Multisensory Research Group
Focus: The anatomical, physiological, behavioral, and computational bases for the development and expression of multisensory integration.
Decoding and interpreting incoming sensory information are among the brain's most important tasks. These are ongoing processes that make it possible for us not only to know the world in which we live, but to plan and initiate behaviors that are appropriate for a particular circumstance. Because survival depends on the speed and accuracy of such processes, it is not surprising to find that encoding, decoding, and evaluating sensory information have been powerful driving forces in evolution. Consequently, extant organisms have an impressive array of specialized sensory systems.
Having multiple sensory systems provides significant benefits; it allows an organism to monitor simultaneously a host of environmental cues, and also provides a means of substituting one sensory system for another when necessary (e.g., hearing and/or touch can substitute for vision in the dark). The ability to monitor and process multiple sensory cues in “parallel” not only increases the likelihood that a given stimulus will be detected, but, because the information carried along each sensory channel reflects a different feature of that stimulus, it increases the chances that the stimulus will be properly identified. Stimuli that may be difficult to distinguish by means of a single sensory modality (e.g., how they look) can become quite distinct via information from another modality (how they sound or feel).
Of particular benefit is the brain’s ability to use the information carried by these different sensory channels synergistically. Thus, different sensory inputs can enhance one another’s effectiveness, increasing the likelihood that an event will be detected, properly identified, and that an appropriate response is initiated as fast as is possible.
Our research goal is to determine how information from different senses is pooled in making decisions, and how the brain develops this remarkable capacity. We use two interrelated neural models to do this: one in the midbrain superior colliculus (SC) and one in association cortex. The midbrain SC has proved to be a most effective model, but its principal features have been shown also to be operative in cortex. Its advantage is not only its host of sensory inputs (visual, auditory, somatosensory), but its many multisensory neurons, and its distinct behavioral function: faciliatating the detection, localization and orientation to external events.
Current Projects:
Contrasts In How The Brain Integrates Within-Modal and Cross-Modal Information:Despite the substantial literature describing the impact of multisensory integration in multiple brain areas, and the importance of this process for perception and behavior, a fundamental question has been largely ignored: does the fusion of information from different sensory source yield a product that is different from the fusion of information from the same sensory source? We are investigating this question at physiological and behavioral levels.
Anatomical Bases of Multisensory Integration: Physiological and behavioral studies have revealed that SC multisensory integration depends on the functional integrity of converging projections that descend from different regions of association cortex. We are currently investigating the nature of these projections and the development of this cortico-SC circuit using modern neuroanatomical tracing techniques and electron microscopy.
Computational Bases of Multisensory Integration: Recent evidence suggests that multisensory integration at the physiological level involves both linear and nonlinear computations. We are currently developing and testing a neural network model that seeks to explain a multitude of empirical findings within a single framework.
Effects of Multisensory Integration on Response Timing and Information: The magnitude of the physiological impact of integration at the single neuron level has traditionally been measured as a change (usually expressed as a % change) in the total number of stimulus-elicited impulses. We have recently found that concordant cross-modal stimuli not only produce more robust responses, but significantly speeds these responses. In addition, we have found that integration produces substantial enhancements in information transmission; conveying not only more information, but information at a faster rate.
Similarities and Differences in Integration Across Species: The traditional animal model of SC multisensory integraiton is the cat, and the anatomical circuit underlying integration has been well-described in this model. We have recently begun evaluating the generality of this anatomical circuit across mammalian species.
Experiential and Anatomical Dependencies of the Development of Integration:Our recent evidence suggests that capacity to engage in multisensory integration is not innate capabiility, but rather one that the brain develops after birth in an experience-dependent fashion. We are currently investigating the constraints guiding its appearance and maturation; in particular, the anatomical circuits involved, the essential properties of the cues that are critical to link them to one another, and whether the strategies of integration change during maturation.
Multisensory Integration in Motion Perception: Natural environments are dynamic, and salient targets are frequently in motion. Animals interact appropriately with these targets by estimating their velocity and direction of movement. We are current investigating how the brain combines information from different senses to affect and improve these decisions.
