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THE ROLE OF BIOLOGICAL RESEARCH IN THE DEVELOPMENT OF FACILITIES 1 Michael H. Robinson The National Zoological Park, Smithsonian Institution, Washington, DC 2 0 0 0 8 ABSTRACT Despite great improvement, zoos basically have not been fully responsive to biological imperatives. The reasons for this are suggested, and the potential and actual contributions of biological research in improving facility design are assessed. Biological research has a high potential for enhancing conditions for the animals and visitors alike. Zoos can become important resources for advancing biological science. (Key Words: Animals, Collections, Zoo Animals, Biological Techniques.) J. Anita. Sci. 1989.67:2441-2451 were available. In addition, poor knowledge of the social requirements of many species Zoos have made tremendous progress in the reinforced the tendency toward unnatural last several decades. Until recently, most zoos groupings that resulted from collectionism. In were "collections" that consisted of a wide the middle period of zoo design, the appearrange of vertebrates. Because they were based ance of the enclosures, cages or exhibits also on the principle of being synoptic, they suffered because of yet other factors. Knowlinvolved small numbers of individuals of a edge of the environmental needs of exotic large number of species. This "art gallery" species lagged far behind even the inadequate approach was one factor that resulted ulti- knowledge of their social requirements. It still mately in assemblages of unnatural groups of does, as we shall see later. animals in unnatural surroundings. But other Today it is possible to eliminate the tiled, factors contributed to making zoos look like sterile look, and most zoos do exhibit natural penitentiaries, and later like public bathrooms. social groupings in surroundings that look The final stage in this progression was for zoos natural to our eyes. This progress is partly due to become "naturalistic" enclosures designed to advances in exotic-animal veterinary medito meet the visitors' conception of nature, cine, and also to the application of the results rather than to reflect the animals' perceptual of biological studies of animal behavior. world. These trends were not solely a reflec- However, it would be a mistake to assume that tion of misguided directorial philosophies. these advances are, by and large, the driving Because zoological medicine was in its infan- forces of change. Instead, they have largely cy, indoor enclosures were tiled to permit enabled change to occur, but the motivation cleaning and disinfecting. This "sterile" envi- came from architects and exhibit designers ronment prolonged longevity of the animals who were concerned primarily with appearbefore antibiotics and worming medications ance, public tastes and the dictates of public presentation. The time for a comprehensively biological approach to zoo design has yet to come. The reasons that it has not yet occurred 1presentedat a symposiumtitled"Strategiesfor Coping are complex, very important and worthy of with the PhysicalEnvirronment"at the ASAS 80th Annu. analysis. They are historical, managerial (adMtg., New Brunswick,NJ. ministrative) and sociological. Recent reviews ReceivedOctober6, 1988. of the history of zoo architecture (e.g., AcceptedJanuary20, 1989. Introduction 2441 2442 ROBINSON Polakowski, 1987) seem largely to miss the point when they concentrate on the influence of changing design concepts. The historical origins of zoos provided an original predisposition against their either being, or becoming, biologically inspired institutions. This state of affairs has been maintained by their longstanding social function and the character of their direction. In the last analysis, design concepts have been determined by mission. And the mission, for a very substantial part of z o o history, has concerned itself with providing spectacle for the public. I have stated elsewhere (Robinson, 1987a, b, 1988a) my views on the functional/philosophic dichotomy between botanic gardens, on the one hand, and zoos and aquariums, on the other. In essence, the botanic collection started as science, whereas the animal collection started as spectacle. Historically, even the ancient botanic gardens arose with a strong connection to herbal medicine and agrieulturet hordculmre. From the start, they had a "scientific," or at the very least a "learned," function. Zoos, on the other hand, arose from menageries, and their function almost certainly was nonutilitarian. Zoos were symbols of conspicuous consumption, collections of stares-enhancing "wonders," part of the wideranging appurtenances of imperial power. They were not resources for scholarship. The spectacle of animals in the Roman arena is the progenitor of the spectacle of lions, bears, tigers, elephants and giraffes in present-day zoos. People are attracted to certain animal species for reasons that defy simple explanation (Robinson, 1988b). People still ask for white tigers, black leopards and albino gorillas. Kellert's studies (1980, 1987) are patiently uncovering some of our feelings about these issues. There is little doubt that the way people are moved by large exotic animals, on the one hand, differs from the way they respond to plants, on the other. Whatever may be its basis, it is a fact that a greater proportion of botanic gardens have research departments than zoos do. For