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At least 1,081 records · Page 60Linked to original sources
PubMed2003

Crystallographic analysis of the thermal motion of the inclusion complex of cyclomaltoheptaose (beta-cyclodextrin) with hexamethylenetetramine.

The crystal structure of the inclusion complex of cyclomaltoheptaose (beta-cyclodextrin) with hexamethylenetetramine was determined at temperatures of 123, 173, 223, and 293 K. The rigid-body motion of the host and guest molecules was evaluated by means of the TLS method that represents the molecular motion in terms of translation, libration, and screw motion. In increasing the temperature from 123 to 293 K, the amplitude of the rigid body vibration of the host molecule was increased from 1.0 to 1.3 degrees in the rotational motion and from 0.16 to 0.17 A in the translational motion. The cyclomaltoheptaose molecule has the flexibility in seven alpha-(1-->4)-linkages, and each glucose unit was in the rotational vibration around an axis through two glycosidic oxygen atoms. As a result, the rigid-body parameters of cyclomaltoheptaose were considered to be overestimated because of including the contribution from the local motion of glucose units. In contrast, for the guest molecule having no structural flexibility, the TLS analysis demonstrated that the atomic thermal vibration was mostly derived from the rigid body motion. The rotational amplitude of hexamethylenetetramine was changed from 5.2 to 6.6 degrees in increasing the temperature from 123 to 293 K, while the change of the translational amplitude was from 0.20 to 0.23 A. The translational motion of the guest molecule was hindered by the inside wall of the host cavity. The molecular motion was characterized by the rotational vibration around the axis through two nitrogen atoms that were involved in the hydrogen-bond formation.

Crystallography, X-Ray↗
PubMed2003

Perception of biological motion in parietal patients.

Three unilateral parietal patients were tested on their perception of biological motion, a special case of form-from-motion. Two patients had the lesion in the right, and one in the left parietal area. All patients could easily perform a classical form-from-motion task [Neuron 32 (2001) 985], but they were severely impaired in a visual search task using biological motion sequences. In particular, the left parietal patient showed a more severe loss. He was unable to identify even a single item. Overall our patients seemed to perform differently from the classical motion-blind patients described in the literature [Visual Cognition 3 (1996) 363; Eur. J. Neurol. 9 (2002) 463; Visual Neurosci. 5 (1990) 353] whose lesions included the visual cortical area V5. Since our patients' low-level motion mechanisms are preserved, we suggest that the perception of biological motion relies on a high-level description of dynamic patterns [Cognition 80 (2001) 47], a mechanism that is impaired in parietal lobe patients. We discuss our results at the light of the recent theories suggesting that biological motion is performed by visual associative areas outside the classical motion pathways and that it is an active process dependent on attentional resources [Cognition 80 (2001) 47].

Aged↗
PubMed2001

Cardinal axes for radial and circular motion, revealed by summation and by masking.

Both electro-physiological and psychophysical studies point to the existence of detectors specialised for the analysis of optic flow. However, it is unclear whether these detectors are tuned to specific 'cardinal directions' (such as radial and circular motion), or whether they respond equally to all directions of optic-flow motion, including intermediate spiral motions. Here summation and masking studies of motion coherence sensitivity are reported that suggest that optic flow may be tuned to radial and circular cardinal directions. Strong summation was found between two orthogonal directions of spiral motion, but much weaker summation between radial and circular motion. As orthogonal spiral motions always contain a common radial or circular component, the stronger summation for these motions implies that detectors are tuned to radial and circular directions. Similarly, the most effective masking stimuli (placed adjacent to but not superimposed on the test stimuli) tended to be those in the radial or circular directions, even for spiral targets, further suggesting that flow-field motion is detected and discriminated by mechanisms tuned to these 'cardinal' directions.

Discrimination, Psychological↗
PubMed2001

Lines and dots: characteristics of the motion integration process.

