fMRI Adaptation Reveals Separate Mechanisms for First-Order and Second-Order Motion

2007 ◽  
Vol 97 (2) ◽  
pp. 1319-1325 ◽  
Author(s):  
Hiroshi Ashida ◽  
Angelika Lingnau ◽  
Matthew B. Wall ◽  
Andrew T. Smith

A key unresolved debate in human vision concerns whether we have two different low-level mechanisms for encoding image motion. Separate neural mechanisms have been suggested for first-order (luminance modulation) and second-order (e.g., contrast modulation) motion in the retinal image but a single mechanism could handle both. Human functional magnetic resonance imaging (fMRI) has not so far convincingly revealed separate anatomical substrates. To examine whether two separate but co-localized mechanisms might exist, we used the technique of fast fMRI adaptation. We found direction-selective adaptation independently for each type of motion in the motion area V5/MT+ of the human brain. However, there was a total absence of cross-adaptation between first-order and second-order motion stimuli. This was true in both of the two subcomponents of MT+ (MT and MST) and similar results were found in V3A. This pattern of adaptation was consistent with psychophysical measurements of detection thresholds in similar stimulus sequences. The results provide strong evidence for separate neural populations that are responsible for detecting first- and second-order motion.

Perception ◽  
1994 ◽  
Vol 23 (10) ◽  
pp. 1211-1219 ◽  
Author(s):  
Timothy Ledgeway ◽  
Andrew T Smith

The magnitude of the motion aftereffect (MAE) obtained following adaptation to first-order or to second-order motion was measured by estimating its duration. The second-order adaptation stimulus was composed of contrast-modulated noise produced by multiplying two-dimensional (2-D) noise by a drifting 1 cycle deg−1 sine grating. The first-order adaptation stimulus was composed of luminance-modulated noise produced by summing, rather than multiplying, the noise and the sine grating. The test stimuli were directionally ambiguous motion patterns composed of either two oppositely drifting sine gratings added to noise or the contrast-modulated equivalent. The adaptation and test stimuli were equated for visibility by presenting them at the same multiple of direction-identification threshold. All possible combinations of first-order and second-order adaptation and test stimuli were examined in order to compare the magnitudes of the MAEs obtained following same adaptation and cross adaptation. After adaptation the test stimuli always appeared to drift coherently in the direction opposite to that of adaptation and the magnitudes of this MAE were very similar for all conditions examined. Statistical analyses of the results showed that there was no significant difference between the durations of the MAEs obtained in the same-adaptation and cross-adaptation conditions. The cross-adaptation effects suggest that either first-order or second-order motion are detected by a common low-level mechanism, or that separate parallel motion-detecting mechanisms exist, for the two types of motion, that interact at some later stage of processing.


2006 ◽  
Vol 95 (2) ◽  
pp. 862-881 ◽  
Author(s):  
Jonas Larsson ◽  
Michael S. Landy ◽  
David J. Heeger

Second-order textures—patterns that cannot be detected by mechanisms sensitive only to luminance changes—are ubiquitous in visual scenes, but the neuronal mechanisms mediating perception of such stimuli are not well understood. We used an adaptation protocol to measure neural activity in the human brain selective for the orientation of second-order textures. Functional MRI (fMRI) responses were measured in three subjects to presentations of first- and second-order probe gratings after adapting to a high-contrast first- or second-order grating that was either parallel or orthogonal to the probe gratings. First-order (LM) stimuli were generated by modulating the stimulus luminance. Second-order stimuli were generated by modulating the contrast (CM) or orientation (OM) of a first-order carrier. We used four combinations of adapter and probe stimuli: LM:LM, CM:CM, OM:OM, and LM:OM. The fourth condition tested for cross-modal adaptation with first-order adapter and second-order probe stimuli. Attention was diverted from the stimulus by a demanding task at fixation. Both first- and second-order stimuli elicited orientation-selective adaptation in multiple cortical visual areas, including V1, V2, V3, V3A/B, a newly identified visual area anterior to dorsal V3 that we have termed LO1, hV4, and VO1. For first-order stimuli (condition LM:LM), the adaptation was no larger in extrastriate areas than in V1, implying that the orientation-selective first-order (luminance) adaptation originated in V1. For second-order stimuli (conditions CM:CM and OM:OM), the magnitude of adaptation, relative to the absolute response magnitude, was significantly larger in VO1 (and for condition CM:CM, also in V3A/B and LO1) than in V1, suggesting that second-order stimulus orientation was extracted by additional processing after V1. There was little difference in the amplitude of adaptation between the second-order conditions. No consistent effect of adaptation was found in the cross-modal condition LM:OM, in agreement with psychophysical evidence for weak interactions between first- and second-order stimuli and computational models of separate mechanisms for first- and second-order visual processing.


Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 345-345
Author(s):  
A J Schofield ◽  
M A Georgeson

Human vision can detect spatiotemporal information conveyed by first-order modulations of luminance and by second-order, non-Fourier modulations of image contrast. Models for second-order motion have suggested two filtering stages separated by a rectifying nonlinearity. We explore here the encoding of stationary first-order and second-order gratings, and their interaction. Stimuli consisted of 2-D broad-band static visual noise sinusoidally modulated in luminance (first-order, LM) or contrast (second-order, CM). Modulation thresholds were measured in a two-interval forced-choice staircase procedure. With increasing noise contrast, first-order sensitivity decreased (owing to masking) but sensitivity to contrast modulation increased. Weak background gratings present in both intervals produced order-specific facilitation: LM background facilitated LM detection (the ‘dipper function’) and CM facilitated CM detection. LM did not facilitate CM, nor vice versa, and this is strong evidence that LM and CM are detected via different mechanisms. Nevertheless, suprathreshold LM gratings masked CM detection, but not vice versa. High-amplitude CM masks had little or no effect on CM or LM detection. A broadly tuned divisive gain-control mechanism applied to the first-order filtering stage has been proposed by Foley (1994 Journal of the Optical Society of America A11 1710 – 1719) to account for masking of luminance gratings, and this might also explain the masking of second-order by first-order stimuli. First-order maskers would drive down the effective contrast of the carrier, thus reducing second-order sensitivity. But for second-order maskers the mean contrast, and hence contrast gain, remained constant, independent of modulation depth. Thus second-order gratings would produce no masking effects, as observed.


2010 ◽  
Vol 50 (17) ◽  
pp. 1766-1774 ◽  
Author(s):  
Claire V. Hutchinson ◽  
Timothy Ledgeway

PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0243430
Author(s):  
Takeshi Miyamoto ◽  
Kenichiro Miura ◽  
Tomohiro Kizuka ◽  
Seiji Ono

A large number of psychophysical and neurophysiological studies have demonstrated that smooth pursuit eye movements are tightly related to visual motion perception. This could be due to the fact that visual motion sensitive cortical areas such as meddle temporal (MT), medial superior temporal (MST) areas are involved in motion perception as well as pursuit initiation. Although the directional-discrimination and perceived target velocity tasks are used to evaluate visual motion perception, it is still uncertain whether the speed of visual motion perception, which is determined by visuomotor reaction time (RT) to a small target, is related to pursuit initiation. Therefore, we attempted to determine the relationship between pursuit latency/acceleration and the visual motion RT which was measured to the visual motion stimuli that moved leftward or rightward. The participants were instructed to fixate on a stationary target and press one of the buttons corresponding to the direction of target motion as soon as possible once the target starts to move. We applied five different visual motion stimuli including first- and second-order motion for smooth pursuit and visual motion RT tasks. It is well known that second-order motion induces lower retinal image motion, which elicits weaker responses in MT and MST compared to first-order motion stimuli. Our results showed that pursuit initiation including latency and initial eye acceleration were suppressed by second-order motion. In addition, second-order motion caused a delay in visual motion RT. The better performances in both pursuit initiation and visual motion RT were observed for first-order motion, whereas second-order (theta motion) induced remarkable deficits in both variables. Furthermore, significant Pearson’s correlation and within-subjects correlation coefficients were obtained between visual motion RT and pursuit latency/acceleration. Our findings support the suggestion that there is a common neuronal pathway involved in both pursuit initiation and the speed of visual motion perception.


2010 ◽  
Vol 6 (6) ◽  
pp. 1041-1041
Author(s):  
H. Ashida ◽  
A. Lingnau ◽  
M. B. Wall ◽  
A. T. Smith

2011 ◽  
Vol 105 (5) ◽  
pp. 2121-2131 ◽  
Author(s):  
Luke E. Hallum ◽  
Michael S. Landy ◽  
David J. Heeger

A variety of cues can differentiate objects from their surrounds. These include “first-order” cues such as luminance modulations and “second-order” cues involving modulations of orientation and contrast. Human sensitivity to first-order modulations is well described by a computational model involving spatially localized filters that are selective for orientation and spatial frequency (SF). It is widely held that first-order modulations are represented by the firing rates of simple and complex cells (“first-order” neurons) in primary visual cortex (V1) that, likewise, have spatially localized receptive fields that are selective for orientation- and SF. Human sensitivity to second-order modulations is well described by a filter-rectify-filter (FRF) model, with first- and second-order filters selective for orientation and SF. However, little is known about how neuronal activity in visual cortex represents second-order modulations. We tested the FRF model by using an functional (f)MRI-adaptation protocol to characterize the selectivity of activity in visual cortex to second-order, orientation-defined gratings of two different SFs. fMRI responses throughout early visual cortex exhibited selective adaptation to these stimuli. The low-SF grating was a more effective adapter than the high-SF grating, incompatible with the FRF model. To explain the results, we extended the FRF model by incorporating normalization, yielding a filter-rectify-normalize-filter model, in which normalization enhances selectivity for second-order SF but only for low spatial frequencies. We conclude that neurons in human visual cortex are selective for second-order SF, that normalization (surround suppression) contributes to this selectivity, and that the selectivity in higher visual areas is simply fed forward from V1.


