary (from bottom to top) are floor, tier 1, tier 2, and tier 3 (nest boxes). UV lights were placed right above feed trough. Source: Zhao, Yang & Zhao, Deiling & Xin, Hongwei. 2013. Characterizing Manure and Litter Properties and Their Carbon Dioxide Production in an Aviary Laying-Hen Housing System. American Society of Agricultural and Biological Engineers Annual International Meeting 2013, ASABE 2013. 4. 10.13031/aim.20131618601.

    To know whether light intensity was similar across treatments, it was measured at 3 locations at approximately bird level in each aviary section (middle of floor area, middle of tier 1, and middle of tier 2) using a light meter (cal-LIGHT 400, The Cooke Corp., San Diego, CA).

    Video Data Collection, Spatial Distribution, and Behavior Analysis

    Dome CCTV cameras with 4k ultra-HD resolution (LNE9292B, LOREX Corp., Linthicum, MD) and an NVR recording system (N882A63B, LOREX Corp., Linthicum, MD) were used, with 4 cameras per section, for 12 total cameras per room. Two cameras were mounted on the wall to record each tier of the aviary, one mounted on the ceiling for an aerial view of the floor area, and one on the backside of the aviary to record tier 1 and floor area underneath system. This set up enabled video recordings of almost the entire housing system, visibility was reduced in some areas due to space limitations of aviary equipment.

    To determine the spatial distribution of hens, video recordings were observed by one observer at 1-min intervals during a 12-min observation period (6-min pre-treatment and 6-min post-treatment) per camera. Hens observed within the system and floor area were counted at each time point. In order to be counted, hens had to be clearly visible in the video frame. Then, the difference of hens for floor area was calculated by subtracting the number of hens pre- and post-treatment application.

    Hen behavior was observed to determine if treatments altered behavior. The behavior categories were preening, dust bathing, wing flapping, perching, and standing alert (Table 1). Standing alert was considered a stress-related behavior (Campler et al., 2009; Bhania and Bahndauria, 2018). Perching behavior is a normal behavior observed in laying hens (Dİkmen, 2014), but was considered a stress-related behavior in this study because it provides a place of refuge from aggressors or stressful situations (Yan et al., 2014; Hartcher and Jones, 2017). Preening, dust bathing and wing flapping were considered natural comfort behaviors (Zimmerman et al., 2011; Bhanja and Bhandauria, 2018). Behavior data was collected via instantaneous scan sampling. Video recordings were observed by one observer with an observation period of 5-min pre-treatment and a second observation period of 10-min post-treatment, totaling a 15-min observation block per camera. The 5-min pretreatment observation period was divided into 20 sets of 15-sec intervals and 40 sets of 15-sec intervals for the 10-min post-treatment application.

    Table 1. Ethogram of the 5 behaviors evaluated during the observation period.

    Behavior category Behavior Description
    Positive- comfort Preening1,2 Bird uses beak to groom feathers on different regions of the body; sometimes uses oil from uropygial gland to groom feathers.
    Dust bathing2 Bird may scratch or squat on the litter, uses different body movements to force the litter to coat the feathers.
    Wing flapping1 Bird is in upright position, extending its wings in fast, repeated movements.
    Negative- stress Standing alert2,3 Bird is in upright position, with the neck extended upright
    Perching4,5 Bird holds onto the perch with feet. May be seen in an upright position or breast may be in contact with the perch.
    1

    Zimmerman, P. H., S. Buijs, A. F., Bolhuis, J. E., and L. J. Keeling. 2011. Behaviour of domestic fowl in anticipation of positive and negative stimuli. Anim. Behav. 81:569–577. https://doi.org/10.1016/J.ANBEHAV.2010.11.028

    .

    2

    Bhanja, S. K., and P. Bhadauria. 2018. Behaviour and welfare concepts in laying hens and their association with housing systems. Ind. J. Poult. Sci. 53:1. https://doi.org/10.5958/0974-8180.2018.00009.0

    .

    3

    Campler, M., M. Jöngren, and P. Jensen. 2009. Fearfulness in red junglefowl and domesticated White Leghorn chickens. Behav. Process. 81:39–43. https://doi.org/10.1016/J.BEPROC.2008.12.018

    .

    4

    Dİkmen, B. Y. 2014. Laying hen behaviour and welfare in housing systems. 25th Scientific-Experts Congress on Agriculture and Food Industry.

    5

    Hartcher, K. M., and B. Jones. 2017. The welfare of layer hens in cage and cage-free housing systems. World’s Poult. Sci. J. 73:767–782. https://doi.org/10.1017/S0043933917000812

    .

