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	<title>cortical plasticity &#8211; Science</title>
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	<title>cortical plasticity &#8211; Science</title>
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		<title>A Hidden Vision Workout May Speed Up How Fast Adults Read</title>
		<link>https://scienmag.com/a-hidden-vision-workout-may-speed-up-how-fast-adults-read/</link>
		
		<dc:creator><![CDATA[Glenn Wilkins]]></dc:creator>
		<pubDate>Wed, 23 Sep 2026 21:38:11 +0000</pubDate>
				<category><![CDATA[Psychology & Psychiatry]]></category>
		<category><![CDATA[adult reading speed improvement]]></category>
		<category><![CDATA[attention and perception in literacy]]></category>
		<category><![CDATA[contour integration]]></category>
		<category><![CDATA[cortical mechanisms of rapid visual processing]]></category>
		<category><![CDATA[cortical plasticity]]></category>
		<category><![CDATA[dyslexia]]></category>
		<category><![CDATA[eye movement and oculomotor control]]></category>
		<category><![CDATA[Gabor patches]]></category>
		<category><![CDATA[home-based visual search exercises]]></category>
		<category><![CDATA[lexical decision]]></category>
		<category><![CDATA[magnocellular-dorsal hypothesis]]></category>
		<category><![CDATA[magnocellular-dorsal system]]></category>
		<category><![CDATA[neural pathways involved in reading]]></category>
		<category><![CDATA[oculomotor control]]></category>
		<category><![CDATA[perceptual and attentional processes in reading]]></category>
		<category><![CDATA[perceptual learning]]></category>
		<category><![CDATA[psychophysics]]></category>
		<category><![CDATA[reading efficiency enhancement]]></category>
		<category><![CDATA[reading speed]]></category>
		<category><![CDATA[speed reading interventions]]></category>
		<category><![CDATA[visual attention]]></category>
		<category><![CDATA[visual processing in reading]]></category>
		<category><![CDATA[visual search]]></category>
		<category><![CDATA[visual search training]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=210485</guid>

					<description><![CDATA[A nine-day home-based visual search training program using Gabor patches sped up some timed reading tasks in typical adult readers, with the most perceptually demanding task versions producing the clearest effects.]]></description>
										<content:encoded><![CDATA[<p>Reading feels effortless for most adults, yet beneath the smooth glide of the eyes across a page lies a demanding cascade of perceptual, attentional, and oculomotor operations. A new study published in the journal Attention, Perception, &amp; Psychophysics asks a deceptively simple question: if those underlying visual skills can be sharpened through practice, might reading itself get faster, even in people who already read normally? Researchers led by Francesco Carabba and Luca Battaglini of the University of Padova designed a home-based training program built entirely around visual search, the everyday act of scanning a cluttered scene to find a target, and deliberately stripped away every phonological, orthographic, and reading-related element. The idea was to test whether exercising the visual machinery alone could leave a measurable fingerprint on timed reading tasks in adult typical readers.</p>
<p>The theoretical motivation comes from the magnocellular-dorsal hypothesis of reading. This framework proposes that a neural pathway specialized for rapid temporal processing and spatial attention, the occipito-parietal &#8220;where&#8221; pathway, plays a crucial role in distributing attentional resources across text. Spatial attention supported by this system is thought to be fundamental for processing letters at different positions, converting orthographic codes into phonological ones, and accessing meaning quickly from visual input. Previous work has linked difficulties in visuo-spatial attention to reading difficulties, and studies of dyslexia have reported less stable binocular fixation and weaker control over eye muscles during reading. The magnocellular theory has faced criticism, and many researchers argue that dyslexia cannot be reduced to a single cause, but substantial evidence supports a genuine involvement of perceptual and visuo-spatial skills in reading.</p>
<p>The Padova team reasoned that if reading depends partly on these visual capacities, then visual perceptual learning, the well-documented phenomenon in which repeated practice on a perceptual task produces long-lasting improvement, might transfer to reading. Visual perceptual learning is a manifestation of cortical plasticity and has already yielded positive outcomes in clinical populations including hemianopia, amblyopia, and macular degeneration, as well as in dyslexic readers. Earlier training studies have exercised the magnocellular stream through coherent motion detection, direction discrimination with sine-wave gratings, and combined oculomotor and search batteries. One particularly relevant study reported that a single ten-minute session combining eye-movement exercises with visual search was followed by faster reading in French children with dyslexia, but that design could not isolate the contribution of the search component. The new study set out to do exactly that, using a single task family with no oculomotor exercises at all.</p>
