Abstract
Background
Variation in management across elephant camps likely has differential effects on the well-being of elephants.
Methods
This study calculated body condition, foot health and skin wound scores (WSs) for 122 elephants from 15 elephant camps in Chiang Mai province, and examined relationships to management factors using a multi-variable modeling approach.
Results
The majority of elephants had high body condition scores (BCS) indicative of being overweight or obese, mild foot problems, but few visible wounds. Females had higher BCSs than males, as did elephants provided a water source at night. Increasing age was associated with higher foot and WSs. Higher WSs were observed in about a quarter of the cases where mahouts carried a hook. Wounds related to saddle riding were rare. Elephants that rested on sand floors at night had a decreased risk of high WSs compared to elephants that rested on compact dirt floors.
Discussion
Findings emphasize the need for elephant camps to adjust management activities that negatively affect body condition (e.g., feeding too many sweet treats), foot health (e.g., hard substrates) and wounding (e.g., misuse of equipment) to improve health and welfare of this population.
Keywords: Health, Welfare, Management, Asian elephant, Thailand, Elephant camp
Introduction
The elephant is important to Thai society and has been a national icon for centuries. Initially used for teak harvesting following a 1989 logging ban, elephants were brought in to permanent camps that catered to tourists by providing rides, animal encounters and entertainment through shows (Bansiddhi et al., 2019). Today, there are 3,783 captive elephants in Thailand with almost 95% of them privately owned (Asian Elephant Specialist Group, 2017). According to data sources from the National Institution of Elephant Research and Health Service, in 2017 there were 2,673 elephants working in 223 tourism venues throughout the country. Chiang Mai is the largest city in the north and has the highest numbers, with 892 elephants in 82 venues (Bansiddhi, 2019).
The welfare of captive elephants has been a recent topic of debate among animal managers, conservationists, scientists, the general public, animal welfare/rights groups and the media. Common concerns centering on the welfare of elephants in tourism in particular are complex in their nature and impact, and call for urgent scientific evaluation to identify realistic solutions to ensure the sustainable and ethical management of captive elephants in the future (Asian Captive Elephant Working Group, 2017). In Thailand, the conditions for working elephants and their access to accommodation, appropriate food and veterinary care are highly variable (Duffy & Moore, 2011), with no enforceable standards. Our survey of elephant camps in northern Thailand revealed considerable variation in management practices; that is, work activities (e.g., feeding, bathing, walking, riding and shows) and hours, housing and rest areas, floor types during the day and night, chaining restraint, use of hooks, diets and nutrition, feeding regimens and watering (Bansiddhi et al., 2018). Such variation likely has differential effects on the well-being of these elephants, which can be assessed through evaluations of welfare indicators like body condition, foot health and wounding.
In recent years, studies of management factors related to the health and welfare of elephants have been conducted in western zoo settings, identifying obesity, poor foot health, ovarian acyclicity and stereotypies as significant problems (Carlstead et al., 2013; Harris, Sherwin & Harris, 2008). A recent epidemiological approach in the U.S. evaluated husbandry and management factors impacting animal-based indicators; that is, physical (body condition, foot and musculoskeletal health), behavioral (stereotypies, walking, recumbence) and physiological (ovarian cycling, prolactin, cortisol) outcomes. Results suggest that, for zoo elephants, good welfare is supported by exercise and walking opportunities, unpredictable feeding schedules, natural substrates, large and compatible social groups, high diversity in feeding and enrichment, large and complex enclosures, and positive elephant-keeper relationships (Greco et al., 2017; Haspeslagh et al., 2013; Meehan et al., 2016; Morfeld & Brown, 2017).
A few studies have examined factors affecting the welfare of tourist elephants in Asia, but none comparable to the large-scale zoo studies. In India, Varadharajan, Krishnamoorthy & Nagarajan (2016) examined husbandry practices and daily routines, including the type of activity (e.g., ceremonial rituals), conspecific socialization, duration of chaining, resting, feeding, bathing, walking and drinking. They found that stereotypic behavior (i.e., weaving, head bobbing and pacing) significantly increased with daily rituals in temples, resting and to some extent feeding. It was suggested that elephants become frustrated with performing daily rituals and when chained during non-working time. In Thailand, a study conducted two decades ago by Chatkupt, Sollod & Sarobol (1999) assessed body condition of elephants in Chiang Mai, Phuket, Bangkok and Ayutthaya. Body condition was better in elephants from Chiang Mai where elephants usually received adequate shade, were housed on softer surfaces, and tended to work fewer hours. Common health problems associated with working conditions in Thailand are wounds, particularly those associated with riding and restraint equipment. Magda et al. (2015) found the prevalence of cutaneous lesions in anatomical regions in contact with saddle-related equipment (i.e., neck, girth, back, tail) was related to the use of rice sacks as padding material, longer working days and the provision of a break (possibly because elephants with active lesions were rested more often). Another effect of work and husbandry practices on captive elephants is foot problems (Angkawanish et al., 2009; Lahiri-Choudhury, 2008). Chronically wet or dirty conditions and steep inclines on trekking trails present physical hazards that can damage the elephants’ feet (Chatkupt, Sollod & Sarobol, 1999).
Given the need for more comprehensive, objective, science-based evaluations of elephant welfare in tourism, the objectives of this study were to: (1) assess body condition, foot health and the prevalence of skin wounds of elephants used in tourism in Northern Thailand; and (2) determine how these health parameters are related to tourist camp management factors using a multi-variable modeling approach.
Materials and Methods
Study animals and work activities
This study was approved by the Institutional Animal Care and Use Committee, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, Thailand (license number; S43/2559). All experiments were performed in accordance with relevant guidelines and regulations. Data were obtained on 122 healthy elephants (33 males and 89 females) from 15 elephant camps in Chiang Mai (Table 1). The age of elephants ranged from 5 to 65 years. There were five types of work or tourist activities that elephants were involved in (Table 1): riding with a saddle, riding bareback, no riding but some tourist interactions, observation only, and elephant shows as described by Bansiddhi et al. (2018). There were five elephants from two camps that did not work or interact with tourists at all. One was a bull used only for breeding that was tethered most of the time in a shed structure and walked ∼1 km for exercise and to forage for 25 min/day. Four elephants were too aggressive to engage in any camp activities. They were kept in a nearby camp under the control of their mahouts during the day, in enclosures at night, and were walked for 20–30 min/day (∼2 km).
Table 1. Summary of elephants in 15 elephant camps in Chiang Mai province.
Camp No. | Number of total elephants | Number of participating elephants | Number of elephants in each type of work | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Male | Female | Total | Riding with a saddle | Riding bareback | No riding | Observation | Show | No work | ||
1 | 4 | 0 | 3 | 3 | 3 | |||||
2 | 5 | 2 | 3 | 5 | 5 | |||||
3 | 5 | 0 | 4 | 4 | 4 | |||||
4 | 6 | 0 | 5 | 5 | 5 | |||||
5 | 6 | 2 | 3 | 5 | 1 | 3 | 1 | |||
6 | 7 | 1 | 4 | 5 | 5 | |||||
7 | 9 | 0 | 5 | 5 | 4 | 1 | ||||
8 | 10 | 1 | 5 | 6 | 3 | 3 | ||||
9 | 15 | 1 | 5 | 6 | 6 | |||||
10 | 35 | 3 | 9 | 12 | 12 | |||||
11 | 46 | 5 | 9 | 14 | 13 | 1 | ||||
12 | 52 | 6 | 6 | 12 | 10 | 2 | ||||
13 | 65 | 0 | 15 | 15 | 4 | 7 | 4 | |||
14 | 66 | 6 | 6 | 12 | 12 | |||||
15 | 76 | 6 | 7 | 13 | 12 | 1 | ||||
Total | 33 | 89 | 122 | 40 | 46 | 20 | 7 | 4 | 5 |
Questionnaire interviews
Elephant camps were a subset of those in a previous study (Bansiddhi et al., 2018). Questionnaire interviews with camp owners, managers, and/or camp veterinarians were performed to record information about camp activities, location, programs for tourists, numbers of elephants and elephant management (e.g., nutrition, feeding, water, rest area, working and health care) (S1). Questionnaire interviews with mahouts gathered information on management of their specific elephants: work routine, restraint, rest area, feeding, watering and health care (S2). Interviewers and observers were veterinarians experienced in working with captive elephants from the Faculty of Veterinary Medicine, Chiang Mai University.