Local motion detectors can only provide the velocity component perpendicular to a moving line that crosses their receptive field, leading to an ambiguity known as the "aperture problem". This problem is solved exactly for rigid objects translating in the screen plane via the intersection of constraints (IOC). In natural scenes, however, object motions are not restricted to fronto-parallel translations, and several objects with distinct motions may be present in the visual space. Under these conditions the usual IOC construction is no longer valid, which raises questions as its use as a basis for spatial integration and selection of motion signals in uniform and non-uniform velocity fields. The influence of the motion of random dots on the perceived direction of a horizontal line grating was measured, when dots and lines are seen through different apertures. The random dots were mapped on a plane that translates in a fronto-parallel plane (uniform 2D translation) or in depth (3D, corresponding to a non-uniform projected velocity field, either expanding or contracting). The grating was either moving rigidly with the dots or in the opposite direction. Subjects' responses show that the direction of line grating movement was reliably influenced only in conditions consistent with rigid motion; where there was a reliable influence, the perceived direction was consistent with the dot motion pattern. This finding points to the existence of a motion-based selection mechanism that operates prior to the disambiguation of the line movement direction. Disambiguation could occur for both uniform and non-uniform velocity fields, even though in the last case none of the individual dots indicated the proper direction in 2D velocity space. Finally, the capture by non-uniform motion patterns was less robust than that by uniform 2D translations, and could be disrupted by manipulations of the shape and size of the apertures.

Adult↗
PubMed2001

Neural dynamics of motion integration and segmentation within and across apertures.

A neural model is developed of how motion integration and segmentation processes, both within and across apertures, compute global motion percepts. Figure-ground properties, such as occlusion, influence which motion signals determine the percept. For visible apertures, a line's terminators do not specify true line motion. For invisible apertures, a line's intrinsic terminators create veridical feature-tracking signals. Sparse feature-tracking signals can be amplified before they propagate across position and are integrated with ambiguous motion signals within line interiors. This integration process determines the global percept. It is the result of several processing stages: directional transient cells respond to image transients and input to a directional short-range filter that selectively boosts feature-tracking signals with the help of competitive signals. Then, a long-range filter inputs to directional cells that pool signals over multiple orientations, opposite contrast polarities, and depths. This all happens no later than cortical area MT. The directional cells activate a directional grouping network, proposed to occur within cortical area MST, within which directions compete to determine a local winner. Enhanced feature-tracking signals typically win over ambiguous motion signals. Model MST cells that encode the winning direction feed back to model MT cells, where they boost directionally consistent cell activities and suppress inconsistent activities over the spatial region to which they project. This feedback accomplishes directional and depthful motion capture within that region. Model simulations include the barberpole illusion, motion capture, the spotted barberpole, the triple barberpole, the occluded translating square illusion, motion transparency and the chopsticks illusion. Qualitative explanations of illusory contours from translating terminators and plaid adaptation are also given.

Computer Simulation↗
PubMed2002

Early unilateral enucleation disrupts motion processing.

Previous research has shown that unilaterally enucleated observers demonstrate better luminance-defined form perception compared to monocularly viewing controls, and similar performance to control observers viewing binocularly (Vision Res. 37(17) (1997) 2465). In Experiment 1 we asked whether the perception of form, where form is defined by other attributes than luminance, is also improved compared to monocularly viewing controls. We tested 16 enucleated observers and 25 controls viewing monocularly and binocularly for their ability to detect and recognize form from texture (texture-defined (TD) form) and form from motion (motion-defined (MD) form). There was no difference between the three groups for TD form perception. However, enucleated observers had significantly poorer MD form perception than did binocularly viewing controls. In Experiment 2 we asked whether poor performance on the perception of MD form might be due to a general reduction in motion processing abilities. To examine this possibility, we used a motion coherence task. We tested eight unilaterally enucleated and 14 monocularly and binocularly viewing control observers on a horizontal coherent motion discrimination task. The monocularly viewing controls showed no naso-temporal asymmetry in direction discrimination for coherent motion. In contrast, the enucleated group showed an asymmetry in direction discrimination where temporalward motion coherence thresholds were significantly higher than those for nasalward motion. These latter findings are discussed in terms of the absence of binocular competition during the development of motion processing pathways.

Adolescent↗
PubMed2002

Orientation sensitivity in human visual motion processing.

Orientation tuning of receptive fields is well documented in the spatial domain, but considerable variability exists amongst published estimates of orientation sensitivity of motion receptive fields. We used a two-frame motion sequence, in which one frame was binary noise and the other was a horizontally displaced and filtered version of the same noise field, to examine the orientation sensitivity of human motion mechanisms. Initially, orientations orthogonal to the direction of motion were removed from each filtered frame. Observers indicated perceived direction of motion in a single interval, binary choice task. D(max) was determined for different amounts of removed orientations, and found to remain constant across the removal of energy up to approximately +/-60 deg from vertical. In a second experiment, the orientations removed were now parallel to the direction of motion of the stimulus. D(max) fell as a cosine function with increasing removal of orientation information, in agreement with off-orientation looking or matched filtering predictions. The two experiments show the presence of mechanisms both broadly tuned and more narrowly tuned for orientation. A control experiment introduced an interstimulus interval between the two frames of our motion sequence. Performance on the direction discrimination task was severely degraded, indicating that the original results are not explicable in terms of a feature-tracking or long-range motion process. The presence of both broadly and narrowly tuned mechanisms implies multiple possible solutions to the processing of coherent plaid motion.

