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Hunt, G. R., Gray R.D., & Taylor, A. H. (2013). Why is tool use rare in animals? (Boesch C C. J. anz C, Ed.). Cambridge, MA.: Cambridge University Press.
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BRYSON, J. O. A. N. N. A. J. EVIDENCE OF MODULARITY FROM PRIMATE ERRORS DURING TASK LEARNING. Retrieved May 14, 2024, from http://dx.doi.org/10.1142/9789812701886_0031
Abstract: The last two decades have seen a great deal of theorising and speculation about
the modular nature of human intelligence, as well as a rise in use of modular
architectures in artificial intelligence. Nevertheless, whether such models of natural
intelligence are well supported is still an issue of debate. In this paper, I propose
that the most important criteria for modularity is specialised representations. I
present a modular model of primate learning of the transitive inference task, and
propose an extension to this model which would explain task-learning results in
other domains. I also briefly relate this work to both neuroscience and established
AI learning architectures.
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Lieberman, D. (1993).
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Robins, A., & Phillips, C. (2009). Lateralised visual processing in domestic cattle herds responding to novel and familiar stimuli. Laterality, 15(5), 514–534.
Abstract: We investigated whether cattle exhibit preferences to monitor challenging and novel stimuli. Experiments were conducted on dairy and beef cattle herds and revealed significant left eye preferences in the cattle for viewing an experimenter walking to repeatedly split the herd through its centre. Visual lateralisation was demonstrated in the preference to use the left monocular field to monitor the experimenter, alone or equipped with a range of novel stimuli. This finding is consistent with left eye preferences found in various species of mammals, birds, and amphibians responding to predators and novel stimuli. A cohort of the familiarised cattle herds was then subjected to additional herd-splitting tests with the same stimuli and demonstrated a reversal of viewing preferences, preferring to monitor the experimenter and stimuli within the right and not left monocular field. This directional shift in viewing preferences is consistent with experience-dependent learning found in lateralised visual processing in other, non-mammalian, species, and to our knowledge is the first of such studies to suggest that such lateralised learning processes also exist in mammals. Together the data support a number of key hypotheses concerning the evolution and conservation of lateralised brain function in vertebrates, and also provide important considerations for livestock handling.
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Siniscalchi, M., Cirone, F., Guaricci, A. C., & Quaranta, A. (2013). Catecholamine plasma levels, IFN-γ serum levels and antibodies production induced by rabies vaccine in dogs selected for their paw preference. Laterality: Asymmetries of Body, Brain and Cognition, 19(5), 522–532.
Abstract: To explore the possible role of the sympathetic nervous activity in the asymmetrical crosstalk between the brain and immune system, catecholamine (E, NE) plasma levels, Interferon-? (IFN-?) serum levels and production of antibodies induced by rabies vaccine in dogs selected for their paw preference were measured. The results showed that the direction of behavioural lateralization influenced both epinephrine levels and immune response in dogs. A different kinetic of epinephrine levels after immunization was observed in left-pawed dogs compared to both right-pawed and ambidextrous dogs. The titers of antirabies antibodies were lower in left-pawed dogs than in right-pawed and ambidextrous dogs. Similarly, the IFN-? serum levels were lower in left-pawed dogs than in the other two groups. Taken together, these findings showed that the left-pawed group appeared to be consistently the different group stressing the fundamental role played by the sympathetic nervous system as a mechanistic basis for the crosstalk between the brain and the immune system.
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Whishaw, I. Q. (2015). Absence of population asymmetry in the American Quarter Horse (Equus ferus caballus) performing skilled left and right manoeuvres in reining competition. Laterality, 20(5), 604–617.