Physical health and welfare parameters
Elephants were examined every 2–3 months for a total of six times between February 2016 and May 2017, and given scores for body condition, foot health and skin wounds. One author (PB) performed all veterinary examinations. At the time of each examination, current management and work activity information was recorded for each elephant.
Body condition score
A 5-point scale developed by Morfeld et al. (2016) was used to assess a body condition, with 1 representing the lowest and 5 representing the highest levels of body fat.
Foot health score
Foot health was scored using a scale adapted from Harris, Sherwin & Harris (2008) and the British and Irish Association of Zoos and Aquariums Elephant Welfare Group described by Todd (2015) (Table 2). Each foot was given a score of 0 (no problem), 1 (mild problems), 2 (moderate problems) or 3 (severe problems). The overall score of each elephant was the highest score from all four feet as described by Todd (2015). The number, location and direction of nail cracks were noted.
Table 2. Scoring system for assessing foot health adapted from Harris, Sherwin & Harris (2008) and the British and Irish Association of Zoos and Aquariums (BIAZA) Elephant Welfare Group as described by Todd (2015).
Score | Description |
---|---|
0 (normal) | No lesions, normal nails |
1 (mild) | Uncomplicated nail cracks (small cracks which did not extend into the cuticle), mild overgrowth of nails or cuticles, mild dry cuticles, mild disfigured nails or mild injuries |
2 (moderate) | Complicated nail cracks (nail cracks exposing underlying tissue), moderate overgrowth of nails or cuticles, moderate dry cuticles, infection or moderate injuries |
3 (severe) | Underlying tissues exposed plus evidence of purulent discharge, deep pododermatitis, nail loss or severe injuries |
Wound score
The wound score (WS) scale was developed by Schein et al. (2013) (Table 3). Each elephant was given a score of 0 (no wound), 1 (minor wounds), or 2 (major wounds). The number, location, types and causes of any open wounds were noted. Wounds were classified into six types: abrasion (the epidermis has been rubbed off); ulcer (a local excavation of the tissue surface that contains inflammatory exudate); abscess (a collection of pus enclosed in an area of inflamed tissue); laceration (irregular shaped wound with possible tissue loss); penetrating (a wound caused by a sharp, usually slender object that passes through the skin into the underlying tissues); and incision (a cut in the skin caused by sharp, cutting materials) (Scorer, 2014; Studdert, Gay & Blood, 2011).
Table 3. Scoring system for assigning wound scores based on Schein et al. (2013).
Score | Description |
---|---|
0 | No lesions |
1 (minor) | Minor wounds such as scrapes, scratches, superficial wounds or mild bleeding, some serous discharge |
2 (major) | Major wounds such as severe bleeding, severe infection with pus, deep destruction of tissue, exposing muscle or bone |
Statistical analysis
Median and percentage data were calculated for body condition, foot health and skin WSs. Generalized estimating equations (GEE) were conducted for fitting marginal regression models using an R program (R Development Core Team, 2018), package multgee, function ordLORgee, which is appropriate for repeated multinomial variables with ordinal response categories (Touloumis, 2015) like the factors associated with physical health and welfare. Mean ± SD and range were used to describe the continuous variables. Management factors were selected as covariates in relation to Body condition score (BCS), Foot health score (FS) and WS (Table 4). Selection of variables for BCS and FS was adapted from Morfeld et al. (2016) and Miller, Hogan & Meehan (2016), respectively. Camps were treated as random effects. The selection process began by a univariate analysis of each variable. Any variable having a significant univariate test at P < 0.15 was selected as a candidate for the multivariate analysis, statistical significance for which was set at P < 0.05. Sex and Age were included in the multivariate model as confounders. Outputs from the GEE analysis were interpreted by using Odds Ratio (OR), which were calculated by the exponential value of the estimate.
Table 4. Explanatory variables for GEE models of body condition score (BCS), foot score (FS), and wound score (WS), and descriptive statistics of the continuous variables.
Variable name | Description | Mean ± SD | Range | GEE Models | ||
---|---|---|---|---|---|---|
BCS | FS | WS | ||||
Sex | Female or male | ✓ | ✓ | ✓ | ||
Age | Age of elephant (years) | 33.9 ± 11.2 | 5–65 | ✓ | ✓ | ✓ |
Work hour | Duration of work when elephants interacted with tourists per day (h) | 5.3 ± 2.1 | 0–9 | ✓ | ✓ | ✓ |
Chain hour | Duration of chaining per day (h) | 14.9 ± 7.3 | 0–23.5 | ✓ | ✓ | |
Walk distance day | Walking distance during working period per day (m) | 4,215.0 ± 3,295.8 | 10–12,000 | ✓ | ✓ | ✓ |
Walk time day | Walking time during working period per day (min) | 121.2 ± 86.3 | 10–450 | ✓ | ✓ | ✓ |
Roughage day | Amount of roughage per day (kg) | 142.7 ± 55.8 | 12–500 | ✓ | ||
Supplement day | Amount of supplement per day (kg) | 21.1 ± 19.3 | 5–100 | ✓ | ||
Free foraging | Ability to forage in the forest or grass field everyday | ✓ | ||||
Feed day | Number of feedings of roughage during the day | ✓ | ||||
Feed night | Number of feedings of roughage during the night | ✓ | ||||
Feed total | Sum of feedings of roughage during the day and night | ✓ | ||||
Water night | Ability to access water during the night; yes or no | ✓ | ||||
Floor day | Type of floor in rest area during daytime; ground or concrete | ✓ | ||||
Floor night | Type of floor in rest area during nighttime; ground, concrete, or sand | ✓ | ✓ | |||
Floor work | Type of floor during working; ground only or mix between ground and concrete | ✓ | ||||
Hill | Walking up or down hill during working or exercise; yes or no | ✓ | ||||
Hook | Using a hook to control an elephant; yes or no | ✓ |
Note:
Data from elephants during periods of musth (n = 9) and pregnancy (n = 2) were excluded.
Data for elephants during periods of musth and gestation were excluded from analysis because of alterations in nutrition and working management; that is, isolation of bulls, increased food provisioning and reduced work load for females. During the study period, nine bulls came into musth and two females conceived; only months associated with these states were excluded.
Results
Descriptive statistics of physical health and welfare parameters
Over the 1-year study, a total of 638 observations were obtained on 122 elephants. The mean number of observations per elephant was 5.2 ± 1.4 (range, 1–6). Median BCS was 4 (range 2–5). The majority of elephants were BCS >3, and none were BCS = 1 (Table 5). Across elephants, BCS increased as the study progressed from 18.9% at Time 1–46.5% at Time 6. Median and mean FS were both 1 (range 0–3: Table 5). In 61% of the observations (n = 106 elephants across 387 observations), nail cracks were observed. Of those, 79% (n = 304 observations) involved one to two nail cracks. Nail cracks were more common in the hind feet (left 65%; right 70% of the observations) than front feet (left 22%; right 21%) and developed in a vertical (97%) rather than horizontal direction (9%) (Fig. 1). Median WS was 0 (range 0–2), with the majority of elephants having no visible wounds. Wounds were noted in 23% of the observations (n = 65 elephants across 145 observations) (Table 5). The most common wounds were abrasions (59% of the observations), found mainly in temporal region next to forehead, and were most likely related to hook use (Fig. 2). A total of 73 elephants (60% of the elephants, n = 365 observations) were controlled by hooks. Of those, 27% of the observations (n = 53 elephants across 97 observations) involved wounds in the temporal area (74%, n = 72 observations), ears (11%, n = 10), forehead (9%, n = 9), legs (1%, n = 1), tail (1%, n = 1) and multiple areas (4%, n = 4). Types of hook wounds included abrasions (80%, n = 77 observations) (Fig. 3A), lacerations (12%, n =12) (Fig. 3B), ulcer (4%, n = 4), abscess (3%, n = 3) and multiple types (1%, n = 1). A total of 40 elephants (n = 200 observations) were used in a saddle riding program, and in only 5% of the observations (n = 6 elephants across nine observations) were wounds observed; these included ulcers on the back (56%, n = 5 observations) (Fig. 3C) or chest (44%, n = 4) (Fig. 3D), areas that were in contact with saddle pads or chest pieces.
