Dissociation of first- and second-order motion systems by perceptual learning

Published in final edited form as: Atten Percept Psychophys. 2012 July ; 74(5): 1009–1019. doi:10.3758/s13414-012-0290-3.Previous studies investigating transfer of perceptual learning between luminance-defined (LD) motion and texture-contrast-defined (CD) motion tasks have found little or no transfer from LD to CD motion tasks but nearly perfect transfer from CD to LD motion tasks. Here, we introduce a paradigm that yields a clean double dissociation: LD training yields no transfer to the CD task, but more interestingly, CD training yields no transfer to the LD task. Participants were trained in two variants of a global motion task. In one (LD) variant, motion was defined by tokens that differed from the background in mean luminance. In the other (CD) variant, motion was defined by tokens that had mean luminance equal to the background but differed from the background in texture contrast. The task was to judge whether the signal tokens were moving to the right or to the left. Task difficulty was varied by manipulating the proportion of tokens that moved coherently across the four frames of the stimulus display. Performance in each of the LD and CD variants of the task was measured as training proceeded. In each task, training produced substantial improvement in performance in the trained task; however, in neither case did this improvement show any significant transfer to the nontrained task.This work was supported in part by NSF Award BCS-0843897 to Dr. Chubb and in part by Award Number RO1NS064100 from the National Institutes of Health, National Institute of Neurological Disorders and Stroke to Dr. Vaina. (BCS-0843897 - NSF; RO1NS064100 - National Institutes of Health, National Institute of Neurological Disorders and Stroke)Accepted manuscrip

High-capacity preconscious processing in concurrent groupings of colored dots.

Grouping is a perceptual process in which a subset of stimulus components (a group) is selected for a subsequent-typically implicit-perceptual computation. Grouping is a critical precursor to segmenting objects from the background and ultimately to object recognition. Here, we study grouping by color. We present subjects with 300-ms exposures of 12 dots colored with the same but unknown identical color interspersed among 14 dots of seven different colors. To indicate grouping, subjects point-click the remembered centroid ("center of gravity") of the set of homogeneous dots, of heterogeneous dots, or of all dots. Subjects accurately judge all of these centroids. Furthermore, after a single stimulus exposure, subjects can judge both the heterogeneous and homogeneous centroids, that is, subjects simultaneously group by similarity and by dissimilarity. The centroid paradigm reveals the relative weight of each dot among targets and distractors to the underlying grouping process, offering a more detailed, quantitative description of grouping than was previously possible. A change detection experiment reveals that conscious memory contains less than two dots and their locations, whereas an ideal detector would have to perfectly process at least 15 of 26 dots to match the subjects' centroid judgments-indicating an extraordinary capacity for preconscious grouping. A different color set yielded identical results. Grouping theories that rely on predefined feature maps would fail to explain these results. Rather, the results indicate that preconscious grouping is automatic, flexible, and rapid, and a far more complex process than previously believed

Measuring the spatial frequency selectivity of second-order texture mechanisms

AbstractRecent investigations of texture and motion perception suggest two early filtering stages: an initial stage of selective linear filtering followed by rectification and a second stage of linear filtering. Here we demonstrate that there are differently scaled second-stage filters, and we measure their contrast modulation sensitivity as a function of spatial frequency. Our stimuli are Gabor modulations of a suprathreshold, bandlimited, isotropic carrier noise. The subjects' task is to discriminate between two possible orientations of the Gabor. Carrier noises are filtered into four octave-wide bands, centered at m = 2, 4, 8, and 16 c/deg. The Gabor test signals are w = 0.5, 1, 2, 4 and 8 c/deg. The threshold modulation of the test signal is measured for all 20 combinations of m and w. For each carrier frequency m, the Gabor test frequency w to which subjects are maximally sensitive appears to be approximately 3–4 octaves below m. The consistent m × w interaction suggests that each second-stage spatial filter may be differentially tuned to a particular first-stage spatial frequency. The most sensitive combination is a second-stage filter of 1 c/deg with first-stage inputs of 8–16 c/deg. We conclude that second-order texture perception appears to utilize multiple channels tuned to spatial frequency and orientation, with channels tuned to low modulation frequencies appearing to be best served by carrier frequencies 8 to 16 times higher than the modulations they are tuned to detect

Two mechanisms that determine the Barber-Pole Illusion

AbstractIn the Barber-Pole Illusion (BPI), a diagonally moving grating is perceived as moving vertically because of the narrow, vertical, rectangular shape of the aperture window through which it is viewed. This strong shape–motion interaction persists through a wide range of parametric variations in the shape of the window, the spatial and temporal frequencies of the moving grating, the contrast of the moving grating, complex variations in the composition of the grating and window shape, and the duration of viewing. It is widely believed that end-stop-feature (third-order) motion computations determine the BPI, and that Fourier motion-energy (first-order) computations determine failures of the BPI. Here we show that the BPI is more complex: (1) In a wide variety of conditions, weak-feature stimuli (extremely fast, low contrast gratings, 21.5Hz, 4% contrast) that stimulate only the Fourier (first-order) motion system actually produce a slightly better BPI illusion than classical strong-feature gratings (2.75Hz, 32% contrast). (2) Reverse-phi barber-pole stimuli are seen exclusively in the feature (third-order) BPI direction when presented at 2.75Hz and exclusively in the opposite (Fourier, first-order) BPI direction at 21.5Hz, indicating that both the first- and the third-order systems can produce the BPI. (3) The BPI in barber poles with scalloped aperture boundaries is much weaker than in normal straight-edge barber poles for 2.75Hz stimuli but not in 21.5Hz stimuli. Conclusions: Both first-order and third-order stimuli produce strong BPIs. In some stimuli, local Fourier motion-energy (first-order) produces the BPI via a subsequent motion-path-integration computation (Journal of Vision (2014) 14, 1--27); in other stimuli, the BPI is determined by various feature (third-order) motion inputs; in most stimuli, the BPI involves combinations of both. High temporal frequency, low-contrast stimuli favor the first-order motion-path-integration computation; low temporal frequency, high-contrast stimuli favor third-order motion computations

