Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2014 Jul 30;9(7):e101877. doi: 10.1371/journal.pone.0101877

Behavioural Repertoire of Working Donkeys and Consistency of Behaviour over Time, as a Preliminary Step towards Identifying Pain-Related Behaviours

Fran H Regan 1, Jo Hockenhull 1, Joy C Pritchard 2,3, Avril E Waterman-Pearson 1, Helen R Whay 1,*
Editor: Martine Hausberger4
PMCID: PMC4116118  PMID: 25076209

Abstract

Background

The donkey has a reputation for stoicism and its behavioural repertoire in clinical contexts is under-reported. Lack of understanding of the norms of donkey behaviour and how it may vary over time can compromise use of behavioural measures as indicators of pain or emotional state. The objective of this study was to find out whether the behaviour of working donkeys was influenced by gender, the time of day or differed between days with a view to assessing how robust these measures are for inclusion in a working donkey ethogram.

Methodology/Principal Findings

Frequency and consistency of postural and event behaviours were measured in 21 adult working donkeys (12 females; 9 males). Instantaneous (scan) and focal sampling were used to measure maintenance, lying, ingestive and investigative behaviours at hourly intervals for ten sessions on each of two consecutive days. High head carriage and biting were seen more frequently in male donkeys than females (P<0.001). Level head carriage, licking/chewing and head-shaking were observed more frequently in female donkeys (P<0.001). Tail position, ear orientation, foot stamping, rolling/lying and head-shaking behaviours were affected by time of day (P<0.001). However, only two variations in ear orientation were found to be significantly different over the two days of observations (P<0.001). Tail swishing, head shaking, foot stamping, and ears held sideways and downwards were significantly correlated (P<0.001) and are assumed to be behaviours to discourage flies.

Conclusions/Significance

All donkeys expressed an extensive behavioural repertoire, although some differences in behaviour were evident between genders. While most behaviours were consistent over time, some behaviours were influenced by time of day. Few behaviours differed between the two test days. The findings can be used to inform the development of a robust, evidence-based ethogram for working donkeys.

Introduction

Donkeys working in developing countries are used for transporting both goods and people, often in extreme heat and humidity, in urban working environments where there are hazards such as heavy traffic, noise, pollution and debris. Working donkeys are usually owned by very poor members of society and seldom receive adequate resources and management to maintain good welfare. During rest periods, donkeys often remain tethered or harnessed alone or in pairs. Consequently, they have little opportunity to engage in truly restorative resting behaviour or to socialise freely.

Domestic donkeys are descended from the African wild ass [1]. Observations of wild ass and populations of feral donkeys provide an insight into donkey behaviour outside of the working environment. The donkey digestive system is very similar to that of the horse, and if unimpeded donkeys will spend a comparable amount of their time grazing, typically 14–16 hours a day [2]. The social organisation of wild ass and feral donkeys can vary with their environment and the resources available [1], [3], [4], with some populations operating resource or territory guarding systems and others guarding females or harems [3]. Although the social lives of working donkeys have yet to be studied, the propensity for donkeys to form pair-bonds or situation –specific groupings demonstrates their social tendencies [5] and lack of opportunity to engage in social behaviour may therefore compromise their welfare further.

Behavioural observation gives the most reliable and immediate insight into the animal's perception of and interaction with its environment [6]. Behavioural divergence from the norm may be clinically significant, for example may indicate pain or pathology. It is likely that many working donkeys suffer from pain associated with multiple acute and/or chronic clinical conditions. Donkeys behave differently to horses [7], and while a number of equid ethograms exist, e.g. [8], they typically focus exclusively on horse behaviour. Little is published regarding the behavioural repertoire of the domestic donkey, particularly under working conditions. As a result, it is challenging to identify when donkey behaviour changes from the norm, compromising the use of behaviour as a welfare indicator in this species.

Research investigating consistency of behavioural parameters has examined natural behaviour and treatment effects in a range of species including horses [9], dairy cows [10], red deer [11] and lambs [12]. Consistency of behaviour can be defined as a percentage agreement between behavioural observations over time. Studying the influence of time on behaviour enables researchers to identify the behaviours most suitable for measurement during short observation periods, making them practical for use in clinical situations.