Table 5. Percentage of elephant body condition score, foot score, and wound score categories from six times of scoring.
Score | Category | Time 1 | Time 2 | Time 3 | Time 4 | Time 5 | Time 6 | Total | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
n = 106 | % | n = 108 | % | n = 111 | % | n = 105 | % | n = 107 | % | n = 101 | % | n = 638 | % | ||
Body condition score | 1 | 0 | 0.0 | 0 | 0.0 | 0 | 0.0 | 0 | 0.0 | 0 | 0.0 | 0 | 0.0 | 0 | 0.0 |
2 | 2 | 1.9 | 5 | 4.6 | 9 | 8.1 | 6 | 5.7 | 6 | 5.6 | 4 | 4.0 | 32 | 5.0 | |
3 | 30 | 28.3 | 27 | 25.0 | 28 | 25.2 | 32 | 30.5 | 29 | 27.1 | 19 | 18.8 | 165 | 25.9 | |
4 | 54 | 50.9 | 53 | 49.1 | 48 | 43.2 | 34 | 32.4 | 36 | 33.6 | 31 | 30.7 | 256 | 40.1 | |
5 | 20 | 18.9 | 23 | 21.3 | 26 | 23.4 | 33 | 31.4 | 36 | 33.6 | 47 | 46.5 | 185 | 29.0 | |
Foot score | 0 | 34 | 32.1 | 42 | 38.9 | 39 | 35.1 | 50 | 47.6 | 32 | 29.9 | 33 | 32.7 | 230 | 36.1 |
1 | 41 | 38.7 | 40 | 37.0 | 51 | 45.9 | 48 | 45.7 | 54 | 50.5 | 44 | 43.6 | 278 | 43.6 | |
2 | 29 | 27.4 | 22 | 20.4 | 19 | 17.1 | 6 | 5.7 | 20 | 18.7 | 21 | 20.8 | 117 | 18.3 | |
3 | 2 | 1.9 | 4 | 3.7 | 2 | 1.8 | 1 | 1.0 | 1 | 0.9 | 3 | 3.0 | 13 | 2.0 | |
Wound score | 0 | 70 | 66.0 | 78 | 72.2 | 89 | 80.2 | 87 | 82.9 | 86 | 80.4 | 83 | 82.2 | 493 | 77.3 |
1 | 27 | 25.5 | 23 | 21.3 | 17 | 15.3 | 15 | 14.3 | 14 | 13.1 | 14 | 13.9 | 110 | 17.2 | |
2 | 9 | 8.5 | 7 | 6.5 | 5 | 4.5 | 3 | 2.9 | 7 | 6.5 | 4 | 4.0 | 35 | 5.5 |
Note:
Data from elephants during periods of musth (n = 9) and pregnancy (n = 2) were excluded.
Figure 1. Characteristics of nail cracks of 387 observations from six times evaluation over a 15-month period.
(A) Percentage of observations with nail cracks by the total number of cracks. (B) Percentage of observations with nail cracks by foot location. (C) Percentage of observations with nail cracks with vertical and horizontal cracks.
Figure 2. Characteristics of wounds of 387 observations from six times evaluation over a 15-month period (percentage).
(A) Wound location, (B) Wound type and (C) Cause of wound.
Figure 3. Skin lesions from inappropriate restraining method and improper use of equipment.
(A) Abrasion wounds and (B) A laceration wound in the head region caused by hooks. (C) Ulcers in the back and (D) Breast region caused by saddle equipment. Photography by Pakkanut Bansiddhi.
Factors associated with physical health and welfare parameters
Results of univariate and multivariate GEE analyses of variables associated with BCS (Table 6), FS (Table 7) and WS (Table 8) are presented. Variables affecting BCS in the univariate analysis were sex, chain hour, supplement day, free foraging, feed night, feed total and water night. In the final multivariate analysis, the combination of sex and water night were associated with higher BCS. Females were 4.394 times more likely to have a higher BCS compared to males (P < 0.001). Elephants that did not have the ability to access water during the night had an 87% decreased risk of having high BCS as compared to elephants that did have access water at night (OR = 0.130, P = 0.001) (Table 6). Variables associated with FS in the univariate analysis were work hour, walk distance day and floor work. Age was the only variable significant in the multivariate model. Increasing age was found to be associated with an increased odds of having a high FS (OR = 1.023, P = 0.031) (Table 7). Variables affecting WS in the univariate analysis were sex, age, hook and floor night. In the multivariate analysis, the combination of age, hook and floor night significantly affected WS. Increasing age was found to be associated with an increased odds of having a higher WS (OR = 1.040, P = 0.001). Elephants that were not controlled by hooks had a 70% decreased risk of having a higher WS as compared to elephants that were controlled by hooks (OR = 0.298, P < 0.001). Elephants that rested on a sand floor (n = 19 elephants) had an 85% decreased risk of having a high WS compared to elephants that rested on a compact dirt floor (OR = 0.146, P = 0.006) (Table 8).
Table 6. Univariate and multivariate GEE analyses of variables associated with body condition score.
Variable | N | Univariate analysis | Multivariate analysis | ||||
---|---|---|---|---|---|---|---|
Estimate | Odds ratio | P-value | Estimate | Odds ratio | P-value | ||
Sex | |||||||
Male | 33 | Reference | |||||
Female | 89 | 1.664 | 5.282 | <0.001 | 1.480 | 4.394 | <0.001 |
Age | 122 | −0.001 | 0.999 | 1.000 | −0.019 | 0.981 | 0.163 |
Work hour | 122 | 0.007 | 1.007 | 0.736 | |||
Chain hour | 122 | −0.056 | 0.946 | 0.001 | −0.008 | 0.992 | 0.706 |
Walk distance day | 122 | −0.001 | 0.999 | 0.615 | |||
Walk time day | 122 | 0.001 | 1.001 | 0.965 | |||
Roughage day | 122 | 0.003 | 1.003 | 0.243 | |||
Supplement day | 122 | 0.014 | 1.014 | 0.075 | 0.012 | 1.012 | 0.212 |
Free foraging | |||||||
Yes | 43 | Reference | |||||
No | 79 | −0.702 | 0.496 | 0.020 | −0.609 | 0.544 | 0.079 |
Feed day | |||||||
1 | 11 | Reference | |||||
2 | 39 | 0.064 | 1.066 | 0.876 | |||
3 | 30 | −0.252 | 0.777 | 0.537 | |||
4 | 29 | −0.571 | 0.565 | 0.193 | |||
5 | 13 | 0.179 | 1.196 | 0.732 | |||
Feed night | |||||||
Yes | 86 | Reference | |||||
No | 36 | 1.274 | 3.573 | <0.001 | 0.211 | 1.235 | 0.618 |
Feed total | |||||||
2 | 25 | Reference | |||||
3 | 31 | −0.728 | 0.483 | 0.102 | −0.294 | 0.745 | 0.562 |
4 | 36 | −0.889 | 0.411 | 0.037 | −0.473 | 0.623 | 0.326 |
5 | 20 | −1.125 | 0.325 | 0.037 | −0.902 | 0.406 | 0.089 |
6 | 10 | −0.804 | 0.448 | 0.137 | 0.305 | 1.356 | 0.584 |
Water night | |||||||
Yes | 19 | Reference | |||||
No | 103 | −2.046 | 0.129 | <0.001 | −2.037 | 0.130 | 0.001 |
Note:
Data from elephants during periods of musth (n = 9) and pregnancy (n = 2) were excluded.
Variables having a P-value < 0.15 in the univariate analysis were included in the multivariate analysis.
Table 7. Univariate and multivariate GEE analyses of variables associated with foot score.
