20 found
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  1. Survival with an asymmetrical brain: Advantages and disadvantages of cerebral lateralization.Giorgio Vallortigara & Lesley J. Rogers - 2005 - Behavioral and Brain Sciences 28 (4):575-589.
    Recent evidence in natural and semi-natural settings has revealed a variety of left-right perceptual asymmetries among vertebrates. These include preferential use of the left or right visual hemifield during activities such as searching for food, agonistic responses, or escape from predators in animals as different as fish, amphibians, reptiles, birds, and mammals. There are obvious disadvantages in showing such directional asymmetries because relevant stimuli may be located to the animal's left or right at random; there is no a priori association (...)
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  2.  36
    Modularity and spatial reorientation in a simple mind: encoding of geometric and nongeometric properties of a spatial environment by fish.Valeria Anna Sovrano, Angelo Bisazza & Giorgio Vallortigara - 2002 - Cognition 85 (2):B51-B59.
  3.  11
    Sensitive periods for social development: Interactions between predisposed and learned mechanisms.Orsola Rosa-Salva, Uwe Mayer, Elisabetta Versace, Marie Hébert, Bastien S. Lemaire & Giorgio Vallortigara - 2021 - Cognition 213 (C):104552.
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  4.  20
    Young children do not succeed in choice tasks that imply evaluating chances.Vittorio Girotto, Laura Fontanari, Michel Gonzalez, Giorgio Vallortigara & Agnès Blaye - 2016 - Cognition 152 (C):32-39.
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  5.  11
    Complementary Specializations of the Left and Right Sides of the Honeybee Brain.Lesley J. Rogers & Giorgio Vallortigara - 2019 - Frontiers in Psychology 10.
    Honeybees show lateral asymmetry in both learning about odours associated with reward and recalling memory of these associations. We have extended this research to show that bees exhibit lateral biases in their initial response to odours: viz., turning towards the source of an odour presented on their right side and turning away from it when presented on their left side. The odours we presented were the main component of the alarm pheromone, iso-amyl acetate (IAA), and four floral scents. The significant (...)
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  6.  8
    Animals' use of landmarks and metric information to reorient: effects of the size of the experimental space.Valeria Anna Sovrano, Angelo Bisazza & Giorgio Vallortigara - 2005 - Cognition 97 (2):121-133.
  7.  17
    Piece of Evidence. Commentary: Ancestral Mental Number Lines: What Is the Evidence?Rosa Rugani, Giorgio Vallortigara, Konstantinos Priftis & Lucia Regolin - 2016 - Frontiers in Psychology 7.
  8.  13
    Response: “Newborn chicks need no number tricks. Commentary: Number-space mapping in the newborn chick resembles humans' mental number line”.Rosa Rugani, Giorgio Vallortigara, Konstantinos Priftis & Lucia Regolin - 2016 - Frontiers in Human Neuroscience 10.
  9.  27
    Social cognition and learning mechanisms: Experimental evidence in domestic chicks.Jonathan N. Daisley, Orsola Rosa Salva, Lucia Regolin & Giorgio Vallortigara - 2011 - Interaction Studies 12 (2):208-232.
    In this paper we review the literature on social learning mechanisms in the domestic chick, focusing largely on work from our own laboratories. The domestic chicken is a social-living bird that searches for food in flocks, avoids predators by following warnings from other flock members, and forms (stable) social hierarchies. All of these behaviors develop throughout ontogeny, largely during the very early stages post-hatch. Newly hatched chicks appear to have predispositions to orient towards and to pay greatest attention to the (...)
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  10.  26
    Social cognition and learning mechanisms: Experimental evidence in domestic chicks.Jonathan N. Daisley, Orsola Rosa Salva, Lucia Regolin & Giorgio Vallortigara - 2011 - Interaction Studies 12 (2):208-232.
  11.  15
    Social cognition and learning mechanisms.Jonathan N. Daisley, Orsola Rosa Salva, Lucia Regolin & Giorgio Vallortigara - 2011 - Interaction Studies. Social Behaviour and Communication in Biological and Artificial Systemsinteraction Studies / Social Behaviour and Communication in Biological and Artificial Systemsinteraction Studies 12 (2):208-232.
    In this paper we review the literature on social learning mechanisms in the domestic chick, focusing largely on work from our own laboratories. The domestic chicken is a social-living bird that searches for food in flocks, avoids predators by following warnings from other flock members, and forms social hierarchies. All of these behaviors develop throughout ontogeny, largely during the very early stages post-hatch. Newly hatched chicks appear to have predispositions to orient towards and to pay greatest attention to the biologically (...)
