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	<title>2017 &#8211; PISAVISIONLAB</title>
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	<link>https://www.pisavisionlab.org</link>
	<description>Research centre dedicated to frontier, interdisciplinary research of human perception</description>
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		<title>Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations, Neural Plast, (2017), 6724631.</title>
		<link>https://www.pisavisionlab.org/2019/12/22/short-term-monocular-deprivation-enhances-physiological-pupillary-oscillations-neural-plast-2017-6724631/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sun, 22 Dec 2019 08:10:46 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[CLAUDIA LUNGHI]]></category>
		<category><![CDATA[PAOLA BINDA]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1128</guid>

					<description><![CDATA[Binda, P. &#038; Lunghi, C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations, Neural Plast, (2017), 6724631.</strong></h2>



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<p><em>Short-term monocular deprivation alters visual perception in adult humans, increasing the dominance of the deprived eye, for example, as measured with binocular rivalry. This form of plasticity may depend upon the inhibition/excitation balance in the visual cortex. Recent work suggests that cortical excitability is reliably tracked by dilations and constrictions of the pupils of the eyes. Here, we ask whether monocular deprivation produces a systematic change of pupil behavior, as measured at rest, that is independent of the change of visual perception. During periods of minimal sensory stimulation (in the dark) and task requirements (minimizing body and gaze movements), slow pupil oscillations, &#8220;hippus,&#8221; spontaneously appear. We find that hippus amplitude increases after monocular deprivation, with larger hippus changes in participants showing larger ocular dominance changes (measured by binocular rivalry). This tight correlation suggests that a single latent variable explains both the change of ocular dominance and hippus. We speculate that the neurotransmitter norepinephrine may be implicated in this phenomenon, given its important role in both plasticity and pupil control. On the practical side, our results indicate that measuring the pupil hippus (a simple and short procedure) provides a sensitive index of the change of ocular dominance induced by short-term monocular deprivation, hence a proxy for plasticity.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations, Neural Plast, (2017), 6724631.</strong></h2>
<!-- /wp:heading -->

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<!-- wp:paragraph -->
<p><em>Short-term monocular deprivation alters visual perception in adult humans, increasing the dominance of the deprived eye, for example, as measured with binocular rivalry. This form of plasticity may depend upon the inhibition/excitation balance in the visual cortex. Recent work suggests that cortical excitability is reliably tracked by dilations and constrictions of the pupils of the eyes. Here, we ask whether monocular deprivation produces a systematic change of pupil behavior, as measured at rest, that is independent of the change of visual perception. During periods of minimal sensory stimulation (in the dark) and task requirements (minimizing body and gaze movements), slow pupil oscillations, "hippus," spontaneously appear. We find that hippus amplitude increases after monocular deprivation, with larger hippus changes in participants showing larger ocular dominance changes (measured by binocular rivalry). This tight correlation suggests that a single latent variable explains both the change of ocular dominance and hippus. We speculate that the neurotransmitter norepinephrine may be implicated in this phenomenon, given its important role in both plasticity and pupil control. On the practical side, our results indicate that measuring the pupil hippus (a simple and short procedure) provides a sensitive index of the change of ocular dominance induced by short-term monocular deprivation, hence a proxy for plasticity.</em></p>
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		<item>
		<title>Renewed Attention on the Pupil Light Reflex, Trends Neurosci.</title>
		<link>https://www.pisavisionlab.org/2019/12/22/renewed-attention-on-the-pupil-light-reflex-trends-neurosci/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sun, 22 Dec 2019 08:16:29 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[PAOLA BINDA]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1132</guid>

					<description><![CDATA[Binda, P. &#038; Gamlin, P. D. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Renewed Attention on the Pupil Light Reflex, Trends Neurosci</strong>.</h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2020/10/Binda-Renewed-Attention.pdf">Binda-Renewed-Attention</a><a href="https://www.pisavisionlab.org/wp-content/uploads/2020/10/Binda-Renewed-Attention.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>In a recent study, Ebitz and Moore described how subthreshold electrical microstimulation of the macaque frontal eye fields (FEF) modulates the pupillary light reflex. This elegant study suggests that the influence of the FEF and prefrontal cortex on attentional modulation of cortical visual processing extends to the subcortical circuit that mediates a very basic reflex, the pupillary light reflex.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Renewed Attention on the Pupil Light Reflex, Trends Neurosci</strong>.</h2>
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>In a recent study, Ebitz and Moore described how subthreshold electrical microstimulation of the macaque frontal eye fields (FEF) modulates the pupillary light reflex. This elegant study suggests that the influence of the FEF and prefrontal cortex on attentional modulation of cortical visual processing extends to the subcortical circuit that mediates a very basic reflex, the pupillary light reflex.</em></p>
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		<item>
		<title>Pupil response components: attention-light interaction in patients with Parinaud&#8217;s syndrome, Sci Rep, 1 (7), 10283.</title>
		<link>https://www.pisavisionlab.org/2019/12/22/pupil-response-components-attention-light-interaction-in-patients-with-parinauds-syndrome-sci-rep-1-7-10283/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sun, 22 Dec 2019 08:18:22 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[PAOLA BINDA]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1136</guid>

					<description><![CDATA[Binda, P., Strasser, T., Stingl, K., Richter, P., Peters, T., Wilhelm, H., et al. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Pupil response components: attention-light interaction in patients with Parinaud&#8217;s syndrome, Sci Rep, 1 (7), 10283.</strong></h2>



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<p><em>Covertly shifting attention to a brighter or darker image (without moving one&#8217;s eyes) is sufficient to evoke pupillary constriction or dilation, respectively. One possibility is that this attentional modulation involves the pupillary light response pathway, which pivots around the olivary pretectal nucleus. We investigate this possibility by studying patients with Parinaud&#8217;s syndrome, where the normal pupillary light response is strongly impaired due to lesions in the pretectal area. Four patients and nine control participants covertly attended (while maintaining fixation at the center of a monitor screen) to one of two disks located in the left and right periphery: one brighter, the other darker than the background. Patients and control subjects behaved alike, showing smaller pupils when attending to the brighter stimulus (despite no eye movements); consistent results were obtained with a dynamic version of the stimulus. We interpret this as proof of principle that attention to bright or dark stimuli can dynamically modulate pupil size in patients with Parinaud&#8217;s syndrome, suggesting that attention acts independently of the pretectal circuit for the pupillary light response and indicating that several components of the pupillary response can be isolated &#8211; including one related to the focus of covert attention.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Pupil response components: attention-light interaction in patients with Parinaud's syndrome, Sci Rep, 1 (7), 10283.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1137,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_parinaudssindrome.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Covertly shifting attention to a brighter or darker image (without moving one's eyes) is sufficient to evoke pupillary constriction or dilation, respectively. One possibility is that this attentional modulation involves the pupillary light response pathway, which pivots around the olivary pretectal nucleus. We investigate this possibility by studying patients with Parinaud's syndrome, where the normal pupillary light response is strongly impaired due to lesions in the pretectal area. Four patients and nine control participants covertly attended (while maintaining fixation at the center of a monitor screen) to one of two disks located in the left and right periphery: one brighter, the other darker than the background. Patients and control subjects behaved alike, showing smaller pupils when attending to the brighter stimulus (despite no eye movements); consistent results were obtained with a dynamic version of the stimulus. We interpret this as proof of principle that attention to bright or dark stimuli can dynamically modulate pupil size in patients with Parinaud's syndrome, suggesting that attention acts independently of the pretectal circuit for the pupillary light response and indicating that several components of the pupillary response can be isolated - including one related to the focus of covert attention.</em></p>
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		<item>
		<title>Binocular rivalry in children on the autism spectrum, Autism Res,</title>
		<link>https://www.pisavisionlab.org/2019/12/23/binocular-rivalry-in-children-on-the-autism-spectrum-autism-res/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Mon, 23 Dec 2019 06:45:00 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[CLAUDIA LUNGHI]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1222</guid>

					<description><![CDATA[Karaminis, T., Lunghi, C., Neil, L., Burr, D. &#038; Pellicano, E. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Binocular rivalry in children on the autism spectrum, Autism Res,</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_binocularRivarlyinChilderontheautism.pdf">2017_binocularRivarlyinChilderontheautism</a><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_binocularRivarlyinChilderontheautism.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>When different images are presented to the eyes, the brain is faced with ambiguity, causing perceptual bistability: visual perception continuously alternates between the monocular images, a phenomenon called binocular rivalry. Many models of rivalry suggest that its temporal dynamics depend on mutual inhibition among neurons representing competing images. These models predict that rivalry should be different in autism, which has been proposed to present an atypical ratio of excitation and inhibition [the E/I imbalance hypothesis; Rubenstein &amp; Merzenich, 2003]. In line with this prediction, some recent studies have provided evidence for atypical binocular rivalry dynamics in autistic adults. In this study, we examined if these findings generalize to autistic children. We developed a child-friendly binocular rivalry paradigm, which included two types of stimuli, low- and high-complexity, and compared rivalry dynamics in groups of autistic and age- and intellectual ability-matched typical children. Unexpectedly, the two groups of children presented the same number of perceptual transitions and the same mean phase durations (times perceiving one of the two stimuli). Yet autistic children reported mixed percepts for a shorter proportion of time (a difference which was in the opposite direction to previous adult studies), while elevated autistic symptomatology was associated with shorter mixed perception periods. Rivalry in the two groups was affected similarly by stimulus type, and consistent with previous findings. Our results suggest that rivalry dynamics are differentially affected in adults and developing autistic children and could be accounted for by hierarchical models of binocular rivalry, including both inhibition and top-down influences.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Binocular rivalry in children on the autism spectrum, Autism Res,</strong></h2>
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>When different images are presented to the eyes, the brain is faced with ambiguity, causing perceptual bistability: visual perception continuously alternates between the monocular images, a phenomenon called binocular rivalry. Many models of rivalry suggest that its temporal dynamics depend on mutual inhibition among neurons representing competing images. These models predict that rivalry should be different in autism, which has been proposed to present an atypical ratio of excitation and inhibition [the E/I imbalance hypothesis; Rubenstein &amp; Merzenich, 2003]. In line with this prediction, some recent studies have provided evidence for atypical binocular rivalry dynamics in autistic adults. In this study, we examined if these findings generalize to autistic children. We developed a child-friendly binocular rivalry paradigm, which included two types of stimuli, low- and high-complexity, and compared rivalry dynamics in groups of autistic and age- and intellectual ability-matched typical children. Unexpectedly, the two groups of children presented the same number of perceptual transitions and the same mean phase durations (times perceiving one of the two stimuli). Yet autistic children reported mixed percepts for a shorter proportion of time (a difference which was in the opposite direction to previous adult studies), while elevated autistic symptomatology was associated with shorter mixed perception periods. Rivalry in the two groups was affected similarly by stimulus type, and consistent with previous findings. Our results suggest that rivalry dynamics are differentially affected in adults and developing autistic children and could be accounted for by hierarchical models of binocular rivalry, including both inhibition and top-down influences.</em></p>
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		<item>
		<title>Touch Accelerates Visual Awareness, Iperception, 1 (8), 2041669516686986.</title>
		<link>https://www.pisavisionlab.org/2019/12/23/touch-accelerates-visual-awareness-iperception-1-8-2041669516686986/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Mon, 23 Dec 2019 06:46:30 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[CLAUDIA LUNGHI]]></category>
		<category><![CDATA[LUCA LO VERDE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1225</guid>