Exploring attention-based explanations for some violations of Hick’s law for aimed movements

Choice reaction time generally increases linearly with the logarithm of the number of potential stimulus–response alternatives, a regularity known as Hick’s law. Two apparent violations of this generalization, which have been reported for aimed eye movements (Kveraga, Boucher, & Hughes, Experimental Brain Research, 146, 307–314, 2002), and arm movements (Wright, Marino, Belovsky, & Chubb, Experimental Brain Research, 179, 475–496, 2007), occurred when the indicator stimulus was an abrupt change at the location that was the target of the to-be-made movement. We report two experiments that examined and rejected the hypothesis that these abrupt-onset indicator stimuli triggered a shift in exogenous attention and that this led to unusually small uncertainty effects. Each experiment compared this indicator stimulus with a single alternative: Experiment 1 tested an indicator stimulus at all locations other than the target; Experiment 2 tested a central pointer to the target. Neither alternative led to an uncertainty effect for pointing responses that was of the size typically observed for other responses using the same stimuli

Response Bias Modulates the Speech Motor System during Syllable Discrimination

Recent evidence suggests that the speech motor system may play a significant role in speech perception. Repetitive transcranial magnetic stimulation (TMS) applied to a speech region of premotor cortex impaired syllable identification, while stimulation of motor areas for different articulators selectively facilitated identification of phonemes relying on those articulators. However, in these experiments performance was not corrected for response bias. It is not currently known how response bias modulates activity in these networks. The present functional magnetic resonance imaging experiment was designed to produce specific, measureable changes in response bias in a speech perception task. Minimal consonant-vowel stimulus pairs were presented between volume acquisitions for same-different discrimination. Speech stimuli were embedded in Gaussian noise at the psychophysically determined threshold level. We manipulated bias by changing the ratio of same-to-different trials: 1:3, 1:2, 1:1, 2:1, 3:1. Ratios were blocked by run and subjects were cued to the upcoming ratio at the beginning of each run. The stimuli were physically identical across runs. Response bias (criterion, C) was measured in individual subjects for each ratio condition. Group mean bias varied in the expected direction. We predicted that activation in frontal but not temporal brain regions would co-vary with bias. Group-level regression of bias scores on percent signal change revealed a fronto-parietal network of motor and sensory-motor brain regions that were sensitive to changes in response bias. We identified several pre- and post-central clusters in the left hemisphere that overlap well with TMS targets from the aforementioned studies. Importantly, activity in these regions covaried with response bias even while the perceptual targets remained constant. Thus, previous results suggesting that speech motor cortex participates directly in the perceptual analysis of speech should be called into question

Studies on Some Immunological Aspects of Australian Infectious Bronchitis Viruses

Prior to 1962, infectious bronchitis (IB) virus had not been identified in Australia. Certainly the disease syndrome caused by IB virus, as seen in Europe and America (Beister and Schwarte, 1959) had not been described in Australia (Gilchrist, 1962, Hungerford, 1962), although reports by Hart (1946), Newton and Simmons (1963) and Gilchrist (1962), all describe syndromes which had some aspects reminiscent of IB infections. One of the prominent poultry diseases at that time had been characterised by a breakdown in kidney function producing a 'uraemia' or nephritis (Hungerford, 1969). This syndrome had been seen since 1948 and was thought possibly to be caused by some nutritional factor (Beilharz and McDonald, 1960). In 1962, Cumming isolated a virus from cases of nephritis and suggested the virus to be IB. This was confirmed by Cumming (1963, 1964), Gilchrist (1963), and Gilchrist and Sinkovic (1964). Supporting serological evidence for the identity of the virus being IB was given by cross neutralisation studies with American IB viruses (Winterfield et al., 1964a), British IB viruses (Berry and Stokes, 1968) and some German IB viruses (von Bulow, 1967). Berry and Stokes (1968) also confirmed the Australian IB virus as a corona-virus by electron microscopy. ... The main approach to the disease problem associated with IB virus infections in the past has been based on the serum neutralisation relationships of the viruses involved and the ability of vaccine viruses to induce these antibodies in birds. The approach to the problem used in this thesis has been based on the ability of virus infections to induce resistance in birds to the affects of virulent IB virus challenge and to evaluate the relationship of this resistance to antibody production. This approach has been aided by, the characteristic of Australian IB viruses to cause death with nephritis under controlled experimental conditions