Variable | N | Univariate analysis | Multivariate analysis | ||||
---|---|---|---|---|---|---|---|
Estimate | Odds ratio | P-value | Estimate | Odds ratio | P-value | ||
Sex | |||||||
Male | 33 | Reference | |||||
Female | 89 | −0.089 | 0.915 | 0.757 | −0.141 | 0.868 | 0.615 |
Age | 122 | 0.016 | 1.016 | 0.159 | 0.023 | 1.023 | 0.031 |
Work hour | 122 | 0.045 | 1.046 | 0.093 | 0.031 | 1.032 | 0.372 |
Chain hour | 122 | −0.001 | 0.999 | 0.976 | |||
Walk distance day | 122 | 0.001 | 1.001 | 0.147 | 0.001 | 1.001 | 0.539 |
Walk time day | 122 | 0.001 | 1.001 | 0.638 | |||
Floor day | |||||||
Ground | 66 | Reference | |||||
Concrete | 56 | −0.074 | 0.928 | 0.769 | |||
Floor night | |||||||
Ground | 50 | Reference | |||||
Concrete | 53 | 0.183 | 1.201 | 0.515 | |||
Sand | 19 | −0.344 | 0.709 | 0.338 | |||
Floor work | |||||||
Ground | 76 | Reference | |||||
Ground and concrete | 46 | 0.477 | 1.612 | 0.070 | 0.507 | 1.661 | 0.066 |
Hill | |||||||
Yes | 91 | Reference | |||||
No | 31 | −0.314 | 0.730 | 0.284 |
Note:
Data from elephants during periods of musth (n = 9) and pregnancy (n = 2) were excluded.
Variables having a P-value < 0.15 at the univariate analysis were included in the multivariate analysis.
Table 8. Univariate and multivariate GEE analyses of variables associated with wound score.
Variable | N | Univariate analysis | Multivariate analysis | ||||
---|---|---|---|---|---|---|---|
Estimate | Odds ratio | P-value | Estimate | Odds ratio | P-value | ||
Sex | |||||||
Male | 33 | Reference | |||||
Female | 89 | −0.824 | 0.439 | 0.005 | −0.546 | 0.579 | 0.063 |
Age | 122 | 0.023 | 1.023 | 0.048 | 0.039 | 1.040 | 0.001 |
Work hour | 122 | −0.062 | 0.940 | 0.164 | |||
Walk distance day | 122 | −0.001 | 0.999 | 0.536 | |||
Walk time day | 122 | 0.001 | 1.001 | 0.428 | |||
Hook | |||||||
Yes | 73 | Reference | |||||
No | 49 | −1.778 | 0.169 | <0.001 | −1.212 | 0.298 | <0.001 |
Floor night | |||||||
Ground | 50 | Reference | |||||
Concrete | 53 | 0.398 | 1.489 | 0.154 | 0.212 | 1.236 | 0.423 |
Sand | 19 | −2.567 | 0.077 | <0.001 | −1.926 | 0.146 | 0.006 |
Note:
Data from elephants during periods of musth (n = 9) and pregnancy (n = 2) were excluded.
Variables having a P-value < 0.15 at the univariate analysis were included in the multivariate analysis.
Discussion
This is the first study to examine the effect of management practices on the health and welfare of tourist elephants by using an epidemiological approach. Study subjects were followed over time with repeated monitoring of risk factors and outcomes; that is, BCS, FS and WS, which made observing changes more robust.
When using a 5-point scale, the “ideal/normal” BCS = 3; BCS = 1–2 equates to “underweight/thin” and “overweight/obese” includes BCS = 4–5 (Morfeld et al., 2016). BCS of elephants in this study was generally high with a median BCS = 4, which was comparable to elephants in North American zoos (Morfeld et al., 2016), but higher than free-ranging elephants in India (Pokharel, Seshagiri & Sukumar, 2017) that used the same scoring system. However, proportionally, Thailand elephants were in better body condition compared to zoo elephants, with 69% at a BCS of four or five compared to 74% in North American zoos. Captive elephants, on average, have higher body condition than free ranging elephants, presumably because of more consistent, high quality diets, but also fewer exercise opportunities. For that reason, comparatively, the majority of western zoo elephants are overweight or obese (Harris, Sherwin & Harris, 2008; Morfeld et al., 2016). While the proportion of FSs and WSs were stable throughout the study period, the percentage of elephants with a BCS of five more than doubled, from 18.9% at Time 1–46.5% at Time 6. One reason for this may be that work duration, walking distance and walking time decreased as the study progressed, while the amount of roughage and supplements remained constant. The decrease in working intensity may have been related to lower tourist numbers in those months of the study. Although those data were not available, in October 2016, TripAdvisor and its booking service, Viator, announced they will no longer sell tickets to hundreds of attractions where travelers come into contact with wild animals or endangered species held in captivity. This announcement could have led to a decrease in tourist numbers during Time 4–6 (October 2016 – May 2017), which then resulted in higher observed BCSs. If so, this effect deserves further investigation, and management adjustments may be needed to account for it.
In our study, females had higher BCS than males, which is similar to Asian elephants in North American zoos (Morfeld et al., 2016). Fat deposits enable a female mammal to bear the energy costs of gestation and lactation, which is important to reproductive success (Heldstab, Van Schaik & Isler, 2017). In addition, male elephants lose weight during musth because of decreased foraging and active interest in females in relation to elevated androgens, and to subsequent catabolism of triglycerides (Goodwin et al., 2015). From our interview, mahouts reported keeping body condition of males lower in an effort to control musth symptoms and reduce aggressive behavior.
Having a water source at night was a significant factor related to higher body condition in elephants. Although one management goal is to reduce the risk of a high BCS because of associated health concerns (Morfeld & Brown, 2016; Morfeld & Brown, 2017; Morfeld et al., 2016), water is important for maintaining adequate body condition in underweight elephants. We were unable to correlate amounts of water consumed per day to BCS, but this could be important for proper welfare management. One of the “Five Freedoms” for animals is the freedom from hunger and thirst by providing adequate and ready access to fresh water (Farm Animal Welfare Council, 1979). Dunkin et al. (2013) found that cutaneous evaporative water loss increased with increasing air temperature across the body of elephants and they used additional water sources to increase evaporative cooling. Because of the high physical activity experienced by some elephants in the tourist industry and the hot, tropical climate in Thailand, providing water both day and night might help to maintain full health and vigor. We were not expecting a relationship between what we consider to be an unhealthy BCS and access to water at night. Further evaluation of the data suggests it might be related to other management practices, and not a direct cause and effect. Specifically, we found elephants that had access to water at night also received greater amounts of roughage and high-calorie supplements during the day, worked fewer hours and exercised less than those that did not have water at night. So, more food and a lower work intensity is more likely the cause of higher BCSs rather than having access to water at night. A surprising finding from the management survey (Bansiddhi et al., 2018) was that only 18% of camps had a water source for elephants at night, so understanding how this limitation affects long-term health and welfare is warranted.
The amount of supplement offered to elephants was associated with higher BCS in the univariate analysis. The most common supplements for elephants in this population were bananas and sugarcane (Bansiddhi et al., 2018), which possess high concentrations of sucrose and other soluble sugars that could contribute to weight problems (Norkaew et al., 2018). Limiting the amount of high-calorie treats and using lower calorie supplements, such as tamarind, watermelon, pumpkin, pineapple and cucumber, which are easy to obtain locally (Bansiddhi et al., 2018; Phuangkum, Lair & Angkawanith, 2005), is recommended if tourists must feed elephants.