Diurnal variations in the behaviour of different groups of horses and ponies have previously been investigated, for example see [13] and [14], studies of Przewalski's horse and New Forest ponies respectively. Few peer reviewed studies could be found on diurnal patterns or consistency of measured behaviours in domestic donkeys, although detailed studies of diurnal variations in activity [15] grazing behaviour [16] and physiological measures [17] in small samples of donkeys have been published. Posture and event behaviours have been used in livestock research to assess pain [12], [18], fear [19], [20], distress [21], anxiety and adaptation to novel environments or stimuli [22]. The lack of information regarding the normal behaviour of donkeys hinders progress towards recognition of abnormal behaviour indicative of pain, fear or distress. Improving our understanding of what constitutes normal postural and event behaviours for donkeys will enable us to detect more readily when behaviour diverges from the norm, and facilitate the use of behaviour as an indicator of pain and emotional state in this species.

The study objective was to find out whether the posture and event behaviours recorded in working donkeys were influenced by gender or time of day and whether they differed between consecutive days. In addition, an avoidance test was used to gauge reaction towards approaching humans [23].

Materials and Methods

Ethics statement

The study was carried out in Lahore, Pakistan during November 2005, under ethical approval from the University of Bristol Faculty of Medical and Veterinary Sciences Ethics Committee (Investigation number UB/05/017) and was compliant with Pakistan law regarding ethical use of animals in science.

Donkey selection and acclimatisation to study environment

Twenty-one working donkeys were recruited from within a 15 km catchment area of Shadara fodder market, Lahore. Inclusion criteria for the study included: non-pregnant females, entire males, minimum body condition score of 1.5 (1 (very thin) - 5 (very fat) [24], donkeys over 3 yrs of age but under 10 years, no acute traumatic injury or severe chronic injury, no wounds or minor body wounds only, no obvious lameness, and intact ears and nostrils. Bodyweight was recorded using an electronic weighbridge (Ezi-weigh, Tru-test Ltd, New Zealand). Donkeys were loose-housed individually in 3 m×3 m shaded pen enclosures with both physical and visual contact with another donkey. They were bedded on dry straw, offered water ad libitum and a food ration twice daily of crushed grains and chopped roughage formulated to aid malnourished animals. An acclimatisation period of 18 h enabled animals to recover from any acute stress, fear, hunger or thirst resulting from their daily working lives and familiarised them with the environment prior to starting behavioural observations.

Behavioural observation period

The ethogram used in this study (see Table 1) was developed through pilot studies with working and non-working donkeys and included all possible behaviour that a donkey might display [25]. Behavioural observations were made for ten minutes at hourly intervals (excluding 12:00) for ten sessions on two consecutive days. Behaviours were recorded directly onto a check sheet by a single observer (FHR) seated 3.5 metres outside the pen. Observations consisted of:

Table 1. Ethogram of behaviours observed in domestic (including working) donkeys at rest* organised by the observation type used in the current study.