					<description><![CDATA[Lunghi, C., Lo Verde, L. &#038; Alais, D. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Touch Accelerates Visual Awareness, Iperception, 1 (8), 2041669516686986.</strong></h2>



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<p><em>To efficiently interact with the external environment, our nervous system combines information arising from different sensory modalities. Recent evidence suggests that cross-modal interactions can be automatic and even unconscious, reflecting the ecological relevance of cross-modal processing. Here, we use continuous flash suppression (CFS) to directly investigate whether haptic signals can interact with visual signals outside of visual awareness. We measured suppression durations of visual gratings rendered invisible by CFS either during visual stimulation alone or during visuo-haptic stimulation. We found that active exploration of a haptic grating congruent in orientation with the suppressed visual grating reduced suppression durations both compared with visual-only stimulation and to incongruent visuo-haptic stimulation. We also found that the facilitatory effect of touch on visual suppression disappeared when the visual and haptic gratings were mismatched in either spatial frequency or orientation. Together, these results demonstrate that congruent touch can accelerate the rise to consciousness of a suppressed visual stimulus and that this unconscious cross-modal interaction depends on visuo-haptic congruency. Furthermore, since CFS suppression is thought to occur early in visual cortical processing, our data reinforce the evidence suggesting that visuo-haptic interactions can occur at the earliest stages of cortical processing.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Touch Accelerates Visual Awareness, Iperception, 1 (8), 2041669516686986.</strong></h2>
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>To efficiently interact with the external environment, our nervous system combines information arising from different sensory modalities. Recent evidence suggests that cross-modal interactions can be automatic and even unconscious, reflecting the ecological relevance of cross-modal processing. Here, we use continuous flash suppression (CFS) to directly investigate whether haptic signals can interact with visual signals outside of visual awareness. We measured suppression durations of visual gratings rendered invisible by CFS either during visual stimulation alone or during visuo-haptic stimulation. We found that active exploration of a haptic grating congruent in orientation with the suppressed visual grating reduced suppression durations both compared with visual-only stimulation and to incongruent visuo-haptic stimulation. We also found that the facilitatory effect of touch on visual suppression disappeared when the visual and haptic gratings were mismatched in either spatial frequency or orientation. Together, these results demonstrate that congruent touch can accelerate the rise to consciousness of a suppressed visual stimulus and that this unconscious cross-modal interaction depends on visuo-haptic congruency. Furthermore, since CFS suppression is thought to occur early in visual cortical processing, our data reinforce the evidence suggesting that visuo-haptic interactions can occur at the earliest stages of cortical processing.</em></p>
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		<item>
		<title>Consciousness is more than meets the eye: a call for a multisensory study of subjective experience, Neuroscience of Consciousness, 1-8.</title>
		<link>https://www.pisavisionlab.org/2019/12/23/consciousness-is-more-than-meets-the-eye-a-call-for-a-multisensory-study-of-subjective-experience-neuroscience-of-consciousness-1-8/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Mon, 23 Dec 2019 06:47:59 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[CLAUDIA LUNGHI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1228</guid>

					<description><![CDATA[Faivre, N., Arzi, A., Lunghi, C. &#038; Salomon, R. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Consciousness is more than meets the eye: a call for a multisensory study of subjective experience, Neuroscience of Consciousness, 1-8.</strong></h2>



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<p><em>Over the last 30 years, our understanding of the neurocognitive bases of consciousness has improved, mostly through studies employing vision. While studying consciousness in the visual modality presents clear advantages, we believe that a comprehensive scientific account of subjective experience must not neglect other exteroceptive and interoceptive signals as well as the role of multisensory interactions for perceptual and self-consciousness. Here, we briefly review four distinct lines of work which converge in documenting how multisensory signals are processed across several levels and contents of consciousness. Namely, how multisensory interactions occur when consciousness is prevented because of perceptual manipulations (i.e. subliminal stimuli) or because of low vigilance states (i.e. sleep, anesthesia), how interactions between exteroceptive and interoceptive signals give rise to bodily self-consciousness, and how multisensory signals are combined to form metacognitive judgments. By describing the interactions between multisensory signals at the perceptual, cognitive, and metacognitive levels, we illustrate how stepping out the visual comfort zone may help in deriving refined accounts of consciousness, and may allow cancelling out idiosyncrasies of each sense to delineate supramodal mechanisms involved during consciousness.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Consciousness is more than meets the eye: a call for a multisensory study of subjective experience, Neuroscience of Consciousness, 1-8.</strong></h2>
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Over the last 30 years, our understanding of the neurocognitive bases of consciousness has improved, mostly through studies employing vision. While studying consciousness in the visual modality presents clear advantages, we believe that a comprehensive scientific account of subjective experience must not neglect other exteroceptive and interoceptive signals as well as the role of multisensory interactions for perceptual and self-consciousness. Here, we briefly review four distinct lines of work which converge in documenting how multisensory signals are processed across several levels and contents of consciousness. Namely, how multisensory interactions occur when consciousness is prevented because of perceptual manipulations (i.e. subliminal stimuli) or because of low vigilance states (i.e. sleep, anesthesia), how interactions between exteroceptive and interoceptive signals give rise to bodily self-consciousness, and how multisensory signals are combined to form metacognitive judgments. By describing the interactions between multisensory signals at the perceptual, cognitive, and metacognitive levels, we illustrate how stepping out the visual comfort zone may help in deriving refined accounts of consciousness, and may allow cancelling out idiosyncrasies of each sense to delineate supramodal mechanisms involved during consciousness.</em></p>
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		<item>
		<title>Serial dependencies act directly on perception, J Vis, 14 (17), 6.</title>
		<link>https://www.pisavisionlab.org/2019/12/24/serial-dependencies-act-directly-on-perception-j-vis-14-17-6/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Tue, 24 Dec 2019 14:20:42 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[GUIDO MARCO CICCHINI]]></category>
		<category><![CDATA[KYRIAKI MIKELLIDOU]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1458</guid>

					<description><![CDATA[Cicchini, G. M., Mikellidou, K. &#038; Burr, D. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Serial dependencies act directly on perception, J Vis, 14 (17), 6.</strong></h2>



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<p><em>There is good evidence that biological perceptual systems exploit the temporal continuity in the world: When asked to reproduce or rate sequentially presented stimuli (varying in almost any dimension), subjects typically err toward the previous stimulus, exhibiting so-called &#8220;serial dependence.&#8221; At this stage it is unclear whether the serial dependence results from averaging within the perceptual system, or at later stages. Here we demonstrate that strong serial dependencies occur within both perceptual and decision processes, with very little contribution from the response. Using a technique to isolate pure perceptual effects (Fritsche, Mostert, &amp; de Lange, 2017), we show strong serial dependence in orientation judgements, over the range of orientations where theoretical considerations predict the effects to be maximal. In a second experiment we dissociate responses from stimuli to show that serial dependence occurs only between stimuli, not responses. The results show that serial dependence is important for perception, exploiting temporal redundancies to enhance perceptual efficiency.</em></p>]]></content:encoded>
					
		
		
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<h2><strong>Serial dependencies act directly on perception, J Vis, 14 (17), 6.</strong></h2>
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<p><em>There is good evidence that biological perceptual systems exploit the temporal continuity in the world: When asked to reproduce or rate sequentially presented stimuli (varying in almost any dimension), subjects typically err toward the previous stimulus, exhibiting so-called "serial dependence." At this stage it is unclear whether the serial dependence results from averaging within the perceptual system, or at later stages. Here we demonstrate that strong serial dependencies occur within both perceptual and decision processes, with very little contribution from the response. Using a technique to isolate pure perceptual effects (Fritsche, Mostert, &amp; de Lange, 2017), we show strong serial dependence in orientation judgements, over the range of orientations where theoretical considerations predict the effects to be maximal. In a second experiment we dissociate responses from stimuli to show that serial dependence occurs only between stimuli, not responses. The results show that serial dependence is important for perception, exploiting temporal redundancies to enhance perceptual efficiency.</em></p>
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		<item>
		<title>Distinct Neural Signatures for Very Small and Very Large Numerosities, Frontiers in Human Neuroscience, (11).</title>
		<link>https://www.pisavisionlab.org/2019/12/27/distinct-neural-signatures-for-very-small-and-very-large-numerosities-frontiers-in-human-neuroscience-11/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 07:45:21 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[MICHELE FORNACIAI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1611</guid>