<p>Eighty-five adult native Italian speakers took part, all classified as typical readers on the basis of self-reported history, with normal or corrected vision. Forty-two were randomly assigned to one of three training versions, fourteen per group, while forty-three served as a no-training control group who completed only the pretest and posttest. The larger control group was a deliberate methodological choice: it sharpened the estimate of the no-training trajectory, including practice effects and measurement noise, and increased statistical power for the central comparisons between each training group and the controls. Reading was assessed with a word-reading test and a nonword-reading test from the DDE-2 battery, plus a lexical decision test requiring participants to silently scan lists of sixty words and sixty nonwords and mark the nonwords. Speed and accuracy were recorded as separate dependent variables, with no error penalty applied to time scores.</p>
<p>The training itself revolved around Gabor patches, stimuli produced by combining a sine-wave luminance grating with a circular Gaussian envelope, presented at roughly five cycles per degree and 95 percent contrast. For nine consecutive days, participants completed seven daily blocks of 144 search displays, each containing more than a hundred Gabor stimuli and remaining on screen until a response was given or ten seconds elapsed. The three versions differed in how the target was defined. In the orientation version, the target was a single Gabor tilted orthogonally to all distractors, an easy target that pops out of the display. In the phase version, the target matched the distractors in orientation but had an inverted phase, a reversal of its black and white luminance pattern, making it highly camouflaged and forcing detailed scrutiny of individual stimuli. In the configuration version, the target was not a single patch but a circular arrangement of multiple Gabors, requiring contour integration and perceptual grouping, a choice inspired by earlier findings that reading acquisition itself enhances early contour integration and that illiterate adults struggle to group circularly arranged patches into a single percept.</p>
<p>The training data confirmed that the three tasks sat at genuinely different difficulty levels. Sensitivity, indexed by the signal-detection measure d-prime, improved significantly across the nine days, and response times fell, classic signatures of perceptual learning. The orientation task produced the highest d-prime values and the fastest responses, the phase task the lowest sensitivity, the slowest responses, and the most timeouts, with the configuration task falling in between. All pairwise group differences were significant after correction, and the phase group showed the steepest improvement slope in response times. Because the task included both target-present and target-absent trials, the researchers also tracked response criterion to distinguish genuine gains in discriminability from simple shifts in the willingness to report a target. Together, these measures established that any downstream differences between groups could be interpreted against a clearly characterized gradient of perceptual demand.</p>
<p>The critical test compared posttest reading performance across groups while statistically controlling for each participant&#8217;s pretest baseline. The results were strikingly outcome-specific. The phase group, which had endured the most perceptually demanding task, showed significantly lower adjusted posttest reading times than the no-training group on the word-reading test, corresponding to roughly four seconds faster, and on the lexical decision test, roughly nine seconds faster. The configuration group showed significantly lower adjusted posttest times on the nonword-reading test, about three and a half seconds faster, a task that relies heavily on grapheme-to-phoneme conversion. The easy orientation task produced no reliable advantage on any timed measure. Notably, no consistent training-related benefit emerged for accuracy on any test, a pattern the authors interpret cautiously given that the accuracy component of the DDE-2 has weaker test-retest reliability and that skilled adult readers commit so few errors that variability is severely restricted.</p>
<p>An exploratory correlation analysis added an intriguing wrinkle. If transfer to reading were driven simply by how much an individual improved at visual search, then gains in d-prime from day one to day nine should predict gains in reading speed. They did not. Correlations between individual search improvement and reading-speed change were near zero for word reading, nonword reading, and lexical decision alike. This does not undermine the group-level effects, but it signals that the mechanism of transfer is not a straightforward linear relationship between perceptual sensitivity and reading speed. The authors suggest that other factors, such as search strategy, response criterion, general visual-attentional engagement, or sheer time on task, may have contributed, and that the present design cannot adjudicate among them.</p>