Category Behaviour Description
Pen Position Back of pen Head and forelimbs in back half of pen (irrespective of orientation)
Front of pen Head and forelimbs in front half of pen (irrespective of orientation)
Postural Behaviours (instantaneous (scan) sampling):
Lying down Lying sternally Lying down on sternum, legs folded underneath body frame
Lying laterally Lying on side with legs outstretched, head and neck may be in contact with ground
Standing Standing on 4 feet Weight-bearing on all 4 limbs with no preferred loading
Standing on 3 feet Weight-bearing on 3 limbs with a hind limb resting
Pointing Placing a foot in a forwards position outside of the main body frame (minimum 1 hoof length) with reduced weight-bearing
Knuckled Forwards bend of one or both fore limbs with the knee bent in front of the placed foot or fetlock joint
Ear position Forwards Both ears facing forwards with ear cups fully visible when facing the donkey head-on
Sideways Both ears facing sideways with ear cup orientated approximately 90 degrees laterally from forwards-facing position
Backwards Both ears facing backwards with ear cups visible when standing behind the donkey
Combinations Each ear in a different orientation, e.g. one facing forwards, one facing backwards
Ear level Down Tip of ear level with or below level of base of ear, drooping downwards in any orientation
Up Tip of ear above base of ear, in any orientation
Head carriage High Poll higher than top of withers
Level Poll level with top of withers
Low Base of ears below top of withers
Very low Nose contact with ground
Head direction No turn Straight head carriage, no turning of head towards self, object or stimuli
Turn to belly Head is turned towards or makes contact with either side of abdomen
Turn to flank Head is turned towards or makes contact with either flank
Turn to limb/foot Head is turned towards or makes contact with either fore/hind limb/foot
Turn to look Head is orientated away from a straight position with attention drawn towards environmental stimuli and not directed towards a body part/region
Tail position Relaxed Tail held in a relaxed position, hanging freely in a vertical line from its body base
Lifted out Tail held in a fixed position, sticking out more than 45 degrees from the vertical line
Tucked Tail held tightly against the rump in a fixed position, with tip of tail tucked between hind legs
Swishing Tail moves swiftly from its base in a side-to-side flicking manner around the hind quarters
Event behaviours (focal sampling):
Body Rolling From lying down laterally or sternally, vigorous rolling and wriggling movement of whole body over onto back
Transition up/down From lying down laterally or sternally to standing, or vice versa
Feet Walking Forwards, backwards or sideways movement of limbs to a new position
Pawing Repetitive lifting and backwards dragging or scraping of pointed hoof
Leg lifting Temporary lifting of any limb from the ground with hesitant replacement near to its original position, often repetitive
Weight shifting Weight temporarily off-loaded from a fore or hind limb onto the remaining 3 limbs, accompanied by subtle body rock
Foot stamping Sudden lifting and forceful replacement of any limb in its original position
Oral Eating Prehension of food into the mouth, with repetitive chewing and swallowing
Drinking Muzzle touches water source followed by at least 1 visible swallow
Sniffing Movement of muzzle towards object, ground or body, followed by inhalation and movement of nostrils
Flehmen response Upper lip curls back to expose gums with incisors meeting, head tips back and rapidly points muzzle upwards
Licking and chewing Repetitive licking and chewing motion in the absence of any food in the mouth
Yawning Mouth opens wide, eyes close, head rises, tips back and shakes, lower jaw grinds and closes
Biting** Grasps object, self or another donkey in open mouth and bites or chews with single or repeated jaw closures
Head Head shaking Vigorous rotational shake of head and neck resulting in ears flapping against sides
Head tossing Rapid up and down movements of neck with successive nods of head
Vocal Snorting Quick forced exhalation of air through nostrils making an audible noise
Braying Series of short duration, loud inhalations, followed by a prolonged noisy exhalation
Sighing Prolonged deep inhalation with a noticeable rise of the body, followed by a short burst of expiration, then gradual release of air
Groaning Similar to a sigh, but accompanied by a monotone prolonged vocalization and often head is turned towards body part
Coughing Distinctive short duration exhalation from the lungs, deep and often moist in sound, often accompanied by a body heave
Maintenance Self grooming Repeated grooming movement of mouth and incisors directed at own body parts
Rubbing Moving a body part against another (e.g. eye rubbing on fore leg) or repeatedly moving a body part back and forth against any object
Stretching Head tucks into neck, mouth opens slightly, eyes often close, whole body contracts and rises up noticeably with inhalation
Dozing State of body stillness with eyes closed, head lowered and standing on all 4 feet, or standing on 3 feet and resting a leg
Eliminative Defaecating Elimination of faeces
Urinating Elimination of urine
Play Playing Lifting up and tipping/ holding objects with mouth, rearing, broncing, bucking or attempted interaction

*NB: the ethogram contains behaviours that may be observed in domestic donkeys, and is not limited to those seen in working donkeys and/or those that were possible in the context of this study.