the latter the function of public spectacle remains a key factor. Spectacle does not need the broad overview of biology to sustain and maintain it. Rather than biology, it was the support of husbandry-knowledge that proved essential after animals no longer could be collected easily from the wild. In a sense the ecological crisis that ended the zoocollector, Frank Buck phenomenon helped start us all toward a biological approach. None of this is meant to detract from the pioneering studies of zoo-based biologists like Hediger (1955, 1964). Neither should it detract from the biological impact of some classic animal collectors. Stories of collecting from the wild, as reported by highly literate naturalist/collectors such as Gerald Durrell (1960) and David Attenborough (1956), probably inspired many of us with our first major interest in wildlife. The separation between the technical prowess of animal-keeping, on the one hand, and biology, on the other, is still reflected in many zoos. An informal survey of zoo directors in the U.S. reveals that those with a training in biological research are a small minority. (Of course, most modern zoos are businesses and it could be argued that biologists cannot become efficient business administrators. It is interesting to contrast zoos with botanic gardens here). However, this is not the place to consider why we are where we are, but rather to look at how and where biology has changed our approaches and where it could affect the future evolution of live animal exhibitry. Avenues for Input How can biological research affect the development of exhibits? This simple question has extensive and complex answers. They fall into a number of overlapping categories. A diagram helps to clarify some of this (Figure 1). The issue is complicated because there are at least two subjects for analysis. First, one can look at the outcome, or effector end, of the research. This is classification by application. Equally well, one can specify the subdisciplines of biology that can be used in facility planning. This is classification by field of enquiry. Because the threads of enquiry are so complex and their interconnections are manifold, they are difficult to conceptualize. The tabulation below reinforces and expands the conceptualization shown in Figure 1; it is given as a prototype to provoke discussion. Only part of it is covered in this paper. Some Research That Has Been Applied, Some Research That Should Be Applied, And Some Research That Needs To Be Done In a relatively short treatment of a large subject, selectivity is essential. Accordingly, I BIOLOGICAL RESEARCH AND ZOO FACILITIES Exhibit Design Promote Enjoyment and Education 1. Highlight beauty/activity and wonder 2. Promote reverence for life on earth 3. Promote biological viewpoint by combatting i. anthropomorphism ii. dorninionistic attitudes Enhance Improve Conservation Quality of Life 1. Reduce stress 2. Reduce aberrant behavior 3. Increase 'normal' activity 4. prolong life, promote health 5. Increase reproduction 1. Increase reproduction 2. Maintain genetic diversity 3. Maintain survival behaviors 4. Maximize economy Ecological Research Genetic Research Behavioral and Neurophysiologica Research Figure 1. Ways in which biological research can affect the development of zoological exhibits. 2443 2444 ROBINSON have chosen not to review the literature but simply to highlight some case-histories that illustrate what I consider to be important points. This makes the approach idiosyncratic and personal. To define the scope of this treatment I take the "development of facilities" to include not merely (or even mainly) the physical/structural aspects of zoo exhibits but also the management of their biotic components. This means that I arbitrarily ignore such matters as the height of enclosing fences, the width of moats, the regulation of temperature and humidity, and the placement of visitors' visual access in relation to flight distances and so on. These are the conventional stuff of exhibit design. Many of these matters already are well-regulated because they can be dealt with by simple pragmatism, and wisdom about them has accumulated and is even codified (for instance, International Zoo Year Book 1959 to present, Crandall, 1964; Collins, 1973; AAZK, 1985). Trial and error has played a major part in this, and insights from field studies, though potentially important, are much rarer than might be expected. Although a considerable literature does exist, it is noteworthy that a case could be made for the paradox that most zoos have learned more about biology from designing exhibits than they have learned about designing exhibits from biology. (It is worth re-reading Hediger's [1955] classic studies with this revisionist heterodoxy in mind.) Research That Has Been Applied To choose case histories in this category, I have concentrated on work carried out at the National Zoo. I made this choice because the familiar is easier to expound. Reviews of the field by Crockett and Hutchins (1978) and Markowitz (1982) and a host of papers in the International Zoo Yearbook and the journal Zoo Biology will correct my selectivity. As an illustration, our National Zoo coati exhibit forms an instructive example. In this case there was a conjunction between exhibit-based research, a monographic field study and some very simple innovations. The entire process involving the improvement of an existing exhibit, is detailed by Clevenger (1987). The changes greatly enhanced the exhibit, both for the animals and the visitors, without involving any structural changes. The starting point was simple. The important details are that the enclosure is a roughly octagonal, suspended, welded wire enclosure varying from 33' to 36" in diameter, it is 8' high at the edges and rises to 13' to 15' at the peaks. At the time we instituted changes, the entire exhibit was subject to direct sunlight and high temperatures in summer and had a floor of soil and little interior furniture. Prior to the changes, the enclosure had housed a variety of small mammals, including kit foxes, skunks and raccoons. All these animals are nocturnal, so their activity periods peaked when visitor presence was at its lowest. Thus it was an entirely unsuccessful exhibit. Because it could most successfully house small mammals, we chose coatis because they are diurnally active and social. All that was necessary was to provide the right exhibit conditions to give the animals an ambience conducive to activity, naturalness and social harmony. Two factors were key; these were the results of extensive field studies of coati ecology and behavior carried out at the Smithsonian Tropical Research Institute by Kaufman (1962) and Russell (1981, 1983) and pragmatic adjustments as the exhibit progressed. From the research, it was clear that the coati is an omnivore that finds abundant quantities of invertebrates by foraging on the forest floor but also that it spends a considerable time in trees (Kaufman, 1962; Russell, 198t, 1983). Furthermore, it is clear from the same sources that males are solitary, whereas females and young may form very large social groupings that live together in relative harmony. Bearing these two factors in mind, we produced an entirely valid and successful exhibit. We grouped only females together and removed the top layers of soil, replacing them with bark mulch to a depth of 4" to 6". This simulated the leaf-litter of the rainforest. In the center, within a circle of about 12', we provided a substrate of dried pine needles. In addition, we provided extensive climbing surfaces above the ground, particularly in the form of horizontal branches. When we first introduced the animals to the newly changed exhibits, a clear problem arose. This was quickly solved by simple pragmatism, although it could have been anticipated by a careful reading of the biology. The animals needed shade and would not remain active in the hot sun. The shortterm solution was to cover the cage top with tennis netting cloth; later, grapevines were encouraged to grow all over the sides anti roof. BIOLOGICAL RESEARCH AND ZOO FACILITIES As a result of the vine's growth, the coatis subsequently added grapes to their diet! Foraging activity was encouraged by distributing food pans throughout the exhibit, and burying it in the substrate. Additionally, during peak visitor hours, supplemental feedings of mealworms, crickets, raisins and grapes are broadcast into the mulch and leaf-litter. The effect of all this is striking: animals are visible more than 95% of the visitor day and 65% of the time are indulging in such active behaviors as exploring, social interaction, walking and climbing (Clevenger, 1987). Another study of considerable interest that dramatically affected the perceived quality of exhibits is that conducted on regurgitation and re-ingestion behavior (herein abbreviated as r/r behavior) in gorillas (Gould and Bres, 1986a,b). This behavior is very common in zoo exhibits: gorillas regurgitate their food onto the floor, or into their hands and then lick it up. This behavior looks highly aberrant and certainly produces adverse visitor reactions. Our study of the r/r phenomenon involved direct observations on gorillas as well as an extensive survey, by questionnaire, of gorilla behavior at 17 other zoos, The biological studies were illuminated by discussions with investigators of the human rumination phenomenon, which appears in many ways equivalent to r/r behavior (Gould and Bres, 1986a,b). The studies eventually led to a relatively simple solution that does not seem to be directly relevant to the probable causation of the aberrant behavior. R/r behavior is considered to be correlated with the occurrence of social deficits during early development. In particular, wild-caught and hand-reared captive born gorillas show a higher incidence of r/r than mother-reared infants do. Feeding browse reduced r/r behavior very considerably in three adult gorillas at the National Zoological Park. It is not clear why this should be the case, except perhaps that eating browse substitutes for the time that gorillas in the wild spend daily foraging and feeding. Missed Opportunities: Research That Should Be Applied One of the most distressing reactions of the public to zoo conditions is anthropomorphism. This leads to objections to zoo conditions that are based on fallacious attitudes, including the application of the philosophical concept of 2445 "freedom" to both the presumed wild state of animals and their "captivity." I have dealt with this "Rousseau Fallacy" elsewhere (Robinson, 1988c). Here is worth stressing that because some visitors see many animals in human terms, they fail to see them as living in their own different world with their own imperafives. From this spectators conclude that animals are "bored" if they sleep, "stressed out" if they lie on their backs, and "imprisoned" if