					<description><![CDATA[Fornaciai, M. &#038; Park, J. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Distinct Neural Signatures for Very Small and Very Large Numerosities, Frontiers in Human Neuroscience, (11)</strong>.</h2>



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<p><em>Behavioral studies of numerical cognition have shown that perceptual threshold for numerosity discrimination depends on the range of numerical values to be estimated. Discrimination threshold is constant when comparing very small numerosities via the mechanism called subitizing, while it increases as a function of numerosity for numbers beyond that range governed by subitizing. However, when numerosity gets so large that the individual elements start to form a cluttered ensemble, discrimination threshold increases as a function of the square root of numerosity. These behavioral patterns suggest that our sense of number is not based on a unitary mechanism and is rather based on multiple numerosity processing mechanisms depending on the absolute numerosity to be estimated. In this study, we demonstrate neurophysiological evidence for such multiple mechanisms. Participants electroencephalogram (EEG) was recorded while they viewed arrays containing either very small (1-4) or very large (100-400) number of dots with systematic variations in non-numerical cues. A linear model that tested the effects of numerical and non-numerical cues on the visual-evoked potentials (VEPs) revealed strong neural sensitivity to numerosity around 160-180 ms over right occipito-parietal sites irrespective of the numerical range presented. In contrast, earlier neural responses (~100 ms) showed markedly distinct patterns across the different numerical ranges tested. These results indicate that differences in behavioral response patterns in numerosity estimation across various numerical ranges may arise from the differences in the first stages of visual analysis. Collectively, the findings provide a firmer ground for the idea that there exists a brain system specifically dedicated for numerosity processing, yet they also suggest that multiple early visual cortical mechanisms converge to that numerosity processing stage later in the visual stream.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Distinct Neural Signatures for Very Small and Very Large Numerosities, Frontiers in Human Neuroscience, (11)</strong>.</h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1612,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_EEGnumerosity.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Behavioral studies of numerical cognition have shown that perceptual threshold for numerosity discrimination depends on the range of numerical values to be estimated. Discrimination threshold is constant when comparing very small numerosities via the mechanism called subitizing, while it increases as a function of numerosity for numbers beyond that range governed by subitizing. However, when numerosity gets so large that the individual elements start to form a cluttered ensemble, discrimination threshold increases as a function of the square root of numerosity. These behavioral patterns suggest that our sense of number is not based on a unitary mechanism and is rather based on multiple numerosity processing mechanisms depending on the absolute numerosity to be estimated. In this study, we demonstrate neurophysiological evidence for such multiple mechanisms. Participants electroencephalogram (EEG) was recorded while they viewed arrays containing either very small (1-4) or very large (100-400) number of dots with systematic variations in non-numerical cues. A linear model that tested the effects of numerical and non-numerical cues on the visual-evoked potentials (VEPs) revealed strong neural sensitivity to numerosity around 160-180 ms over right occipito-parietal sites irrespective of the numerical range presented. In contrast, earlier neural responses (~100 ms) showed markedly distinct patterns across the different numerical ranges tested. These results indicate that differences in behavioral response patterns in numerosity estimation across various numerical ranges may arise from the differences in the first stages of visual analysis. Collectively, the findings provide a firmer ground for the idea that there exists a brain system specifically dedicated for numerosity processing, yet they also suggest that multiple early visual cortical mechanisms converge to that numerosity processing stage later in the visual stream.</em></p>
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		<item>
		<title>Ensemble perception of emotions in autistic and typical children and adolescents, Developmental Cognitive Neuroscience, (24), 51-62.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/nsemble-perception-of-emotions-in-autistic-and-typical-children-and-adolescents-developmental-cognitive-neuroscience-24-51-62/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 13:52:11 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[MARCO TURI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1614</guid>

					<description><![CDATA[Karaminis, T., Neil, L., Manning, C., Turi, M., Fiorentini, C., Burr, D., et al. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading">E<strong>nsemble perception of emotions in autistic and typical children and adolescents, Developmental Cognitive Neuroscience, (24), 51-62.</strong></h2>



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<p><em>Ensemble perception, the ability to assess automatically the summary of large amounts of information presented in visual scenes, is available early in typical development. This ability might be compromised in autistic children, who are thought to present limitations in maintaining summary statistics representations for the recent history of sensory input. Here we examined ensemble perception of facial emotional expressions in 35 autistic children, 30 age- and ability-matched typical children and 25 typical adults. Participants received three tasks: a) an ‘ensemble’ emotion discrimination task; b) a baseline (single-face) emotion discrimination task; and c) a facial expression identification task. Children performed worse than adults on all three tasks. Unexpectedly, autistic and typical children were, on average, indistinguishable in their precision and accuracy on all three tasks. Computational modelling suggested that, on average, autistic and typical children used ensemble-encoding strategies to a similar extent; but ensemble perception was related to non-verbal reasoning abilities in autistic but not in typical children. Eye-movement data also showed no group differences in the way children attended to the stimuli. Our combined findings suggest that the abilities of autistic and typical children for ensemble perception of emotions are comparable on average.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2>E<strong>nsemble perception of emotions in autistic and typical children and adolescents, Developmental Cognitive Neuroscience, (24), 51-62.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1615,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_ensemblePerceptionofEmotions.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Ensemble perception, the ability to assess automatically the summary of large amounts of information presented in visual scenes, is available early in typical development. This ability might be compromised in autistic children, who are thought to present limitations in maintaining summary statistics representations for the recent history of sensory input. Here we examined ensemble perception of facial emotional expressions in 35 autistic children, 30 age- and ability-matched typical children and 25 typical adults. Participants received three tasks: a) an ‘ensemble’ emotion discrimination task; b) a baseline (single-face) emotion discrimination task; and c) a facial expression identification task. Children performed worse than adults on all three tasks. Unexpectedly, autistic and typical children were, on average, indistinguishable in their precision and accuracy on all three tasks. Computational modelling suggested that, on average, autistic and typical children used ensemble-encoding strategies to a similar extent; but ensemble perception was related to non-verbal reasoning abilities in autistic but not in typical children. Eye-movement data also showed no group differences in the way children attended to the stimuli. Our combined findings suggest that the abilities of autistic and typical children for ensemble perception of emotions are comparable on average.</em></p>
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		<item>
		<title>Plasticity of Visual Pathways and Function in the Developing Brain: Is the Pulvinar a Crucial Player?, Front Syst Neurosci, (11), 3.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/plasticity-of-visual-pathways-and-function-in-the-developing-brain-is-the-pulvinar-a-crucial-player-front-syst-neurosci-11-3/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 13:55:07 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1618</guid>

					<description><![CDATA[Karaminis, T., Neil, L., Manning, C., Turi, M., Fiorentini, C., Burr, D., et al. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Plasticity of Visual Pathways and Function in the Developing Brain: Is the Pulvinar a Crucial Player?, Front Syst Neurosci, (11), 3.</strong> </h2>



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<p><em>The pulvinar is the largest of the thalamic nuclei in the primates, including humans. In the primates, two of the three major subdivisions, the lateral and inferior pulvinar, are heavily interconnected with a significant proportion of the visual association cortex. However, while we now have a better understanding of the bidirectional connectivity of these pulvinar subdivisions, its functions remain somewhat of an enigma. Over the past few years, researchers have started to tackle this problem by addressing it from the angle of development and visual cortical lesions. In this review, we will draw together literature from the realms of studies in nonhuman primates and humans that have informed much of the current understanding. This literature has been responsible for changing many long-held opinions on the development of the visual cortex and how the pulvinar interacts dynamically with cortices during early life to ensure rapid development and functional capacity Furthermore, there is evidence to suggest involvement of the pulvinar following lesions of the primary visual cortex (V1) and geniculostriate pathway in early life which have far better functional outcomes than identical lesions obtained in adulthood. Shedding new light on the pulvinar and its role following lesions of the visual brain has implications for our understanding of visual brain disorders and the potential for recovery.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Plasticity of Visual Pathways and Function in the Developing Brain: Is the Pulvinar a Crucial Player?, Front Syst Neurosci, (11), 3.</strong> </h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1619,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_plasticityAndPulvinar.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>The pulvinar is the largest of the thalamic nuclei in the primates, including humans. In the primates, two of the three major subdivisions, the lateral and inferior pulvinar, are heavily interconnected with a significant proportion of the visual association cortex. However, while we now have a better understanding of the bidirectional connectivity of these pulvinar subdivisions, its functions remain somewhat of an enigma. Over the past few years, researchers have started to tackle this problem by addressing it from the angle of development and visual cortical lesions. In this review, we will draw together literature from the realms of studies in nonhuman primates and humans that have informed much of the current understanding. This literature has been responsible for changing many long-held opinions on the development of the visual cortex and how the pulvinar interacts dynamically with cortices during early life to ensure rapid development and functional capacity Furthermore, there is evidence to suggest involvement of the pulvinar following lesions of the primary visual cortex (V1) and geniculostriate pathway in early life which have far better functional outcomes than identical lesions obtained in adulthood. Shedding new light on the pulvinar and its role following lesions of the visual brain has implications for our understanding of visual brain disorders and the potential for recovery.</em></p>
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		<item>
		<title>Saccadic suppression is embedded within extended oscillatory modulation of sensitivity</title>
		<link>https://www.pisavisionlab.org/2019/12/27/saccadic-suppression-is-embedded-within-extended-oscillatory-modulation-of-sensitivity-j-neurosci/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 13:57:14 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[ALESSANDRO BENEDETTO]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1621</guid>

					<description><![CDATA[Benedetto, A. &#038; Morrone, M.C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"></h2>



