Tool-use for drinking water by immature chimpanzees of Mahale: prevalence of an unessential behavior

Use of leaves or sticks for drinking water has only rarely been observed during long-term study of wild chimpanzees (Pan troglodytes schweinfurthii) at Mahale. Recently, however, we observed 42 episodes of tool-use for drinking water (73 tools and two cases of using tool-sets) between 1999 and 2004. Interestingly, all of the performers were immature chimpanzees aged from 2 to 10 years. Immature chimpanzees sometimes observed the tool-using performance of others and subsequently reproduced the behavior, while adults usually paid no attention to the performance. This tool-use did not seem to occur out of necessity: (1) chimpanzees often used tools along streams where they could drink water without tools, (2) they used tools for drinking water from tree holes during the wet season when they could easily obtain water from many streams, and (3) the tool-using performance sometimes contained playful aspects. Between-site comparisons revealed that chimpanzees at drier habitats used tools for drinking water more frequently and in a more conventional manner. However, some variations could not be explained by ecological conditions. Such variations and the increase in this tool-use in recent years at Mahale strongly suggest that social learning plays an important role in the process of acquiring the behavior. We should note here that such behaviors that lack obvious benefits or necessity can be prevalent in a group.     

The conditions for tool use in primates: implications for the evolution of material culture

In order to identify the conditions that favored the flourishing of primate tool use into hominid technology, we examine inter- and intraspecific variation in manufacture and use of tools in extant nonhuman primates, and develop a model to account for their distribution. We focus on tools used in acquiring food, usually by extraction. Any model for the evolution of the use of feeding tools must explain why tool use is found in only a small subset of primate species, why many of these species use tools much more readily in captivity, why routine reliance on feeding tools is found in only two species of ape, and why there is strong geographic variation within these two species. Because ecological factors alone cannot explain the distribution of tool use in the wild, we develop a model that focuses on social and cognitive factors affecting the invention and transmission of tool-using skills. The model posits that tool use in the wild depends on suitable ecological niches (especially extractive foraging) and the manipulative skills that go with them, a measure of intelligence that enables rapid acquisition of complex skills (through both invention and, more importantly, observational learning), and social tolerance in a gregarious setting (which facilitates both invention and transmission). The manipulative skills component explains the distribution across species of the use of feeding tools, intelligence explains why in the wild only apes are known to make and use feeding tools routinely, and social tolerance explains variation across populations of chimpanzees and orangutans. We conclude that strong mutual tolerance was a key factor in the explosive increase in technology among hominids, probably intricately tied to a lifestyle involving food sharing and tool-based processing or the acquisition of large, shareable food packages.     

Oral tool use by captive orangutans (Pongo pygmaeus)

Eight captive orangutans (Pongo pygmaeus) were given wooden blocks embedded with raisins and bamboo as raw material for tool making in a study of manual laterality. In about three quarters of the raisin extraction bouts, the orangutans held the tool in the lips or teeth rather than in their hands. Three adult males and 2 adult females showed extreme (> or =92%) preference for oral tool use, a subadult male and an adult female used oral tools about half the time, and 1 adult female preferred manual tool use. Most oral tool users made short tools (approx. 4-10 cm long) that were held in the lips and (probably) supported by the tongue. Preference for oral tool use does not correlate with body weight, age or sex, but it may be related to hand size or individual preference. This is the first report of customary oral tool use as the norm in captive orangutans; it resembles the behavioral patterns reported by van Schaik et al. and Fox et al. in nature.     

Drinking tools of wild chimpanzees at Bossou

Use of drinking tools by wild chimpanzees (Pan troglodytes) and the context in which the tools were used were studied at Bossou, Republic of Guinea, West Africa. During the middle to late dry season and early wet season liquids are available occasionally in the holes of trees. Chimpanzees drank water or sap using a leaf (or fiber) as a sponge or spoon. When the chimpanzees were on the ground, they tended to use one of a few kinds of soft, hairless leaves, if they were available nearby. Females, particularly juveniles and adolescents, were thought to be the main users of the drinking tool. In a few episodes, a tool set was used to procure liquid. Once a chimpanzee used a stick to push a leaf sponge into a water hole and to pull it out from the hole. In addition, three chimpanzees used a pestle to squeeze sap from an oil-palm tree before using a fiber sponge. © 1995 Wiley-Liss, Inc.     

