Interaction between primary and secondary mechanisms in human motion perception
References (58)
A short-range process in apparent motion
Vision Research
(1974)- et al.
Interattribute apparent motion
Vision Research
(1989) - et al.
Illusory motion in visual displays
Vision Research
(1984) Biological image motion processing: A review
Vision Research
(1985)- et al.
Assimilation and contrast in motion perception: Explorations in cooperativity
Vision Research
(1990) Visual processing of four kinds of relative motion
Vision Research
(1986)Orientation discrimination for objects defined by relative motion and objects defined by luminance contrast
Vision Research
(1989)- et al.
Dissociation of orientation discrimination from form detection for motion-defined bars and luminance-defined bars: Effects of dot lifetime and presentation duration
Vision Research
(1992) - et al.
Extension of displacement limits in multiple-exposure sequences of apparent motion
Vision Research
(1989) - et al.
Temporal and spatial integration in dynamic random-dot stimuli
Vision Research
(1992)
Theta motion: A paradoxical stimulus to explore higher order motion extraction
Vision Research
Human vision favours centrifugal motion
Perception
Detecting visual motion: Theory and models
Motion may be seen but not used
Current Biology
Differentiation and integration in motion perception
Perception
Motion: The long and short of it
Spatial Vision
Cooperative phenomena in apparent movement perception of random-dot cinematograms
Vision Research
Drift-balanced random stimuli: A general basis for studying non-Fourier motion perception
Journal of the Optical Society of America A
Second-order motion perception: Space-time separable mechanisms
Two motion perception mechanisms revealed through distance-driven reversal of apparent motion
Spatiotemporal integration in the detection of coherent motion
Vision Research
Visual areas of the mammalian cerebral cortex
Motion perception in the peripheral visual field
Graefes Archiv
Single visual neurons code opposing motion independent of direction
Science
The ecological approach to visual perception
Inhomogeneities and anisotropies of the visual fields for motion detection
Investigative Ophthalmology and Visual Science
Incremental rigidity scheme for recovering structure from motion: Position-based versus velocity-based formulations
Journal of the Optical Society of America A
Motion defined exclusively by second-order characteristics does not evoke optokinetic nystagmus
Visual Neuroscience
The “motion-blind” patient: Low-level spatial and temporal filters
Journal of Neuroscience
Cited by (16)
A visual field dependent architecture for second order motion processing
2011, Neuroscience LettersDistinct visual motion processing impairments in aging and Alzheimer's disease
2011, Vision ResearchCitation Excerpt :In young people, the visual motion processing of naturalistically large stimuli is supported by spatial and temporal cue integration that influence direction (Fredericksen, Verstraten, & van, 1994; Graham & Robson, 1987) and speed discrimination (Andersen & Saidpour, 2002). Declines in motion coherence, created by the addition of random motion, impairs the processing of such stimuli (Zanker & Hupgens, 1994). Aging has been associated with increases in optic flow heading thresholds, thought to be attributable to declines in central visual processing (Atchley & Andersen, 1998, 1999; Warren, Blackwell, & Morris, 1989).
Chapter 15 Contour discontinuities subserve two types of form analysis that underlie motion processing
2006, Progress in Brain ResearchCitation Excerpt :This would be expected if second-order filters detect or are influenced by contour, texture, or form information, because form can be defined using first-order cues. Wilson et al. (1992; see also Derrington et al., 1993; Zanker and Huepgens, 1994) suggested that first-order motion is processed foremost in V1, whereas second-order motion also requires processing in V2, with both streams converging in MT. This was supported by the finding that 87% of sampled cells in MT in the alert macaque are tuned to second-order motion as well as first-order motion (Albright, 1992, see also Olavarria et al., 1992; but compare O’Keefe and Movshon, 1998 who found <25% such cells in MT in the anaesthetized macaque; for second-order motion tuning in cat cortex see Mareschal and Baker, 1998, 1999; Zhou and Baker, 1993, 1994, 1996). Albright (1992) suggested that these cells may underlie form–cue invariant motion processing (see also, Buracas and Albright, 1996).
Perceptual learning in primary and secondary motion vision
1999, Vision Research