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<p></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1622,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_saccadicSuppressionOscillations.pdf"} -->
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<!-- wp:paragraph -->
<p></p>
<!-- /wp:paragraph --></content><journal_conference_workshops>Journal of Neuroscience, 37(13), 3661–3670.</journal_conference_workshops>
<abstract>Action and perception are intimately coupled systems. One clear case is saccadic suppression, the reduced visibility around the time of saccades, which is important in mediating visual stability; another is the oscillatory modulation of visibility synchronized with hand action. To suppress effectively the spurious retinal motion generated by the eye movements, it is crucial that saccadic suppression and saccadic onset be temporally synchronous. However, the mechanisms that determine this temporal synchrony are unknown. We investigated the effect of saccades on contrast discrimination sensitivity over a long period stretching over &gt;1 s before and after saccade execution. Human subjects made horizontal saccades at will to two stationary saccadic targets separated by 20°. At a random interval, a brief Gabor patch was displayed between the two fixations in either the upper or lower visual field and the subject had to detect its location. Strong saccadic suppression was measured between −50 and 50 ms from saccadic onset. However, the suppression was systematically embedded in a trough of oscillations of contrast sensitivity that fluctuated rhythmically in the delta range (at ∼3 Hz), commencing ∼1 s before saccade execution and lasting for up to 1 s after the saccade. The results show that saccadic preparation and visual sensitivity oscillations are coupled and the coupling might be instrumental in temporally aligning the initiation of the saccade with the visual suppression. SIGNIFICANCE STATEMENT Saccades are known to produce a suppression of contrast sensitivity at saccadic onset and an enhancement after saccadic offset. Here, we show that these dynamics are systematically embedded in visual oscillations of contrast sensitivity that fluctuate rhythmically in the delta range (at ∼3 Hz), commencing ∼1 s before saccade execution and lasting for up to 1 s after the saccade. The results show that saccadic preparation and visual sensitivity oscillations are coupled and the coupling might be instrumental in aligning temporally the initiation of the saccade with the visual suppression.</abstract>
<autori>Benedetto, A., &amp; Morrone, M. C.</autori>
<pdf>https://www.pisavisionlab.org/2019/12/27/saccadic-suppression-is-embedded-within-extended-oscillatory-modulation-of-sensitivity-j-neurosci/3661-full/</pdf><doi>https://doi.org/10.1523/JNEUROSCI.2390-16.2016</doi>
	</item>
		<item>
		<title>Visual information from observing grasping movement in allocentric and egocentric perspectives: development in typical children, Exp Brain Res.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/visual-information-from-observing-grasping-movement-in-allocentric-and-egocentric-perspectives-development-in-typical-children-exp-brain-res/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:00:26 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[FRANCESCA TINELLI]]></category>
		<category><![CDATA[MARCO TURI]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1624</guid>

					<description><![CDATA[Tinelli, F., Cioni, G., Sandini, G., Turi, M. &#038; Morrone, M. C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Visual information from observing grasping movement in allocentric and egocentric perspectives: development in typical children, Exp Brain Res</strong>.</h2>



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<p><em>Development of the motor system lags behind that of the visual system and might delay some visual properties more closely linked to action. We measured the developmental trajectory of the discrimination of object size from observation of the biological motion of a grasping action in egocentric and allocentric viewpoints (observing action of others or self), in children and adolescents from 5 to 18 years of age. Children of 5-7 years of age performed the task at chance, indicating a delayed ability to understand the goal of the action. We found a progressive improvement in the ability of discrimination from 9 to 18 years, which parallels the development of fine motor control. Only after 9 years of age did we observe an advantage for the egocentric view, as previously reported for adults. Given that visual and haptic sensitivity of size discrimination, as well as biological motion, are mature in early adolescence, we interpret our results as reflecting immaturity of the influence of the motor system on visual perception.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Visual information from observing grasping movement in allocentric and egocentric perspectives: development in typical children, Exp Brain Res</strong>.</h2>
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Development of the motor system lags behind that of the visual system and might delay some visual properties more closely linked to action. We measured the developmental trajectory of the discrimination of object size from observation of the biological motion of a grasping action in egocentric and allocentric viewpoints (observing action of others or self), in children and adolescents from 5 to 18 years of age. Children of 5-7 years of age performed the task at chance, indicating a delayed ability to understand the goal of the action. We found a progressive improvement in the ability of discrimination from 9 to 18 years, which parallels the development of fine motor control. Only after 9 years of age did we observe an advantage for the egocentric view, as previously reported for adults. Given that visual and haptic sensitivity of size discrimination, as well as biological motion, are mature in early adolescence, we interpret our results as reflecting immaturity of the influence of the motor system on visual perception.</em></p>
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		<item>
		<title>A Matched Comparison Across Three Different Sensory Pairs of Cross-Modal Temporal Recalibration From Sustained and Transient Adaptation, i-Perception, 4 (8), 204166951771869.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/a-matched-comparison-across-three-different-sensory-pairs-of-cross-modal-temporal-recalibration-from-sustained-and-transient-adaptation-i-perception-4-8-204166951771869/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:02:59 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[HAO TAM HO]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1627</guid>

					<description><![CDATA[Alais, D., Ho, T., Han, S. e. &#038; Van der Burg, E. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>A Matched Comparison Across Three Different Sensory Pairs of Cross-Modal Temporal Recalibration From Sustained and Transient Adaptation, i-Perception, 4 (8), 204166951771869.</strong></h2>



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<p></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>A Matched Comparison Across Three Different Sensory Pairs of Cross-Modal Temporal Recalibration From Sustained and Transient Adaptation, i-Perception, 4 (8), 204166951771869.</strong></h2>
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		<title>Pitch contour impairment in congenital amusia: New insights from the Self-paced Audio-visual Contour Task (SACT), Plos One, 6 (12), e0179252.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/pitch-contour-impairment-in-congenital-amusia-new-insights-from-the-self-paced-audio-visual-contour-task-sact-plos-one-6-12-e0179252/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:11:17 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[HAO TAM HO]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1630</guid>

					<description><![CDATA[Lu, X., Sun, Y., Ho, H. T. &#038; Thompson, W. F. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Pitch contour impairment in congenital amusia: New insights from the Self-paced Audio-visual Contour Task (SACT), Plos One, 6 (12), e0179252.</strong></h2>



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<p></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Pitch contour impairment in congenital amusia: New insights from the Self-paced Audio-visual Contour Task (SACT), Plos One, 6 (12), e0179252.</strong></h2>
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<p></p>
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		<item>
		<title>Pitch discrimination associated with phonological awareness: Evidence from congenital amusia, Scientific Reports, 1 (7).</title>
		<link>https://www.pisavisionlab.org/2019/12/27/pitch-discrimination-associated-with-phonological-awareness-evidence-from-congenital-amusia-scientific-reports-1-7/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:12:33 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[HAO TAM HO]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1633</guid>

					<description><![CDATA[Sun, Y., Lu, X., Ho, H. T. &#038; Thompson, W. F. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Pitch discrimination associated with phonological awareness: Evidence from congenital amusia, Scientific Reports, 1 (7)</strong>.</h2>



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<p></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Pitch discrimination associated with phonological awareness: Evidence from congenital amusia, Scientific Reports, 1 (7)</strong>.</h2>
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<p></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Psychophysical evidence for the number sense, Philos Trans R Soc Lond B Biol Sci, 1740 (373).</title>
		<link>https://www.pisavisionlab.org/2019/12/27/psychophysical-evidence-for-the-number-sense-philos-trans-r-soc-lond-b-biol-sci-1740-373/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:15:11 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[GIOVANNI ANOBILE]]></category>
		<category><![CDATA[ROBERTO ARRIGHI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1636</guid>

					<description><![CDATA[Burr, D. C., Anobile, G. &#038; Arrighi, R. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong><em>Psychophysical evidence for the number sense</em>, Philos Trans R Soc Lond B Biol Sci, 1740 (373).</strong> </h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017Anobile_Psychophysical-evidence-for-the-number-sense.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>It is now clear that most animals, including humans, possess an ability to rapidly estimate number. Some have questioned whether this ability arises from dedicated numerosity mechanisms, or is derived indirectly from judgements of density or other attributes. We describe a series of psychophysical experiments, largely using adaptation techniques, which demonstrate clearly the existence of a number sense in humans. The number sense is truly general, extending over space, time and sensory modality, and is closely linked with action. We further show that when multiple cues are present, numerosity emerges as the natural dimension for discrimination. However, when element density increases past a certain level, the elements become too crowded to parse, and the scene is perceived as a texture rather than array of elements. The two different regimes are psychophysically discriminable in that they follow distinct psychophysical laws, and show different dependencies on eccentricity, luminance levels and effects of perceptual grouping. The distinction is important, as the ability to discriminate numerosity, but not texture, correlates with formal maths skills.This article is part of the discussion meeting issue &#8216;The origins of numerical abilities&#8217;.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong><em>Psychophysical evidence for the number sense</em>, Philos Trans R Soc Lond B Biol Sci, 1740 (373).</strong> </h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1637,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017Anobile_Psychophysical-evidence-for-the-number-sense.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>It is now clear that most animals, including humans, possess an ability to rapidly estimate number. Some have questioned whether this ability arises from dedicated numerosity mechanisms, or is derived indirectly from judgements of density or other attributes. We describe a series of psychophysical experiments, largely using adaptation techniques, which demonstrate clearly the existence of a number sense in humans. The number sense is truly general, extending over space, time and sensory modality, and is closely linked with action. We further show that when multiple cues are present, numerosity emerges as the natural dimension for discrimination. However, when element density increases past a certain level, the elements become too crowded to parse, and the scene is perceived as a texture rather than array of elements. The two different regimes are psychophysically discriminable in that they follow distinct psychophysical laws, and show different dependencies on eccentricity, luminance levels and effects of perceptual grouping. The distinction is important, as the ability to discriminate numerosity, but not texture, correlates with formal maths skills.This article is part of the discussion meeting issue 'The origins of numerical abilities'.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Spatiotopic coding during dynamic head tilt, J Neurophysiol, 2 (117), 808-817.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/spatiotopic-coding-during-dynamic-head-tilt-j-neurophysiol-2-117-808-817/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:16:42 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[KYRIAKI MIKELLIDOU]]></category>
		<category><![CDATA[MARCO TURI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1639</guid>