<p>Indeed, the authors are careful to frame the study as exploratory and to enumerate its limits. The three search tasks differed not only in difficulty but also in target definition and the search strategy they likely encouraged. Under a contemporary framework distinguishing priority guidance, in which a salient target is selected from a priority map, from clump scanning, in which observers systematically inspect contiguous groups of items, the orientation task probably rewarded simple priority guidance while the phase task demanded systematic scrutiny and the configuration task engaged grouping processes. Without manipulating set size, estimating search slopes, or recording eye movements, the observed reading effects cannot be uniquely attributed to difficulty, search mode, or any specific mechanism. Training dose also varied, since the phase condition consumed roughly ninety minutes daily against thirty for orientation, a consequence of slower responses and more timeouts rather than extra trials. A sensitivity analysis based on ten thousand simulations showed the study was powered only to detect relatively large effects, and for two error measures no plausible effect could achieve adequate power at all.</p>
<p>Even so, the study delivers a genuinely provocative preliminary result: a training program containing no letters, no sounds, and no reading whatsoever was associated with faster performance on some timed reading-related outcomes in adults who already read normally, with the most demanding visual tasks producing the clearest transfer. The effects are modest in absolute terms and their clinical or educational significance remains unproven, particularly because the sample consisted of typical adult readers reading in Italian, a language with highly transparent orthography whose findings may not generalize to deeper orthographies. The authors argue that establishing baseline effects in the neurotypical brain is a necessary foundation before testing dyslexic populations, whose brain structures and connectivity may differ and require protocol adaptations. The next steps they propose are clear: larger samples, preregistered analyses, designs that manipulate difficulty within a single search paradigm while controlling training dose, and extension to children and readers with dyslexia. If those replications hold, the humble Gabor patch could become an unexpected tool in the science of reading enhancement.</p>
<p><strong>Subject of Research:</strong> Visual search training and its effects on reading speed in adult typical readers</p>
<p><strong>Article Title:</strong> Probing the use of visual search as a tool to enhance reading speed</p>
<p><strong>Article References:</strong> Carabba, F., Borsati, C., Fontana, G., Altieri, E., Vicovaro, M., &amp; Battaglini, L. (2026). Probing the use of visual search as a tool to enhance reading speed. <em>Attention, Perception, &amp;amp; Psychophysics, 88</em>(7), Article 190. <a href="https://doi.org/10.3758/s13414-026-03336-2" rel="noopener noreferrer">https://doi.org/10.3758/s13414-026-03336-2</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3758/s13414-026-03336-2" rel="noopener noreferrer">10.3758/s13414-026-03336-2</a></p>
<p><strong>Keywords:</strong> visual search, reading speed, perceptual learning, magnocellular-dorsal system, Gabor patches, dyslexia, visual attention, contour integration, psychophysics, oculomotor control, lexical decision, cortical plasticity</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">210485</post-id>	</item>
		<item>
		<title>Brain Activity Geometry Sets the Limits of Human Learning</title>
		<link>https://scienmag.com/brain-activity-geometry-sets-the-limits-of-human-learning/</link>
		
		<dc:creator><![CDATA[Cassandra Pierce]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 18:25:35 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[brain activity and learning efficiency]]></category>
		<category><![CDATA[brain activity high-dimensional space]]></category>
		<category><![CDATA[brain scaffolding for skill acquisition]]></category>
		<category><![CDATA[brain-computer interfaces]]></category>
		<category><![CDATA[cortical plasticity]]></category>
		<category><![CDATA[functional brain imaging for learning]]></category>
		<category><![CDATA[functional MRI]]></category>
		<category><![CDATA[geometric models of brain function]]></category>
		<category><![CDATA[geometry]]></category>
		<category><![CDATA[high-dimensional neural coding]]></category>
		<category><![CDATA[human neuroscience]]></category>
		<category><![CDATA[intrinsic brain activity structure]]></category>
		<category><![CDATA[latent variable models]]></category>
		<category><![CDATA[motor learning]]></category>
		<category><![CDATA[motor learning and neural geometry]]></category>
		<category><![CDATA[neural]]></category>
		<category><![CDATA[Neural activity geometry in human learning]]></category>
		<category><![CDATA[neural dimensionality]]></category>
		<category><![CDATA[neural dynamics and skill mastery]]></category>
		<category><![CDATA[neural geometry]]></category>
		<category><![CDATA[neural manifold organization]]></category>
		<category><![CDATA[neural manifolds]]></category>
		<category><![CDATA[neural population activity patterns]]></category>
