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	<title>brain information processing &#8211; Science</title>
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		<title>Localized recurrent connections control neural activity dimensionality across brain regions</title>
		<link>https://scienmag.com/localized-recurrent-connections-control-neural-activity-dimensionality-across-brain-regions/</link>
		
		<dc:creator><![CDATA[Cassandra Pierce]]></dc:creator>
		<pubDate>Wed, 19 Aug 2026 12:16:30 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[brain information processing]]></category>
		<category><![CDATA[brain region connectivity]]></category>
		<category><![CDATA[cortical and subcortical neural interactions]]></category>
		<category><![CDATA[dimensionality reduction in neuroscience]]></category>
		<category><![CDATA[feedback mechanisms in neural circuits]]></category>
		<category><![CDATA[high-dimensional brain activity]]></category>
		<category><![CDATA[localized feedback connections in neural networks]]></category>
		<category><![CDATA[neural activity dimensionality]]></category>
		<category><![CDATA[neural activity structure]]></category>
		<category><![CDATA[neural network stability]]></category>
		<category><![CDATA[neural population dynamics]]></category>
		<category><![CDATA[stable neural pattern formation]]></category>
		<guid isPermaLink="false">https://scienmag.com/localized-recurrent-connections-control-neural-activity-dimensionality-across-brain-regions/</guid>

					<description><![CDATA[A new study suggests that the brain’s neural activity may be governed by a surprisingly simple principle: strong, highly localized feedback connections can sharply limit the number of dimensions available to neural populations, even when those populations contain thousands or millions of neurons. The finding, reported by David Dahmen, Stefano Recanatesi, X. Jia and colleagues [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>A new study suggests that the brain’s neural activity may be governed by a surprisingly simple principle: strong, highly localized feedback connections can sharply limit the number of dimensions available to neural populations, even when those populations contain thousands or millions of neurons. The finding, reported by David Dahmen, Stefano Recanatesi, X. Jia and colleagues in <em>Nature Neuroscience</em>, offers a fresh explanation for why brain activity often occupies a compact, structured space rather than wandering freely through every possible combination of neuronal states. The work could help explain how different brain areas remain flexible enough to process complex information while still maintaining stable, recognizable patterns of activity.</p>
<p>At first glance, the brain appears to be an almost impossibly high-dimensional system. Every neuron can change its firing rate independently, at least in principle, creating a vast mathematical space in which the collective activity of a neural population could evolve. If a network contains thousands of neurons, the number of possible activity patterns becomes astronomically large. Yet experiments repeatedly show that real neural activity is far more constrained. When researchers record many neurons simultaneously, they often find that the activity can be described using a relatively small number of coordinated patterns, known as neural dimensions. These dimensions do not represent individual neurons; instead, they capture collective modes in which groups of cells rise, fall or interact together.</p>
<p>The new research focuses on recurrence, the process by which neural signals feed back into the same network or return to a nearby circuit after passing through other neurons. Recurrence is a defining feature of biological brains. Unlike a simple one-way chain of information processing, the brain is filled with loops. A signal can influence a local population, alter its future state, and then be fed back into the circuit milliseconds later. Such feedback can amplify activity, stabilize it, or push the network into a new configuration. The study argues that the strength and spatial organization of these recurrent connections are crucial in determining how many independent patterns of activity a brain area can support.</p>
<p>The central result is that strong recurrence does not necessarily make a network more complex in the sense of increasing its effective dimensionality. Instead, when recurrent interactions are concentrated among nearby or functionally related neurons, they can compress the network’s activity into a smaller set of dominant modes. In mathematical terms, the network’s activity becomes confined to a lower-dimensional manifold within the full space defined by all individual neurons. A manifold can be imagined as a curved surface embedded in a much larger space: although countless coordinates are available, the system’s actual states remain close to a restricted structure. This compression may be one of the ways the brain turns enormous biological complexity into manageable computation.</p>