					<description><![CDATA[Mikellidou, K., Turi, M. &#038; Burr, D. C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Spatiotopic coding during dynamic head tilt, J Neurophysiol, 2 (117), 808-817.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_spatiotopicCodingDuringDynamicHeadTilt.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>Humans maintain a stable representation of the visual world effortlessly, despite constant movements of the eyes, head, and body, across multiple planes. Whereas visual stability in the face of saccadic eye movements has been intensely researched, fewer studies have investigated retinal image transformations induced by head movements, especially in the frontal plane. Unlike head rotations in the horizontal and sagittal planes, tilting the head in the frontal plane is only partially counteracted by torsional eye movements and consequently induces a distortion of the retinal image to which we seem to be completely oblivious. One possible mechanism aiding perceptual stability is an active reconstruction of a spatiotopic map of the visual world, anchored in allocentric coordinates. To explore this possibility, we measured the positional motion aftereffect (PMAE; the apparent change in position after adaptation to motion) with head tilts of approximately 42 degrees between adaptation and test (to dissociate retinal from allocentric coordinates). The aftereffect was shown to have both a retinotopic and spatiotopic component. When tested with unpatterned Gaussian blobs rather than sinusoidal grating stimuli, the retinotopic component was greatly reduced, whereas the spatiotopic component remained. The results suggest that perceptual stability may be maintained at least partially through mechanisms involving spatiotopic coding.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Spatiotopic coding during dynamic head tilt, J Neurophysiol, 2 (117), 808-817.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1640,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_spatiotopicCodingDuringDynamicHeadTilt.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Humans maintain a stable representation of the visual world effortlessly, despite constant movements of the eyes, head, and body, across multiple planes. Whereas visual stability in the face of saccadic eye movements has been intensely researched, fewer studies have investigated retinal image transformations induced by head movements, especially in the frontal plane. Unlike head rotations in the horizontal and sagittal planes, tilting the head in the frontal plane is only partially counteracted by torsional eye movements and consequently induces a distortion of the retinal image to which we seem to be completely oblivious. One possible mechanism aiding perceptual stability is an active reconstruction of a spatiotopic map of the visual world, anchored in allocentric coordinates. To explore this possibility, we measured the positional motion aftereffect (PMAE; the apparent change in position after adaptation to motion) with head tilts of approximately 42 degrees between adaptation and test (to dissociate retinal from allocentric coordinates). The aftereffect was shown to have both a retinotopic and spatiotopic component. When tested with unpatterned Gaussian blobs rather than sinusoidal grating stimuli, the retinotopic component was greatly reduced, whereas the spatiotopic component remained. The results suggest that perceptual stability may be maintained at least partially through mechanisms involving spatiotopic coding.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Active Vision: Dynamic Reformatting of Visual Information by the Saccade-Drift Cycle, Curr Biol, 9 (27), R341-R344.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/active-vision-dynamic-reformatting-of-visual-information-by-the-saccade-drift-cycle-curr-biol-9-27-r341-r344/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:18:03 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1642</guid>

					<description><![CDATA[Kagan, I. &#038; Burr, D. C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong> Active Vision: Dynamic Reformatting of Visual Information by the Saccade-Drift Cycle, Curr Biol, 9 (27), R341-R344.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burr_activevisiondynamic.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>Visual processing depends on rapid parsing of global features followed by analysis of fine detail. A new study suggests that this transformation is enabled by a cycle of saccades and fixational drifts, which reformat visual input to match the spatiotemporal sensitivity of fast and slow neuronal pathways.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong> Active Vision: Dynamic Reformatting of Visual Information by the Saccade-Drift Cycle, Curr Biol, 9 (27), R341-R344.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1643,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burr_activevisiondynamic.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Visual processing depends on rapid parsing of global features followed by analysis of fine detail. A new study suggests that this transformation is enabled by a cycle of saccades and fixational drifts, which reformat visual input to match the spatiotemporal sensitivity of fast and slow neuronal pathways.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Audio-visual temporal perception in children with restored hearing, Neuropsychologia, (99), 350-359.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/audio-visual-temporal-perception-in-children-with-restored-hearing-neuropsychologia-99-350-359/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 14:20:50 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1645</guid>

					<description><![CDATA[Gori, M., Chilosi, A., Forli, F. &#038; Burr, D. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Audio-visual temporal perception in children with restored hearing, Neuropsychologia, (99), 350-359.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burr_audiovisualtemporalperception.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>It is not clear how audio-visual temporal perception develops in children with restored hearing. In this study we measured temporal discrimination thresholds with an audio-visual temporal bisection task in 9 deaf children with restored audition, and 22 typically hearing children. In typically hearing children, audition was more precise than vision, with no gain in multisensory conditions (as previously reported in Gori et al. (2012b)). However, deaf children with restored audition showed similar thresholds for audio and visual thresholds and some evidence of gain in audio-visual temporal multisensory conditions. Interestingly, we found a strong correlation between auditory weighting of multisensory signals and quality of language: patients who gave more weight to audition had better language skills. Similarly, auditory thresholds for the temporal bisection task were also a good predictor of language skills. This result supports the idea that the temporal auditory processing is associated with language development.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Audio-visual temporal perception in children with restored hearing, Neuropsychologia, (99), 350-359.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1646,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burr_audiovisualtemporalperception.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>It is not clear how audio-visual temporal perception develops in children with restored hearing. In this study we measured temporal discrimination thresholds with an audio-visual temporal bisection task in 9 deaf children with restored audition, and 22 typically hearing children. In typically hearing children, audition was more precise than vision, with no gain in multisensory conditions (as previously reported in Gori et al. (2012b)). However, deaf children with restored audition showed similar thresholds for audio and visual thresholds and some evidence of gain in audio-visual temporal multisensory conditions. Interestingly, we found a strong correlation between auditory weighting of multisensory signals and quality of language: patients who gave more weight to audition had better language skills. Similarly, auditory thresholds for the temporal bisection task were also a good predictor of language skills. This result supports the idea that the temporal auditory processing is associated with language development.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Hemispheric language organization after congenital left brain lesions: A comparison between functional transcranial Doppler and functional MRI, J Neuropsychol.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/hemispheric-language-organization-after-congenital-left-brain-lesions-a-comparison-between-functional-transcranial-doppler-and-functional-mri-j-neuropsychol/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:29:54 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[MARCO TURI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1648</guid>

					<description><![CDATA[Chilosi, A. M., Bulgheroni, S., Turi, M., Cristofani, P., Biagi, L., Erbetta, A., et al. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Hemispheric language organization after congenital left brain lesions: A comparison between functional transcranial Doppler and functional MRI, J Neuropsychol.</strong></h2>



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<p><em>This study investigated whether functional transcranial Doppler ultrasound (fTCD) is a suitable tool for studying hemispheric lateralization of language in patients with pre-perinatal left hemisphere (LH) lesions and right hemiparesis. Eighteen left-hemisphere-damaged children and young adults and 18 healthy controls were assessed by fTCD and fMRI to evaluate hemispheric activation during two language tasks: a fTCD animation description task and a fMRI covert rhyme generation task. Lateralization indices (LIs), measured by the two methods, differed significantly between the two groups, for a clear LH dominance in healthy participants and a prevalent activation of right hemisphere in more than 80% of brain-damaged patients. Distribution of participants in terms of left, right, and bilateral lateralization was highly concordant between fTCD and fMRI values. Moreover, right hemisphere language dominance in patients with left hemispheric lesions was significantly associated with severity of cortical and subcortical damage in LH. This study suggests that fTCD is an easily applicable tool that might be a valid alternative to fMRI for large-scale studies of patients with congenital brain lesions.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Hemispheric language organization after congenital left brain lesions: A comparison between functional transcranial Doppler and functional MRI, J Neuropsychol.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1649,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_turi_hemisfericlanguageorganization.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>This study investigated whether functional transcranial Doppler ultrasound (fTCD) is a suitable tool for studying hemispheric lateralization of language in patients with pre-perinatal left hemisphere (LH) lesions and right hemiparesis. Eighteen left-hemisphere-damaged children and young adults and 18 healthy controls were assessed by fTCD and fMRI to evaluate hemispheric activation during two language tasks: a fTCD animation description task and a fMRI covert rhyme generation task. Lateralization indices (LIs), measured by the two methods, differed significantly between the two groups, for a clear LH dominance in healthy participants and a prevalent activation of right hemisphere in more than 80% of brain-damaged patients. Distribution of participants in terms of left, right, and bilateral lateralization was highly concordant between fTCD and fMRI values. Moreover, right hemisphere language dominance in patients with left hemispheric lesions was significantly associated with severity of cortical and subcortical damage in LH. This study suggests that fTCD is an easily applicable tool that might be a valid alternative to fMRI for large-scale studies of patients with congenital brain lesions.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>The light-from-above prior is intact in autistic children, J Exp Child Psychol, (161), 113-125.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/the-light-from-above-prior-is-intact-in-autistic-children-j-exp-child-psychol-161-113-125/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:32:28 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1651</guid>

					<description><![CDATA[Croydon, A., Karaminis, T., Neil, L., Burr, D. &#038; Pellicano, E. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong><em>The light-from-above prior is intact in autistic children</em>, J Exp Child Psychol, (161), 113-125.</strong></h2>