Elephants that had a chance to forage regularly had an increased risk for high BCS in the univariate analysis. For underweight elephants, this can help improve their body condition. Having foraging opportunities is important to elephants as it can increase the variety of foods and herbs they eat and is supportive of natural behavior. Foraging enrichment is considered one of the most effective strategies to improve welfare and reduce stereotypies and other abnormal repetitive behaviors in captive animals (Van Zeeland et al., 2013), including elephants (Morfeld et al., 2016). Thus, to maintain good body condition, elephant camps should promote foraging and not feed elephants a lot of supplementary treats. An increase in the number of feedings per day and feeding elephants at night, however, were associated with lower BCS in the univariate analysis. In animal experiments, Anderson et al. (1980) found significantly less body weight gain with higher eating frequency in rat pups. In humans, it is a common practice for clinicians to recommend increasing meal frequency as a strategy for weight management and to improve metabolic parameters. Frequent meals have been further proposed to reduce the occurrence of excess caloric consumption and provide better glucose control and reduced insulin secretion (Kulovitz et al., 2014). Another important factor associated with BCS in zoo elephants is feeding schedules; an unpredictable schedule was associated with a 69% decrease risk of BCS four or five as compared to elephants with a predictable feeding schedule (Morfeld et al., 2016). For tourist elephants, most were fed roughage by their mahouts on a fairly predictable feeding schedule, although feeding of supplementary treats by tourists was on an unpredictable schedule. Thus, it is unclear if a similar relationship between BCS and unpredictable feeding schedules applies to tourist elephants.
One unexpected finding in the univariate analysis was that elephants not constrained by prolonged chaining had an increased risk for high BCS. One consequence of chaining in elephants is the development of stereotypic behaviors (Friend & Parker, 1999; Gruber et al., 2000; Schmid, 1995; Varadharajan, Krishnamoorthy & Nagarajan, 2016), which consist of repetitive movements that may burn more calories. Data on this population showed that elephants that presented stereotypic behaviors had lower BCS than elephants that did not (GEE, n = 122, P = 0.02).
In examinations of foot health, the majority of observations (44%) found mild problems with uncomplicated nail cracks or injuries; in only 2% of the observations were severe foot problems observed. These results were comparable to a study by Todd (2015) that scored 74 elephants in three camps in Chiang Mai by the same system and found the majority (64%) had mild and 3% had severe foot problems. In our study, more than half of observations (61%) had nail cracks. This finding was similar to a survey of tourist elephants in India that found nail cracks in 61% (Sasmal, 2018). Foot problems do occur in wild elephants, but they are not common (Fowler, 2001). Benz (2005) noted that captive elephants have a thinner sole and pad horn layer in the weight-bearing surface in comparison to wild elephants, which encourages foot disorders in captive elephants and is caused by a floor in zoos that is too hard and abrasive. That study also evaluated wild elephants and found no evidence of cracks, fissures, holes or other pathological alterations. However, micro-cracks were apparent in all animals, both captive and wild, suggesting they result from normal wear. According to assertions by various vets working in the wild in Sri Lanka and South Africa, wild elephants’ foot problems are usually related to trauma (penetration by shot, traps or sharp objects on the ground, but also burn wounds) and resulting infections (Benz, 2005).
We did not find the forelimbs to be more affected by nail cracks than the hind limbs, despite bearing a greater proportion (about 61%) of body weight in a standing position (Genin et al., 2010) or higher in mean peak pressure magnitudes (by about 5%) when walking on flat concrete (Panagiotopoulou et al., 2012). In fact, the opposite was true, and a majority of cracks were in the hind feet. However, during quadrupedal walking in most animals, the hind limbs become almost entirely responsible for providing propulsion to push themselves forward while the front limbs provide more braking (Granatosky et al., 2018; Tefera, 2012). The pressure from propulsion might induce nail cracks in the hind limbs, especially when elephants walk up hill. Similar to our findings, West (2001) found that nail cracks are common in hind feet in circus and zoo elephants. We found vertical cracks more often than horizontal cracks, which are generally caused by nail overgrowth, digging, kicking, or obesity (Fowler, 1993; Rutkowski, Marion & Hopper, 2001). Horizontal cracks, while more unusual, were found in 9% of elephants with nail cracks in this study. In horses, horizontal cracks are usually the result of an injury and rarely spread like vertical cracks (Thomas, 2006).
Increasing age was found to be associated with higher FS in the final model. Older elephants frequently develop foot problems, likely due to diseases like arthritis, and to reduced activity levels (West, 2001). Elderly captive elephants are predisposed to pododermatitis, an infectious process of the foot that takes 5–8 weeks longer to recover from in older elephants (Silva & Dangolla, 2006). In humans, age-associated nail changes and disorders are common in elderly patients. There is usually a tendency of the normally smooth nail plate texture to become progressively more friable with increasing age, resulting in fissuring, splitting and longitudinal superficial or deep striations (Cohen & Scher, 1992; Singh, Haneef & Uday, 2005).
In the univariate analysis, work hours and walking distance were associated with an increased risk of a high FS, possibly because an elephant’s foot and nail supports more weight and pressure when active than when standing still (Fowler, 2001). However, regular physical exercise, such as walking, does benefit captive elephants as it promotes muscle tone, flexibility, agility, stamina and a healthy weight, and it provides enrichment; lack of exercise is one of the alleged causes of foot problems (Fowler, 2008; Olson, 2004). Walking distances have been reported to range from 3.2 to 8.9 km per day in wild Asian elephants (Rowell, 2014) and 5.3 km per day in North American zoo elephants (Holdgate et al., 2016). Although the mean walking distance of 4.2 km per day in this study was comparable, there were elephants that walked up to 12 km per day. Those elephants that walked more than four km per day had a higher percentage of moderate to severe foot problems (FS of two and three) than elephants that walked less than four km per day (18%). However, Holdgate et al. (2016) and Miller, Hogan & Meehan (2016) found no correlations between walking distance and foot health in elephants in North American zoos. The authors noted that those data were not collected at the same time, whereas they were in this study. So, it is possible that measures of foot health taken coincident with walking distance measurements more accurately reveal these associations. It must be noted that walking distance and walking time in this study were estimated by mahouts and only during the working period, not during free-foraging or when taken for bathing and drinking during rest periods.
Having concrete floors in walking routes was associated with higher FS in the univariate analysis. Similarly, a study in zoo elephants demonstrated a significant relationship between time spent on hard substrate and foot problems (Miller, Hogan & Meehan, 2016). In farm animals (e.g., cattle and pigs), excessive walking on concrete causes foot and claw disorders, stretches in the white line (lamina horn that connects the sole to the hoof wall) and wearing down of the sole, thus weakening the junction between the wall and sole of the foot (Mills & Marchant-Forde, 2010; Ribo & Serratosa, 2009).
Most wounds were found in the head region; that is, the forehead and temporal area next to the forehead, and the ears, all places where equipment (e.g., hooks) is used. We also found penetrating and incision wounds caused by knives, the other tool commonly carried by mahouts. It was not possible to determine misuse of hooks in sensitive areas of the elephant’s skin (less than one cm thick), including inside the ears or mouth, behind the ears, in and around anus, under the chin and around the feet (Doyle, 2014; Shoshani, 1982), but it is possible they may be present. Using hooks where skin is thicker (e.g., around the forehead), may require more force that can lead to pronounced injuries. It must be noted that in 73% of the observations where mahouts carried a hook, the elephants had no associated wounds. Thus, misuse of hooks may not be as widespread as animal protection groups suggest. Still, our findings indicate there is overuse of equipment to control elephants in some camps or with some elephants. As such, using hooks was found to be associated with higher WSs. Therefore, it is imperative that mahouts be trained in proper use of the hook and how to control elephants without resorting to painful punishment. The knife should never be used to control an elephant, except when human life is in danger. The primary purpose of the bush knife is to cut food for the elephant, clear pathways, and cut firewood for the mahout (Phuangkum, Lair & Angkawanith, 2005), not to control elephants.
Skin lesions related to contact with saddle-related equipment were found in only 5% of observations at camps with a saddle program, which indicates that saddle use caused wounds in only a few elephants. This is much lower than a prevalence of 64% reported by Magda et al. (2015), which conducted a survey on 194 elephants from 18 tourism camps across Thailand. Their results showed that the use of a rice sack as padding was a significant risk factor for having an active lesion. It may be that camps have heeded recommendations from that study and made the changes necessary to avoid saddle injuries. Beside using gunnysacks, camps in northern Thailand generally use hammered bark, blankets, or sponge material as saddle padding (Bansiddhi et al., 2018), which might reduce the incidence of injuries. Shape of the backbone can also be a factor, with higher ridgelines being more susceptible to saddle injuries if saddles are not well designed, although this has yet to be studied in detail.