<p>The researchers distinguish between the number of neurons in a region and the number of dimensions that are actually used by its activity. These quantities are not equivalent. A population may contain a large number of cells but behave collectively as if it were controlled by only a few variables. For example, many neurons may vary their activity in highly correlated ways, meaning that their signals carry overlapping rather than independent information. Strong local recurrence can generate precisely this type of coordination. Instead of allowing every neuron to fluctuate separately, feedback links can synchronize or organize subsets of cells, reducing the effective degrees of freedom while preserving meaningful dynamics.</p>
<p>This mechanism may also explain why dimensionality differs across brain areas. Regions involved in fast sensory encoding may require a broad repertoire of activity patterns to represent rapidly changing features of the outside world. Other areas, including circuits involved in memory, decision-making or motor planning, may benefit from more constrained dynamics that can stabilize internal states and guide behavior over time. According to the study’s framework, these differences do not require every region to follow a completely separate design. They can emerge from variations in the strength, range and localization of recurrent connectivity. A small change in how strongly nearby neurons influence one another could alter the geometry of the entire population’s activity.</p>
<p>The result has implications for how scientists interpret neural recordings. A common approach is to calculate the dimensionality of a population by examining the covariance or correlation structure of its activity. If many neurons fluctuate together, the data can be summarized by a small number of principal components. But correlations alone do not reveal why those patterns exist. The new work connects the observed dimensionality to the underlying architecture of the network, showing how local feedback can shape the spectrum of collective activity. In such a network, a few modes may become especially dominant, while other potential patterns are suppressed because recurrent interactions pull the system back toward preferred configurations.</p>
<p>The findings may help bridge two seemingly conflicting views of the brain. One view emphasizes the immense richness and flexibility of neural computation; the other highlights the strong regularities and constraints visible in large-scale recordings. Local recurrent circuits could provide both. Their feedback may reduce unnecessary variation, making neural states more robust against noise, while still allowing the network to switch between multiple stable or metastable patterns. In this picture, low dimensionality is not a sign that the brain is performing a simple computation. Rather, it may indicate that the computation has been organized efficiently, with a limited set of coordinated variables carrying the information most relevant to the task.</p>
<p>The study also raises questions about how neural dimensionality changes with learning, development and disease. Learning may modify recurrent weights, strengthening some local loops and weakening others, thereby reshaping the activity manifold without requiring large-scale anatomical rewiring. Development could progressively tune these circuits so that different brain areas acquire distinct computational roles. Conversely, disorders that disrupt excitation, inhibition or the spatial structure of connectivity might cause neural activity to become either excessively constrained or abnormally diffuse. Conditions associated with altered network stability, including epilepsy, schizophrenia or neurodegenerative disease, could therefore involve changes not only in how strongly neurons fire but also in the dimensionality of the collective dynamics.</p>
<p>For artificial intelligence, the work offers an appealing design principle. Artificial neural networks often become difficult to control when feedback is added, because recurrent loops can produce unstable or chaotic activity. The brain’s strategy suggests that carefully localized recurrence may provide a way to obtain stable, low-dimensional dynamics without sacrificing the ability to represent complex sequences. Engineers could use this principle to build more efficient recurrent systems in which strong local interactions create reliable computational states, while longer-range connections preserve flexibility and communication between modules. The broader message is that intelligence may not require every unit in a network to remain independently expressive; it may depend on organizing many units into a small number of powerful, coordinated dynamical modes.</p>