Abstract: Use of the right hand by humans for speech-related hand gestures, writing and throwing exemplifies motoric asymmetry. There are reports of asymmetry in many other animal species, including reports of left preference in emotional responsivity, spontaneous behaviour and the trained performance of the horse, Equus ferus caballus. The present study used the novel approach of using judges' scores to examine asymmetry in an equestrian event. The study analysed the scores of five judges evaluating the reining performance of 482, three-year-old American Quarter Horses competing in a major competition. Reining requires that the horses perform the manoeuvres of spin, circle and stop directed to either the left or right and symmetrical performance is featured in the judging criteria. The scores were sensitive to performance level, sex and manoeuvre, but there was no evidence of a population asymmetry in the left vs. right direction of the manoeuvres. The results are discussed in relation to need of using a large number of subjects in measuring asymmetry, the expression of individual vs. population asymmetry as a function of morphological and behavioural measures, and the influence of behavioural training on asymmetry.
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Siniscalchi, M., Padalino, B., Aubé, L., & Quaranta, A. (2015). Right-nostril use during sniffing at arousing stimuli produces higher cardiac activity in jumper horses. Laterality, 20(4), 483–500.
Abstract: Lateralization in horses, Equus caballus, has been reported at both motor and sensory levels. Here we investigated left- and right-nostril use in 12 jumper horses freely sniffing different emotive stimuli. Results revealed that during sniffing at adrenaline and oestrus mare urine stimuli, horses showed a clear right-nostril bias while just a tendency in the use of the right nostril was observed during sniffing of other odours (food, cotton swab and repellent). Sniffing at adrenaline and urine odours was also accompanied by increasing cardiac activity and behavioural reactivity strengthening the role of the right hemisphere in the analysis of intense emotion and sexual behaviour.
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Krueger, K. (2017). Perissodactyla Cognition. In J. Vonk, & T. Shackelford (Eds.), Encyclopedia of Animal Cognition and Behavior (pp. 1–10). Cham: Springer International Publishing.
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Krueger, K., Marr, I., & Farmer, K. (2017). Equine Cognition. In J. Vonk, & T. Shackelford (Eds.), Encyclopedia of Animal Cognition and Behavior (pp. 1–11). Cham: Springer International Publishing.
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Panksepp, J. (2005). Affective consciousness: Core emotional feelings in animals and humans. Conscious Cogn, 14(1), 30–80.
Abstract: The position advanced in this paper is that the bedrock of emotional feelings is contained within the evolved emotional action apparatus of mammalian brains. This dual-aspect monism approach to brain-mind functions, which asserts that emotional feelings may reflect the neurodynamics of brain systems that generate instinctual emotional behaviors, saves us from various conceptual conundrums. In coarse form, primary process affective consciousness seems to be fundamentally an unconditional “gift of nature” rather than an acquired skill, even though those systems facilitate skill acquisition via various felt reinforcements. Affective consciousness, being a comparatively intrinsic function of the brain, shared homologously by all mammalian species, should be the easiest variant of consciousness to study in animals. This is not to deny that some secondary processes (e.g., awareness of feelings in the generation of behavioral choices) cannot be evaluated in animals with sufficiently clever behavioral learning procedures, as with place-preference procedures and the analysis of changes in learned behaviors after one has induced re-valuation of incentives. Rather, the claim is that a direct neuroscientific study of primary process emotional/affective states is best achieved through the study of the intrinsic (“instinctual”), albeit experientially refined, emotional action tendencies of other animals. In this view, core emotional feelings may reflect the neurodynamic attractor landscapes of a variety of extended trans-diencephalic, limbic emotional action systems-including SEEKING, FEAR, RAGE, LUST, CARE, PANIC, and PLAY. Through a study of these brain systems, the neural infrastructure of human and animal affective consciousness may be revealed. Emotional feelings are instantiated in large-scale neurodynamics that can be most effectively monitored via the ethological analysis of emotional action tendencies and the accompanying brain neurochemical/electrical changes. The intrinsic coherence of such emotional responses is demonstrated by the fact that they can be provoked by electrical and chemical stimulation of specific brain zones-effects that are affectively laden. For substantive progress in this emerging research arena, animal brain researchers need to discuss affective brain functions more openly. Secondary awareness processes, because of their more conditional, contextually situated nature, are more difficult to understand in any neuroscientific detail. In other words, the information-processing brain functions, critical for cognitive consciousness, are harder to study in other animals than the more homologous emotional/motivational affective state functions of the brain.
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