1997 ◽  
Vol 36 (04/05) ◽  
pp. 315-318 ◽  
Author(s):  
K. Momose ◽  
K. Komiya ◽  
A. Uchiyama

Abstract:The relationship between chromatically modulated stimuli and visual evoked potentials (VEPs) was considered. VEPs of normal subjects elicited by chromatically modulated stimuli were measured under several color adaptations, and their binary kernels were estimated. Up to the second-order, binary kernels obtained from VEPs were so characteristic that the VEP-chromatic modulation system showed second-order nonlinearity. First-order binary kernels depended on the color of the stimulus and adaptation, whereas second-order kernels showed almost no difference. This result indicates that the waveforms of first-order binary kernels reflect perceived color (hue). This supports the suggestion that kernels of VEPs include color responses, and could be used as a probe with which to examine the color visual system.


2017 ◽  
Vol 9 (3) ◽  
pp. 17-30
Author(s):  
Kelly James Clark

In Branden Thornhill-Miller and Peter Millican’s challenging and provocative essay, we hear a considerably longer, more scholarly and less melodic rendition of John Lennon’s catchy tune—without religion, or at least without first-order supernaturalisms (the kinds of religion we find in the world), there’d be significantly less intra-group violence. First-order supernaturalist beliefs, as defined by Thornhill-Miller and Peter Millican (hereafter M&M), are “beliefs that claim unique authority for some particular religious tradition in preference to all others” (3). According to M&M, first-order supernaturalist beliefs are exclusivist, dogmatic, empirically unsupported, and irrational. Moreover, again according to M&M, we have perfectly natural explanations of the causes that underlie such beliefs (they seem to conceive of such natural explanations as debunking explanations). They then make a case for second-order supernaturalism, “which maintains that the universe in general, and the religious sensitivities of humanity in particular, have been formed by supernatural powers working through natural processes” (3). Second-order supernaturalism is a kind of theism, more closely akin to deism than, say, Christianity or Buddhism. It is, as such, universal (according to contemporary psychology of religion), empirically supported (according to philosophy in the form of the Fine-Tuning Argument), and beneficial (and so justified pragmatically). With respect to its pragmatic value, second-order supernaturalism, according to M&M, gets the good(s) of religion (cooperation, trust, etc) without its bad(s) (conflict and violence). Second-order supernaturalism is thus rational (and possibly true) and inconducive to violence. In this paper, I will examine just one small but important part of M&M’s argument: the claim that (first-order) religion is a primary motivator of violence and that its elimination would eliminate or curtail a great deal of violence in the world. Imagine, they say, no religion, too.Janusz Salamon offers a friendly extension or clarification of M&M’s second-order theism, one that I think, with emendations, has promise. He argues that the core of first-order religions, the belief that Ultimate Reality is the Ultimate Good (agatheism), is rational (agreeing that their particular claims are not) and, if widely conceded and endorsed by adherents of first-order religions, would reduce conflict in the world.While I favor the virtue of intellectual humility endorsed in both papers, I will argue contra M&M that (a) belief in first-order religion is not a primary motivator of conflict and violence (and so eliminating first-order religion won’t reduce violence). Second, partly contra Salamon, who I think is half right (but not half wrong), I will argue that (b) the religious resources for compassion can and should come from within both the particular (often exclusivist) and the universal (agatheistic) aspects of religious beliefs. Finally, I will argue that (c) both are guilty, as I am, of the philosopher’s obsession with belief. 


2009 ◽  
Vol 74 (1) ◽  
pp. 43-55 ◽  
Author(s):  
Dennis N. Kevill ◽  
Byoung-Chun Park ◽  
Jin Burm Kyong

The kinetics of nucleophilic substitution reactions of 1-(phenoxycarbonyl)pyridinium ions, prepared with the essentially non-nucleophilic/non-basic fluoroborate as the counterion, have been studied using up to 1.60 M methanol in acetonitrile as solvent and under solvolytic conditions in 2,2,2-trifluoroethan-1-ol (TFE) and its mixtures with water. Under the non- solvolytic conditions, the parent and three pyridine-ring-substituted derivatives were studied. Both second-order (first-order in methanol) and third-order (second-order in methanol) kinetic contributions were observed. In the solvolysis studies, since solvent ionizing power values were almost constant over the range of aqueous TFE studied, a Grunwald–Winstein equation treatment of the specific rates of solvolysis for the parent and the 4-methoxy derivative could be carried out in terms of variations in solvent nucleophilicity, and an appreciable sensitivity to changes in solvent nucleophilicity was found.


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