<p>The authors’ conclusion places recurrence at the center of a major question in neuroscience: how does anatomy become computation? The answer emerging from this work is that the spatial arrangement of feedback may be just as important as the number of neurons or the strength of their individual responses. When recurrence is strong and localized, it can act like an invisible sculptor, shaping the high-dimensional activity of a neural population into a smaller and more functional form. Brain areas may therefore differ in their computational capacities not simply because they contain different cell types, but because their recurrent architecture channels activity through different geometric spaces. By linking microscopic connectivity with macroscopic neural dynamics, the study provides a potential framework for understanding how the brain remains both extraordinarily complex and remarkably organized.</p>
<p><strong>Subject of Research</strong>: The influence of strong, localized recurrent connectivity on the dimensionality and organization of neural activity across brain areas.</p>
<p><strong>Article Title</strong>: Strong and localized recurrence controls the dimensionality of neural activity across brain areas.</p>
<p><strong>Article References</strong>: Dahmen, D., Recanatesi, S., Jia, X. <i>et al.</i> Strong and localized recurrence controls the dimensionality of neural activity across brain areas. <i>Nature Neuroscience</i> (2026). <a href="https://doi.org/10.1038/s41593-026-02395-w">https://doi.org/10.1038/s41593-026-02395-w</a></p>
<p><strong>Image Credits</strong>: AI Generated</p>
<p><strong>DOI</strong>: <a href="https://doi.org/10.1038/s41593-026-02395-w">https://doi.org/10.1038/s41593-026-02395-w</a></p>
<p><strong>Keywords</strong>: neural activity, recurrent networks, brain connectivity, neural dimensionality, population dynamics, low-dimensional manifolds, computational neuroscience, brain areas, localized recurrence, neural computation</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">180225</post-id>	</item>
		<item>
		<title>BU Researcher Receives Prestigious CAREER Award</title>
		<link>https://scienmag.com/bu-researcher-receives-prestigious-career-award/</link>
		
		<dc:creator><![CDATA[Cassandra Pierce]]></dc:creator>
		<pubDate>Sat, 01 Aug 2026 08:22:22 +0000</pubDate>
				<category><![CDATA[Science Education]]></category>
		<category><![CDATA[Boston University neuroscience faculty]]></category>
		<category><![CDATA[brain information processing]]></category>
		<category><![CDATA[early-career neuroscience researcher]]></category>
		<category><![CDATA[foundational neuroscience research]]></category>
		<category><![CDATA[interdisciplinary neuroscience education]]></category>
		<category><![CDATA[neural basis of purposeful behavior]]></category>
		<category><![CDATA[neural circuit research]]></category>
		<category><![CDATA[neurobiology research funding]]></category>
		<category><![CDATA[NSF CAREER Award]]></category>
		<category><![CDATA[role of neural circuits in decision-making]]></category>
		<category><![CDATA[sensory integration in the brain]]></category>
		<category><![CDATA[transforming sensory information]]></category>
		<guid isPermaLink="false">https://scienmag.com/bu-researcher-receives-prestigious-career-award/</guid>

					<description><![CDATA[(Boston)—Chandramouli “Chand” Chandrasekaran, PhD, an assistant professor whose appointments span anatomy and neurobiology at Boston University Chobanian &#38; Avedisian School of Medicine and psychological and brain sciences at the University’s College of Arts and Sciences, has received a Faculty Early Career Development Program, or CAREER, award from the National Science Foundation. The award provides at [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>(Boston)—Chandramouli “Chand” Chandrasekaran, PhD, an assistant professor whose appointments span anatomy and neurobiology at Boston University Chobanian &amp; Avedisian School of Medicine and psychological and brain sciences at the University’s College of Arts and Sciences, has received a Faculty Early Career Development Program, or CAREER, award from the National Science Foundation. The award provides at least $400,000 over five years, supporting a research and education program focused on one of the brain’s most fundamental challenges: transforming sensory information and situational context into timely, purposeful behavior.</p>
<p>The NSF CAREER award is regarded as the agency’s most prestigious honor for early-career faculty. It is designed for researchers who demonstrate exceptional potential in both research and education and who can serve as academic role models within their institutions and communities. Awardees are selected across a wide range of scientific disciplines, with emphasis placed on the originality of their research, the significance of the questions they address, and their ability to connect discovery with teaching and public engagement. For Chandrasekaran, the award will provide a platform to investigate how neural circuits evaluate incoming information before selecting and executing an action.</p>