**The donkeys in this study did not have physical access to other donkeys during the observation period; therefore biting in this context refers to biting objects or self.

  1. instantaneous (scan) sampling at one minute intervals throughout each ten minute observation period, recording the anatomical components of posture (ear orientation, head carriage, feet position, and tail carriage), general activity category (standing, walking, lying, rolling, and eating) and the donkey's location in the pen (front or back; standing at the front of the pen would allow visual contact with other donkeys) at the scan time point.

  2. focal sampling of pre-defined event behaviours, such as snorting, braying and leg lifting, recording all occurrences throughout the 10 minute period. Some event behaviours were recorded if a single occurrence was observed (for example cough, snort, leg-lift), and others if the behaviour continued for a minimum of 3 s (such as licking/chewing, body-rubbing, walking).

The ethogram (Table 1) is organised to reflect the two types of observations made in the study.

Avoidance tests

An avoidance test was developed by adapting measures of fear in livestock [26], [27]. Following pilot testing, score system [27] was modified so that the observer (FHR) approached each donkey, loose within its pen, from a distance of 3 meters by walking slowly towards the side (shoulder area) of the donkey avoiding direct eye contact. The stage at which the donkey withdrew was then scored (for description of scores see Table 2). The avoidance test was carried out once during the acclimatisation period and twice a day at 12 hour intervals (before and after behavioural observations) on the two consecutive test days.

Table 2. Descriptors used to score reaction to the avoidance test in working donkeys, modified from [22].

Score Description
−1 Donkey does not allow observer to enter pen, aggression displayed
0 Donkey withdraws at observer's approach (1 metre)
1 Donkey allows observer to approach but withdraws at shoulder touch
2 Donkey allows observer to touch shoulder but withdraws at head touch
3 Donkey allows observer to touch head and does not withdraw

Statistical Analysis

All data were converted into total number of observations of each posture or event behaviour per 10 minute observation period and per day for each donkey. Data were not normally distributed, so non-parametric tests were used for all analyses. Data were tested for significant gender differences using the Mann-Whitney U test. Friedman analysis of variance (ANOVA) with chi-squared statistic was used to investigate the effect of time of day on observed behaviours. The Wilcoxon Signed Rank test was used to test for differences between matched observation periods on day 1 and day 2. Kendalls coefficient of concordance was used to look for associations within groups of behaviours hypothesised to be related to each other. Statistical analysis was performed using SPSS version 19.0 (SPSS Inc., Illinois, USA) and the significance level was set at P<0.05. Holm's sequentially rejective multiple test procedure [28] was used to reduce the risk of Type I errors through the multiple tests conducted, with only the variables meeting the adjusted P value denoted by the procedure retaining their significance and being reported as such.

Results

Body condition and body weight

The mean +/− s.d. age of the 21 donkeys in years was 5.7+/−1.7. Mean bodyweight was 120 kg+/−19 and the median body condition score was 2: thin (min = 1 very thin, max = 2.5 thin/medium). There were no significant differences in bodyweight (Mann Whitney U = 43.5; median male 116.5 kg; median female 118 kg; P = 0.464), age (Mann Whitney U = 53; median male 5 years; median female 6 years; P = 0.972) and body condition score (Mann Whitney U = 56.5; median male 2; median female 1.75; P = 0.862) between male and female donkeys.

Behaviour

During the observation period the donkeys stood for a median (min-max) of 78.4% (48.2–94.5%) of the sampling points. Walking was observed for a median of 5.7% (1.6–13.4%) and lying for 12.3% (0–40%) with some donkeys not seen lying at all. A median of 56.6 (20.0–84.0) occurrences of eating behaviour were observed throughout the period. Maintenance behaviours, such as rolling, self-grooming and stretching were rarely observed with medians of 0.9 (0–6.8%), 3.5 (2–10 occurrences) and 0 (0–1.5 occurrences) respectively.