    Statistical Analysis

    Data analyses were carried out using the GLM procedure of SPSS 27 (IBM, Armonk, NY). The study was a completely randomized design, and the experimental unit was an aviary section (N = 3 aviary sections/room). Data were examined for normality and analyzed for interaction between treatment, position in aviary, and main treatment effects, distribution time of day, time post treatment. Statistical significance was considered at P ≤ 0.05. Means were separated with Tukey’s Least Significant Difference Test.

    RESULTS AND DISCUSSION

    Spatial Distribution of Hens

    Spatial distribution results are presented as means ± standard error of the mean (S.E.M). No difference was detected in the spatial distribution of hens before treatments were applied. For the AM application, at min 0 (i.e., immediate time period that followed treatment application), there was a significant difference (P =0.001) between treatments, with DF + UV treatment having the highest difference of hens in floor area (i.e., more hens in the floor area after treatment application) compared to the other treatments (Table 2). At min 1, C, DF, and UV treatments were comparable between one another but had a lower difference (P < 0.001) than DF + UV treatment. Min 2, 3, 4, and 5 followed a similar trend to min 1, meaning C, DF, and UV treatments had a mean comparable between one another but significantly lower than DF + UV (P < 0.001; P = 0.005 in min 5). DF + UV treatment had the overall highest difference of hens located in floor area at each timepoint when compared to the other treatments, with highest occurrence at min 2 (Table 2).

    Table 2. Mean difference of the number of hens (pre- and post-treatment application) located in floor area in AM application.

    Empty Cell Treatments1 Empty Cell
    Min Control ± SEM DF ± SEM UV ± SEM DF+UV ± SEM P-value2
    0 5.3a ± 0.7 27.0ab ± 4.9 37.3b ± 2.4 71.7c ± 13.0 0.001
    1 10.0a ± 3.2 23.0a ± 4.0 38.0a ± 9.2 71.3b ± 7.2 <0.001
    2 11.0a ± 1.5 20.3a ± 6.4 33.0a ± 10.8 102.7b ± 14.2 <0.001
    3 8.7a ± 0.7 13.0a ± 3.5 33.0a ± 6.2 75.0b ± 10.3 <0.001
    4 11.7a ± 4.6 15.3a ± 5.5 30.3a ± 3.7 78.3b ± 10.7 <0.001
    5 13.0a ± 3.6 21.7a ± 6.1 27.0a ± 7.0 67.3b ± 11.9 0.005
    1

    Control=control, nothing was applied; DF=the floor of the system and tier 1 were darkened; UV= UV lights turned on for 10-sec; DF+UV=the floor of the system was darkened plus UV lights turned on for 10-sec.

    2

    Means within a row lacking a common superscript differ (P≤ 0.05).

    For the PM application, at min 0 DF + UV treatment had a higher difference of hens located in floor area (P = 0.017) than C treatment; DF and UV treatments had a similar difference of hens when compared individually to C and DF + UV treatments (Table 3). Min 1, 2 and 4 followed a similar trend from min 0, meaning that a lower difference (P = 0.025 in min 1; P = 0.044 in min 2; P = 0.021 in min 4) was detected in C treatment when compared to DF + UV treatment, but DF and UV treatments had a difference of hens similar to C and DF + UV treatments when compared individually. At min 3 and 5 no significant differences were detected between treatments (P = 0.103 in min 3; P = 0.109 in min 5). In PM application, the DF+UV treatment had an overall higher difference of hens located floor area when compared to C treatment, but was the same compared to other treatments, with exception of min 3 and 5 (Table 3).

    Table 3. Mean difference of the number of hens (pre- and post-treatment application) located in floor area in PM application.

    Empty Cell Treatments1 Empty Cell
    Min Control ± SEM DF ± SEM UV ± SEM DF+UV ± SEM P-value2
    0 12.0a ± 1.2 22.0ab ± 5.0 31.0ab ± 8.3 55.3b ± 11.1 0.017
    1 9.3a ± 2.9 23.7ab ± 5.7 31.0ab ± 7.5 53.0b ± 12.1 0.025
    2 11.3a ± 1.7 26.7ab ± 7.1 29.7ab ± 10.4 47.3b ± 6.6 0.044
    3 15.3 ± 4.7 20.0 ± 4.0 25.0 ± 8.4 37.0 ± 3.5 0.103
    4 9.3a ± 0.9 29.0ab ± 3.8 33.3ab ± 7.8 48.3b ± 10.2 0.021
    5 17.3 ± 2.4 24.0 ± 2.1 39.7 ± 10.3 43.0 ± 10.0 0.109
    1

    Control=control, nothing was applied; DF=the floor of the system and tier 1 were darkened; UV= UV lights turned on for 10-sec; DF+UV=the floor of the system was darkened plus UV lights turned on for 10-sec.

