1. Introduction
Despite considerable research efforts, there remain gaps in the knowledge of zoo and aquarium animal nutrition [
1]. Zoological collections are faced with the challenge of not only providing food that is nutritionally comparable to the wild diet, but also encouraging animals to express naturalistic feeding behaviours. To further compound this challenge, many zoo-housed species have yet to be formally studied in the wild or in captivity [
2,
3]. This limits the availability of keepers and aquarists to provide the most nutritionally suitable diets for their animals.
The science of food presentation has been gathering interest recently [
1]. Some food presentation techniques may provide opportunities for animals to engage in species-specific, natural behaviours, such as gnawing, carcass manipulation or plucking of food [
4,
5,
6]. Careful consideration of feed presentation styles may therefore provide animals with enrichment opportunities.
One method of feeding zoo animals is to present the diet chopped into cubes [
5]. Whilst frequently used in zoos globally, there is limited evidence available to suggest that animals benefit from chopped food items [
7,
8]. Anecdotally, it has been suggested that chopped food may limit aggression between animals and promote sharing [
1]. However, behavioural research has demonstrated that providing whole-food items tended to reduce aggression [
1,
7,
8]. Additionally, chopping food may increase the speed of nutrient breakdown, desiccation and bacterial contamination of food items [
5,
9].
Research has been conducted into the effect of chopped food for a range of mammals including primates [
1,
8,
10], tapirs, and coatis (
Nasua nasua) [
7]. However, there is limited research available on the effect of chopped food on avian behaviour, despite the fact they are the most speciose taxon in zoological collections globally [
11]. Related research on food pellet size suggests that oversized pellets improved food manipulation and gnawing behaviour in Orange-winged Parrot (
Amazona amazonica) [
12,
13]. In preference and motivation studies, the Amazon parrots were willing to lift weights in excess of 100 g to gain access to over-sized pellets, even when the smaller but nutritionally identical pellets were also available [
12,
13]. Extensions of this research could be conducted on species that are frugivorous. Whole fruit and vegetables may therefore be valuable in promoting natural behaviours for some zoo-housed birds.
The Turacos (Family Musophagidae) are a group of 23 bird species which occur throughout Africa [
14]. The majority of turaco species are specialist frugivores in the wild, with some species feeding exclusively on fruit items [
15,
16,
17]. However, some turacos also supplement their diet with small amounts of leaves, flowers or galls, depending on preference and seasonal fruit availability [
18,
19]. The Great Blue Turaco (
Corythaeola cristata), for example, is believed to have the highest leaf intake, with leaves making up roughly 25% of the diet [
19]. In the wild, turacos are selective in terms of their fruit consumption, appearing to choose hexose-rich fruits over fruits which are high in fat or nitrogen [
18,
19].
Hexose-rich fruits are easily digested, and turacos possess rapid food transit times as a result [
15,
16]. Studies have investigated the effects of seed size on food transit times in the gut [
15,
16], revealing that for some species, larger seed sizes result in even faster food passage rates. Wild turacos search for food by travelling between fruiting trees and then pecking large food items or swallowing small food items whole [
18]. Turacos generally forage throughout the day, and take many regular, small meals rather than one single, large meal [
19,
20]. In captivity, this means that turacos are often fed ad libitum, with constant access throughout the day to their food source.
Over 1500 Musophagidae individuals are found in zoos, according to a search of the Zoological Information Management System (ZIMS) in May 2021 [
19]. While this is not a large population in comparison to other zoo-housed avian taxa, such as flamingos or penguins [
19], turacos are a specialist group and are of interest to the zoo biologist. Turacos are often provided with chopped food diets in captivity, making them a good model for food presentation research.
The aim of this project was to identify whether a change in food presentation would affect the feeding behaviours of zoo-housed turacos. Additionally, this study aimed to determine the effects on keeper workload when changing from a chopped-food to whole-food diet.