Behaviour: effect of gender

Table 3 shows behaviours which differed significantly between male and female donkeys. Standing, walking, lying, rolling, head turning, tail position and location in pen were not influenced by gender. Some patterns were found with head carriage: female donkeys held their heads in the level position (poll level with withers) (Mann-Whitney U = 339.5; P<0.001) more frequently than male donkeys. Male donkeys more frequently held their heads in the high position (poll above withers) (Mann-Whitney U = 39.0; P<0.001), indicating a more vigilant posture. Lying and maintenance behaviours were unaffected by gender. Biting (Mann-Whitney U = 120.0; P<0.001) was more frequently demonstrated by male donkeys while head-shaking (Mann-Whitney U = 325.0; P<0.001) and licking/chewing were seen more frequently in females (Mann-Whitney U = 387.0; P<0.001).

Table 3. Postural and event behaviours significantly more frequently observed in male (n = 9) or female (n = 12) working donkeys (bold cells denote gender where the behaviour was most frequently observed).

Behaviour Mann-Whitney U statistic (significance, p) Male donkeys Median (min-max) Female donkeys Median (min-max)
Postural behaviours:
High head carriage 39.0 (<0.001) 18.18 (0–100) 4.54 (0–90.91)
Level head carriage 399.5 (<0.001) 18.18 (0–90.91) 40.91 (0–100)
Event behaviours:
Licking and chewing 387.0 (<0.001) 0 (0–5) 1 (0–10)
Head shaking 325.0 (<0.001) 0 (0–9) 1 (0–12)
Biting object/self 120.0 (<0.001) 0 (0–13) 0 (0–0)

Behaviour: effect of time

Table 4 shows the behaviours which were significantly affected by the time of day. Tail position (relaxed, tucked and swishing) and ear orientation (one ear forwards, one sideways; one sideways, one backwards; and both ears sideways and facing down) differed significantly across the day (Friedman χ2 =  from 33.8 to 204.3; P<0.001). Lying down/rolling and foot stamping were also significantly affected by time of day. The majority of event behaviours were consistent over time, with the exception of head-shaking which was influenced by time of day (Friedman χ2 = 91.7; P<0.001).

Table 4. Postural and event behaviours which differed in frequency within a single day in 21 working donkeys.

Behaviour Number of observations for all time points on 2 consecutive days Median (min-max) Difference in frequency of observations between 10 time points across a single day Friedman ANOVA with Chi squared statistic (significance, p)
Postural behaviours:
General
Lying down/rolling 0 (0–95.45) 36.869 (<0.001)
Tail position
Relaxed 47.73 (0–100) 111.502 (<0.001)
Tucked 0 (0–100) 41.011 (<0.001)
Swishing 40.91 (0–95.45) 204.296 (<0.001)
Feet position
Foot stamping 0 (0–22.73) 39.346 (<0.001)
Ear orientation
Combination: FF/SS 0 (0–22.73) 40.431 (<0.001)
Combination: SS/BB 0 (0–22.73) 33.831 (<0.001)
Combination: SD/SD 0 (0–100) 51.276 (<0.001)
Event behaviours:
Head shaking 0 (0–12) 91.692 (<0.001)

Ear orientation: FF/SS  =  one ear forwards, one sideways; SS/BB  =  one ear sideways, one backwards; SD/SD  =  both ears sideways and facing down.

Only two measures were found to significantly differ across the two test days: both ears sideways (Wilcoxon −3.945; median Day 1 = 18.18, median Day 2 = 13.64; P<0.001) and both ears sideways and down (Wilcoxon 3.602; median Day 1 = 18.18, median Day 2 = 22.73; P<0.001). All other postural behaviours and event behaviours were consistent across the test days.

Using the Kendall's coefficient test, foot-stamping, tail swishing, ears held sideways facing down and headshaking were all positively associated with each other (R = 0.780, P<0.001).