Wild capuchins (Cebus capucinus) fail to use tools in an experimental field study

From September through November 2000 we conducted an experimental field study of tool use in a group of 15 wild white-faced capuchins (Cebus capucinus) in Costa Rica. The problem presented to the capuchins involved the use of wooden dowels as probes to obtain a food reward (two bananas) located inside a clear Plexiglas box. Specifically, the task required the capuchins to manually insert a dowel into any of six holes drilled into the box in order to push the bananas off a shelf. The banana could then be retrieved through a large opening at the bottom of the box. The capuchins visited the tool-use platform 702 times over the course of 55 consecutive days and under several experimental conditions. During the first 21 days of the study, they explored the box but made no attempt to touch or pick up the dowels. Even after we placed the dowels in the holes, the capuchins only occasionally manipulated them. Overall, the results indicate that the capuchins did not use a tool to solve this novel foraging problem.     

Use of a barbed tool by an adult and a juvenile woodpecker finch (Cactospiza pallida)

Here we describe the modification and use of a new tool type in the woodpecker finch (Cactospiza pallida). This species is known to habitually use twigs or cactus spines to extract arthropods out of tree holes. We observed an adult and a juvenile bird using several barbed twigs from introduced blackberry bushes (Rubus niveus) which the adult bird had first modified by removing leaves and side twigs. The barbs of blackberry tools provide a novel functional feature not present in tools made from native plants and de-leafing of twigs never has been observed before. Both birds were observed using several of these tools to extract prey from under the bark of the native scalesia tree (Scalesia penduculta). They oriented the twigs such that the barbs pointed towards themselves; this rendered the barbs functional as they could be used to drag prey out of a crevice. The juvenile bird first watched the adult using the tool and then used the tool that the adult bird had left under the bark at the same location and in the same way as the adult. Our observation highlights the fact that opportunities for the transmission of social information do occur in the wild and indicates that woodpecker finches are flexible in their choice of tool material and tool modification.     

Geographic variation in tool use on Neesia fruits in orangutans

Geographic variation in the presence of skilled behavior may reflect geographic variation in genetic predispositions or ecological conditions (accompanied by reliable expression during development), or it may reflect the vagaries of invention and the appropriate social conditions for persistence. In this study, we compare the feeding techniques and tool-using skills used by orangutans to extract the nutritious seeds from Neesia fruits between Suaq Balimbing on Sumatra and Gunung Palung on Borneo, and map the distribution of Neesia tool use in Sumatran swamps. We show that neither genetics nor ecology is sufficient to explain the distribution of this tool use, confirming earlier findings on chimpanzees. We conclude that the ability to learn to use tools determines the geographic distribution. It is impossible to distinguish between the history of invention and the conditions for social transmission as the causal factors, but the high density and the social tolerance at Suaq Balimbing create propitious conditions for the maintenance of the skill as a tradition once it has been invented. High orangutan densities in the other Sumatran coastal swamps with Neesia tool use support the conclusion that suitable transmission conditions are the critical factor to explain the geographic distribution of skills such as feeding tool use.     

Cognitive abilities related to tool use in the woodpecker finch, Cactospiza pallida

Woodpecker finches are famous for their spontaneous tool use behaviour in the wild. They use twigs or cactus spines to pry arthropods out of crevices and use this ability more than any other tool-using species known. We experimentally investigated the cognitive abilities related to tool use. We chose three experimental designs that have been used to test several primate species (trap tube task and modification task) and New Caledonian crows (tool length task). One of six woodpecker finches was able to solve the trap tube task, and several individuals modified tools and chose twigs of appropriate length. Most subjects mastered these new tasks quickly, but we found no evidence that they were able to assess the problems in advance. These findings resemble those obtained for primates in these tasks.     

Do woodpecker finches acquire tool-use by social learning?