their enclosures look small from our scale. This also goes with criticism of nonnaturalistic exhibits and an idyllic view of life in the wild. We certainly have enough evidence from behavior studies to know that the perceptual worlds of many animals are extraordinarily different from our own. Some of the most relevant studies, still valid, are those of Von Uexkull (1934), English translation in Schiller (1957), and Tinbergen (1951). In addition, we know that biological reality means that predation, parasitism and competition (often mediated through territoriality and dominance orders) may make life extremely stressful for the great majority of animals. All these aspects of anthropomorphism and biological misunderstanding in part are encouraged by the fact that zoos present a human-eye view of animals to their visitors. I have developed this theme in considerable detail elsewhere (Robinson, 1987c, 1986b), but here are some reiterations that I think are important. First, a number of facilities need to be built that show that the conceptual worlds of animals are, in reality, very different from our own. This means building exhibits that are black and white to show that some animals do not have color vision, or exhibits that have a "color balance" different from our own, showing that animals can have a very different world (red/ green color blindness, for instance) even though they can see color. A further step would be to scale up an exhibit area so that it is presented at a small-animal eye view, not that of a large erect-standing human. (This is the kind of thing that Hollywood has done for sensation in films such as "The Incredible Shrinking Man." This technique could be reversed for perhaps more respectable scientific purposes.) Another aspect of biology that needs to be highlighted to present a valid view of animals concerns predation, killing and death. We cannot persist with the idyllic view of nature that we present in zoos without this resulting 2446 ROBINSON in further seriously distorted public attitudes. Too many other sources of popular animal lore already reflect nonbiological attitudes of a benign world of nature. Present tastes may prevent us from having anything resembling prey capture occur in our vertebrate exhibits, but we probably can design invertebrate exhibits in which an octopus eats live shrimp, anemones capture crabs, and micro-organisms prey upon each other in a biologically valid system. We have, in fact, just added to our reptile house specimens of the species of frog that recently figured in research on a whole new family of antibiotics. Explanatory graphics point out that there is a constant "arms race" between different organisms, and that where this is the most intense and most complex (i.e., in the tropics) is exactly where we expect to find the most useful new weapons in our fight against viruses, bacteria, fungi and other pests. Apart from such broad issues, there are some results of pragmatic studies of animal exhibits that need broader application. We need to recognize that the presence of the masses of zoo visitors is an important intrusion into the animal's environment. In studies at NZP, both Baldwin (unpublished data) and Carlstead (unpublished data) have noted that zoo animal activity is altered by visitor disturbance, and even by janitorial noises. The acoustic environment is important to the exhibit ambience. Most nocturnal houses that reverse the animals' subjective day/night regimen by lighting do not manipulate the acoustic day/night regimen even though acoustic cycles characteristically are as distinct as visual cycles. Thus, nocturnal animals in "twilight exhibits" may be receiving contradictory signals. Low light signals night, whereas high noise levels signal day. To correct this, we can synthesize appropriate sound regimens to match the light regimens and mask external noises (L. Gilbert, personal communication). Furthermore, we need to recognize that species of animals differ considerably in their responses to environmental complexity and variability. Some animals are capable of coping with new environmental stimuli in an opportunistic manner that almost certainly has been subject to natural selection. Others find novelty stressful; these animals can be described as neophobic. Greenberg (1983, 1984a,b) have done extensive studies on the foraging behavior of birds. In these experi- ments, differences between species in their ability to explore new situations have been tested extensively. The results provide us with insights that are of great potential importance in developing criteria for the choice of species for zoo exhibits. In some cases, neophobic species should be avoided, but in other circumstances neophobia perhaps could be utilized in confining certain kinds of animals by creating a psychological barrier of unfamiliarity. If this does not provoke escape by panic, it could be effective for that period needed to break down the fear of the new and different. Research on the golden lion tamarin led to the creation of a new exhibit that has been enormously successful. This species essentially was rescued from near-extinction by a zoo-based breeding program (Kleiman et al., 1986). The results of reintroduction efforts suggested that deficits in foraging, food recognition and feeding behaviors found in zoo-bred specimens were considerable, so extensive training regimes were used to prepare the animals for the wild. Additionally, there