    2

    Means within a row lacking a common superscript differ (P≤ 0.05).

    Based on the location of UV lights (i.e., to stimulate hens’ movement towards the floor area) the UV light may had been perceived as an environmental stressor that was followed by a fleeing response from hens’ movement to the floor area to escape the UV light. There may be 2 possible explanations as to why hens reacted in such a manner. When an animal encounters a short-term challenge (i.e., predation attempt or change to the immediate environment) “the physiological stress response, coordinated by the activation of the hypothalamic-pituitary-adrenal axis, provides an essential mechanism for survival designed to help the animal escape the stressor and return to stable conditions” (Pusch et al., 2018). The first explanation is related to the personality of brown hens (i.e., proactive personality) (Cockrem, 2013; Pusch et al., 2018). Personality is defined here as “birds’ response to changes in their immediate environment that is consistent with individual behavioral and physiological responses” (Cockrem, 2013). Proactive animals tend to have a bold and fast response to unfamiliar environments or stimuli (i.e., quick explorers, less fearful and more aggressive) and produce smaller physiological responses (e.g., corticosterone elevations) to acute stressors (Cockrem, 2013; Pusch et al., 2018).

    A second explanation for the hens’ reaction could be related to the flicker rate of the UV lights. While a statement can be found in the manual of UV lights used, stating that these lights do not flicker, and no flickering was detected by the naked human eye, the avian eye can perceive rapid movements (high flicker fusion frequency) (Rubene et al., 2010; Korbel, 2012; Lisney et al., 2012). Flicker fusion frequency is defined as “the rate of successive light flashes from a stationary light source at which the sensation of flicker disappears, and the light becomes ‘steady’” (Simonson and Brozek, 1952). In the study by Lisney et al., (2012) the retina of adult laying hens was examined, via electroretinograms, to determine whether the chicken retina can detect flicker at higher frequencies. The results showed the retina of hens can at least respond to flicker frequencies in the 100 to 200 Hz range, although Lisney et al., 2011, found that hens do not appear to be able to consciously detect flicker above approximately 90 Hz. The retina’s ability to respond to flicker frequencies higher than 100 Hz may result in distress for the animals (Lisney et al., 2012). Although a light meter was not used to determine if flickering was apparent in the UV lights, there was a quick and effective way this was resolved by, using the slow-motion video setting (240 frames per second) in a standard iPhone. While the frequency of the flicker cannot be determined with this procedure, flickering can be detected and indeed, the UV light did flicker. Therefore, flickering may have caused hens to experience general stress and move to the floor area away from UV light (Greenwood et al., 2004; Lisney et al., 2011). A second plausible explanation, related to light flickering, may give insight as to why hens reacted to such an extent. Rubene et al., (2010) concluded that when some UV light is added to regular white light, birds can detect higher frequencies of flickering light, compared to only white light, meaning that the temporal resolution was enhanced by the addition of UV wavelengths. Because hens in the present study had no prior exposure to UV light, it may be plausible that the UV light flash caused some distress due to improved temporal resolution during those 10-sec.

    When examining the mean difference of hens in floor area between AM and PM application (Table 2 and Table 3, respectively), it is evident that treatments had a stronger effect on hens in the AM application than PM application. A potential justification for this is that in AM application, treatments were novel to hens as they did not have prior exposure to UV lights. In a study conducted by Jones (1977), 909 male chicks were separated into groups that were presented with different rearing cues (red crosses or black circles) on the walls of their home environment from 2 to 7 d old; behaviors were measured during an open field test in absence or presence of familiar rearing cues. After chicks reached 7 d of age, they were tested individually in a test box; the researcher found fearfulness (freezing, sitting time, lying time, and time spent with eyes closed) was reduced in the presence of familiar rearing cue, meaning that familiarity decreased fearfulness (Zajonc et al., 1974; Jones, 1977). An interesting finding was that when chicks were in the presence of their familiar cue, they spent more time drinking and eating, which could potentially support notion that chicks were less fearful (Jones, 1977). Campbell et al. (2016a) studied hen pattern movements between the aviary system and floor area at various times (morning, afternoon, and evening) throughout 2 different flock cycles (peak lay, mid lay, and end of lay). For both flocks, more hens per unit moved from the system onto floor area in the morning period as soon as hens gained access to it; but a higher occupancy of the floor area was more apparent and consistent during afternoon period (Campbell et al., 2016a).