2. Materials and Methods
2.1. Study Subjects
Prior to this study commencing, this project was ethically reviewed and approved by the University Centre Sparsholt Ethical Review Committee (code TUR210919). Three groups of birds were observed for this study: two housed at Sparsholt College’s Animal Management Centre (AMC) in Hampshire and one at The Living Rainforest in Berkshire. The two groups at Sparsholt College consisted of one trio of juvenile White-cheeked Turacos (
Tauraco leucotis), and one adult pair of White-cheeked Turacos. Both groups were housed in aviaries with both a heated indoor and outdoor area. The exhibits were sparsely planted with small shrubs and bamboo, along with elevated perches. During the observation period for the White-cheeked Turaco groups, the temperature ranged from 3 to 13 °C and the humidity from 65 to 97%. The group at the Living Rainforest were an adult pair of Fischer’s Turacos (
Tauraco fischeri) who were housed in a well planted aviary containing tropical plants such as a large
Monstera deliciosa. The exhibit was inside a temperature-controlled (between 25–26 °C) and humidity-controlled (80–85%) glass house (
Figure 1). Light levels were not analysed for either group, but as the Living Rainforest exhibit was inside, light levels were generally lower. Both adult pairs included in this study were bonded male and female pairs who had been housed together for several years (
Table 1). The researcher was able to differentiate between subjects by the coloured bands on their legs and by subtle differences in markings.
Data were collected between November 2019 and January 2020 and behavioural observations were carried out from the beginning of morning feeding at 09:00–12:00 at Sparsholt College, and at morning and afternoon feeds at The Living Rainforest from 09:00 to 12:00 and from 14:00 to 16:00. A total of 30 h was collected for each group, totalling 90 h of observations.
2.2. Behaviour
All observations were conducted by the same observer (BG), who sat quietly a minimum of five meters away from the study subjects for all observations. An ethogram for state behaviours (
Table 2) was created for the purpose of this study as there were no published ethograms specifically for turaco species. Some of the behaviours defined in the ethograms were adapted from work by Almeida et al. [
21], Barrera et al. [
22] and Blanchett [
23], all of which studied a range of avian species.
Subject state behaviour was recorded using instantaneous focal sampling at one-minute intervals and continuous focal sampling was used for recording event behaviours. Weather conditions, temperature, and humidity were recorded using a local weather forecast, and presence of students, staff or visitors was also recorded.
2.3. Food Intake
In both conditions, the fruit and vegetables provided were weighed before and after the observation period to measure how much was consumed. Measurements were undertaken using an Ascher 200 g Portable Digital Pocket Scale: this scale allowed measurements to be measured to the closest 0.001 g. A sample of the same foods was prepared in the same manner (chopped or whole) and was weighed before and after placement in a nearby, vacant enclosure. This extra portion acted as a correction factor, to determine whether excessive rain or desiccation had changed the weight of the food. When this control was analysed, the results were ±0.1, so food samples were affected minimally by the environment. Quantities of food items for each group involved can be seen in
Table 3. It was not possible to measure the weights of foods for Fischer’s Turaco group due to accessibility issues.
2.4. Diet Preparation
There were two conditions for this study: the chopped-food condition consisted of fruits and vegetables being cut up into approximately 1 cm × 1 cm cubes, and in the whole-food-condition fruits and vegetables were provided either entirely whole or cut in half. The birds had previously been provided with whole fruit as enrichment (the diet was normally provided in a chopped format) and no new fruits or vegetables were used as part of this study. The conditions were provided on a randomised schedule to remove order effect. Pelleted feed was always provided in metal bowls (both groups at Sparsholt College) or in coconut bowls (The Living Rainforest) as per the normal husbandry routine. In the chopped-food condition, the fruits and vegetables were provided in a separate metal bowl to the pelleted feed. The whole foods were presented speared on nails or skewers (either hanging or attached to the walls) and were scattered throughout the enclosures. Fruit provided included apples, bananas, pears, papaya, grapes, blueberries, and plums, and the vegetables included sweet potato, broccoli, courgette, and butternut squash. Vegetables were steamed for both the chopped and whole conditions as per the standard husbandry regime. The skins of fruits were included when food was presented in the whole condition.
The amount of time required to prepare the diet was also recorded. One of the researchers (BG) used a timer to record the number of seconds it took for keepers to prepare the diet (including weighing out pelleted feeds and washing equipment after preparation had taken place).
2.5. Data Analysis
Data were compiled onto an Excel™ 2016 spreadsheet, and then uploaded to Minitab, version 19, for analysis. Data on ‘time taken to prepare diets’ were tested for normality. Data were normally distributed, and a two-sample t test was run to determine whether the diet type (chopped or whole) affected the amount of time taken to prepare the diet.
The amount of food eaten was calculated by deducting the amount of food remaining at the end of each observation from the amount of food offered. A correction factor was applied to account for changes in food weight as a result of environmental conditions (rain or desiccation) (
Table 1). The ‘food eaten’ data were not normally distributed. As a result, a Kruskal–Wallis test was used to investigate the effect of group (Fischer’s, juvenile White-cheeked or adult White-cheeked) and diet condition (chopped or whole) on the amount food eaten. Pairwise post hoc tests were run; these were either Mann–Whitney U tests (when comparing between adults and juveniles) or Wilcoxon tests (comparing between chopped and whole conditions).