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<p><em>Sensory information is inherently ambiguous. The brain disambiguates this information by anticipating or predicting the sensory environment based on prior knowledge. Pellicano and Burr (2012) proposed that this process may be atypical in autism and that internal assumptions, or &#8220;priors,&#8221; may be underweighted or less used than in typical individuals. A robust internal assumption used by adults is the &#8220;light-from-above&#8221; prior, a bias to interpret ambiguous shading patterns as if formed by a light source located above (and slightly to the left) of the scene. We investigated whether autistic children (n=18) use this prior to the same degree as typical children of similar age and intellectual ability (n=18). Children were asked to judge the shape (concave or convex) of a shaded hexagon stimulus presented in 24 rotations. We estimated the relation between the proportion of convex judgments and stimulus orientation for each child and calculated the light source location most consistent with those judgments. Children behaved similarly to adults in this task, preferring to assume that the light source was from above left, when other interpretations were compatible with the shading evidence. Autistic and typical children used prior assumptions to the same extent to make sense of shading patterns. Future research should examine whether this prior is as adaptable (i.e., modifiable with training) in autistic children as it is in typical adults.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong><em>The light-from-above prior is intact in autistic children</em>, J Exp Child Psychol, (161), 113-125.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1652,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burr_thelightfromabove.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Sensory information is inherently ambiguous. The brain disambiguates this information by anticipating or predicting the sensory environment based on prior knowledge. Pellicano and Burr (2012) proposed that this process may be atypical in autism and that internal assumptions, or "priors," may be underweighted or less used than in typical individuals. A robust internal assumption used by adults is the "light-from-above" prior, a bias to interpret ambiguous shading patterns as if formed by a light source located above (and slightly to the left) of the scene. We investigated whether autistic children (n=18) use this prior to the same degree as typical children of similar age and intellectual ability (n=18). Children were asked to judge the shape (concave or convex) of a shaded hexagon stimulus presented in 24 rotations. We estimated the relation between the proportion of convex judgments and stimulus orientation for each child and calculated the light source location most consistent with those judgments. Children behaved similarly to adults in this task, preferring to assume that the light source was from above left, when other interpretations were compatible with the shading evidence. Autistic and typical children used prior assumptions to the same extent to make sense of shading patterns. Future research should examine whether this prior is as adaptable (i.e., modifiable with training) in autistic children as it is in typical adults.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Temporally Evolving Gain Mechanisms of Attention in Macaque Area V4, J Neurophysiol, jn 00522 02016.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/temporally-evolving-gain-mechanisms-of-attention-in-macaque-area-v4-j-neurophysiol-jn-00522-02016/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:34:09 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1654</guid>

					<description><![CDATA[Sani, I., Santandrea, E., Morrone, M. C. &#038; Chelazzi, L. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Temporally Evolving Gain Mechanisms of Attention in Macaque Area V4, J Neurophysiol, jn 00522 02016.</strong></h2>



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<p><em>Cognitive attention and perceptual saliency jointly govern our interaction with the environment. Yet, we still lack a universally accepted account of the interplay between attention and luminance contrast &#8211; a fundamental dimension of saliency. We measured the attentional modulation of V4 neurons&#8217; Contrast Response Functions (CRFs) in awake, behaving macaque monkeys and applied a new approach which emphasizes the temporal dynamics of cell responses. We found that attention modulates CRFs via different gain mechanisms during subsequent epochs of visually driven activity: an early contrast-gain &#8211; strongly dependent on pre-stimulus activity changes (baseline shift), a time-limited stimulus-dependent multiplicative modulation, reaching its maximal expression around 150 ms after stimulus onset, and a late resurgence of contrast-gain modulation. Attention produced comparable time-dependent attentional gain changes on cells heterogeneously coding contrast, supporting the notion that the same circuits mediate attention mechanisms in V4 regardless of the form of contrast selectivity expressed by the given neuron. Surprisingly, attention was also sometimes capable of inducing radical transformations in the shape of CRFs. These findings offer important insights into the mechanisms that underlie contrast coding and attention in primate visual cortex and a new perspective on their interplay, one in which time becomes a fundamental factor.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Temporally Evolving Gain Mechanisms of Attention in Macaque Area V4, J Neurophysiol, jn 00522 02016.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1655,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_temporallyevolinggainmechanism.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Cognitive attention and perceptual saliency jointly govern our interaction with the environment. Yet, we still lack a universally accepted account of the interplay between attention and luminance contrast - a fundamental dimension of saliency. We measured the attentional modulation of V4 neurons' Contrast Response Functions (CRFs) in awake, behaving macaque monkeys and applied a new approach which emphasizes the temporal dynamics of cell responses. We found that attention modulates CRFs via different gain mechanisms during subsequent epochs of visually driven activity: an early contrast-gain - strongly dependent on pre-stimulus activity changes (baseline shift), a time-limited stimulus-dependent multiplicative modulation, reaching its maximal expression around 150 ms after stimulus onset, and a late resurgence of contrast-gain modulation. Attention produced comparable time-dependent attentional gain changes on cells heterogeneously coding contrast, supporting the notion that the same circuits mediate attention mechanisms in V4 regardless of the form of contrast selectivity expressed by the given neuron. Surprisingly, attention was also sometimes capable of inducing radical transformations in the shape of CRFs. These findings offer important insights into the mechanisms that underlie contrast coding and attention in primate visual cortex and a new perspective on their interplay, one in which time becomes a fundamental factor.</em></p>
<!-- /wp:paragraph --></content>	</item>
		<item>
		<title>Autism is associated with reduced ability to interpret grasping actions of others, Sci Rep, 1 (7), 12687.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/autism-is-associated-with-reduced-ability-to-interpret-grasping-actions-of-others-sci-rep-1-7-12687/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:35:59 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[FRANCESCA TINELLI]]></category>
		<category><![CDATA[MARCO TURI]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1657</guid>

					<description><![CDATA[Turi, M., Muratori, F., Tinelli, F., Morrone, M. C. &#038; Burr, D. C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong><em>Autism is associated with reduced ability to interpret grasping actions of others</em>, Sci Rep, 1 (7), 12687.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_Turi-etAl_AutismIsAssociatedWithReducedAbilityToInterpretGraspingActionsOfOthers_SciRep2017.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>We investigated the ability of children with ASD to discriminate a small cylinder from a large cube by observing a point-light movie of an actor grasping the object, either from an allocentric or egocentric viewpoint (observing action of others or self). Compared with typically developing controls, high functioning autistic children showed a strong selective impairment in this task, but only with the allocentric viewpoint, where thresholds were twice as high: egocentric thresholds were similar to age- and ability-matched controls. The magnitude of the impairment correlated strongly with the degree of symptomology (R2 = 0.5). The results suggest that children with ASD might be impaired in their ability to predict and infer the consequences of others&#8217; movements, which could be related to the social-communicative deficits often reported in autism.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong><em>Autism is associated with reduced ability to interpret grasping actions of others</em>, Sci Rep, 1 (7), 12687.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1658,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_Turi-etAl_AutismIsAssociatedWithReducedAbilityToInterpretGraspingActionsOfOthers_SciRep2017.pdf"} -->
<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_Turi-etAl_AutismIsAssociatedWithReducedAbilityToInterpretGraspingActionsOfOthers_SciRep2017.pdf" class="wp-block-file__button" download>Download</a></div>
<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>We investigated the ability of children with ASD to discriminate a small cylinder from a large cube by observing a point-light movie of an actor grasping the object, either from an allocentric or egocentric viewpoint (observing action of others or self). Compared with typically developing controls, high functioning autistic children showed a strong selective impairment in this task, but only with the allocentric viewpoint, where thresholds were twice as high: egocentric thresholds were similar to age- and ability-matched controls. The magnitude of the impairment correlated strongly with the degree of symptomology (R2 = 0.5). The results suggest that children with ASD might be impaired in their ability to predict and infer the consequences of others' movements, which could be related to the social-communicative deficits often reported in autism.</em></p>
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		<item>
		<title>Evidence for a number sense, Behavioral and Brain Sciences, (40), 18-19.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/evidence-for-a-number-sense-behavioral-and-brain-sciences-40-18-19/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:37:21 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1660</guid>

					<description><![CDATA[Burr, D. C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Evidence for a number sense, Behavioral and Brain Sciences, (40), 18-19.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burrsenseofnumber.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>Numerosity is inherently confounded by related stimulus attributes such as density and area, and many studies have reported interactions of various strengths between area, density, and numerosity. However, direct measurements of sensitivity within the area-density-numerosity space show that numerosity emerges as the most spontaneous and sensitive dimension, strongly supporting the existence of a dedicated number sense.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Evidence for a number sense, Behavioral and Brain Sciences, (40), 18-19.</strong></h2>
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<!-- wp:file {"id":1661,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burrsenseofnumber.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Numerosity is inherently confounded by related stimulus attributes such as density and area, and many studies have reported interactions of various strengths between area, density, and numerosity. However, direct measurements of sensitivity within the area-density-numerosity space show that numerosity emerges as the most spontaneous and sensitive dimension, strongly supporting the existence of a dedicated number sense.</em></p>
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		<item>
		<title>Evidence for a number sense, Perceiving numerosity from birth, Behavioral and Brain Sciences, (40), 21-22.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/evidence-for-a-number-sense-perceiving-numerosity-from-birth-behavioral-and-brain-sciences-40-21-22/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:40:38 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[ELISA CASTALDI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1663</guid>

					<description><![CDATA[de Hevia, M. D., Castaldi, E., Streri, A., Eger, E. &#038; Izard, V. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Perceiving numerosity from birth, Behavioral and Brain Sciences, (40), 21-22.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burrsenseofnumber-1.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>Leibovich et al. opened up an important discussion on the nature and origins of numerosity perception. The authors rightly point out that non-numerical features of stimuli influence this ability. Despite these biases, there is evidence that from birth, humans perceive and represent numerosities, and not just non-numerical quantitative features such as item size, density, and convex hull.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Perceiving numerosity from birth, Behavioral and Brain Sciences, (40), 21-22.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1664,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_burrsenseofnumber-1.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Leibovich et al. opened up an important discussion on the nature and origins of numerosity perception. The authors rightly point out that non-numerical features of stimuli influence this ability. Despite these biases, there is evidence that from birth, humans perceive and represent numerosities, and not just non-numerical quantitative features such as item size, density, and convex hull.</em></p>
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		<item>
		<title>Area Prostriata in the Human Brain, Curr Biol, 19 (27), 3056-3060 e3053.</title>
		<link>https://www.pisavisionlab.org/2019/12/27/area-prostriata-in-the-human-brain-curr-biol-19-27-3056-3060-e3053/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Fri, 27 Dec 2019 17:43:04 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[JAN KURZAWSKI]]></category>
		<category><![CDATA[KYRIAKI MIKELLIDOU]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1667</guid>