were deficits in the avoidance of harmful entities (predators, dangerous animals and potentially poisonous foods) and in locomotory behavior (including apparent neophobia and reduced exploration). All these factors, in conjunction with the nest-site dependence of family groups, suggested that if a socially harmonious grouping of tamarins were released into an area of forest within our zoo, they would remain there unbounded by physical barrier as long as they had food and a nest-site (Beck actually made this proposal). This idea was tested in 1987, and again in 1988. Not only was it an outstanding success as a "cageless" exhibit, but it has proved to be an interesting and inexpensive way to prepare tamarins for eventual reintroduction to their homeland. With time they learn the necessary survival skills. The group has remained outdoors from May to late September, and has maintained excellent physical condition. The sight of these gloriously colored small monkeys freely ranging within the trees has been extremely satisfying to all concerned. (There is an important caveat to make here. The fact that zoo-bred tamarins have deficits in their survival behavior should not lead anyone to assume that zoo conditions are inimical to these animals. Nor should we conclude that the tamarins in zoos are more stressed in their enclosures than in the wiM. Zoo-raised tamar- BIOLOGICAL RESEARCH AND ZOO FACILITIES ins live longer than those in the wild and they probably raise more young more frequently. In the wild they almost certainly die violently, or from starvation or painful disease, in contrast to the zoo situation.) The fact that their survival behavior has become deficient in zoo conditions is highly instructive. It supports the inference that learning paradigms in tamarins are adaptively tailored to allow them to be flexible in a variable environment and that i~: the course of evolution such flexibility has been the subject of selection. Natural behavior thus is learned in a manner that fits it to the circumstances. This is an important area for fundamental research that has not been exploited. Lorenz (1965) first drew attention to the very real consequences of what he called "the innate schoolteacher": evolutionarily based proscriptions on learning. We now have an exciting new technique that could yield insights in this field. Surrogate mothers of in vitro fertilized young can be of a related, but different, species. Young thus produced can be studied to see what is hard-wired vs what is acquired in utero. Research That Needs To Be Done Zoos are remarkable and greatly underutilized resources for biological research. Comparative studies frequently are high-yield tools for the elucidation of evolutionary problems, and zoos may offer unique opportunities for broad-spectrum comparisons. In studies' of social behavior, for instance, it seldom is possible for a field researcher to make broad comparisons within a wide range of species. It would be impossible to directly compare similar behavior units in the same place for all four genera of apes. But in many zoos, this would be possible, looking from gorilla, to chimpanzee, to orang and to the gibbons and siamangs, literally on the same day. It also is possible to do such a zoo study and know the precise genetic, medical and personal history of each individual animal, another thing that seldom is possible in the wild. Of course there are drawbacks; large animals may not be in sufficiently large enclosures to fully express their behavioral repertory, nor may they be entirely wild after being habituated to or born under zoo conditions. Despite these caveats, great research opportunities exist. One that is relatively untapped is the chance to look at the complexities of the reactions between animals 2447 and the biotic elements of their environment other than their own species. We have little knowledge of the environmental factors that are relevant to the lives of most animals. Social behavior has been widely studied and it is a natural focus for ethological investigation. In part, this is due to the fact that much of social behavior is mediated through highly evolved and often conspicuous and stereotyped signals. Precisely because they are signals (displays, etc.), they attract the attention not only of their intended recipients, but our attention, too. Because they evolved to communicate, they are more easily interpreted by alien species (us) than are many aspects of noncommunicative behavior. The bias for intraspecific studies not only reflects these factors, and our sensory biases (there are fewer studies of olfactory communication than of acoustic or visual communication), but a/so other research-procedural factors. It is easier to observe, experiment upon, and manipulate social interactions than to do the same to many subject/environment interactions. Such study is vital to our understanding of behavior and ecology to know what is relevant to survival in each animal's surroundings. As Tinbergen (1963) pointed out so forcefully, we have little idea what most animals (young birds, for example) need to learn about their environment as they mature. The golden lion tamarin reintroductions discussed above show how great are the behavioral survival deficits found in zoo-born animals kept in static environments with predictable flushes of food and absence of predators. The tamarins cannot adequately cope with finding or processing unaccustomed food, with locomotion among unaccustomed substrates (real trees!), finding shelter or avoiding predators. Studies of survival behavior vis-a-vis environmental factors are technically extremely difficult in the field, and the difficulty increases with increasing complexity of habitat. Most wild habitats cannot be modified for experimentation without massive logistic problems, but zoo habitats can. Thus there is an untapped potential for direct investigations of what could be called "environmental relevance." Some of the questions that have hardly been posed but that arise inevitably out of our attempts to create artificial habitats conducive to the well-being of animals are crucial. They are raised in simple form by the naive anthropomorphism of zoo visitors, and in another context, more 2448 ROBINSON obliquely, by animal welfare activists in relation to the conditions of domestic animals in the food industry. The same basic ignorance of what really is the relationship between animals and their environmental needs lie behind questions such as, "How would you like to be imprisoned in a concrete cage without the sight of trees and the blue sky? and How would you like to be shut up in an overcrowded hen-house with no freedom? These questions are naive and we tend to answer them by pointing out that they reflect aberrant conceptions, but they are part of a sophisticated problem. As scientists we cannot say with any degree of assurance whether monkeys react to trees as trees with the intertwined stimulus effects of leaves, bark, branches, color, form, odor, movement, sound and so on, or whether a tree is merely an avenue from one food source to the next, a mating platform or an arboreal minaret from which to greet the dawn. From what we know of stimulus filtering in social contexts, we could feel justified in arguing that a tamarin should be as happy in an aerial maze of plastic tubes, with sliced food provided regularly in dishes, as it is in the Brazilian jungle. It is consistent with our knowledge of ethology to consider that in the real jungle the tamarins do not see the jungle, but just a mosaic of challenges, stresses and opportunities. Dawkins (1980) has brilliantly analyzed the problems involved in assessing animal welfare matters in fanning from this angle. In a penetrating analysis, that otherwise represents a new level of sophisticated discussion for this subject, she largely misses or muffles the point about our ignorance about the "natural" state of animal/environment interaction and environmental relevance. Preference tests between environments are advocated as a means of study. This of course is an extraordinary powerful tool in many instances. However, the influence of early learning on the outcome of such tests should not be underrated; clearly, zoo-raised tamarins could be expected to prefer enclosures to the terrifying state of the wild. Incidental spin-offs from studies, often involving preference tests, with a direct animal husbandry orientation also cast light on environmental relevance. Many examples are reviewed by Dawkins (1980). We need to apply concepts derived from fundamental studies to the assessment of animal husbandry conditions in modem farming. We also need to use these insights in designing further research in this field. For instance, it is not enough to study whether battery hens are more stressed than free-range hens; we also should be looking to which elements of the natural world are attended to influence domestic animals. Do hens find the world of the open air, sunshine, blue skies, green fields and bucolic rural scenes satisfying? This question is not a reductio ad absurdum, there is a very real issue at stake here. The issue is susceptible to study. Studies of animal-environment interaction need expansion, both as part of the corpus of ethology and throughout the zoo world. They have an immediate relevance to animal welfare issues. But it is essential that the researchers who carry them out should be aware of their broader, more theoretical and academic implications. For example, we have recently carded out studies at the National Zoo on the effects of the presence of visitors on the behavior of zoo animals. In one study, visitors were barred from pathways giving access to certain outdoor cages, and animal activity was monitored in situations with vs without visitors. A simple loop trail that passed our separate serval and leopard exhibits was closed for this experiment (Baldwin, unpublished data). Serval activity increased by up to 30%, but activity of the male leopard actually went down by more than 20%. Studies on leopard cats and fennec foxes in the small mammal house (Carlstead, unpublished data) showed a marked effect of high visitor rates and noisy janitorial activities on pacing behavior. These studies immediately feed information into exhibit design, but they also have extensive implications for understanding what components of their environments animals may attend to. The experimental studies of Greenberg (1983, 1984a,b) show that ingenious experimentation is possible in this field. We clearly need to expand it. There probably are other areas for research as potentially important to exhibit design as the ones that I have stressed. Many will be obvious from my tabulation (Table 1). One may not seem important but in future will become so. We can now collect urine from the floor to exhibit enclosures and assay it for a variety of biochemical factors. Urinary hormone analysis of zoo animals has become relatively routine. With this has arisen the possibility of detecting compounds associated with stress and consequently of objectively BIOLOGICAL RESEARCH AND ZOO FACILITIES o O 23 =1 I= Z O .