To consider the differences between species and housing conditions, behavioural data for Fischer’s Turaco and White-cheeked Turaco were analysed separately. For Fischer’s Turaco, the effect of chopped or whole-food condition on behaviour was analysed using either paired t tests or Wilcoxon’s tests, depending on whether data were normally distributed. For the White-cheeked Turaco, the effects of food condition and social group were analysed using a series of Friedman’s ANOVAs, as all data were determined to be non-parametric. Where significant differences were identified, pairwise post hoc Wilcoxon’s tests were run to determine where significant differences lay.
4. Discussion
Overall, there was no significant difference between the amount eaten for turacos under either the chopped or whole-food conditions: significant differences were found only in the amount of food eaten by juveniles versus adult birds. Food condition significantly affected the amount of preening and feeding seen in Fischer’s turacos, and no behaviours in White-cheeked Turacos. Keepers spent significantly less time preparing diets that contained whole fruits and vegetables, thus saving time for other duties.
4.1. Behaviour
Two behaviours were significantly affected by food condition for Fischer’s turacos: these were food manipulation, feeding and preening. Preening behaviour decreased when whole foods were provided, whereas feeding increased. The reduction in preening behaviour may be as a result of increased feeding: birds required more time to process food, so had less time to engage in preening. Locomotion, whilst not significant, also increased slightly for Fischer’s turaco pair when whole foods were provided.
For the White-cheeked Turacos, the results are more complex. While two results (allo-feeding and preening) were significant, post hoc analysis revealed that the significant differences were between adult and juvenile pairs for preening, with adults spending more time preening. Allo-feeding occurred in adults but not in juveniles: this is because allo-feeding is related to pair-bonding [
19]. The change in preening behaviour is also attributable to differences between adult birds and juveniles. Additionally, there were differences in feeding between juveniles and adults in response to the whole-food condition. While the trend toward increased time spent feeding was seen for all birds with whole foods, the juvenile turacos appeared to increase their time spent feeding more than adults. This is important to note, because it suggests that birds of particular life stages may be more sensitive to food condition changes. It is therefore important to monitor all bird life stages, rather than focus solely on adults [
22,
23].
Across both species, the amount of time spent feeding increased when whole foods were provided. The whole-food items may have required more time to process and therefore presented a greater challenge than the traditional diet. Wild turacos feed on a variety of different fruit species [
15,
18,
19], encompassing a range of different sizes and textures. Some of the fruits encountered in the wild are similar in size to chopped food items. For both wild and captive turacos, these food items were generally swallowed whole. In this study, the larger food items required turacos to peck at the food and gouge out portions of fruit using their beaks. This required the turacos to expend a little more energy in the processing of their food and is reflective of some of the larger fruit items that may be encountered in their African forest habitat [
18]. In this study, relatively soft fruits were used: some wild fruits may have much tougher skins and rinds that require further processing [
19].
Food interaction times have increased in other zoo studies when foods are provided whole (e.g., in tapirs and macaques [
1]). In Amazon parrots, preference has also been seen for larger food items, even when both large and small items are of the same nutritional value [
12,
13]. This extended period of time engaging in food manipulation and feeding may have some enrichment value for the birds [
24,
25]. An increase in these behaviours may also have some benefit for public engagement in a zoo environment, as increased animal activity has been shown to have a significant bearing on visitor interest [
26].
Inactivity was not affected by food condition. The differences in inactivity level appeared to be much greater between individuals than as a result of food condition. Increased activity levels are often considered beneficial for zoo animals, particularly for species that become inactive in captivity. It is not clear that food presentation style affected the inactivity levels of the birds. If the aim is to increase activity levels, the change of a predominantly whole-food diet may not satisfy this aim [
26,
27].
Overall, the feeding of whole-food items had relatively little influence on behaviour, aside from feeding behaviour. From one perspective, this suggests that the food condition has limited impact on the behaviour and welfare of the birds. Many birds are neophobic when changes are made to their diets [
21], so it is promising to note that the birds did not show clear signs of aggression or distress when whole-food items were provided. If birds showed few behavioural responses to the change in feeding style, it is likely that the food condition did not impact bird welfare.