People:
Current Members
- Dr. Barry E. Stein - Professor and Chair. Interests: Multisensory integration, its circuitry and critical experiential and developmental antecedents.
- Dr. Ramanyran Ramachandran - Assistant Professor. Interests: Auditory signal processing, computational methods, motion perception.
- Dr. Benjamin Rowland - Assistant Professor. Interests: Computational bases of multisensory integration, temporal dynamics of integration.
- Dr. J. "Bill" Vaughan - Assistant Professor. Interests: Developmental antecedents of multisensory integration, physiological correlates of behavior.
- Dr. Thomas Perrault, Jr. – Assistant Professor. Cortical-subcortical interactions in multisensory integration.
- Dr. Juan Carlos Alvarado - Postdoctoral Fellow. Interests: How the brain integrates within- vs.cross-modal stimuli: physiology.
- Dr. Veronica Fuentes-Santamaria - Postdoctoral Fellow. Interests: Anatomical bases of multisensory integration, synaptic morphology.
- Dr. Guy Gingras - Postdoctoral Fellow. Interests: Behavioral assessment of within-modal and cross-modal integration.
- Dr. J. "Chad" Smith - Postdoctoral Fellow. Interests: Cross-species similarities and differences in multisensory integration.
Collaborators
Educational Resources:
Books
- Stein, B.E. & Meredith, M.A. (1993). The merging of the senses. MIT Press: Cambridge, MA.
- Calvert, G.A., Spence, C., & Stein, B.E. (2004). The handbook of multisensory processes. MIT Press: Cambridge, MA.
Recent Publications (2007): Updated 06/22/2007
Rowland BA, Stanford TR, and Stein BE (2007) A model of the neural mechanisms underlying multisensory integration in the superior colliculus. Perception (In Press).
Rowland BA, Stanford TR, and Stein BE (2007) A Bayesian model unifies multisensory spatial localization with the physiological properties of the superior colliculus. Exp. Brain Res. 180(1):153-61. [PDF]
Jiang W, Jiang H, Rowland BA, and Stein BE (2007) Multisensory orientation behavior is disrupted by neonatal cortical ablation. J. Neurophysiol. 97:557-562. [PDF]
Burnett LR, Stein BE, Perrault TJ, and Wallace MT (2007) Excitotoxic lesions of the superior colliculus preferentially impacts multisensory neurons and multisensory integration. Exp. Brain Res. 179:325-338. [PDF]
Rowland BA, Quessy S, Stanford TR, and Stein BE (2007) Multisensory integration shortens physiological response latencies. J. Neurosci. 27: 5879-5884. [PDF]
Stanford TR and Stein BE (2007) Superadditivity in multisensory integration: putting the computation in context. Neuroreport 18: 787-792. [PDF]
Alvarado JC, Vaughan JW, Stanford TR, and Stein BE (2007) Multisensory versus unisensory integration: contrasting modes in the superior colliculus. J. Neurophysiol. 97: 3193-3205. [PDF]
Wallace MT and Stein BE (2007) Early experience determines how the senses will interact. J. Neurophysiol. 97: 921-926. [PDF]
Wallace MT, Carriere BN, Perrault TJ, Jr, Vaughan JW, and Stein BE (2006) The development of cortical multisensory integration. J. Neurosci. 26:11844-11849. [PDF]
Jiang W, Jiang H, and Stein BE (2006) Neonatal cortical ablation disrupts multisensory development in the superior colliculus. J. Neurophysiol. 95:1380-1396. [PDF]
McHaffie JG, Jiang H, May PJ, Coizet V, Overton PG, Stein BE, and Redgrave P (2006) A direct projection from the superior colliculus to substantia nigra pars compacta in the cat. Neuroscience 138: 221-234. [PDF]
Fuentes-Santamaria V, Stein BE, and McHaffie JG (2006) Neurofilament proteins are preferentially expressed in descending output neurons of the cat superior colliculus: A study using SMI-32. Neuroscience 138: 55-68. [PDF]
Gabriele ML, Smoot JE, Jiang H, Stein BE, and McHaffie JG (2006) Early establishment of adult-like nigrotectal architecture in the neonatal cat: A double-labeling study using carbocyanine dyes. Neuroscience 137: 1309-1319. [PDF]
McHaffie JG, Stanford TR, Stein BE, Coizet V, and Redgrave P (2005) Subcortical loops through the basal ganglia? Trends Neurosci. 28: 401-407.