<p>At the center of his research is a problem that appears simple in daily life but is extraordinarily complex in the brain. Consider a driver approaching an intersection: visual signals indicate the color of a traffic light, sounds may provide information about nearby vehicles or pedestrians, and memory and expectations establish the broader context. The brain must combine these sources, determine what matters, estimate when an action should occur, and generate an appropriate movement. Chandrasekaran’s work examines how this process unfolds, including how the nervous system decides whether to turn left or right, accelerate, stop, or wait when conditions change.</p>
<p>The research program combines electrophysiology, behavioral analysis, optogenetics, and computational modeling. Electrophysiological techniques allow researchers to record the electrical activity of neurons as animals perceive sensory cues, interpret context, and make decisions. Behavioral experiments reveal how those neural signals relate to choices, reaction times, learning, and movement. Optogenetics provides a way to test causality by using light-sensitive proteins to activate or inhibit precisely defined populations of neurons. Computational methods then help translate complex patterns of activity into models of how the brain represents evidence, weighs competing possibilities, and transforms decisions into coordinated motor commands.</p>
<p>This approach is particularly important because sensory processing and decision-making are not separate stages that operate independently. The significance of a visual or auditory signal depends on the circumstances in which it appears. A sound that signals danger in one environment may be irrelevant in another, while the same visual cue can prompt different behaviors depending on an individual’s goals or prior experience. Chandrasekaran’s research seeks to clarify how neural systems integrate sensory evidence with context, allowing the brain to distinguish between information that requires immediate action and information that can be ignored.</p>
<p>His interest in this question developed through an international and interdisciplinary scientific training path. Chandrasekaran earned a master’s degree in neural and behavioral sciences through the International Max Planck Research School at the University of Tübingen in Germany. He later completed his PhD at Princeton University under the mentorship of Asif Ghazanfar, PhD. During his doctoral work, he investigated multisensory integration, the process by which the brain combines information arriving through different senses, such as sight and hearing, to form a more reliable interpretation of the world.</p>
<p>Multisensory integration is a central feature of perception and behavior. Visual and auditory signals often reach the brain at different speeds and may vary in reliability, yet the nervous system must merge them into a coherent estimate of what is happening. Chandrasekaran’s earlier work examined the neural mechanisms that support this integration, providing a foundation for his current focus on how combined sensory information guides decisions and action. The questions are relevant not only to basic neuroscience but also to conditions in which perception, attention, decision-making, or movement is disrupted.</p>
<p>Following his doctoral training, Chandrasekaran became a postdoctoral fellow with the late Krishna Shenoy, PhD, at Stanford University. There, he developed computational and experimental approaches to studying how the brain makes decisions and controls everyday movements. His work at Boston University builds on that foundation by examining the dynamic relationship between sensory signals, internal context, neural computation, and behavior. Through the NSF-supported program, he will pursue a more detailed account of how the brain selects the right action at the right moment—a process that underlies everything from navigating an intersection to responding to unexpected events. The award also reflects the broader goal of training students to connect rigorous experimentation with quantitative models of brain function.</p>
<p><strong>Subject of Research</strong>: How the brain integrates sensory input and contextual information to make decisions and generate appropriately timed actions.</p>
<p><strong>Article Title</strong>: Boston University Neuroscientist Receives NSF CAREER Award to Study How the Brain Converts Sensory Information Into Action</p>
<p><strong>References</strong>: National Science Foundation CAREER award program; Boston University Chobanian &amp; Avedisian School of Medicine announcement.</p>
<p><strong>Keywords</strong>: neuroscience, brain research, sensory integration, multisensory integration, decision-making, motor control, electrophysiology, optogenetics, computational neuroscience, National Science Foundation CAREER Award</p>
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