Avoidance scores

Three female donkeys did not let the observer enter the pen to start the test on each test session and so scored −1 for each test. For those that did let the observer start the test, avoidance scores did not differ significantly with time of day (Wilcoxon 1242.0; median am = 3, median pm = 3; P = 0.242) or the day of testing (Wilcoxon 1714.0; median day 1 = 3, median day 2 = 3; P = 0.184). There was a significant difference in avoidance test scores between genders (Mann-Whitney U = 1162.5; median male = 3, median female = 2; P = 0.003)

Discussion

The results of this study confirm that donkeys have an extensive behavioural repertoire, as found in previous studies [25], although some behaviours are observed much more frequently than others. Several behaviours varied between male and female donkeys and this should be accounted for when assessing behavioural signs of pain in working donkeys. Some behaviours of working donkeys are not consistent over time, which may make them unsuitable for use in a tool for recognising pain behaviour in clinical situations.

The donkeys spent the majority of the observational period standing with very little time spent on maintenance behaviours. Gender-specific patterns for a number of postural and event behaviours were found, with the strongest differences seen in head carriage. In male donkeys high head carriage and biting were seen, suggesting a focus on the external environment. These are components of a normal social and sexual behaviour repertoire [29], [30] and are indicative of the male donkeys' strong motivation to investigate surroundings and interact with con-specifics. Female donkeys appeared to be less focused on the external environment than the males, expressed by their level head carriage. Headshaking was significantly more frequent in females and may suggest that they react more vigorously than male donkeys to the presence of flies. No comparable published behavioural research could be found, therefore the results of this study can only be considered in the context of this study group and environment.

This study has also helped refine the working donkey ethogram by investigating changes in behaviours over time, enabling inclusion of the behaviours which are most robust and useable in the field at any time of day. The majority of foot and limb positions, head carriage positions and event behaviours were found to be consistent over time. Strong time-dependent effects on headshaking, foot stamping and tail swishing were hypothesised to be due to the presence of flies, which was greatest in the middle of the day, although in this study fly levels were not recorded directly. This supports the finding that free ranging Przewalski's horses increase their activity and feeding budgets at night compared to daytime levels in the summer months, due to high temperatures and disturbance by flying insects [13]. Lying down/rolling varied significantly across the eleven hour observation period. In a study of adult feral donkeys in California lying posture during daylight hours in hot months was never observed, suggesting that donkeys may change their lying behaviour to reduce the risk of heat stress [30]. The donkeys in the present study also spent a relatively short time lying down during the daylight observation periods; although they were observed informally to be recumbent during hours of darkness. Working donkeys are rarely allowed to rest un-harnessed and have little or no opportunity to lie down during a typical day, which may contribute to chronic fatigue.

Only two variants of ear orientation were found to differ significantly across test days, with the remaining postural and all event behaviours proving to be consistent. This provides strong evidence for the robustness of these behaviours over time and their inclusion in a working donkey ethogram.

Behavioural observations in the current study were limited to daylight hours; pilot studies using video-recording of behaviour at night were unsuccessful due to an erratic power supply. Observation of behaviour over only two consecutive days was a further limitation caused by the need to return donkeys to their owners after a relatively short period of time. However, the behaviour observed would not be expected to change markedly given an extended observation period.

The avoidance scoring method generated results comparable with previous research. The present study found that 57% of donkeys achieved the top score (allowing their head to be touched by an approaching observer), in agreement with the 56% of working donkeys rated in a previous study [24] as either non-responsive or eliciting a friendly response. The present study found that 24% of donkeys showed a negative reaction (aggression towards or avoidance of the test observer), fewer than the 44% of donkeys reported by [24] although still a cause for concern. This could be due to the difference in test environments: donkeys in the current study were loose in a pen, having rested, eaten food and received gentle handling (i.e. avoiding practices commonly seen during the donkey's working day such as shouting, slapping and hitting the donkeys with sticks) prior to testing, while the donkeys in the previous study described above [24] were scored as found during their working day. A consistent negative avoidance test score (−1) was exhibited by three of the 21 donkeys in the present study and the observer could not safely enter the pen to start the test. Prolonged or persistent fear can be a serious compromise to an animal's welfare and can result in depression, chronic fatigue, restlessness and anorexia [31]. Female donkeys scored significantly lower in the test than males and the three donkeys that consistently had a negative score in the avoidance tests were all female. Gender differences in emotional reactivity have been identified in horses, with mares being more easily panicked and aggressive than geldings [32]; our findings suggest similar gender differences in donkeys.