Stanford TR, Quessy S, and Stein BE (2005) Evaluating the operations underlying multisensory integration in cat superior colliculus. J. Neurosci. 25: 6499-6508.
Stein BE (2005) The development of a dialogue between cortex and midbrain to integrate multisensory information. Exp. Brain Res. 166: 305-315.
Laurienti P, Perrault TJ, Jr, Stanford TR, Wallace MT, and Stein BE (2005) On the use of superadditivity as a metric for characterizing multisensory integration in functional neuroimaging studies. Exp. Brain Res. 166: 289-297.
Perrault TJ, Jr, Vaughan JW, Stein BE, and Wallace MT (2005) Superior colliculus neurons use distinct operational modes in the integration of multisensory stimuli. J. Neurophysiol. 93: 2575-2586.
Wallace MT, Perrault TJ, Jr, Hairston WD, and Stein BE (2004) Visual experience is necessary for the development of multisensory integration. J. Neurosci. 24: 9580-9584.
Wallace MT, Roberson G, Hairston WD, Stein BE, and Schirillo JA (2004) Unifying multisensory signals across time and space. Exp. Brain Res. 158: 252-258.
Wallace MT, Ramachandran R, and Stein BE (2004) A revised view of sensory cortical parcellation. Proc. Natl. Acad. Sci. (PNAS) 101: 2167-2172.
Burnett LR, Stein BE, Chaponis D, and Wallace MT (2004) Superior colliculus (SC) lesions preferentially disrupt multisensory orientation. Neuroscience 124: 535-547.
Perrault TJ, Jr, Vaughan JW, Stein BE, and Wallace MT (2003) Neuron-specific response characteristics predict the magnitude of multisensory integration. J. Neurophysiol. 90: 4022-4026.
Jiang W and Stein BE (2003) Cortex controls multisensory depression in superior colliculus. J. Neurophysiol. 90: 2123-2135.
Lovelace CT, Stein BE, and Wallace MT (2003) An irrelevant light enhances auditory detection in humans: A psychophysical analysis of multisensory integration in stimulus detection. Cognitive Brain Research 17: 447-453.
Jiang H, Stein BE, and McHaffie JG (2003) Opposing basal ganglia processes shape midbrain visuomotor activity bilaterally. Nature 423: 982-986.
Laurienti PJ, Wallace MT, Maldjian JA, Susi CM, Stein BE, and Burdette JH (2003) Cross-modal sensory processing in the anterior cingulate and medial prefrontal cortices. Human Brain Mapping 19: 213-223.
Hairston D, Wallace MT, Vaughan JW, Stein BE, Norris JL, and Schirillo JA (2003) Visual localization ability influences cross-modal bias. J. Cognitive Neurosci. 15: 20-29.
Jiang W, Jiang H, and Stein BE (2002) Two corticotectal areas mediate multisensory orientation behavior. J. Cognitive Neurosci., 4: 1240-1255.
Stein BE, Wallace MT, Stanford TR, and Jiang W (2002) Cortex governs multisensory integration in the midbrain. The Neuroscientist 8: 306-314.
Laurienti PJ, Burdette JH, Wallace MT, Yen Y-F, Field AS, and Stein BE (2002) Deactivation of sensory-specific cortex by cross-modal stimuli. J. Cognitive Neurosci., 14: 420-429.
McHaffie JG, Wang S, Walton N, Stein BE, and Redgrave P. (2002) Covariant maturation of nocifensive oral behaviour and c-fos expression in rat superior colliculus. Neuroscience, 109: 597-607.
Full List of Publications
Links
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