800,215 research outputs found
Neural Models of Motion Integration, Segmentation, and Probablistic Decision-Making
When brain mechanism carry out motion integration and segmentation processes that compute unambiguous global motion percepts from ambiguous local motion signals? Consider, for example, a deer running at variable speeds behind forest cover. The forest cover is an occluder that creates apertures through which fragments of the deer's motion signals are intermittently experienced. The brain coherently groups these fragments into a trackable percept of the deer in its trajectory. Form and motion processes are needed to accomplish this using feedforward and feedback interactions both within and across cortical processing streams. All the cortical areas V1, V2, MT, and MST are involved in these interactions. Figure-ground processes in the form stream through V2, such as the seperation of occluding boundaries of the forest cover from the boundaries of the deer, select the motion signals which determine global object motion percepts in the motion stream through MT. Sparse, but unambiguous, feauture tracking signals are amplified before they propogate across position and are intergrated with far more numerous ambiguous motion signals. Figure-ground and integration processes together determine the global percept. A neural model predicts the processing stages that embody these form and motion interactions. Model concepts and data are summarized about motion grouping across apertures in response to a wide variety of displays, and probabilistic decision making in parietal cortex in response to random dot displays.National Science Foundation (SBE-0354378); Office of Naval Research (N00014-01-1-0624
Laminar Cortical Dynamics of Visual Form and Motion Interactions During Coherent Object Motion Perception
How do visual form and motion processes cooperate to compute object motion when each process separately is insufficient? A 3D FORMOTION model specifies how 3D boundary representations, which separate figures from backgrounds within cortical area V2, capture motion signals at the appropriate depths in MT; how motion signals in MT disambiguate boundaries in V2 via MT-to-Vl-to-V2 feedback; how sparse feature tracking signals are amplified; and how a spatially anisotropic motion grouping process propagates across perceptual space via MT-MST feedback to integrate feature-tracking and ambiguous motion signals to determine a global object motion percept. Simulated data include: the degree of motion coherence of rotating shapes observed through apertures, the coherent vs. element motion percepts separated in depth during the chopsticks illusion, and the rigid vs. non-rigid appearance of rotating ellipses.Air Force Office of Scientific Research (F49620-01-1-0397); National Geospatial-Intelligence Agency (NMA201-01-1-2016); National Science Foundation (BCS-02-35398, SBE-0354378); Office of Naval Research (N00014-95-1-0409, N00014-01-1-0624
Reciprocal Interactions Between Motion and Form Perception
The processes underlying the perceptual analysis of visual form are believed to have minimal interaction with those subserving the perception of visual motion (Livingstone and Hubel, 1987; Victor and Conte, 1990). Recent reports of functionally and anatomically segregated parallel streams in the primate visual cortex seem to support this hypothesis (Ungerlieder and Mishkin, 1982; VanEssen and Maunsell, 1983; Shipp and Zeki, 1985; Zeki and Shipp, 1988; De Yoe et al., 1994). Here we present perceptual evidence that is at odds with this view and instead suggests strong symmetric interactions between the form and motion processes. In one direction, we show that the introduction of specific static figural elements, say 'F', in a simple motion sequence biases an observer to perceive a particular motion field, say 'M'. In the reverse direction, the imposition of the same motion field 'M' on the original sequence leads the observer to perceive illusory static figural elements 'F'. A specific implication of these findings concerns the possible existence of (what we call) motion end-stopped units in the primate visual system. Such units might constitute part of a mechanism for signalling subjective occluding contours based on motion-field discontinuities
Emergence of macroscopic directed motion in populations of motile colloids
From the formation of animal flocks to the emergence of coordinate motion in
bacterial swarms, at all scales populations of motile organisms display
coherent collective motion. This consistent behavior strongly contrasts with
the difference in communication abilities between the individuals. Guided by
this universal feature, physicists have proposed that solely alignment rules at
the individual level could account for the emergence of unidirectional motion
at the group level. This hypothesis has been supported by agent-based
simulations. However, more complex collective behaviors have been
systematically found in experiments including the formation of vortices,
fluctuating swarms, clustering and swirling. All these model systems
predominantly rely on actual collisions to display collective motion. As a
result, the potential local alignment rules are entangled with more complex,
often unknown, interactions. The large-scale behavior of the populations
therefore depends on these uncontrolled microscopic couplings. Here, we
demonstrate a new phase of active matter. We reveal that dilute populations of
millions of colloidal rollers self-organize to achieve coherent motion along a
unique direction, with very few density and velocity fluctuations. Identifying
the microscopic interactions between the rollers allows a theoretical
description of this polar-liquid state. Comparison of the theory with
experiment suggests that hydrodynamic interactions promote the emergence of
collective motion either in the form of a single macroscopic flock at low
densities, or in that of a homogenous polar phase at higher densities.
