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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.
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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.
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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.
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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.
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Brown, C. (2001). Familiarity with the test environment improves escape responses in the crimson spotted rainbowfish, Melanotaenia duboulayi. Anim. Cogn., 4(2), 109–113.
Abstract: Animals that are familiar with their environment have been reported to have greater survivorship for a number of reasons related to their knowledge of the terrain, which they recall from memory. In an initial experiment rainbowfish significantly improved their escape response towards a novel trawl apparatus over a sequence of five runs. Escape latencies were still low during a subsequent exposure 11 months after the initial exposure. While part of the improvement in escape success was certainly due to learning associated with the location of the escape route, it is likely that this was aided by habituation to the tank environment and the experimental protocol. In a follow-up experiment, fish that had been kept in the experimental tank for 3 weeks prior to testing, and had become familiar with the test tank, showed significantly lower escape latencies and escaped more often than fish that were not familiar with the test environment. It is suspected that familiarity with the testing arena decreased stress and enabled individuals to detect novel stimuli and devote more attention to them. These findings have significant implications for experimenters studying aspects of animal cognition, such as learning and memory, in laboratory situations.
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Xitco, M., Gory, J., & Kuczaj, S. (2001). Spontaneous pointing by bottlenose dolphins (Tursiops truncatus). Anim. Cogn., 4(2), 115–123.
Abstract: Two bottlenose dolphins (Tursiops truncatus) participating in a symbolic communication project spontaneously developed behaviors that resembled pointing and gaze alternation. The dolphins' behavior demonstrated several features reminiscent of referential communicative behavior. It was triadic, involving a signaler, receiver, and referent. It was also indicative, specifying a focus of attention. The dolphins' points were distinct from the act of attending to or acting on objects. Spontaneous dolphin pointing was influenced by the presence of a potential receiver, and the distance between that receiver and the dolphin. These findings suggest that dolphins are capable of producing referential gestures.
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López, J. C., Broglio, C., Rodríguez, F., Thinus-Blanc, C., & Salas, C. (1999). Multiple spatial learning strategies in goldfish (Carassius auratus). Anim. Cogn., 2(2), 109–120.
Abstract: There is a considerable amount of evidence that mammals and birds can use different spatial learning strategies based on multiple learning and memory systems. Unfortunately, only a few studies have investigated spatial learning and memory mechanisms in other vertebrates. This study aimed to identify the strategies used by goldfish to solve two different spatial tasks in a series of three experiments. In experiment 1, two groups of goldfish (Carassius auratus) were trained either in a spatial constancy task (SC), in which visual cues signalled the goal indirectly, or in a directly cued task (DC) in which similar cues signalled the goal directly. Transfer tests were conducted to study the effects of discrete cue deletion on the performance in both tasks. In these transfer tests the performance of the animals trained in the DC task dropped to chance level when the cue that signalled the goal directly was removed. In contrast, the removal of any single cue did not disrupt SC performance. In experiment 2, fish trained in the SC or the DC task were trained with the goal reversed. Goldfish in the SC group needed fewer sessions to master the reversal task than DC animals. Finally, experiment 3 investigated the effects of a substantial modification of the geometrical features of the apparatus on the performance of animals trained in the SC or in the DC condition. The performance of DC goldfish was not affected, whereas the same change disrupted performance in the SC animals despite the presence of the visual cues. These results suggest that there are separate spatial learning and memory systems in fish. Whereas the DC animals used a typical guidance strategy, relying only on the cue that signalled the goal directly, SC fish relied on a strategy with the properties of an actual spatial mapping system. Thus, the comparative approach points to the generality of these learning strategies among vertebrates.
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Czeschlik, T. (1998). Animal cognition – the phylogeny and ontogeny of cognitive abilities. Anim. Cogn., 1(1), 1–2.
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Miklósi, Á. (2002). Cecilia Heyes and Ludwig Huber (eds): The Evolution of Cognition. Anim. Cogn., 5(3), 187–189.
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Hare, B. (2001). Can competitive paradigms increase the validity of experiments on primate social cognition? Anim. Cogn., 4(3), 269–280.
Abstract: Experiments vary in their ability to distinguish between competing hypotheses. In tests on primate cognition the majority of this variation is due to an experimenter's ability to test primates in valid settings while providing the adequate amount of experimental control. While experimenters studying primate cognition can use methods of control perfected in captivity, it is still very unclear how to design and then objectively evaluate the external validity of new experimental paradigms. I recommend that more effort be allocated to specify how to create relevant test settings for primates. Primate social life is highly competitive. This means that all aspects of primates themselves, including their cognitive abilities, have likely been shaped by the need to out-compete conspecifics. Based on this hypothesis, sophisticated cognitive abilities of primates might best be demonstrated in competitive contexts. Thus, it is suggested that one possible measure of validity is whether investigators integrate a competitive component into their experimental designs. To evaluate this methodological prediction I review the literature on chimpanzee perspective-taking as a case study including several recent studies that include a competitive component in their experimental designs.
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