Increasing age had an expected association with higher WS, as Magda et al. (2015) also found that older elephants were more likely to have active lesions in association with saddle riding. In humans, many of the protective functions of skin decrease with age. Functional changes in aging skin include altered permeability, diminished sebum production, decreased inflammatory and immunological responsiveness, attenuated thermoregulation and reduced elasticity. These changes affect the rate and quality of healing (Gordon, 2014). Bedsores are one of the most common wounds in the elderly and form where the weight of the person’s body presses the skin against the firm surface of the bed (Kandha Vadivu, 2015). Because of their large body weight, lying down on hard floors might be a risk factor for developing sores in elephants. This was confirmed by our result that resting on sand floors at night was associated with low WS.
In the univariate analysis, males had a higher WS than females (24% of observations vs. 11%, respectively), most of these related to hook injuries. Males generally are more aggressive and need more intensive control. In addition, fights between males over territory or in competition for mates can cause serious wounds; that is, puncture wounds from tusks. We found one female and three males that had laceration, abrasion, or penetrating wounds from fighting.
Conclusions
This is the first study linking tourist camp management practices with specific health and welfare outcomes in Asian elephants. Findings emphasize the need for some elephant camps to adjust management activities that affect body condition, foot health and wounding. It is important to strike a balance between work intensity, exercise opportunities and nutrition to prevent problems associated with obesity. Foot problems could be reduced by limiting walking on hard surfaces and establishing a regular foot care program. Carrying a hook is often necessary for the safety of elephants, mahouts and tourists in free-contact situations. However, protocols need to be enforced that prevent the misuse of equipment and unnecessary wounding. Furthermore, mahouts must be trained to use hooks properly and in a way that is not punitive. Saddles must fit properly to take pressure off the spine and with appropriate padding to prevent abrasions, and occasionally removed during the day to provide rest and relief of any pressure points.
Space and budget limitations may make it difficult for some camps to comply with all of these recommendations, but they must be more proactive to ensure these intelligent animals are managed in a way that meets physical and psychological needs. Simple acts, like changing from concrete to compact dirt or sand floors, especially for old elephants, and managing tourist interactions can make a big difference in the life of an elephant, without being financially onerous to owners. The results of this study will now be used to develop science-based welfare guidelines and elephant camp standards to aid in the management of elephants used in tourism. Future studies will use the survey data to further investigate associations between management factors and other behavioral and physiological welfare indicators to further refine these recommendations. Finally, we will work with elephant camps to help them improve welfare standards by providing education and training opportunities for owners and mahouts.
Supplemental Information
Questionnaire interviews with camp owners, managers and/or camp veterinarians were performed by using this questionnaire sheet to record information about camp activities, location, programs for tourists, numbers of elephants and elephant management.
Questionnaire interviews with mahouts gathered information on management of their specific elephants; that is, work routine, restraint, rest area, feeding, watering and health care by using this questionnaire sheet.
Acknowledgments
This research work is supported by Chiang Mai University. We would like to acknowledge the supports from the Thai Elephant Conservation Center and the National Institute of Elephant Research and Health Service for their data sources. We thank all of the owners, managers and mahouts at the elephant camps for their cooperation. Special thanks to Dr. Chaleamchat Somgird, Dr. Khajohnpat Boonprasert, Dr. Thittaya Janyamathakul, Dr. Pattarawan Thilanun, Dr. Panida Muanghong, Dr. Siripat Khammesri, and Dr. Channarong Srisa-ard for suggestions and cooperation.
Funding Statement
The National Research Council of Thailand (NRCT), the Royal Golden Jubilee Ph.D. program, Thailand Research Fund (TRF), and Chiang Mai University provided research grants. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Contributor Information
Korakot Nganvongpanit, Email: korakot.n@cmu.ac.th.
Chatchote Thitaram, Email: chatchote.thitaram@cmu.ac.th.
Additional Information and Declarations
Competing Interests
The authors declare that they have no competing interests.
Author Contributions
Pakkanut Bansiddhi conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.
Korakot Nganvongpanit conceived and designed the experiments, authored or reviewed drafts of the paper, approved the final draft.
Janine L. Brown conceived and designed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.
Veerasak Punyapornwithaya analyzed the data, prepared figures and/or tables, approved the final draft.
Pornsawan Pongsopawijit contributed reagents/materials/analysis tools, approved the final draft.
Chatchote Thitaram conceived and designed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.
Ethics
The following information was supplied relating to ethical approvals (i.e., approving body and any reference numbers):
This study was approved by the Institutional Animal Care and Use Committee, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, Thailand (license number; S43/2559). All experiments were performed in accordance with relevant guidelines and regulations.
Data Availability
The following information was supplied regarding data availability:
The raw measurements are available in the Supplemental File.
References
- Anderson et al. (1980).Anderson TA, Raffety CJ, Birkhofer KK, Fomon SJ. Effect of feeding frequency on growth and body composition of gastrostomized rat pups. Journal of Nutrition. 1980;110(12):2374–2380. doi: 10.1093/jn/110.12.2374. [DOI] [PubMed] [Google Scholar]
- Angkawanish et al. (2009).Angkawanish T, Boonprasert K, Homkong P, Sombutputorn P, Mahasawangkul S, Jansittiwate S, Keratimanochaya T, Clausen B. Elephant health status in Thailand: the role of mobile elephant clinic and elephant hospital. Gajah. 2009;31:15–20. [Google Scholar]
- Asian Captive Elephant Working Group (2017).Asian Captive Elephant Working Group ACEWG statement. 2017. http://acewg.org/wp-content/uploads/2018/06/ACEWG_Statement_March2017.pdf http://acewg.org/wp-content/uploads/2018/06/ACEWG_Statement_March2017.pdf
- Asian Elephant Specialist Group (2017).Asian Elephant Specialist Group Asian elephant range states meeting, final report. 2017. https://www.asesg.org/PDFfiles/2017/AsERSM%202017_Final%20Report.pdf https://www.asesg.org/PDFfiles/2017/AsERSM%202017_Final%20Report.pdf
- Bansiddhi (2019).Bansiddhi P. Chiang Mai University; 2019. Management factors of elephant camps affecting health and welfare of elephants. Doctoral thesis. [Google Scholar]
- Bansiddhi et al. (2019).Bansiddhi P, Brown JL, Thitaram C, Punyapornwithaya V, Nganvongpanit K. Elephant tourism in Thailand: a review of animal welfare practices and needs. Journal of Applied Animal Welfare Science. 2019 doi: 10.1080/10888705.2019.1569522. Epub ahead of print 28 Janunary 2019. [DOI] [PubMed] [Google Scholar]