Tool-use is widespread among animals, but except in primates the development of this behaviour is poorly known. Here, we report on the first experimental study to our knowledge of the mechanisms underlying the acquisition of tool-use in a bird species. The woodpecker finch Cactospiza pallida, endemic to the Galápagos Islands, is a famous textbook example of tool-use in animals. This species uses modified twigs or cactus spines to pry arthropods out of tree holes. Using nestlings and adult birds from the field, we tested experimentally whether woodpecker finches learn tool-use socially. We show that social learning is not essential for the development of tool-use: all juveniles developed tool-use regardless of whether or not they had a tool-using model. However, we found that not all adult woodpecker finches used tools in our experiments. These non-tool-using individuals also did not learn this task by observing tool-using conspecifics. Our results suggest that tool-use behaviour depends on a very specific learning disposition that involves trial-and-error learning during a sensitive phase early in ontogeny.     

Pestle-pounding behavior of wild chimpanzees at Bossou,Guinea: A newly observed tool-using behavior

A new type of tool-using behavior was observed in a group of wild chimpanzees (Pan troglodytes verus) at Bossou, Guinea. The chimpanzees used the leaf-petiole of oil-palm trees (Elaeis guineensis) as a pounding tool to deepen a hole in the oil-palm crown which appeared after the chimpanzees had pulled out the central young shoots. Finally, the chimpanzees extracted and ate the apical meristem or apical bud of the oil-palm tree which is edible but inaccessible without such tool use. The motor pattern which the chimpanzees employed is similar to that used for termite-nest digging but it is more exaggerated and requires great force. The behavior is reminiscent of pestlepounding. The chimpanzees exploit substantial amounts of food with this tool-using skill, compensating for insufficient fruit foods in the primary forest. This tool-using behavior was first observed in 1990 and, to date, almost half of the group members have been confirmed to use the pestle tool. It appears that this tool-using behavior was invented recently and has since spread widely throughout the group as a habitual one.     

The ant-gathering behaviour by the use of tools among wild chimpanzees of the Mahali Mountains

Chimpanzees of Kasoge use tools in the trees for collecting arboreal ants (Camponotus spp.) mostly in woodland vegetation. Ant-gathering by the use of tools is routine behaviour, at least during the first half of the rainy season. Three kinds of tools were recognized: wiping handkerchief, expelling stick and poking rod. Although the first two types were observed only once, this is the first time that these methods of using plants to obtain insects have been recorded. The poking rods can be divided into five categories which differentiate between the materials used and the way and the degree to which these materials are modified. The use of a mid-rib of the leaf as a rod is a modification peculiar to a chimpanzee of Kasoge. The apparent selectivity of the plant species as the material for a tool was made clear, with special reference to the ethnobotany of the sympatric Batongwe tribe. The tool-using activity of “chimpanzee level” does not require the exclusive specialization of one hand. Ant-gathering was seen during the time when chimpanzees usually take a rest between the two intensive feeding periods of a day. This implies that ant-gathering by use of tools is a kind of luxury.     

Transport of tools and mental representation: is capuchin monkey tool behaviour a useful model of Plio-Pleistocene hominid technology?

Capuchin monkeys display greatly developed tool-using capacities, performing successfully a variety of tool-tasks. Impressed by their achievements in this respect, some investigators have suggested that capuchin tool-using behaviour could be used as a model of the tool behaviour of the first hominids. The transport of tools, a task requiring complex cognitive capabilities, is an essential ingredient in the technological behaviour of the first hominids. In this way, to qualify as another source for modelling hominid behavioural evolution, capuchins had to exhibit proficiency in the transport of tools. We investigated this problem through experiments designed to elicit the transport of objects. The results showed that the monkeys were able to transport food to be processed with the use of tools, but failed when the tools themselves had to be transported. Our hypothesis is that a limited capacity for abstract representation, together with the lack of a regulatory system ensuring that the food would not be lost and consumed by another individual during the search for and transport of the tools, were responsible for such a failure. We conclude that the tool-using behaviour of capuchins presents no functional analogy with the tool behaviour of the Plio-Pleistocene hominids, and that capuchin monkeys are a very inadequate source for modelling Plio-Pleistocene hominid's technological behaviour.     