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  12. Supernatural beliefs : adaptations for social life or by-products of cognitive adaptations?Vittorio Girotto, Telmo Pievani & Giorgio Vallortigara - 2014 - In Frans B. M. De Waal, Patricia Smith Churchland, Telmo Pievani & Stefano Parmigiani (eds.), Evolved Morality: The Biology and Philosophy of Human Conscience. Leiden, The Netherlands: Brill.
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  13.  12
    Cognitive gadgets and cognitive priors.Gian Domenico Iannetti & Giorgio Vallortigara - 2019 - Behavioral and Brain Sciences 42.
    Some of the foundations of Heyes’ radical reasoning seem to be based on a fractional selection of available evidence. Using an ethological perspective, we argue against Heyes’ rapid dismissal of innate cognitive instincts. Heyes’ use of fMRI studies of literacy to claim that culture assembles pieces of mental technology seems an example of incorrect reverse inferences and overlap theories pervasive in cognitive neuroscience.
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  14.  3
    Numerosities and Other Magnitudes in the Brains: A Comparative View.Elena Lorenzi, Matilde Perrino & Giorgio Vallortigara - 2021 - Frontiers in Psychology 12.
    The ability to represent, discriminate, and perform arithmetic operations on discrete quantities (numerosities) has been documented in a variety of species of different taxonomic groups, both vertebrates and invertebrates. We do not know, however, to what extent similarity in behavioral data corresponds to basic similarity in underlying neural mechanisms. Here, we review evidence for magnitude representation, both discrete (countable) and continuous, following the sensory input path from primary sensory systems to associative pallial territories in the vertebrate brains. We also speculate (...)
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  15.  16
    An experimental study of the alphabetical rating.Sergio Cesare Masin, Giuliana Mazzoni & Giorgio Vallortigara - 1987 - Bulletin of the Psychonomic Society 25 (4):259-262.
  16.  25
    Experimental Evidence From Newborn Chicks Enriches Our Knowledge on Human Spatial–Numerical Associations.Rosa Rugani, Giorgio Vallortigara, Konstantinos Priftis & Lucia Regolin - 2017 - Cognitive Science 41 (8):2275-2279.
    Núñez and Fias raised concerns on whether our results demonstrate a linear number-space mapping. Patro and Nuerk urge caution on the use of animal models to understand the origin of the orientation of spatial–numerical association. Here, we discuss why both objections are unfounded.
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  17.  23
    Conjoining information from different modules: A comparative perspective.Giorgio Vallortigara & Valeria Anna Sovrano - 2002 - Behavioral and Brain Sciences 25 (6):701-702.
    The hypothesis that nonhuman species, lacking verbal language, do not really integrate information from different modules, but use instead information sequentially, appears difficult to put under empirical scrutiny. Evidence is discussed showing that in nonhuman species storing of geometric information occurs spontaneously even when landmark information suffices for spatial reorientation, suggesting simultaneous encoding, if not use, of information from different modules.
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  18.  39
    Forming an asymmetrical brain: Genes, environment, and evolutionarily stable strategies.Giorgio Vallortigara & Lesley J. Rogers - 2005 - Behavioral and Brain Sciences 28 (4):615-623.
    The present response elaborates and defends the main theses advanced in the target article: namely, that in order to provide an evolutionary account of brain lateralization, we should consider advantages and disadvantages associated both with the individual possession of an asymmetrical brain and with the alignment of the direction of lateralization at the population level. We explain why we believe that the hypothesis that directional lateralization evolved as an evolutionarily stable strategy may provide a better account than alternative hypotheses. We (...)
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  19.  33
    Minimization of modal contours: An instance of an evolutionary internalized geometric regularity?Giorgio Vallortigara & Luca Tommasi - 2001 - Behavioral and Brain Sciences 24 (4):706-707.
    The stratification in depth of chromatically homogeneous overlapping figures depends on a minimization rule which assigns the status of being “in front” to the figure that requires the formation of shorter modal contours. This rule has been proven valid also in birds, whose visual neuroanatomy is radically different from that of other mammals, thus suggesting an example of evolutionary convergence toward a perceptual universal. [Shepard].
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  20.  25
    Segregation and integration of information among visual modules.Giorgio Vallortigara - 1999 - Behavioral and Brain Sciences 22 (3):398-399.
    It is argued that the alleged cases of cognitive penetration of visual modules actually arise from the integration of information among different modules. This would reflect a general computational strategy according to which constraints to a particular module would be provided by information coming from different modules. Examples are provided from the integration of stereopsis and occlusion and from computation of motion direction.
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