		<category><![CDATA[skill acquisition]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=197344</guid>

					<description><![CDATA[New human neuroimaging research shows that the intrinsic geometry of brain activity, organized into neural manifolds, determines which skills are learned quickly and which remain out of reach.]]></description>
										<content:encoded><![CDATA[<p>Why can some people pick up a new skill in an afternoon while others grind for weeks with little to show for it? A study published in Nature Neuroscience by Busch and colleagues offers a striking answer rooted not in motivation, practice schedules or raw cognitive power, but in the intrinsic shape of brain activity itself. Using functional imaging in humans, the researchers show that the geometry of neural population activity, the way patterns of brain activation are organized in a high-dimensional space, acts as a kind of invisible scaffold for learning. Skills that require the brain to move its activity patterns along directions already embedded in that scaffold are learned readily. Skills that demand excursions outside the existing structure are learned slowly, if at all. The finding, highlighted in an accompanying commentary by Aaron P. Batista of the University of Pittsburgh, reframes learning as a geometric problem, and it may finally explain a puzzle that has haunted motor learning research for more than a decade.</p>
<p>The intellectual foundation of the new work lies in the concept of neural manifolds. When neuroscientists record from many neurons at once, they find that the activity of the population does not explore all of the dimensions theoretically available to it. Instead, the patterns of co-activation are confined to a lower-dimensional subspace, a manifold whose axes reflect the correlated structure of the circuit. Pioneering experiments by Sadtler and colleagues in 2014, using brain-computer interfaces in monkeys, demonstrated that animals could readily learn to control a cursor when the mapping between neural activity and cursor movement stayed within the intrinsic manifold of their motor cortex. When the mapping was altered to require activity patterns outside that manifold, performance collapsed and learning proceeded far more slowly. Subsequent work by Oby and colleagues in 2019 and by Golub and colleagues in 2018 extended this principle, showing that the boundaries of the manifold impose real, measurable constraints on what a brain can learn to do.</p>
<p>Those experiments, however, were performed with invasive recordings in animal models. Whether the same geometric principle governs learning in the intact, behaving human brain remained an open question, and a technically daunting one. Human learning is typically studied with functional magnetic resonance imaging, which measures blood-oxygen-level-dependent signals across the cortex rather than the firing of individual neurons. Busch and colleagues tackled the challenge by extracting the latent structure of whole-brain activity from imaging data, characterizing the manifold of human brain activity at a population level and then asking how that structure changes, or fails to change, as people learn new tasks. Their central result is elegantly asymmetric: learning proceeds smoothly when the required new activity patterns remain within the existing manifold, but is sharply limited when the task demands patterns that lie beyond it.</p>
<p>The technical machinery behind this conclusion deserves attention, because it represents a methodological bridge between two levels of analysis that have long been difficult to reconcile. Dimensionality reduction techniques, such as principal component analysis and related latent variable methods, allow researchers to compress the activity of thousands of voxels into a small number of dominant activity patterns. The geometry of these patterns, their relative positions, orientations and curvatures in the reduced space, constitutes a fingerprint of the brain&#8217;s intrinsic organization. By tracking how task-related activity trajectories move through this space during training, the researchers could quantify precisely how far a learner had to push their neural activity away from its habitual configuration. Distance within the manifold predicted rapid improvement; distance beyond the manifold predicted stagnation. The geometry was not a passive byproduct of learning. It was the variable that best explained the pace of learning itself.</p>
<p>This asymmetry carries profound implications for how neuroscientists think about plasticity. The traditional view of learning emphasizes synaptic modification: connections strengthen or weaken, and behavior changes accordingly. The manifold framework does not contradict that view, but it adds a crucial layer of constraint. Synaptic plasticity may be abundant and readily available, yet if the circuit&#8217;s correlated structure funnels activity along a limited set of axes, then only certain behavioral changes are cheap to produce. Changing the manifold itself, reorganizing the fundamental correlations that define it, appears to be a far more expensive operation for the brain. In effect, the brain possesses two distinct currencies of adaptation: cheap movements within its existing neural geometry, and costly renovations of that geometry. Busch and colleagues provide the strongest human evidence yet that the exchange rate between these currencies governs what we can learn and how fast.</p>