- Bansiddhi et al. (2018).Bansiddhi P, Brown JL, Thitaram C, Punyapornwithaya V, Somgird C, Edwards KL, Nganvongpanit K. Changing trends in elephant camp management in northern Thailand and implications for welfare. PeerJ. 2018;6(3):e5996. doi: 10.7717/peerj.5996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benz (2005).Benz A. University of Zurich; 2005. The elephant’s hoof: macroscopic and microscopic morphology of defined locations under consideration of pathological changes. Doctoral thesis. [Google Scholar]
- Carlstead et al. (2013).Carlstead K, Mench JA, Meehan C, Brown JL. An epidemiological approach to welfare research in zoos: the elephant welfare project. Journal of Applied Animal Welfare Science. 2013;16(4):319–337. doi: 10.1080/10888705.2013.827915. [DOI] [PubMed] [Google Scholar]
- Chatkupt, Sollod & Sarobol (1999).Chatkupt TT, Sollod AE, Sarobol S. Elephants in Thailand: determinants of health and welfare in working populations. Journal of Applied Animal Welfare Science. 1999;2(3):187–203. doi: 10.1207/s15327604jaws0203_2. [DOI] [PubMed] [Google Scholar]
- Cohen & Scher (1992).Cohen PR, Scher RK. Geriatric nail disorders: diagnosis and treatment. Journal of the American Academy of Dermatology. 1992;26(4):521–531. doi: 10.1016/0190-9622(92)70075-Q. [DOI] [PubMed] [Google Scholar]
- Doyle (2014).Doyle C. Captive elephants. In: Gruen L, editor. The Ethics of Captivity. Oxford: Oxford University Press; 2014. pp. 38–56. [Google Scholar]
- Duffy & Moore (2011).Duffy R, Moore L. Global regulations and local practices: the politics and governance of animal welfare in elephant tourism. Journal of Sustainable Tourism. 2011;19(4–5):589–604. doi: 10.1080/09669582.2011.566927. [DOI] [Google Scholar]
- Dunkin et al. (2013).Dunkin RC, Wilson D, Way N, Johnson K, Williams TM. Climate influences thermal balance and water use in African and Asian elephants: physiology can predict drivers of elephant distribution. Journal of Experimental Biology. 2013;216(15):2939–2952. doi: 10.1242/jeb.080218. [DOI] [PubMed] [Google Scholar]
- Farm Animal Welfare Council (1979).Farm Animal Welfare Council Farm animal welfare council press statement. 1979. http://webarchive.nationalarchives.gov.uk/20121010012427/ http://www.fawc.org.uk/freedoms.htm http://webarchive.nationalarchives.gov.uk/20121010012427/ http://www.fawc.org.uk/freedoms.htm
- Fowler (1993).Fowler ME. Foot care in elephants. In: Fowler ME, editor. Zoo and Wild Animal Medicine: Current Therapy 3. Philadelphia: W.B. Saunders Company; 1993. pp. 448–453. [Google Scholar]
- Fowler (2001).Fowler ME. An overview of foot conditions in Asian and African elephants. In: Csuti B, Sargent EL, Bechert US, editors. The Elephant’s Foot: Prevention and Care of Foot Conditions in Captive Asian and African Elephants. Ames: Iowa State University Press; 2001. pp. 3–7. [Google Scholar]
- Fowler (2008).Fowler ME. Foot disorders. In: Fowler M, Mikota SK, editors. Biology, Medicine, and Surgery of Elephants. Ames: Blackwell Publishing; 2008. pp. 271–290. [Google Scholar]
- Friend & Parker (1999).Friend TH, Parker ML. The effect of penning versus picketing on stereotypic behavior of circus elephants. Applied Animal Behaviour Science. 1999;64(3):213–225. doi: 10.1016/S0168-1591(99)00039-8. [DOI] [Google Scholar]
- Genin et al. (2010).Genin JJ, Willems PA, Cavagna GA, Lair R, Heglund NC. Biomechanics of locomotion in Asian elephants. Journal of Experimental Biology. 2010;213(5):694–706. doi: 10.1242/jeb.035436. [DOI] [PubMed] [Google Scholar]
- Goodwin et al. (2015).Goodwin TE, Harelimana IH, MacDonald LJ, Mark DB, Juru AU, Yin Q, Engman JA, Kopper RA, Lichti CF, Mackintosh SG, Shoemaker JD, Sutherland MV, Tackett AJ, Schulte BA. The role of bacteria in chemical signals of elephant musth: proximate causes and biochemical pathways in. In: Schulte BA, Goodwin TE, Ferkin MH, editors. Chemical Signals in Vertebrates 13. New York: Springer International Publishing; 2015. pp. 63–86. [Google Scholar]
- Gordon (2014).Gordon R. Skin disorders. In: Kauffman TL, Scott RW, Barr JO, Moran ML, editors. A Comprehensive Guide to Geriatric Rehabilitation. London: Churchill Livingstone Elsevier; 2014. pp. 369–378. [Google Scholar]
- Granatosky et al. (2018).Granatosky MC, Fitzsimons A, Zeininger A, Schmitt D. Mechanisms for the functional differentiation of the propulsive and braking roles of the forelimbs and hindlimbs during quadrupedal walking in primates and felines. Journal of Experimental Biology. 2018;221(2):jeb162917. doi: 10.1242/jeb.162917. [DOI] [PubMed] [Google Scholar]
- Greco et al. (2017).Greco BJ, Meehan CL, Heinsius JL, Mench JA. Why pace? The influence of social, housing, management, life history, and demographic characteristics on locomotor stereotypy in zoo elephants. Applied Animal Behaviour Science. 2017;194:104–111. doi: 10.1016/j.applanim.2017.05.003. [DOI] [Google Scholar]
- Gruber et al. (2000).Gruber TM, Friend TH, Gardner JM, Packard JM, Beaver B, Bushong D. Variation in stereotypic behavior related to restraint in circus elephants. Zoo Biology. 2000;19(3):209–221. doi: 10.1002/1098-2361(2000)19:3<209::AID-ZOO4>3.0.CO;2-7. [DOI] [Google Scholar]
- Harris, Sherwin & Harris (2008).Harris M, Sherwin C, Harris S. The welfare, housing and husbandry of elephants in uk zoos. Bristol: University of Bristol; 2008. [Google Scholar]
- Haspeslagh et al. (2013).Haspeslagh M, Stevens JMG, De Groot E, Dewulf J, Kalmar ID, Moons CPH. A survey of foot problems, stereotypic behaviour and floor type in Asian elephants (Elephas maximus) in European zoos. Animal Welfare. 2013;22(4):437–443. doi: 10.7120/09627286.22.4.437. [DOI] [Google Scholar]
- Heldstab, Van Schaik & Isler (2017).Heldstab SA, Van Schaik CP, Isler K. Getting fat or getting help? How female mammals cope with energetic constraints on reproduction. Frontiers in Zoology. 2017;14(1):29. doi: 10.1186/s12983-017-0214-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holdgate et al. (2016).Holdgate MR, Meehan CL, Hogan JN, Miller LJ, Soltis J, Andrews J, Shepherdson DJ. Walking behavior of zoo elephants: associations between GPS-measured daily walking distances and environmental factors, social factors, and welfare indicators. PLOS ONE. 2016;11(7):e0150331. doi: 10.1371/journal.pone.0150331. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kandha Vadivu (2015).Kandha Vadivu P. Design and development of portable support surface and multilayered fabric cover for bed sore prevention. Indian Journal of Surgery. 2015;77(S2):576–582. doi: 10.1007/s12262-013-0930-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kulovitz et al. (2014).Kulovitz MG, Kravitz LR, Mermier C, Gibson AL, Conn CA, Kolkmeyer D, Kerksick CM. Potential role of meal frequency as a strategy for weight loss and health in overweight or obese adults. Nutrition. 2014;30(4):386–392. doi: 10.1016/j.nut.2013.08.009. [DOI] [PubMed] [Google Scholar]
- Lahiri-Choudhury (2008).Lahiri-Choudhury DK. Historical lessons for the treatment of foot diseases in captive Asian elephants. In: Csuti B, Sargent EL, Bechert US, editors. The Elephant’s Foot: Prevention and Care of Foot Conditions in Captive Asian and African Elephants. Ames: Iowa State University Press; 2008. pp. 81–84. [Google Scholar]
- Magda et al. (2015).Magda S, Spohn O, Angkawanish T, Smith DA, Pearl DL. Risk factors for saddle-related skin lesions on elephants used in the tourism industry in Thailand. BMC Veterinary Research. 2015;11(1):117. doi: 10.1186/s12917-015-0438-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meehan et al. (2016).Meehan CL, Mench JA, Carlstead K, Hogan JN. Determining connections between the daily lives of zoo elephants and their welfare: an epidemiological approach. PLOS ONE. 2016;11(7):e0158124. doi: 10.1371/journal.pone.0158124. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller, Hogan & Meehan (2016).Miller MA, Hogan JN, Meehan CL. Housing and demographic risk factors impacting foot and musculoskeletal health in African elephants (Loxodonta africana) and Asian elephants (Elephas maximus) in North American zoos. PLOS ONE. 2016;11(7):e0155223. doi: 10.1371/journal.pone.0155223. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mills & Marchant-Forde (2010).Mills DS, Marchant-Forde JN. The encyclopedia of applied animal behaviour and welfare. Cambridge: Cambridge University Press; 2010. [Google Scholar]