Furthermore, hydrodynamics protects the polar-liquid state from the giant
density fluctuations. Our experiments demonstrate that genuine physical
interactions at the individual level are sufficient to set homogeneous active
populations into stable directed motion
Interactions between motion and form processing in the human visual system
The predominant view of motion and form processing in the human visual system assumes that these two attributes are handled by separate and independent modules. Motion processing involves filtering by direction-selective sensors, followed by integration to solve the aperture problem. Form processing involves filtering by orientation-selective and size-selective receptive fields, followed by integration to encode object shape. It has long been known that motion signals can influence form processing in the well-known Gestalt principle of common fate; texture elements which share a common motion property are grouped into a single contour or texture region. However, recent research in psychophysics and neuroscience indicates that the influence of form signals on motion processing is more extensive than previously thought. First, the salience and apparent direction of moving lines depends on how the local orientation and direction of motion combine to match the receptive field properties of motion-selective neurons. Second, orientation signals generated by “motion-streaks” influence motion processing; motion sensitivity, apparent direction and adaptation are affected by simultaneously present orientation signals. Third, form signals generated by human body shape influence biological motion processing, as revealed by studies using point-light motion stimuli. Thus, form-motion integration seems to occur at several different levels of cortical processing, from V1 to STS
Long-Range Acoustic Interactions in Insect Swarms: An Adaptive Gravity Model
The collective motion of groups of animals emerges from the net effect of the interactions between individual members of the group. In many cases, such as birds, fish, or ungulates, these interactions are mediated by sensory stimuli that predominantly arise from nearby neighbors. But not all stimuli in animal groups are short range. Here, we consider mating swarms of midges, which are thought to interact primarily via long-range acoustic stimuli. We exploit the similarity in form between the decay of acoustic and gravitational sources to build a model for swarm behavior. By accounting for the adaptive nature of the midges\u27 acoustic sensing, we show that our \u27adaptive gravity\u27 model makes mean-field predictions that agree well with experimental observations of laboratory swarms. Our results highlight the role of sensory mechanisms and interaction range in collective animal behavior. Additionally, the adaptive interactions that we present here open a new class of equations of motion, which may appear in other biological contexts
Fluctuation-induced collective motion: A single-particle density analysis
In a system of noisy self-propelled particles with interactions that favor
directional alignment, collective motion will appear if the density of
particles increases beyond a certain threshold. In this paper, we argue that
such a threshold may depend also on the profiles of the perturbation in the
particle directions. Specifically, we perform mean-field, linear stability,
perturbative and numerical analyses on an approximated form of the
Fokker-Planck equation describing the system. We find that if an angular
perturbation to an initially homogeneous system is large in magnitude and
highly localized in space, it will be amplified and thus serves as an
indication of the onset of collective motion. Our results also demonstrate that
high particle speed promotes collective motion.Comment: To appear in Physical Review E
Formation and Propagation of Matter Wave Soliton Trains
Attraction between atoms in a Bose-Einstein-Condensate renders the condensate
unstable to collapse. Confinement in an atom trap, however, can stabilize the
condensate for a limited number of atoms, as was observed with 7Li, but beyond
this number, the condensate collapses. Attractive condensates constrained to
one-dimensional motion are predicted to form stable solitons for which the
attractive interactions exactly compensate for the wave packet dispersion. Here
we report the formation or bright solitons of 7Li atoms created in a quasi-1D
optical trap. The solitons are created from a stable Bose-Einstein condensate
by magnetically tuning the interactions from repulsive to attractive. We
observe a soliton train, containing many solitons. The solitons are set in
motion by offsetting the optical potential and are observed to propagate in the
potential for many oscillatory cycles without spreading. Repulsive interactions
between neighboring solitons are inferred from their motion
The Rotating Vicsek Model: Pattern Formation and Enhanced Flocking in Chiral Active Matter
We generalize the Vicsek model to describe the collective behaviour of polar
circle swimmers with local alignment interactions. While the phase transition
leading to collective motion in 2D (flocking) occurs at the same interaction to
noise ratio as for linear swimmers, as we show, circular motion enhances the
polarization in the ordered phase (enhanced flocking) and induces secondary
instabilities leading to structure formation. Slow rotations result in phase
separation whereas fast rotations generate patterns which consist of phase
synchronized microflocks of controllable self-limited size. Our results defy
the viewpoint that monofrequent rotations form a rather trivial extension of
the Vicsek model and establish a generic route to pattern formation in chiral
active matter with possible applications to control coarsening and to design
rotating microflocks.Comment: Contains a Supplementary Materia
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