					<description><![CDATA[Mikellidou, K., Kurzawski, J. W., Frijia, F., Montanaro, D., Greco, V., Burr, D. C., et al. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong><em>Area Prostriata in the Human Brain</em>, Curr Biol, 19 (27), 3056-3060 e3053.</strong></h2>



<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_prostriata.pdf" class="wp-block-file__button" download>Download</a></div>



<p><em>Area prostriata is a cortical area at the fundus of the calcarine sulcus, described anatomically in humans [ 1–5 ] and other primates [ 6–9 ]. It is lightly myelinated and lacks the clearly defined six-layer structure evident throughout the cerebral cortex, with a thinner layer 4 and thicker layer 2 [ 10 ], characteristic of limbic cortex [ 11 ]. In the marmoset and rhesus monkey, area prostriata has cortical connections with MT+ [ 12 ], the cingulate motor cortex [ 8 ], the auditory cortex [ 13 ], the orbitofrontal cortex, and the frontal polar cortices [ 14 ]. Here we use functional magnetic resonance together with a wide-field projection system to study its functional properties in humans. With population receptive field mapping [ 15 ], we show that area prostriata has a complete representation of the visual field, clearly distinct from the adjacent area V1. As in the marmoset, the caudal-dorsal border of human prostriata—abutting V1—represents the far peripheral visual field, with eccentricities decreasing toward its rostral boundary. Area prostriata responds strongly to very fast motion, greater than 500°/s. The functional properties of area prostriata suggest that it may serve to alert the brain quickly to fast visual events, particularly in the peripheral visual field.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong><em>Area Prostriata in the Human Brain</em>, Curr Biol, 19 (27), 3056-3060 e3053.</strong></h2>
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<!-- wp:file {"id":1668,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_prostriata.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Area prostriata is a cortical area at the fundus of the calcarine sulcus, described anatomically in humans [ 1–5 ] and other primates [ 6–9 ]. It is lightly myelinated and lacks the clearly defined six-layer structure evident throughout the cerebral cortex, with a thinner layer 4 and thicker layer 2 [ 10 ], characteristic of limbic cortex [ 11 ]. In the marmoset and rhesus monkey, area prostriata has cortical connections with MT+ [ 12 ], the cingulate motor cortex [ 8 ], the auditory cortex [ 13 ], the orbitofrontal cortex, and the frontal polar cortices [ 14 ]. Here we use functional magnetic resonance together with a wide-field projection system to study its functional properties in humans. With population receptive field mapping [ 15 ], we show that area prostriata has a complete representation of the visual field, clearly distinct from the adjacent area V1. As in the marmoset, the caudal-dorsal border of human prostriata—abutting V1—represents the far peripheral visual field, with eccentricities decreasing toward its rostral boundary. Area prostriata responds strongly to very fast motion, greater than 500°/s. The functional properties of area prostriata suggest that it may serve to alert the brain quickly to fast visual events, particularly in the peripheral visual field.</em></p>
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		<item>
		<title>Spatial localization of sound elicits early responses from occipital visual cortex in humans, Sci Rep, 1 (7), 10415.</title>
		<link>https://www.pisavisionlab.org/2019/12/28/spatial-localization-of-sound-elicits-early-responses-from-occipital-visual-cortex-in-humans-sci-rep-1-7-10415/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sat, 28 Dec 2019 07:59:15 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1671</guid>

					<description><![CDATA[Campus, C., Sandini, G., Concetta Morrone, M. &#038; Gori, M. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Spatial localization of sound elicits early responses from occipital visual cortex in humans, Sci Rep, 1 (7), 10415.</strong></h2>



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<p><em>Much evidence points to an interaction between vision and audition at early cortical sites. However, the functional role of these interactions is not yet understood. Here we show an early response of the occipital cortex to sound that it is strongly linked to the spatial localization task performed by the observer. The early occipital response to a sound, usually absent, increased by more than 10-fold when presented during a space localization task, but not during a time localization task. The response amplification was not only specific to the task, but surprisingly also to the position of the stimulus in the two hemifields. We suggest that early occipital processing of sound is linked to the construction of an audio spatial map that may utilize the visual map of the occipital cortex.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Spatial localization of sound elicits early responses from occipital visual cortex in humans, Sci Rep, 1 (7), 10415.</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1672,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_spatialLocalizationOfSoundElicits.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Much evidence points to an interaction between vision and audition at early cortical sites. However, the functional role of these interactions is not yet understood. Here we show an early response of the occipital cortex to sound that it is strongly linked to the spatial localization task performed by the observer. The early occipital response to a sound, usually absent, increased by more than 10-fold when presented during a space localization task, but not during a time localization task. The response amplification was not only specific to the task, but surprisingly also to the position of the stimulus in the two hemifields. We suggest that early occipital processing of sound is linked to the construction of an audio spatial map that may utilize the visual map of the occipital cortex.</em></p>
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		<item>
		<title>Auditory Sensitivity and Decision Criteria Oscillate at Different Frequencies Separately for the Two Ears, Current Biology,</title>
		<link>https://www.pisavisionlab.org/2019/12/28/auditory-sensitivity-and-decision-criteria-oscillate-at-different-frequencies-separately-for-the-two-ears-current-biology/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sat, 28 Dec 2019 08:01:05 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[HAO TAM HO]]></category>
		<category><![CDATA[MARIA CONCETTA MORRONE]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1674</guid>

					<description><![CDATA[Ho, T. H., Leung, J., Burr, D., Alais, D. &#038; Morrone, M. C. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Auditory Sensitivity and Decision Criteria Oscillate at Different Frequencies Separately for the Two Ears, Current Biology,</strong></h2>



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<p><em>Many behavioral measures of visual perception fluctuate continually in a rhythmic manner, reflecting the influence of endogenous brain oscillations, particularly theta (~4–7 Hz) and alpha (~8–12 Hz) rhythms. However, it is unclear whether these oscillations are unique to vision or whether auditory performance also oscillates. Several studies report no oscillatory modulation in audition, while those with positive findings suffer from confounds relating to neural entrainment. Here, we used a bilateral pitch-identification task to investigate rhythmic fluctuations in auditory performance separately for the two ears and applied signal detection theory (SDT) to test for oscillations of both sensitivity and criterion (changes in decision boundary). Using uncorrelated dichotic white noise to induce a phase reset of oscillations, we demonstrate that, as with vision, both auditory sensitivity and criterion showed strong oscillations over time, at different frequencies: ~6 Hz (theta range) for sensitivity and ~8 Hz (low alpha range) for criterion, implying distinct underlying sampling mechanisms. The modulation in sensitivity in left and right ears was in antiphase, suggestive of attention-like mechanisms sampling alternatively from the two ears.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Auditory Sensitivity and Decision Criteria Oscillate at Different Frequencies Separately for the Two Ears, Current Biology,</strong></h2>
<!-- /wp:heading -->

<!-- wp:file {"id":1675,"href":"https://www.pisavisionlab.org/wp-content/uploads/2019/12/2017_auditoryOscillations.pdf"} -->
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<!-- /wp:file -->

<!-- wp:paragraph -->
<p><em>Many behavioral measures of visual perception fluctuate continually in a rhythmic manner, reflecting the influence of endogenous brain oscillations, particularly theta (~4–7 Hz) and alpha (~8–12 Hz) rhythms. However, it is unclear whether these oscillations are unique to vision or whether auditory performance also oscillates. Several studies report no oscillatory modulation in audition, while those with positive findings suffer from confounds relating to neural entrainment. Here, we used a bilateral pitch-identification task to investigate rhythmic fluctuations in auditory performance separately for the two ears and applied signal detection theory (SDT) to test for oscillations of both sensitivity and criterion (changes in decision boundary). Using uncorrelated dichotic white noise to induce a phase reset of oscillations, we demonstrate that, as with vision, both auditory sensitivity and criterion showed strong oscillations over time, at different frequencies: ~6 Hz (theta range) for sensitivity and ~8 Hz (low alpha range) for criterion, implying distinct underlying sampling mechanisms. The modulation in sensitivity in left and right ears was in antiphase, suggestive of attention-like mechanisms sampling alternatively from the two ears.</em></p>
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		<item>
		<title>Plasticity of the human visual brain after an early cortical lesion, Neuropsychologia.</title>
		<link>https://www.pisavisionlab.org/2019/12/28/plasticity-of-the-human-visual-brain-after-an-early-cortical-lesion-neuropsychologia/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sat, 28 Dec 2019 08:05:47 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[FRANCESCA TINELLI]]></category>
		<category><![CDATA[KYRIAKI MIKELLIDOU]]></category>
		<category><![CDATA[ROBERTO ARRIGHI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1677</guid>

					<description><![CDATA[Mikellidou, K., Arrighi, R., Aghakhanyan, G., Tinelli, F., Frijia, F., Crespi, S., et al. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Plasticity of the human visual brain after an early cortical lesion, Neuropsychologia</strong>.</h2>



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<figure class="wp-block-image"><a href="http://win.pisavisionlab.org/public/Plasticity%20of%20the%20human%20visual%20brain%20after%20an%20early%20cortical%20lesion.pdf" target="_blank" rel="noreferrer noopener"><img decoding="async" src="http://cdn.f1000.com.s3.amazonaws.com/images/badges/badgef1000.gif" alt="Access the recommendation on F1000Prime"/></a></figure>