This study has confirmed that working donkeys have a large behavioural repertoire and identified some behaviours which lack diurnal consistency in their expression. Few behaviours varied significantly across the test days indicating that time of day has a greater impact on behaviour observed than the day itself. This should be taken into consideration in future observational studies.

Acknowledgments

The authors would like to thank the Brooke for supporting this project, Brooke Pakistan staff in Lahore for their assistance, and all the owners who allowed their donkeys to be used in this study. We would also like to thank the academic editor and anonymous reviewers for their constructive feedback on the earlier version of this manuscript.

Funding Statement

The authors received funding from a UK based working equine charity called “The Brooke.” One author (JCP) who contributed to preparation of the manuscript is employed part-time for The Brooke, independently of the current work which was carried out under her second affiliation. The funder had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.

References

  • 1.Rudman R (1998) The social organisation of feral donkeys (Equus asinus) on a small Caribbean island (St. John, US Virgin Islands). Appl Anim Behav Sci 60 211–228.
  • 2.Smith D, Wood S (2008) Donkey Nutrition In The Professional Handbook of the Donkey 4th Ed. Yatesbury: Whittet Books.
  • 3.Moehlman PD (1998) Feral asses (Equus africanus): intraspecific variation in social organization in arid and mesic habitats. Appl Anim Behav Sci 60: 171–195. [Google Scholar]
  • 4.Klingel H (1998) Observations on social organization and behaviour of African and Asiatic Wild Asses Equus africanus and Equus hemionus Appl Anim Behav Sci 60: 103–113. [DOI] [PubMed] [Google Scholar]
  • 5. Murray LMA, Byrne K, D'Eath RB (2013) Pair-bonding and companion recognition in domestic donkeys, Equus asinus. Appl Anim Behav Sci 143: 67–74. [Google Scholar]
  • 6. Gonyou HW (1994) Why the study of animal behaviour is associated with the animal welfare issue. J Anim Sci 72: 2171–2177. [DOI] [PubMed] [Google Scholar]
  • 7.McGreevy PD (2004) Equine Behavior: a guide for veterinarians and equine scientists. Edinburgh: Saunders.
  • 8.McDonnell S (2003) A practical field guide to horse behaviour – The equid ethogram. Lexington: The Blood Horse Inc.
  • 9. Visser EK, Van Reenen CG, Hopster H, Schilder MBH, Knaap JH, et al. (2001) Quantifying aspects of young horses temperament: consistency of behavioural variables. Appl Anim Behav Sci 74: 241–258. [Google Scholar]
  • 10. Schrader L (2002) Consistency of individual behavioural characteristics of dairy cows in their home pen. Appl Anim Behav Sci 77: 255–266. [Google Scholar]
  • 11. Chaya W, Pollard J, Littlejohn R (2006) A note on stability of behavioural reactions to handling in red deer hinds and their calves. Appl Anim Behav Sci 101: 177–182. [Google Scholar]
  • 12. Molony V, Kent JE (1997) Assessment of acute pain in farm animals using behavioural and physiological measurements. J Anim Sci 75: 266–272. [DOI] [PubMed] [Google Scholar]
  • 13. Berger A, Scheibe KM, Eichhorn K, Scheibe A, Streich J (1999) Diurnal and ultradian rhythms of behaviour in a mare group of przewalski horse (Equus ferus przewalski) measured through one year under semi-reserve conditions. Appl Anim Behav Sci 64: 1–17. [Google Scholar]
  • 14.Tyler SJ (1972) The behaviour and social organisation of the New Forest Ponies. Anim Behav Monographs 5: , 85–196. [Google Scholar]
  • 15. Canacoo EA, Avornyo FK (1998) Daytime activities of donkeys at range in the coastal savanna of Ghana. Appl Anim Behav Sci 60: 229–234. [Google Scholar]