=~ b == O ~"~ ~ ==N 9 m ..... o o o "~1 O ~ = . l 9 e ~ o == s ~ ~ 8 ~ o ii 9G ._ 9 < i ~.~ ~.~ ~ ~.~ E "~ .-~ ~ .[ ._~ .s~ . ~= 2 - ~.~ = 8.~ ~ < .~..~. = = <[... .~..~ =1 ,~ ,.4 m # ~-~ ~~ d ' ~ ~; =;z .'-, o ~-o ~ ~ 2449 2450 ROBINSON measuring levels of stress in zoo animals. Up to now we have been able to measure stress by its behavioral indicators, and by inference (Dawkins, 1980). Should a reliable new tool emerge, this will allow us to refine exhibits even further in the interests of our animals. Conclusion Design of facilities at zoos has been less influenced by biological considerations than it ought to have been. Desmond Morris, an ardent proponent of zoos, has analyzed the defects in exhibits and designs that have persisted despite the reforms we have enacted. His analysis (Morris, 1968) has been largely ignored, but it is penetrating and important. Every zoo director should read, or re-read it. What is wrong with zoos according to Morris? The answer is very simple. Having solved the problems concerned with the social milieu of our animals, we have failed to satisfy the exploratory drives of many of them. According to this judgment there are basically two kinds of animal, the specialists and the opportunists. The specialists need an outlet for their finelytuned adaptations, then they can relax; otherwise they exhibit frustration behaviors. In contrast, the opportunists are "forever investigating, always on the move. It is because man, the supreme opportunist, belongs to this category that we find this group so fascinating." In zoos "the opportunists are precisely the animals that find the sterile, restricting life of the zoo so frustrating and so damagi n g . . . T h e nervous system of the opportunist seems to abhor inactivity. And inactivity is just what the zoo cage has to o f f e r . . . w e make it as difficult as possible for him [the zoo animal] by restricting his environment in almost every conceiving way. We rigidify it, limit it, standardize it and sterilize it. Then [we] laugh at the improvisations of the frustrated, inquisitive animals it houses." Morris' old zoo (London) has now, 20 yr later, employed someone specifically to look into habitat enrichment. Before we defensively assert that these strictures are unjust, and we have improved things since then, remember that zoo-born tamarins are deficient in survival behaviors because even the most innovative enclosures are rigidified, standardized and limited. When we put them into a more open system, their behavior expands and flourishes, as we have seen at NZP. We need to think more about creating variety and exploratory opportunities. Like the coatis, we need to nose around for new experiences and new opportunities for our opportunists. It is not imprisonment, or lack of freedom that characterizes a bad exhibit, but boredom, if we were free to anthropomorphize. If we return to the zoo-world's relative inattention to biological research considerations, reasons for which could prove worth a research effort and be of considerable historical interest, we have to say that the potential is high. Zoos could be centers of exhibit-based research on an expanded and expanding scale. Such research would not only enrich our basic biological knowledge but also could enrich the zoo experience for visitors. In addition, it should enhance the health and welfare of the animals. Finally, the ultimate step in the evolution of zoos is to create the biological park to replace the zoological park. This, the zoo-that-is-not, would integrate the plant and animal kingdoms in a new forward step in bioexhibitry. It would be a powerful new tool for education, conservation and recreation. Research would be enhanced by its existence and be necessary for its flowering. To return to Morris (1968) on the need for zoos, let me finish with this account of his first zoo visit: 'q'hat visit did more for my later interest in animals than a hundred films or a thousand books. The animals were real and near. If zoos disappear, I fear that our vast urban populations will become so physically remote from animal life that they will eventually cease to care about it." This is our responsibility, it is enormous, it eventually means the custody of life on earth. We must be worthy of it. Literature Cited AAZK. 1985. Biological Values for Selected Mammals. American Associationof Zoo Keepers, Inc., Topeka, KS. Attenborough, D. 1956. Zoo Quest to Guiana. Scientific Book Club, London. Clevenger, S. 1987.Utilizingnatural history and behavior in exhibit design: Coatis (Nasua nasua) at National Zoological Park. In: Proc. AAZPA Regional Mtg., Syracuse, NY, March 1987. pp 82-89. Collins, L. R. 1973. Monotremes and Marsupials. Smithsonian Institution Press, Washington, DC. Crandall, L. S. 1964. The Managementof Wild Mammalsin Captivity. University of Chicago Press, Chicago. Crockett, C. and M. Hutchins. 1978. Applied Behavioral Research at the Woodland Park Zoological Gardens Seattle, Washington 1977. Pika Press, Seattle. Dawkins, M. S. 1980. Animal Suffering. The Science of BIOLOGICAL RESEARCH AND ZOO FACILITIES Animal Welfare. Chapman and Hall, New York. 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