    Light Intensity

    Mean light intensity (lx) in rooms post-treatment application can be found in Table 4. When comparing light intensity between treatments for floor area, there were no differences (P ≥ 0.05) detected. In tier 1, there were differences (P ≤ 0.05) in light intensity detected between all treatments, with DF treatment having lowest light intensity (1.4 ± 0.03 lx) whereas UV treatment had the highest (7.7 ± 0.4 lx). For tier 2, non-UV light treatments had the same light intensity (C = 3.2 ± 0.2 lx; DF = 3.3 ± 0.1 lx) but differed (P ≤ 0.05) from treatments that utilized UV lights (UV = 8.9 ± 0.3 lx; DF + UV = 8.5 ± 0.3 lx). According to Hy-line (2017) technical bulletin published on poultry lighting for egg producers, light intensity (measured in lux, clux or food candles (fc)) is essential for poultry production. High light intensity (above 50 lx) “may cause nervousness and aberrant behavior, while light intensity below 5 lx is too dark to stimulate proper growth and production” (Hy-line, 2017). For laying hens that have been transferred to layer house, an average of 30 lx at the level of feed trough is recommended (Hy-line, 2017). This recommendation differs from broiler production (Aviagen, 2018). Deep et al. (2013) investigated what was the required minimum standard light intensity needed for optimal production and welfare of broilers, the light intensity explored during study were 0.1, 0.5, 1, 5, and 10 lx (broilers were exposed to 40 lx for first 7 d of age before abruptly switching to treatments). Authors concluded that 0.1 lx was inadequate as it led to lower feed intake and overall higher mortality compared to birds exposed to 1,0.5, 5, and 10 lx, whereas 0.5 to 10 lux did not differ on broiler mortality over treatment period (Deep et al., 2013). Additionally, authors recommended that at least 5 lx be maintained for light intensity for optimal production and welfare, whereas anything less than 1 lx reduces overall productivity and welfare (Deep et al., 2013). Based on findings from present study, it can be inferred that the light intensity in treatment rooms, particularly in aviary tiers, was low and not high, meaning light intensity was not high enough to cause aberrant behaviors.

    Table 4. Mean light intensity in the treatment rooms.

    Empty Cell Light intensity (lx)
    Treatment Floor area1 Tier 1 Tier 2
    Control 35.1 ± 0.4 2.9b ± 0.07 3.2a ± 0.2
    DF 34.5 ± 0.2 1.4a ± 0.03 3.3a ± 0.1
    UV 34.9 ± 1.0 7.7d ± 0.4 8.9b ± 0.3
    DF+UV 35.2 ± 0.4 5.2c ± 0.3 8.5b ± 0.3
    1

    Means within a column lacking a common superscript differ (P≤ 0.05).

    Furthermore, observations of hens’ reaction after UV flash were used revealed that hens who had their backs to the UV light, or had their heads in feed trough, did not react to UV light in the same manner as hens who were in direct contact (i.e., fleeing response). Instead, those hens stayed in aviary system looking around being vigilant.

    Behavioral Data Collected From Hens

    The results for behavioral observations after treatments were applied are shown in Table 5. C treatment had, overall, the highest frequency (P = 0.01) of preening behavior when compared to UV treatment and DF + UV treatment but comparable expression to DF treatment. Hens from both UV light treatments had a lower frequency of preening. For perching behavior, there was a significant difference (P ≤ 0.001) between the DF treatment and other treatments, with DF having the lowest frequency of perching. DF and DF + UV treatments were significantly different (P = 0.007) in frequency of dust bathing behavior between one another, but when each is compared to C and UV treatments, they are comparable in frequency. For wing flapping, C and DF treatments were similar but had higher frequency (P ≤ 0.001) compared to UV and DF + UV treatments. Standing alert was highest in UV treatment and DF + UV treatment when compared to C and DF treatments (P ≤ 0.001).

    Table 5. Mean frequency of occurrence for behavioral observation post-treatment application.

    Empty Cell Behaviors
    Treatments Preening Perching Dust bathing Wing flapping Standing alert
    Control 0.33c ± 0.020 0.23b ± 0.017 0.02ab ± 0.006 0.12c ± 0.009 0.08a ± 0.013
    UV 0.23a ± 0.016 0.22b ± 0.012 0.02ab ± 0.006 0.09ab ± 0.005 0.20b ± 0.016
    DF 0.29bc ± 0.010 0.14a ± 0.007 0.04b ± 0.008 0.11bc ± 0.007 0.10a ± 0.009
    DF + UV 0.25ab ± 0.016 0.24b ± 0.011 0.01a ± 0.004 0.08a ± 0.005 0.21b ± 0.016
    P-value1 0.01 <0.001 0.007 <0.001 <0.001
    1

    Means within a column lacking a common superscript differ (P≤ 0.05).