  • 16. Lamoot I, Callebauta J, Demeulenaerea E, Vandenberghea C, Hoffmann M (2005) Foraging behaviour of donkeys grazing in a coastal dune area in temperate climate conditions. Appl Anim Behav Sci 92: 93–112. [Google Scholar]
  • 17. Ayo JO, Dzenda T, Zakari FO (2008) Individual and Diurnal Variations in Rectal Temperature, Respiration, and Heart Rate of Pack Donkeys during the Early Rainy Season. J. Equine Vet. Sci 28: 281–288. [Google Scholar]
  • 18. Hay M, Vulin A, Genin S, Sales P, Prunier A (2003) Assessment of pain induced by castration in piglets: behavioural and physiological responses over the subsequent five days. Appl Anim Behav Sci 82: 201–218. [Google Scholar]
  • 19. Rushen J, Taylor AA, de Passille AM (1999) Domestic animals fear of humans and its effect on their welfare. Appl Anim Behav Sci 65: 285–303. [Google Scholar]
  • 20. Andersen IL, Boe KE, Foerevik G, Janczak A, Bakken M (2000) Behavioural evaluation of methods for assessing fear responses in weaned pigs. Appl Anim Behav Sci 69: 227–240. [DOI] [PubMed] [Google Scholar]
  • 21. Thornton PD, Waterman-Pearson AE (1999) Quantification of the pain and distress responses to castration in young lambs. Res Vet Sci 66: 107–118. [DOI] [PubMed] [Google Scholar]
  • 22. Hemsworth PH, Price EO, Borgwardt R (1996) Behavioural responses of domestic pigs and cattle to humans and novel stimuli. Appl Anim Behav Sci 50: 43–56. [Google Scholar]
  • 23. Burn CC, Dennison TL, Whay HR (2010) Relationships between behaviour and health in working horses,donkeys, and mules in developing countries. Appl Anim Behav Sci 126: 109–118. [Google Scholar]
  • 24. Pritchard JC, Lindberg AC, Main DCJ, Whay HR (2005) Assessment of the welfare of working horses, mules and donkeys, using health and behaviour parameters. Prev Vet Med 69: 265–283. [DOI] [PubMed] [Google Scholar]
  • 25.Ashley FH, Waterman-Pearson AE, Whay HR (2006) Development of an ethogram to record potential behavioural indicators of pain in working donkeys. In: Proceedings of the 5th International Colloquium on Working Equines, 28th October-3rd November, Addis Ababa, Ethiopia. pp. 15–23.
  • 26. Rousing T, Waiblinger S (2004) Evaluation of on-farm methods for testing the human-animal relationship in dairy herds with cubicle loose housing systems. Test- retest and inter-observer reliability and consistency to familiarity of test person. Appl Anim Behav Sci 85: 215–231. [Google Scholar]
  • 27. Rousing T, Ibsen B, Sorensen JT (2005) A note on: On-farm testing of the behavioural response of group-housed calves towards humans: test-retest and inter-observer reliability and effect of familiarity of test person. Appl Anim Behav Sci 94: 237–243. [Google Scholar]
  • 28. Holm S (1979) A simple sequentially rejective multiple test procedure. Scand J Stat 6: 65–70. [Google Scholar]
  • 29. Henry M, Lodi LD, Gastal MMFO (1998) Sexual behaviour of domesticated donkeys (Equus asinus) breeding under controlled or free range management systems. Appl Anim Behav Sci 60: 263–276. [Google Scholar]
  • 30. Moehlman PD (1998) Behavioural patterns and communication in feral asses (Equus africanus). Appl Anim Behav Sci 60: 125–169. [Google Scholar]
  • 31.Gregory NG (2004) Anxiety and Fear. In: Physiology and behaviour of animal suffering. Oxford: Universities Federation for Animal Welfare, Blackwell Publishing.
  • 32.Gilkeson J, Duberstein KJ (2009) Determination of gender differences in trainability in yearlings. J. Equine Vet. Sci. 29: , 491–493. [Google Scholar]

Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES