|
|
Cook, R. G., Shaw, R., & Blaisdell, A. P. (2001). Dynamic object perception by pigeons: discrimination of action in video presentations. Anim. Cogn., 4(3), 137–146.
Abstract: Two experiments examined the discrimination by pigeons of relative motion using computer-generated video stimuli. Using a go/no-go procedure, pigeons were tested with video stimuli in which the camera's perspective went either “around” or “through” an approaching object in a semi-realistic context. Experiment 1 found that pigeons could learn this discrimination and transfer it to videos composed from novel objects. Experiment 2 found that the order of the video's frames was critical to the discrimination of the videos. We hypothesize that the pigeons perceived a three-dimensional representation of the objects and the camera's relative motion and used this as the primary basis for discrimination. It is proposed that the pigeons might be able to form generalized natural categories for the different kinds of motions portrayed in the videos.
|
|
|
|
Forkman, B. (2000). Domestic hens have declarative representations. Anim. Cogn., 3(3), 135–137.
Abstract: It is generally considered that information can be stored either as a procedural or as a declarative representation. A devaluation technique was used to determine whether hens have declarative representations. Individual hens (Gallus gallus domesticus) were fed in an enclosure with two containers, each with a new food type. One of the food types was devalued by pre-feeding with that food, after which the hens were tested with empty food containers. The pre-feeding should only affect the choice of the hens if they have learned where a particular food type was (declarative representation) rather than “go left when coming into the enclosure” (procedural representation). A significant proportion of the hens went to the location previously occupied by the non-devalued food (seven out of eight). This supports the hypothesis that domestic hens can form declarative representations.
|
|
|
|
De Lillo,, C. De Lillo, Floreano,, D. Floreano, Antinucci,, & F. Antinucci. (2001). Transitive choices by a simple, fully connected, backpropagation neural network: implications for the comparative study of transitive inference. Anim. Cogn., 4(1), 61–68.
Abstract: In search of the minimal requirements for transitive reasoning, a simple neural network was trained and tested on the non-verbal version of the conventional “five-term-series task” – a paradigm used with human adults, children and a variety of non-human species. The transitive performance of the network was analogous in several aspects to that reported for children and animals. The three effects usually associated with transitive choices i.e. “symbolic distance”, “lexical marking” and “end-anchor”, were also clearly shown by the neural network. In a second experiment, where the training conditions were manipulated, the network failed to match the behavioural pattern reported for human adults in the test following an ordered presentation of the premises. However, it mimicked young children's performance when tested with a novel comparison term. Although we do not intend to suggest a new model of transitive inference, we conclude, in line with other authors, that a simple error-correcting rule can generate transitive behaviour similar to the choice pattern of children and animals in the binary form of the five-term-series task without requiring high-order logical or paralogical abilities. The analysis of the training history and of the final internal structure of the network reveals the associative strategy employed. However, our results indicate that the scope of the associative strategy used by the network might be limited. The extent to which the conventional five-term-series task, in absence of appropriate manipulations of training and testing conditions, is suitable to detect cognitive differences across species is also discussed on the basis of our results.
|
|
|
|
Westergaard, G. C., Liv, C., Chavanne, T. J., & Suomi, S. J. (1998). Token-mediated tool-use by a tufted capuchin monkey (Cebus apella). Anim. Cogn., 1(2), 101–106.
Abstract: This research examined token-mediated tool-use in a tufted capuchin monkey (Cebus apella). We conducted five experiments. In experiment 1 we examined the use of plastic color-coded chips to request food, and in experiments 2-5 we examined the use of color-coded chips to request tools. Our subject learned to use chips to request tools following the same general pattern seen in great apes performing analogous tasks, that is, initial discrimination followed by an understanding of the relationship among tokens, tools, and their functions. Our findings are consistent with the view that parallel representational processes underlie the tool-related behavior of capuchins and great apes.
|
|
|
|
Heiling, A. M., & Herberstein, M. E. (1999). The role of experience in web-building spiders (Araneidae). Anim. Cogn., 2(3), 171–177.
Abstract: A typical feature of vertical orb-webs is the 'top/bottom' asymmetry, where the lower web region is larger than the upper web region. This asymmetry may improve prey capture success, because, sitting in the hub of the web, a spider can reach prey entangled below the hub faster than prey entangled in the area above the hub. While web asymmetry is known to vary intraspecifically, we tested if this variation also exists at the individual level and whether it is the result of experience, using two orb-web spider species, Argiope keyserlingi and Larinioides sclopetarius. The results reveal that experienced web-building spiders constructed more asymmetric webs than conspecifics deprived of any prior building experience over a period of several months. Experienced individuals invested more silk material into the web region below the hub, which covered a larger area. Moreover, web asymmetry was also influenced by previous prey capture experiences, as spiders increased the lower region of the web if it intercepted the most prey over a period of 6 days. Consequently, spiders may be able to use long-term web-building experience as well as short-term prey capture experience to build better traps. In contrast to previous views of spiders, experience can contribute to intraspecific as well as to individual variations in web design.
|
|
|
|
Iversen, I. H., & Matsuzawa, T. (2001). Acquisition of navigation by chimpanzees (Pan troglodytes) in an automated fingermaze task. Anim. Cogn., 4(3), 179–192.