    Overall, UV light influenced the behavior of hens as both groups in rooms with UV lights had lower frequencies of preening and wing flapping (comfort behaviors) but had a higher expression of standing alert (stress behavior), whereas more hens exhibited comfort behaviors in the non-UV light treatments. Interestingly, an increase in preening (comfort behavior) expression was anticipated after UV light utilization as disruption to hen environment occurred (i.e., stressful situation), this occurrence is referred to as displacement behavior. Displacement behaviors such as preening, head shaking or vocalization, are behaviors birds will do to show signs of frustration, stress, and overall discomfort (Duncan and Wood-Gush, 1972; Kuhne et al., 2013). Results from present study demonstrated that although hens in UV treatments exhibited signs of stress (i.e., higher standing alert frequency), hens were still comfortable in the environment as displacement behavior, such as preening, was not apparent. Moreover, Zimmerman et al. (2011) conducted a study in 17-wk old hens to find behavioral expressions specific to the anticipation of a positive, neutral, and negative event. The authors observed that anticipation of a positive event was associated with an increase in comfort behaviors (preening, wing flapping, feather ruffling and body scratching), whereas hens in the negative event showed more head movements and higher locomotion. Although hens in the present study were not anticipating a positive or negative event, it could be inferred that natural comfort behaviors are expressed to reflect how well the animal is feeling in the current environment and why lower frequencies of these behaviors were lowest in both UV treatments (Linares and Martin, 2010; Bhanja and Bhadauria, 2018).

    Domestication may have played a role in hens displaying a higher frequency of standing alert behavior. Domestication is defined as a process by which a population of animals becomes adapted to a captive environment by the combination of genetic changes and environmentally induced developmental events (Price, 2002). The Red Junglefowl is considered the wild ancestor of domestic chickens (Fumihito et al., 1994; Hartcher and Jones, 2017; Tixier-Boichard, 2020). In a study conducted by Campler et al., (2009) domesticated White Leghorn chickens and Red Junglefowl were tested for behavioral reactions to 4 different types of potentially fearful stimuli. Results indicated Red Junglefowl had higher fear levels than White Leghorn across the 4 fear tests and performed more stand/sit alert and less locomotion, fly/jump, and vocalizations. Whether it was a conscious or unconscious decision to select for less fearfulness in chickens, domestication contributes to this phenomenon as indicated by the results presented. However, molecular studies show that a consequence of intensive selection is the loss of genetic diversity at the DNA level (Tixier-Boichard, 2020).

    Overall results indicated that a flash of UV light combined with darkened floors (DF + UV treatment) was the most effective in moving hens out of an aviary system and onto floor area. However, the treatment used might not be effective for long term movement because hen concentration varied within a 6-min observation period.

    CONCLUSIONS AND APPLICATIONS

    • 1.

      Utilization of UV lights coupled with darken floors had a stronger reaction on hens, compared to C, UV, and DF treatments. However, this reaction was observed when DF + UV treatment was novel in AM application and not when it was applied in PM application.

    • 2.

      Although the UV light flash caused hens to concentrate in floor area, the technique of UV flash of 10-sec might not be feasible during mass depopulation procedures as hens did not stay concentrated for longer than 6-min.

    • 3.

      Behavioral differences were seen among the 4 lighting treatments with more comfort behaviors (preening and wing flapping) expressed in non-UV treatments when compared to treatments that utilized UV light.

    • 4.

      Future research should focus on usage of UV lights in preventing undesirable behaviors (i.e., floor eggs and piling) because this technique provoked an immediate reaction from hens. Piling behavior is a common concern in laying hens because it can lead to decreased welfare and productivity; yet this is not a concern in younger chicks because it can aid in thermoregulation (Bright and Johnson, 2011; Campbell et al., 2016b; Gray et al., 2020). However, the consequences for long-term use of UV-light flash are not known and should be further explored.

    ACKNOWLEDGMENTS

    This research was funded by Michigan Alliance for Animal Agriculture (grant number AA-19-050).

    DISCLOSURES

    The authors declare no conflicts of interest.

    REFERENCES

    View PDFView articleCrossRefView in ScopusGoogle ScholarAmerican Association of Avian Pathologists (AAAP) 2021

    American Association of Avian Pathologists (AAAP). (2021). Poultry depopulation guide and decision tree. Accessed Dec. 2022https://aaap.memberclicks.net/assets/Positions/2020_Poultry_Depopulation%20Guide%20FINAL%20%202-11-21.pdf20_Poultry_DepopulationGuideFINAL2-11-21.pdf

    American Veterinary Medical Association AVMA, 2019

    American Veterinary Medical Association (AVMA). (2019). Guidelines for depopulation of animals: 2019 edition. Acessed Dec. 2022. https://www.ipic.iastate.edu/information/NPBfiles/AVMAGuidelinesDepopulationofAnimals2019Edition.pdfidelinesDepopulationofAnimals2019Edition.pdf
    .