Complex tool sets for honey extraction among chimpanzees in Loango National Park, Gabon

Homo faber was once proposed as a label for humans specifically to highlight their unique propensity for tool use. However, new observations on complex tool use by the chimpanzees of Loango National Park, Gabon, expand our knowledge about tool-using abilities in Pan troglodytes. Chimpanzees in Loango, when using tools to extract honey from three types of bee nests, were observed to regularly use three- to five-element tool sets. In other words, different types of tools were used sequentially to access a single food source. Such tool sets included multi-function tools that present typical wear for two distinct uses. In addition, chimpanzees exploited underground bee nests and used ground-perforating tools to locate nest chambers that were not visible from the ground surface. These new observations concur with others from Central African chimpanzees to highlight the importance of honey extraction in arguments favoring the emergence of complex tool use in hominoids, including different tool types, expanded tool sets, multifunction tools, and the exploitation of underground resources. This last technique requires sophisticated cognitive abilities concerning unseen objects. A sequential analysis reveals a higher level of complexity in honey extraction than previously proposed for nut cracking or hunting tools, and compares with some technologies attributed to early hominins from the Early and Middle Stone Age. A better understanding of similarities in human and chimpanzee tool use will allow for a greater understanding of tool-using skills that are uniquely human.     

Individual variation in nest size and nest site features of the Bornean orangutans (Pongo pygmaeus)

Nest construction is a daily habit of independent orangutans for sleeping or resting. Data on their nests have been used in various ecological studies (e.g., density estimation, ranging behavior, evolution of material culture) because they are the most observable field signs. We investigated nest size and nest site features of Bornean orangutans in the wild during 10 months' fieldwork at three sites in East Kalimantan, Indonesia: Kutai National Park, Birawa, and Meratus. To examine individual variation, we followed 31 individual orangutans and recorded the 92 nests they made for nest size (diameter) and nest site features (height of nest above ground, tree species used for the nest site, the diameter and height of the tree, whether the nest was new or reused, and nest location within the tree). Analyses taking age–sex classes of the focal individuals into consideration showed significant age–sex differences in nest size and location, but not in nest height or nest tree features (diameter, height of tree, and height of lowest branch). Mature orangutans (adult females, unflanged and flanged males) made larger nests than immatures (juveniles and adolescents). Flanged male orangutans with larger nests used stable locations for nesting sites and reused old nests more frequently than immatures. The overall proportion of nests in open (exposed) locations was higher than in closed (sheltered) locations. Flanged males and immatures frequently made open nests, whereas adult females with an infant preferred closed locations. The good correspondence between nest size and age–sex classes indicates that nest size variation may reflect body size and therefore age–sex variation in the population. Am. J. Primatol. 71:393–399, 2009. © 2009 Wiley‐Liss, Inc.     

New tool use by wild Sumatran orangutans (Pongo pygmaeus abelii)

Two forms of tool use by wild Sumatran orangutans are reported from the Agusan Monitoring Station, a new research site in Indonesia. One form, a branch "hook" used in locomotion, has not been reported previously in wild orangutans. The second form, a leaf "pad" used to protect the hands and feet from thorns while feeding, shares similarities in form and function with a tool type used by orangutans at Ketambe, a nearby research site. Both instances of tool use occurred in areas of disturbance, and appear to be spontaneous inventions under novel conditions, although habitual use of the tool in other ecological contexts is plausible. A summary of the distribution of tool use types in wild orangutans is presented.     

Tool use by captive chimpanzees at an artificial termite mound

This study examines tool use by a colony of captive chimpanzees at an artificial termite mound. The mound, constructed of concrete, simulates the termite mounds which are used as food sources by wild chimpanzees who extract the termites using grass or twig-type tools. In the present study, tool availability was manipulated, specifically the type of tool, and the distance of tool material from the mound. The type of food available in the mound was also varied. Tool-making and tool-using behavior was examined in relation to individual, age, and sex differences. The artificial mound proved to be a viable simulation of the naturally occurring mounds, with most of the chimpanzees exploiting the food in the mound by using tools over the period of study. Interesting individual differences emerged in the way that the chimpanzees selected and used tools, some preferring to move some distance from the mound to collect “off-the-peg” tools, others preferring to sit and fashion a tool from material available nearer the mound. Also, some chimpanzees used both ends of a tool, while others used only one end. There were significant age differences in activity at the mound, the younger chimpanzees spending more time at the mound, using tools previously used by others, and manipulating the mound holes manually. Sex differences, although not significant, were apparent. The artificial mound provides the chimpanzees with a stimulating and rewarding activity, interest and enjoyment for the public, and an opportunity for researchers to study tool use under more controlled conditions than are possible in the field.     