<p><em>In adults, partial damage to V1 or optic radiations abolishes perception in the corresponding part of the visual field, causing a scotoma. However, it is widely accepted that the developing cortex has superior capacities to reorganize following an early lesion to endorse adaptive plasticity. Here we report a single patient case (G.S.) with near normal central field vision despite a massive unilateral lesion to the optic radiations acquired early in life. The patient underwent surgical removal of a right hemisphere parieto-temporal-occipital atypical choroid plexus papilloma of the right lateral ventricle at four months of age, which presumably altered the visual pathways during in utero development. Both the tumor and surgery severely compromised the optic radiations. Residual vision of G.S. was tested psychophysically when the patient was 7 years old. We found a close-to-normal visual acuity and contrast sensitivity within the central 25 degrees and a great impairment in form and contrast vision in the far periphery (40-50 degrees ) of the left visual hemifield. BOLD response to full field luminance flicker was recorded from the primary visual cortex (V1) and in a region in the residual temporal-occipital region, presumably corresponding to the middle temporal complex (MT+), of the lesioned (right) hemisphere. A population receptive field analysis of the BOLD responses to contrast modulated stimuli revealed a retinotopic organization just for the MT+ region but not for the calcarine regions. Interestingly, consistent islands of ipsilateral activity were found in MT+ and in the parieto-occipital sulcus (POS) of the intact hemisphere. Probabilistic tractography revealed that optic radiations between LGN and V1 were very sparse in the lesioned hemisphere consistently with the post-surgery cerebral resection, while normal in the intact hemisphere. On the other hand, strong structural connections between MT+ and LGN were found in the lesioned hemisphere, while the equivalent tract in the spared hemisphere showed minimal structural connectivity. These results suggest that during development of the pathological brain, abnormal thalamic projections can lead to functional cortical changes, which may mediate functional recovery of vision.</em></p>]]></content:encoded>
					
		
		
		<content><!-- wp:heading -->
<h2><strong>Plasticity of the human visual brain after an early cortical lesion, Neuropsychologia</strong>.</h2>
<!-- /wp:heading -->

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<p><em>In adults, partial damage to V1 or optic radiations abolishes perception in the corresponding part of the visual field, causing a scotoma. However, it is widely accepted that the developing cortex has superior capacities to reorganize following an early lesion to endorse adaptive plasticity. Here we report a single patient case (G.S.) with near normal central field vision despite a massive unilateral lesion to the optic radiations acquired early in life. The patient underwent surgical removal of a right hemisphere parieto-temporal-occipital atypical choroid plexus papilloma of the right lateral ventricle at four months of age, which presumably altered the visual pathways during in utero development. Both the tumor and surgery severely compromised the optic radiations. Residual vision of G.S. was tested psychophysically when the patient was 7 years old. We found a close-to-normal visual acuity and contrast sensitivity within the central 25 degrees and a great impairment in form and contrast vision in the far periphery (40-50 degrees ) of the left visual hemifield. BOLD response to full field luminance flicker was recorded from the primary visual cortex (V1) and in a region in the residual temporal-occipital region, presumably corresponding to the middle temporal complex (MT+), of the lesioned (right) hemisphere. A population receptive field analysis of the BOLD responses to contrast modulated stimuli revealed a retinotopic organization just for the MT+ region but not for the calcarine regions. Interestingly, consistent islands of ipsilateral activity were found in MT+ and in the parieto-occipital sulcus (POS) of the intact hemisphere. Probabilistic tractography revealed that optic radiations between LGN and V1 were very sparse in the lesioned hemisphere consistently with the post-surgery cerebral resection, while normal in the intact hemisphere. On the other hand, strong structural connections between MT+ and LGN were found in the lesioned hemisphere, while the equivalent tract in the spared hemisphere showed minimal structural connectivity. These results suggest that during development of the pathological brain, abnormal thalamic projections can lead to functional cortical changes, which may mediate functional recovery of vision.</em></p>
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		<item>
		<title>Connecting Visual Objects Reduces Perceived Numerosity and Density for Sparse but not Dense Patterns, Journal of Numerical Cognition, 4 (3).</title>
		<link>https://www.pisavisionlab.org/2019/12/28/connecting-visual-objects-reduces-perceived-numerosity-and-density-for-sparse-but-not-dense-patterns-journal-of-numerical-cognition-4-3-2/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sat, 28 Dec 2019 08:09:09 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[ANTONELLA POMè]]></category>
		<category><![CDATA[DAVID BURR]]></category>
		<category><![CDATA[GIOVANNI ANOBILE]]></category>
		<category><![CDATA[GUIDO MARCO CICCHINI]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1680</guid>

					<description><![CDATA[Anobile, G., Cicchini, G. M., Pomè, A. &#038; Burr, D. (2017).]]></description>
										<content:encoded><![CDATA[<h2 class="wp-block-heading"><strong>Connecting Visual Objects Reduces Perceived Numerosity and Density for Sparse but not Dense Patterns, Journal of Numerical Cognition, 4 (3)</strong>.</h2>



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<p><em>How is numerosity encoded by the visual system? – directly, or derived indirectly from texture density? We recently suggested that the numerosity of sparse patterns is encoded directly by dedicated mechanisms (which have been described as the “Approximate Number System” ANS). However, at high dot densities, where items become “crowded” and difficult to segregate, “texture-density” mechanisms come into play. Here we tested the importance of item segmentation on numerosity and density perception at various stimulus densities, by measuring the effect of connecting visual objects with thin lines. The results confirmed many previous studies showing that connecting items robustly reduces the apparent numerosity of patterns of moderate density. We further showed that the apparent density of moderate-density patterns is also reduced by connecting the dots. Crucially, we found that both these effects are strongly reduced at higher numerosities. Indeed for density judgments, the effect reverses, so connecting dots in dense patterns increases the apparent density (as expected from the physical characteristics). The results provide clear support for the three-regime framework of number perception, and suggest that for moderately sparse stimuli, numerosity – but not texture-density – is perceived directly.</em></p>]]></content:encoded>
					
		
		
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<h2><strong>Connecting Visual Objects Reduces Perceived Numerosity and Density for Sparse but not Dense Patterns, Journal of Numerical Cognition, 4 (3)</strong>.</h2>
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<p><em>How is numerosity encoded by the visual system? – directly, or derived indirectly from texture density? We recently suggested that the numerosity of sparse patterns is encoded directly by dedicated mechanisms (which have been described as the “Approximate Number System” ANS). However, at high dot densities, where items become “crowded” and difficult to segregate, “texture-density” mechanisms come into play. Here we tested the importance of item segmentation on numerosity and density perception at various stimulus densities, by measuring the effect of connecting visual objects with thin lines. The results confirmed many previous studies showing that connecting items robustly reduces the apparent numerosity of patterns of moderate density. We further showed that the apparent density of moderate-density patterns is also reduced by connecting the dots. Crucially, we found that both these effects are strongly reduced at higher numerosities. Indeed for density judgments, the effect reverses, so connecting dots in dense patterns increases the apparent density (as expected from the physical characteristics). The results provide clear support for the three-regime framework of number perception, and suggest that for moderately sparse stimuli, numerosity – but not texture-density – is perceived directly.</em></p>
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		<title>Different Responses of Spontaneous and Stimulus-Related Alpha Activity to Ambient Luminance Changes</title>
		<link>https://www.pisavisionlab.org/2019/12/28/different-responses-of-spontaneous-and-stimulus-related-alpha-activity-to-ambient-luminance-changes-eur-j-neurosci/</link>
		
		<dc:creator><![CDATA[daniele]]></dc:creator>
		<pubDate>Sat, 28 Dec 2019 08:10:52 +0000</pubDate>
				<category><![CDATA[2017]]></category>
		<category><![CDATA[ALESSANDRO BENEDETTO]]></category>
		<guid isPermaLink="false">https://www.pisavisionlab.org/?p=1682</guid>

					<description><![CDATA[Benedetto, A., Lozano-Soldevilla, D. &#038; VanRullen, R. (2017).]]></description>
										<content:encoded><![CDATA[<div class="wp-block-file"><a href="https://www.pisavisionlab.org/wp-content/uploads/2019/12/Benedetto_et_al-2017-European_Journal_of_Neuroscience.pdf" class="wp-block-file__button" download>Download</a></div>



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<p></p>
<!-- /wp:paragraph --></content><journal_conference_workshops>European Journal of Neuroscience, 48(7), 2599–2608.</journal_conference_workshops>
<abstract>Alpha oscillations are particularly important in determining our percepts and have been implicated in fundamental brain functions. Oscillatory activity can be spontaneous or stimulus-related. Furthermore, stimulus-related responses can be phase- or non-phase-locked to the stimulus. Non-phase-locked (induced) activity can be identified as the average amplitude changes in response to a stimulation, while phase-locked activity can be measured via reverse-correlation techniques (echo function). However, the mechanisms and the functional roles of these oscillations are far from clear. Here, we investigated the effect of ambient luminance changes, known to dramatically modulate neural oscillations, on spontaneous and stimulus-related alpha. We investigated the effect of ambient luminance on EEG alpha during spontaneous human brain activity at rest (experiment 1) and during visual stimulation (experiment 2). Results show that spontaneous alpha amplitude increased by decreasing ambient luminance, while alpha frequency remained unaffected. In the second experiment, we found that under low-luminance viewing, the stimulus-related alpha amplitude was lower, and its frequency was slightly faster. These effects were evident in the phase-locked part of the alpha response (echo function), but weaker or absent in the induced (non-phase-locked) alpha responses. Finally, we explored the possible behavioural correlates of these modulations in a monocular critical flicker frequency task (experiment 3), finding that dark adaptation in the left eye decreased the temporal threshold of the right eye. Overall, we found that ambient luminance changes impact differently on spontaneous and stimulus-related alpha expression. We suggest that stimulus-related alpha activity is crucial in determining human temporal segmentation abilities.</abstract>
<autori>Benedetto, A., Lozano‐Soldevilla, D., &amp; VanRullen, R.</autori>
<pdf>https://www.pisavisionlab.org/2019/12/28/different-responses-of-spontaneous-and-stimulus-related-alpha-activity-to-ambient-luminance-changes-eur-j-neurosci/ejn-13791/</pdf><doi>https://doi.org/10.1111/ejn.13791</doi>
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