    Anderson, 2014

    K.E. Anderson
    Time study examining the effect of range, cage-free, and cage environments on man-hours committed to bird care in 3 brown egg layer strains
    J. Appl. Poult. Res., 23 (2014), pp. 108-115

    View PDFView articleCrossRefView in ScopusGoogle ScholarAviagen, 2018

    Aviagen, Ross broiler management handbook, 2018. Accessed Feb. 2023, Aviagen; Huntsville, AL. Accessed Feb. 2023. https://en.aviagen.com/assets/Tech_Center/Ross_Broiler/Ross-BroilerHandbook2018-EN.pdf
    .
    • Bhanja and Bhadauria, 2018
      S.K. Bhanja, P. Bhadauria
      Behaviour and welfare concepts in laying hens and their association with housing systems
      Indian J. Poult. Sci., 53 (2018), p. 1
    • Brannan and Anderson, 2021
      K.E. Brannan, K.E Anderson
      Examination of the impact of range, cage-free, modified systems, and conventional cage environments on the labor inputs committed to bird care for three brown egg layer strains
      J. Appl. Poult. Res., 30 (2021), pp. 100-118

    Bright and Johnson, 2011

    A. Bright, E.A. Johnson
    Short communications smothering in commercial free-range laying hens: a preliminary investigation
    Vet. Rec., 168 (19) (2011), p. 512

    View in ScopusGoogle ScholarBurkhardt, 1982

    D. Burkhardt
    Birds, berries, and UV
    Naturwissenschaften, 69 (1982), pp. 153-157

    Google ScholarCampbell et al., 2016a

    D.L.M. Campbell, M.M. Makagon, J.C. Swanson, J.M. Siegford
    Laying hen movement in a commercial aviary: enclosure to floor and back again
    Poult. Sci., 95 (2016), pp. 176-187

    View PDFView articleCrossRefView in ScopusGoogle ScholarCampbell et al., 2016b

    D.L.M. Campbell, M.M. Makagon, J.C. Swanson, J.M. Siegford
    Litter use by laying hens in a commercial aviary: dust bathing and piling
    Poult. Sci., 95 (2016), pp. 164-175

    View PDFView articleCrossRefView in ScopusGoogle ScholarCampler et al., 2009

    M. Campler, M. Jöngren, P. Jensen
    Fearfulness in red junglefowl and domesticated White Leghorn chickens
    Behav. Processes, 81 (2009), pp. 39-43

    View PDFView articleView in ScopusGoogle ScholarCockrem, 2013

    J.F. Cockrem
    Corticosterone responses and personality in birds: individual variation and the ability to cope with environmental changes due to climate change
    Gen. Comp. Endocrinol., 190 (2013), pp. 156-163

    View PDFView articleView in ScopusGoogle Scholar

    • de Haas et al., n.d
      de Haas, E., Matthijs, M., Mens, A., Rodenburg, B., & Heerkens, J. (n.d.). Management guide for the care and housing of cage-free egg laying hens in Vietnam.

    Deep et al., 2013

    A. Deep, C. Raginski, K. Schwean-Lardner, B.I. Fancher, H.L. Classen
    Minimum light intensity threshold to prevent negative effects on broiler production and welfare
    Br. Poult. Sci., 54 (2013), pp. 686-694

    View in ScopusGoogle ScholarDİkmen, 2014

    B.Y Dİkmen
    Laying hen behaviour and welfare in housing systems
    25th Scientific-Experts Congress on Agriculture and Food Industry. Accessed Dec. 2022 (2014)

    Duncan and Wood-Gush, 1972

    I.J.H. Duncan, D.G.M. Wood-Gush
    An analysis of displacement preening in the domestic fowl
    Anim. Behav., 20 (1972), pp. 68-71

    View PDFView articleView in ScopusGoogle Scholar

    • Farghly, 2014
      M.F.A. Farghly
      Improvement of productive and reproductive performance of Dandarawi chicken through flash light program
      Egypt. J. Animal. Prod., 51 (2014), pp. 129-144

    Farghly et al., 2017

    M.F.A. Farghly, O.H. El-Garhy, R.M Ali
    Application of flashed lighting program in naked neck chickens (Sharkasi) management. Egypt
    Poult. Sci., 37 (2017), pp. 1063-1089

    Google ScholarFarghly and Makled, 2015

    M.F.A. Farghly, M.N. Makled
    Application of intermittent feeding and flash lighting regimens in broiler chickens management
    Egypt. J. Nutr. Feeds, 18 (2015), pp. 261-276