Animal tool-use

The sight of an animal making and using a tool captivates scientists and laymen alike, perhaps because it forces us to question some of our ideas about human uniqueness. Does the animal know how the tool works? Did it anticipate the need for the tool and make it in advance? To some, this fascination with tools seems arbitrary and anthropocentric; after all, animals engage in many other complex activities, like nest building, and we know that complex behaviour need not be cognitively demanding. But tool-using behaviour can also provide a powerful window into the minds of living animals, and help us to learn what capacities we share with them - and what might have changed to allow for the incontrovertibly unique levels of technology shown by modern humans.     

Spontaneous use of sticks as tools by captive gorillas (Gorilla gorilla gorilla)

The present report describes the spontaneous use of sticks, as tools by young adult gorillas (Gorilla gorilla gorilla) in a social group at the San Diego Wild Animal Park, CA, USA. Three 8-year-old gorillas (one female and two males) threw sticks into the foliage of trees, which the gorillas could not climb due to electric wire, to knock down leaves and seeds. Two of the three gorillas selected sticks that were more suitable (i.e. longer or thicker sticks) for throwing. Moreover, they looked up at the target (i.e. the foliage of the tree) before throwing and grasped the stick at a position appropriate, for throwing (i. e. the end of the stick). They were more likely to throw sticks when particular adult group members were not nearby. These two gorillas also pulled branches of trees toward themselves by using sticks to capture them (branch-pulling), and one of these two beat a branch with a stick to knock down leaves and seeds (branch-beating). One of these two gorillas used much longer sticks for branch-pulling than for stick-throwing, indicating that he was capable of task-dependent selection of sticks. Analyzing the spontaneous use of sticks as tools by gorillas in captivity can lead to a better understanding of not only their cognitive ability but also of their social relationships which may otherwise be concealed.     

Characteristics and utilization of old Black Woodpecker Dryocopus martius holes by hole-nesting species

Old nest holes made by the Black Woodpecker Dryocopus martius were examined in two study areas in Sweden. We found a large variation in nest hole characteristics and that the height in the tree and depth of the hole were important factors in the choice of nest hole by secondary hole nesters. A large proportion of old nest holes remained unoccupied. Many holes were probably of poor quality due to shallow depth, low height or narrow entrance. Nest holes in the vicinity of farmland (<200 m from the field-forest edge) were more often occupied than nest holes deeper into the forest. This was because Jackdaws Corvus monedula , the numerically dominant species, only used nest holes near farmland. Jackdaws usually used the best nest holes, while other subordinate species had to use inferior holes near fields or nest holes in areas with less competition, deeper in the forest. Besides birds, some mammals and bees were found using old Black Woodpecker holes.     

Optimal Sequencing Rules for Some Large-Scale Flexible Manufacturing Problems Under the Manhattan and Chebychev Metrics

The purpose of this paper is to develop optimal tool partitioning policies and strip sequencing strategies for a class of flexible manufacturing problems. The problems under consideration involve a large number of operations to be performed by a series of tools on a two-dimensional object. For example, these operations could consist of drilling holes in a metallic sheet. Tools are arranged in a carousel or along a toolbar according to a predetermined sequence. Operations are performed by repeatedly moving the sheet to bring the hole locations under the tool. During each pass, as all operations involving a series of consecutive tools are executed, two main problems are to be solved: (1) how to move the sheet during each pass, (2) how to partition the tools into blocks of consecutive tools. A strip strategy is used to move the sheet. Given this policy, optimal strip widths and tool partitioning policies are determined jointly. Analytical solutions are derived under two metrics corresponding to different operating modes. A numerical example is provided.