- Morfeld & Brown (2016).Morfeld KA, Brown JL. Ovarian acyclicity in zoo African elephants (Loxodonta africana) is associated with high body condition scores and elevated serum insulin and leptin. Reproduction, Fertility and Development. 2016;28(5):640–647. doi: 10.1071/RD14140. [DOI] [PubMed] [Google Scholar]
- Morfeld & Brown (2017).Morfeld KA, Brown JL. Metabolic health assessment of zoo elephants: management factors predicting leptin levels and the glucose-to-insulin ratio and their associations with health parameters. PLOS ONE. 2017;12(11):e0188701. doi: 10.1371/journal.pone.0188701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morfeld et al. (2016).Morfeld KA, Meehan CL, Hogan JN, Brown JL. Assessment of body condition in African (Loxodonta africana) and Asian (Elephas maximus) elephants in North American zoos and management practices associated with high body condition scores. PLOS ONE. 2016;11(7):e0155146. doi: 10.1371/journal.pone.0155146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Norkaew et al. (2018).Norkaew T, Brown JL, Bansiddhi P, Somgird C, Thitaram C, Punyapornwithaya V, Punturee K, Vongchan P, Somboon N, Khonmee J. Body condition and adrenal glucocorticoid activity affects metabolic marker and lipid profiles in captive female elephants in Thailand. PLOS ONE. 2018;13(10):e0204965. doi: 10.1371/journal.pone.0204965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Olson (2004).Olson D. Elephant husbandry resource guide. Lawrence: Allen Press; 2004. [Google Scholar]
- Panagiotopoulou et al. (2012).Panagiotopoulou O, Pataky TC, Hill Z, Hutchinson JR. Statistical parametric mapping of the regional distribution and ontogenetic scaling of foot pressures during walking in Asian elephants (Elephas maximus) Journal of Experimental Biology. 2012;215(9):1584–1593. doi: 10.1242/jeb.065862. [DOI] [PubMed] [Google Scholar]
- Phuangkum, Lair & Angkawanith (2005).Phuangkum P, Lair RC, Angkawanith T. Elephant care manual for mahouts and camp managers. Lampang: Bannakij Printing; 2005. [Google Scholar]
- Pokharel, Seshagiri & Sukumar (2017).Pokharel SS, Seshagiri PB, Sukumar R. Assessment of season-dependent body condition scores in relation to faecal glucocorticoid metabolites in free-ranging Asian elephants. Conservation Physiology. 2017;5(1):cox039. doi: 10.1093/conphys/cox039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- R Development Core Team (2018).R Development Core Team . R: a language and environment for statistical computing. Vienna: The R Foundation for Statistical Computing; 2018. [Google Scholar]
- Ribo & Serratosa (2009).Ribo O, Serratosa J. History and procedural aspects of the animal welfare risk assessment at efsa. In: Smulders FJM, Algers B, editors. Welfare of Production Animals: Assessment and Management of Risks. Wageningen: Wageningen Academic Publishers; 2009. pp. 305–332. [Google Scholar]
- Rowell (2014).Rowell Z. Locomotion in captive Asian elephants (Elephas maximus) Journal of Zoo and Aquarium Research. 2014;2(4):130–135. doi: 10.19227/jzar.v2i4.50. [DOI] [Google Scholar]
- Rutkowski, Marion & Hopper (2001).Rutkowski C, Marion F, Hopper R. Split nails, abscesses, and cuticular fluid pockets. In: Csuti B, Sargent EL, Bechert US, editors. The Elephant’s Foot: Prevention and Care of Foot Conditions in Captive Asian and African Elephants. Ames: Iowa State University Press; 2001. pp. 85–86. [Google Scholar]
- Sasmal (2018).Sasmal A. Elephants of the Pink City, Jaipur, India: a study of the captive elephant welfare and management practice in ex-situ environmental conditions. Annual Graduate Student Symposium; Cedar Falls: University of Northern Iowa; 2018. [Google Scholar]
- Schein et al. (2013).Schein M, Rogers PN, Leppäniemi A, Rosin D. The wound, the wound. In: Schein M, Rogers PN, Leppäniemi A, Rosin D, editors. Schein’s Common Sense Prevention and Management of Surgical Complications: For Surgeons, Residents, Lawyers, and Even Those Who Never Have Any Complications. Shropshire: tfm Publishing Limited; 2013. [Google Scholar]
- Schmid (1995).Schmid J. Keeping circus elephants temporarily in paddocks - the effects on their behaviour. Animal Welfare. 1995;4(2):87–101. [Google Scholar]
- Scorer (2014).Scorer T. Surgical nursing procedures. In: Aspinall V, editor. Clinical Procedures in Veterinary Nursing - E-Book. Oxford: Elsevier Health Sciences; 2014. pp. 153–176. [Google Scholar]
- Shoshani (1982).Shoshani J. On the dissection of a female Asian elephant (Elephas maximus maxiums linnaeus, 1758) and data from other elephants. Elephant. 1982;2(1):3–93. doi: 10.22237/elephant/1521731887. [DOI] [Google Scholar]
- Silva & Dangolla (2006).Silva I, Dangolla A. Veterinary problems of geographical concern: section viii sri lanka. In: Fowler M, Mikota SK, editors. Biology, Medicine, and Surgery of Elephants. Ames: Blankwell Publishing; 2006. pp. 468–474. [Google Scholar]
- Singh, Haneef & Uday (2005).Singh G, Haneef N, Uday A. Nail changes and disorders among the elderly. Indian Journal of Dermatology, Venereology, and Leprology. 2005;71(6):386–392. doi: 10.4103/0378-6323.18941. [DOI] [PubMed] [Google Scholar]
- Studdert, Gay & Blood (2011).Studdert VP, Gay CC, Blood DC. Saunders comprehensive veterinary dictionary e-book. Philadelphia: Elsevier Health Sciences; 2011. [Google Scholar]
- Tefera (2012).Tefera M. Kinematics and comparative anatomy of somelimb bones of the African elephant (Loxodonta africana) and large domestic animals. Journal of Veterinary Anatomy. 2012;5(2):15–31. [Google Scholar]
- Thomas (2006).Thomas HS. Understanding equine hoof care: your guide to horse health care and management. Lexington: Blood-Horse Publications; 2006. [Google Scholar]
- Todd (2015).Todd H. London: Royal Veterinary College; 2015. Comparing the foot and locomotory health of Asian elephants (Elephas maximus) of northern Thailand to the UK and Ireland. Research project report. [Google Scholar]
- Touloumis (2015).Touloumis A. R package multgee: a generalized estimating equations solver for multinomial responses. Journal of Statistical Software. 2015;64(8):1–14. doi: 10.18637/jss.v064.i08. [DOI] [Google Scholar]
- Van Zeeland et al. (2013).Van Zeeland YRA, Schoemaker NJ, Ravesteijn MM, Mol M, Lumeij JT. Efficacy of foraging enrichments to increase foraging time in grey parrots (Psittacus erithacus erithacus) Applied Animal Behaviour Science. 2013;149(1–4):87–102. doi: 10.1016/j.applanim.2013.09.005. [DOI] [Google Scholar]
- Varadharajan, Krishnamoorthy & Nagarajan (2016).Varadharajan V, Krishnamoorthy T, Nagarajan B. Prevalence of stereotypies and its possible causes among captive Asian elephants (Elephas maximus) in Tamil Nadu, India. Applied Animal Behaviour Science. 2016;174:137–146. doi: 10.1016/j.applanim.2015.10.006. [DOI] [Google Scholar]
- West (2001).West G. Occurrence and treatment of nail/foot abscess, nail cracks, and sole abscesses in captive elephants. In: Csuti B, Sargent EL, Bechert US, editors. The Elephant’s Foot: Prevention and Care of Foot Conditions in Captive Asian and African Elephants. Ames: Iowa State University Press; 2001. pp. 93–97. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Questionnaire interviews with camp owners, managers and/or camp veterinarians were performed by using this questionnaire sheet to record information about camp activities, location, programs for tourists, numbers of elephants and elephant management.
Questionnaire interviews with mahouts gathered information on management of their specific elephants; that is, work routine, restraint, rest area, feeding, watering and health care by using this questionnaire sheet.
Data Availability Statement
The following information was supplied regarding data availability:
The raw measurements are available in the Supplemental File.