    View in ScopusGoogle ScholarFumihito et al., 1994

    A. Fumihito, T. Miyake, S.I. Sumi, M. Takada, S. Ohno, N. Kondo
    One subspecies of the red junglefowl (Gallus gallus gallus) suffices as the matriarchic ancestor of all domestic breeds
    Proc. Nat. Acad. Sci. USA, 91 (1994), pp. 12505-12509

    View in ScopusGoogle Scholar

    • Gerpe et al., 2021
      C. Gerpe, A. Stratmann, R. Bruckmaier, J.M. Toscano
      Examining the catching, carrying, and crating process during depopulation of end-of-lay hens
      J. Appl. Poult. Res., 30 (2021), pp. 100-115

    Gray et al., 2020

    H. Gray, R. Davis, A. Bright, A. Rayner, L. Asher
    Why do hens pile? Hypothesizing the causes and consequences
    Front. Vet. Sci., 7 (2020), Article 616836

    Google ScholarGreenwood et al., 2004

    V.J. Greenwood, E.L. Smith, A.R. Goldsmith, I.C. Cuthill, L.H. Crisp, M.B. Walter-Swan, A.T.D. Bennett
    Does the flicker frequency of fluorescent lighting affect the welfare of captive European starlings?
    Appl. Anim. Behav. Sci., 86 (2004), pp. 145-159

    View PDFView articleView in ScopusGoogle Scholar

    Hy-line, 2017

    Hy-line. (2017). Understanding poultry lighting: a guide to LED bulbs and other sources of light for egg production. Accessed Feb. 2023. https://www.hyline.com/ViewFile?id=481427a2-82a3-420f-b830-58eb9b4d3442

    Jones, 1977

    R.B. Jones
    Open-field responses of domestic chicks in the presence or absence of familiar cues
    Behav. Processes, 2 (1977), pp. 315-323

    View PDFView articleView in ScopusGoogle ScholarKnowles and Wilkins, 1998

    T.G. Knowles, L.J. Wilkins
    The problem of broken bones during the handling of laying hens-a review
    Poult. Sci., 77 (1998), pp. 1798-1802

    View PDFView articleCrossRefView in ScopusGoogle Scholar

    Kuhne et al., 2013

    F. Kuhne, A.F.C. Sauerbrey, S. Adler
    The discrimination-learning task determines the kind of frustration-related behaviours in laying hens (Gallus gallus domesticus)
    App. Anim. Behav. Sci., 148 (2013), pp. 192-200

    View PDFView articleView in ScopusGoogle ScholarLewis and Gous, 2009

    P.D. Lewis, R.M. Gous
    Responses of poultry to ultraviolet radiation
    World’s Poult. Sci. J., 65 (2009), pp. 499-510

    Google ScholarLinares and Martin, 2010

    Linares J.A. and Martin M., Poultry: behavior and welfare assessment, Pages 750–756 in Encyclopedia of AnimalBehavior, 2010, doi:10.1016/B978-0-08-045337-8.00088-7
    . Accessed Dec. 2022. Academic Press publishing

    Lisney et al., 2012

    T.J. Lisney, B. Ekesten, R. Tauson, O. Håstad, A. Ödeen
    Using electroretinograms to assess flicker fusion frequency in domestic hens Gallus gallus domesticus
    Vision Res., 62 (2012), pp. 125-133

    View PDFView articleView in ScopusGoogle ScholarLisney et al., 2011

    T.J. Lisney, D. Rubene, J. Rózsa, H. Løvlie, O. Håstad, A. Ödeen
    Behavioural assessment of flicker fusion frequency in chicken Gallus gallus domesticus
    Vision Res., 51 (2011), pp. 1324-1332

    View PDFView articleView in ScopusGoogle ScholarMaddocks et al., 2001

    S.A. Maddocks, I.C. Cuthill, A.R. Goldsmith, C.M. Sherwin
    Behavioural and physiological effects of absence of ultraviolet wavelengths for domestic chicks
    Anim. Behav., 62 (2001), pp. 1013-1019

    View PDFView articleView in ScopusGoogle ScholarMellor and Webster, 2014

    D.J. Mellor, J.R. Webster
    Development of animal welfare understanding drives change in minimum welfare standards
    Rev. Sci. Tech., 33 (2014), pp. 121-130

    View in ScopusGoogle ScholarOchs et al., 2019

    D. Ochs, C.A. Wolf, N.J. Widmar, C. Bir
    Is there a “Cage-Free” lunch in U.S. egg production? Public views of laying-hen housing attributes
    J. Agric. Resour. Econ., 44 (2019), pp. 345-361