Abstract: These experiments investigated how chimpanzees learn to navigate visual fingermazes presented on a touch monitor. The aim was to determine whether training the subjects to solve several different mazes would establish a generalized map-reading skill such that they would solve new mazes correctly on the first presentation. In experiment 1, two captive adult female chimpanzees were trained to move a visual object (a ball) with a finger over the monitor surface toward a target through a grid of obstacles that formed a maze. The task was fully automated with storage of movement paths on individual trials. Training progressed from very simple mazes with one obstacle to complex mazes with several obstacles. The subjects learned to move the ball to the target in a curved path so as to avoid obstacles and blind alleys. After training on several mazes, both subjects developed a high level of efficiency in moving the ball to the target in a path that closely approached the ideal shortest path. New mazes were then presented to determine whether the subjects had acquired a more generalized maze-solving performance. The subjects solved 65–100% of the new mazes the first time they were presented by moving the ball around obstacles to the target without making detours into blind alleys. In experiment 2, one of the chimpanzees was trained using mazes with two routes to the target. One of the routes was blocked at one of many possible locations. After training to avoid the blind alley in different mazes, new mazes were presented that also had one route blocked. The subject correctly solved 90.7% of the novel mazes. When the mazes had one short and one long open route to the target the subject preferred the shorter route. When the short route was blocked, the subject solved only 53.3% of the mazes because of the preference for the shorter route even when blocked. The overall results suggest that with the training methods used the subjects learned to solve specific mazes with a trial-and-error method. Although both subjects were able to solve many of the novel mazes they did not fully develop a more general “map-reading” skill.
|
|
|
|
Byrne, R. W. (1999). Imitation without intentionality. Using string parsing to copy the organization of behaviour. Anim. Cogn., 2(2), 63–72.
Abstract: A theory of imitation is proposed, string parsing, which separates the copying of behavioural organization by observation from an understanding of the cause of its effectiveness. In string parsing, recurring patterns in the visible stream of behaviour are detected and used to build a statistical sketch of the underlying hierarchical structure. This statistical sketch may in turn aid the subsequent comprehension of cause and effect. Three cases of social learning of relatively complex skills are examined, as potential cases of imitation by string parsing. Understanding the basic requirements for successful string parsing helps to resolve the conflict between mainly negative reports of imitation in experiments and more positive evidence from natural conditions. Since string parsing does not depend on comprehension of the intentions of other agents or the everyday physics of objects, separate tests of these abilities are needed even in animals shown to learn by imitation.
|
|
|
|
Xia, L., Siemann, M., & Delius, J. D. (2000). Matching of numerical symbols with number of responses by pigeons. Anim. Cogn., 3(1), 35–43.
Abstract: Pigeons were trained to peck a certain number of times on a key that displayed one of several possible numerical symbols. The particular symbol displayed indicated the number of times that the key had to be pecked. The pigeons signalled the completion of the requirement by operating a separate key. They received a food reward for correct response sequences and time-out penalties for incorrect response sequences. In the first experiment nine pigeons learned to allocate 1, 2, 3 or 4 pecks to the corresponding numerosity symbols s1, s2, s3 and s4 with levels of accuracy well above chance. The second experiment explored the maximum set of numerosities that the pigeons were capable of handling concurrently. Six of the pigeons coped with an s1-s5 task and four pigeons even managed an s1-s6 task with performances that were significantly above chance. Analysis of response times suggested that the pigeons were mainly relying on a number-based rather than on a time-based strategy.
|
|
|
|
Hashiya, K., & Kojima, S. (2001). Acquisition of auditory-visual intermodal matching-to-sample by a chimpanzee (Pan troglodytes): comparison with visual-visual intramodal matching. Anim. Cogn., 4(3), 231–239.
Abstract: A chimpanzee acquired an auditory–visual intermodal matching-to-sample (AVMTS) task, in which, following the presentation of a sample sound, the subject had to select from two alternatives a photograph that corresponded to the sample. The acquired AVMTS performance might shed light on chimpanzee intermodal cognition, which is one of the least understood aspects in chimpanzee cognition. The first aim of this paper was to describe the training process of the task. The second aim was to describe through a series of experiments the features of the chimpanzee AVMTS performance in comparison with results obtained in a visual intramodal matching task, in which a visual stimulus alone served as the sample. The results show that the acquisition of AVMTS was facilitated by the alternation of auditory presentation and audio-visual presentation (i.e., the sample sound together with a visual presentation of the object producing the particular sample sound). Once AVMTS performance was established for the limited number of stimulus sets, the subject showed rapid transfer of the performance to novel sets. However, the subject showed a steep decay of matching performance as a function of the delay interval between the sample and the choice alternative presentations when the sound alone, but not the visual stimulus alone, served as the sample. This might suggest a cognitive limitation for the chimpanzee in auditory-related tasks.
|
|
|
|
Call, J., Hare, B. A., & Tomasello, M. (1998). Chimpanzee gaze following in an object-choice task. Anim. Cogn., 1(2), 89–99.
Abstract: Many primate species reliably track and follow the visual gaze of conspecifics and humans, even to locations above and behind the subject. However, it is not clear whether primates follow a human's gaze to find hidden food under one of two containers in an object-choice task. In a series of experiments six adult female chimpanzees followed a human's gaze (head and eye direction) to a distal location in space above and behind them, and checked back to the human's face when they did not find anything interesting or unusual. This study also assessed whether these same subjects would also use the human's gaze in an object-choice task with three types of occluders: barriers, tubes, and bowls. Barriers and tubes permitted the experimenter to see their contents (i.e., food) whereas bowls did not. Chimpanzees used the human's gaze direction to choose the tube or barrier containing food but they did not use the human's gaze to decide between bowls. Our findings allowed us to discard both simple orientation and understanding seeing-knowing in others as the explanations for gaze following in chimpanzees. However, they did not allow us to conclusively choose between orientation combined with foraging tendencies and understanding seeing in others. One interesting possibility raised by these results is that studies in which the human cannot see the reward at the time of subject choice may potentially be underestimating chimpanzees' social knowledge.
|
|