4.2. Food Intake
There was no impact of food presentation style on feed intake. Whilst significant differences were identified, these were between groups (juvenile versus adult White-cheeked Turaco) rather than between feeding styles. Generally, juvenile birds tended to take in more food than the adults, which may be in keeping with higher nutrient requirements for growing birds. Despite the difference in intake between groups, there were not significant difference as a result of diet. This means that the whole food style did not cause birds to overfeed or stop feeding on their fruit. This is important to note because turacos are often also fed a pelleted component in their diets (in this study, T16, leafeater pellets and Zoo Diet A). These pelleted feeds contain much of the vitamin and mineral diet that the birds require for good health. While pellet intake was not directly assessed in this study, it should be noted that food condition change did not appear to affect the quantity of fruit taken, and therefore should not affect the normal amount of pellet eaten per bird.
Feed intake studies are an important tool for assessing the effects of dietary change [
25]: while the diet was strictly speaking not changed, the presentation style was. A sudden decrease in diet may be a sign of either neophobia or unsuitable diet: this was not identified in this study. If the amount of food eaten did not change between conditions, this suggests there was limited impact of diet style on the accessibility of food to the turacos.
4.3. Diet Preparation
Overall, keepers were able to save an average of 151 s of time when preparing whole-food diets. Some of this time was saved because the keepers were not chopping foods: the remainder was saved because keepers were spending less time washing knives and chopping boards. Whilst 151 s initially does not appear to be much time, it should be noted that 2.5 min on average could be saved at every feeding time. For a single turaco exhibit, the total time saved per year using whole food preparation is 15.31 h. This time saving might be multiplied by the number of aviaries containing frugivorous species that could be provided with whole-food diets. The extra time saved might then be devoted to other keeper duties: for example, keepers may be able to spend more time engaged in enrichment activities [
5].
Additionally, there may be some benefits in leaving foods in a whole condition in terms of nutritional quality. It is well recognised in human nutrition studies that chopping of foods increases their metabolic rate, desiccation rate, browning and production of waste products such as ethylene [
28,
29]. The higher the environmental temperature and the smaller the fruit and vegetable pieces, the more rapidly changes in nutritional quality occur [
9]. In exhibits where temperatures remain high (such as rainforest biomes), the effects of chopping impact food quality more rapidly. This may result in food that loses some of its vitamin and nutritional value or tastes unpalatable to the birds. Additionally, cut surfaces are more likely to result in bacterial contamination from food preparation utensils or enclosure furnishings [
24]. Maintaining food in a whole format may therefore result in food staying fresh for longer periods of time.
4.4. Future Directions
There is a growing evidence base that suggests naturalistic feeding styles may be beneficial for welfare [
1,
5,
7]. However, the literature on food presentation, specifically on the chopped versus whole concept, tends to focus on mammal species [
5], even though birds are better represented in zoological collections in terms of numbers of species [
11]. There remain many gaps to be filled in the literature on bird food presentation [
25]. Model species for chopped and whole food presentation research should be species that feed primarily on fruits and vegetables in captivity. Among the birds, the Orders Columbiformes (pigeons and doves), Bucerotiformes (hornbills), Psittaciformes (parrots) and some Passeriformes (songbirds) are good candidates for future study, on account of their diets and representation in captivity [
30]. Research should be undertaken whenever trialling the new feeding style to ensure that food intake and behaviour are not impacted.
Future research should also investigate the ability of birds to process thick peels or shelled fruits and vegetables. In this study, the fruits that were used had thin skins and were easy to gouge. The vegetables used were also steamed in order to make the food softer. As a result, it is beyond the scope of this study to determine whether turacos could process fruits with thicker skins, such as pineapples [
17]. It is likely that some birds, such as macaws, may be better equipped to process tough fruits: the blue-and-yellow macaw is an example [
21,
31]. Future research could determine the thickness and strength of fruit peels, shells and rinds and use this information to identify a bird’s capabilities in terms of food manipulation. Future studies should continue to incorporate control food to account for water accumulation or loss through evaporation.
Previous studies on zoo-housed birds have also showed that other variables, such as temperature, humidity, visitor and keeper presence may affect behaviour [
30]. The potential impact of these extraneous variables was not controlled for in this study. Similarly, it should be acknowledged that there only a small sample size was available for this study. While this small sample size is reflective of the nature of turaco keeping (they are often kept in pairs or singly), future studies should aim to overcome this small sample challenge. To summarise, future multi-zoo studies could take into account the influence of environmental and anthropocentric variables, ensuring they maximise the sample used in their study.