    Google Scholar

    • Patel et al., 2016
      S.J. Patel, A.S. Patel, M.D. Patel, J.H. Patel
      Significance of light in poultry production: a review
      Adv. Life Sci., 5 (2016), pp. 1154-1160
    • Price, 2002
      E.O. Price
      Why study domestication?, Pages 1-21 in Animal Domestication and
      Behavior, CABI Publishing, New York, NY USA (2002)

    Pusch et al., 2018

    E.A. Pusch, A.B. Bentz, D.J. Becker, K.J. Navara
    Behavioral phenotype predicts physiological responses to chronic stress in proactive and reactive birds
    Gen. Comp. Endocrinol., 255 (2018), pp. 71-77

    View PDFView articleView in ScopusGoogle Scholar

    • Rana and Campbell, 2021
      M.S. Rana, D.L.M. Campbell
      Application of ultraviolet light for poultry production: a review of impacts on behavior, physiology, and production
      Front. Anim. Sci., 2 (2021), p. 39

    Rubene et al., 2010

    D. Rubene, O. Håstad, R. Tauson, H. Wall, A. Ödeen
    The presence of UV wavelengths improves the temporal resolution of the avian visual system
    J. Exp. Biol., 213 (2010), pp. 3357-3363

    View in ScopusGoogle ScholarSchutkowski et al., 2013

    A. Schutkowski, J. Krämer, H. Kluge, F. Hirche, A. Krombholz, T. Theumer, G.I. Stangl
    UVB exposure of farm animals: study on a food-based strategy to bridge the gap between current vitamin D intakes and dietary targets
    PLoS ONE, 8 (2013), p. e69418

    View in ScopusGoogle ScholarSeifert et al., 2020

    M. Seifert, T. Baden, D. Osorio
    The retinal basis of vision in chicken
    Semin. Cell Dev. Biol., 106 (2020), pp. 106-115

    View PDFView articleView in ScopusGoogle ScholarSimonson and Brozek, 1952

    E. Simonson, J. Brozek
    Flicker fusion frequency background and applications
    Physiol. Rev., 32 (3) (1952), pp. 349-378

    View in ScopusGoogle ScholarTixier-Boichard, 2020

    M. Tixier-Boichard
    From the jungle fowl to highly performing chickens: are we reaching limits?
    World’s Poult. Sci. J., 76 (2020), pp. 2-17

    View in ScopusGoogle ScholarTrejo-Pech and White, 2021

    C.O. Trejo-Pech, S. White
    Egg production: conventional or cage-free?
    CASE J., 17 (2021), pp. 462-493

    View in ScopusGoogle ScholarUnited Egg Producers n.d

    United Egg Producers. (n.d.). Facts & stats. Accessed Dec. 2022. https://unitedegg.com/facts-stats/

    Wichman et al., 2021

    A. Wichman, R. de Groot, O. Håstad, H. Wall, D. Rubene
    Influence of different light spectrums on behaviour and welfare in laying hens
    Animals, 11 (2021), p. 924

    View in ScopusGoogle ScholarUnited Egg Producers, 2017

    United Egg Producers. (2017). Animal husbandry guidelines for U.S. egg-laying flocks. Acessed Feb. 2023 https://uepcertified.com/wp-content/uploads/2019/09/CF-UEP-Guidelines_17-3.pdf

    World Organization for Animal Health OIE, 2022

    World Organization for Animal Health (OIE). (2022) Animal welfare. Accessed Dec. 2022, https://www.woah.org/en/what-we-do/animal-health-and-welfare/animal-welfare/
    • Wilby et al., n.d
      Wilby, D., Toomey, M. B., Olsson, P., Frederiksen, R., Cornwall, M. C., Oulton, R., Kelber, A., Corbo, J. C., and Roberts, N. W. (2015). Optics of cone photoreceptors in the chicken (Gallus gallus domesticus).

    Yan et al., 2014

    F.F. Yan, P.Y. Hester, H.W. Cheng
    The effect of perch access during pullet rearing and egg laying on physiological measures of stress in White Leghorns at 71 weeks of age
    Poult. Sci., 93 (2014), pp. 1318-1326

    View PDFView articleCrossRefView in ScopusGoogle ScholarZajonc et al., 1974

    R.B. Zajonc, H. Markus, W.R. Wilson
    Exposure, object preference, and distress in the domestic chick
    J. Comp. Physiol. Psychol., 86 (1974), pp. 581-585

    View in ScopusGoogle ScholarZimmerman et al., 2011

    P.H. Zimmerman, S.A.F. Buijs, J.E. Bolhuis, L.J. Keeling
    Behaviour of domestic fowl in anticipation of positive and negative stimuli
    Anim. Behav., 81 (2011), pp. 569-577

    View PDFView articleView in ScopusGoogle Scholar