<p>The findings also resonate with an older literature on muscle synergies and motor primitives. Work by Berger, Gentner, Edmunds, Pai and d&#8217;Avella in 2013 showed that the motor system composes movements from a small repertoire of coordinated activation patterns rather than controlling every muscle independently. If behavior is built from a finite set of building blocks, then learning new behaviors is easiest when the desired behavior can be assembled from blocks already in stock. The manifold results generalize this intuition from muscles to cortex: the brain&#8217;s activity repertoire constrains the behaviors it can readily acquire. Interestingly, the conceptual reach of neural geometry now extends beyond neuroscience altogether. Research in artificial intelligence, notably the work of Elhage and colleagues on features and representations inside neural networks, has revealed that artificial deep networks also organize their computations along low-dimensional manifolds, and that the geometry of these representations shapes what the networks can learn. Brains and machines, it seems, confront the same geometric trade-offs.</p>
<p>For the growing field of brain-computer interfaces, the implications are immediate and practical. A user learning to control a robotic limb or a communication prosthesis is, in geometric terms, being asked to steer their neural activity into configurations that map onto device commands. The new results suggest that interface designers should work with the brain&#8217;s intrinsic geometry rather than against it, aligning decoder mappings with the existing manifold to shorten training times and boost performance. Conversely, when a therapeutic goal requires the brain to adopt genuinely novel activity patterns, clinicians may need to design training protocols that gradually reshape the manifold itself, perhaps through carefully staged practice that pulls the geometry outward over time. Similar reasoning applies to neurorehabilitation after stroke, where recovery may depend on whether the damaged cortex can re-express lost skills within its surviving manifold or must construct new geometric structure from the ground up.</p>
<p>The study also sharpens a question that has lingered since the first manifold experiments: what determines the geometry in the first place? Candidates include the statistics of a lifetime of experience, the anatomical wiring of cortical circuits, developmental programs and genetic constraints. If intrinsic geometry is largely fixed by anatomy and history, then the fastest route to enhanced learning may be to choose training tasks that sit comfortably within a person&#8217;s existing manifold, a principle that could personalize education and skill training. If, on the other hand, geometry is malleable with the right kind of experience, then identifying the activities that expand manifolds becomes a central goal for learning science. Busch and colleagues&#8217; human imaging paradigm provides a tool for testing these possibilities, because it allows researchers to measure manifold structure repeatedly as individuals accumulate different kinds of experience.</p>
<p>Writing in Nature Neuroscience, Batista emphasizes the elegance of the asymmetry at the heart of the new findings: the same geometric framework that explains effortless learning also explains its limits, unifying what previously looked like separate phenomena under a single principle. The work transforms a philosophical question, why some skills come easily and others do not, into a quantitative one, measurable in the coordinates of brain activity. As imaging methods and latent variable models continue to improve, researchers may soon be able to read out an individual&#8217;s neural geometry and predict, before the first practice session, which skills that person will master quickly and which will demand a renovation of the brain&#8217;s deepest structure. Learning, on this view, is not a climb up an abstract ladder of difficulty. It is a journey through a landscape whose contours were drawn long before the journey began, and knowing the map may be the first step toward redrawing it.</p>
<p><strong>Subject of Research:</strong> How the intrinsic geometry of human brain activity constrains and guides learning</p>
<p><strong>Article Title:</strong> Neural geometry guides learning</p>
<p><strong>Article References:</strong> Batista, A. P. (2026). Neural geometry guides learning. <em>Nature Neuroscience</em>. <a href="https://doi.org/10.1038/s41593-026-02442-6" rel="noopener noreferrer">https://doi.org/10.1038/s41593-026-02442-6</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s41593-026-02442-6" rel="noopener noreferrer">10.1038/s41593-026-02442-6</a></p>
<p><strong>Keywords:</strong> neural manifolds, neural geometry, motor learning, functional MRI, brain-computer interfaces, neural dimensionality, cortical plasticity, skill acquisition, latent variable models, human neuroscience, Neural, geometry</p>
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