Humans↗
PubMed2002

Integration of motion information during binocular rivalry.

When two moving gratings are superimposed in normal viewing they often combine to form a pattern that moves with a single direction of motion. Here, we investigated whether the same mechanism underlies pattern motion when drifting gratings are presented independently to the two eyes. We report that, with relatively large circular grating patches (4 deg), there are periods of monocular dominance in which one eye's orientation alone is perceived, usually moving orthogonal to the contours (component motion). But, during the transitions from one monocular view to the other, a fluid mosaic is perceived, consisting of contiguous patches, each containing contours of only one of the gratings. This entire mosaic often appears to move in a single direction (pattern motion), just as when two gratings are literally superimposed. Although this implies that motion signals from the perceptually suppressed grating continue to influence the perception of motion, an alternative possibility is that it reflects a strategy that involves integrating directional information from the contiguous single-grating patches. To test between these possibilities, we performed a second experiment with very small grating stimuli that were about the same size as the contiguous single-grating patches in the mosaic (1-deg diameter). Despite the fact that the form of only one grating was perceived, we report that pattern motion was still perceived on about one third of trials. Moreover, a decrease in the occurrence of pattern motion was apparent when the contrast and spatial frequency of the gratings were made more different from each other. This phenomenon clearly demonstrates an independent binocular interaction for form and motion.

Humans↗
PubMed2003

Adaptation of response transients in fly motion vision. I: Experiments.

Two types of transient responses have been investigated in fly motion-sensitive neurons in the past: the impulse and the step response. In response to a brief motion pulse, cells show a sudden rise in activity followed by an exponential decay ('impulse response'). In response to the onset of a constant velocity stimulus, cells exhibit transient oscillations before settling to a steady-state value ('step response'). Since the impulse response has been shown to shorten when tested after presentation of an adapting motion stimulus, we investigated whether adaptation also occurs during the step response. We tested this hypothesis by recording extracellularly the response of the H1-cell in the lobula plate of the blowfly Calliphora vicina to gratings of varying pattern contrasts and drift velocity. We found that the transient oscillations of the step response strongly depend on the pattern contrast: at low contrasts, oscillations lasted for several seconds, whereas at high contrasts, they settled within fractions of a second. This suggests that motion adaptation occurs during the initial period of the stimulus presentation and is dependent on the contrast of the motion stimulus. Using identical stimulus parameters (contrast and temporal frequency) for the adapting stimulus and testing the impulse response afterwards, we found that the impulse response and the transient period in the step response shortened in a similar way. We then analyzed the dynamic of the transients oscillations produced by ongoing motion of a square wave pattern in the anti-preferred direction (null direction) of H1. As observed for preferred direction motion, we found that the duration and amplitude of those transients shortened as the contrast and the velocity of the pattern increased, and that the oscillations disappeared when a blank screen instead of a pattern was presented before the onset of motion. Under both stimulus conditions, i.e. grating and blank screen before motion onset, the steady-state response level showed the same dependence on the contrast and temporal frequency of the pattern. When we analyzed the responses of the cell to pattern of various sizes and contrasts moving in the preferred direction of the cell, we found that increments in the size affected the overall amplitude of both the transient oscillations and the steady-state response level, whereas the duration of the oscillations only depended on the local pattern contrast. We also tested the impulse response before and after the presentation of an adapting stimulus presented in either the same or a different location of the visual field. The response shortened only when both the adapting and the test stimuli were presented at the same location. These last experiments demonstrate a strictly local mechanism of adaptation affecting the response transients of both the impulse and the step response.

Adaptation, Ocular↗
PubMed1997

Spatio-temporal boundary formation: the role of local motion signals in boundary perception.

Spatio-temporal boundary formation (SBF) refers to a perceptual process responsible for perception of moving, bounded surfaces from sequential changes in spatially separated local elements. Previous research has indicated that this process produces perception of global form, continuous boundaries and global motion from spatially and temporally sparse element changes. In the present paper, we sought to distinguish between two classes of models for SBF: form-precedes-motion and motion-precedes-form models. Experiment 1 tested the effects of the addition of spurious motion signals, a manipulation that should affect a motion-precedes-form computation but not a form-precedes-motion computation. Shape identification in a 10-alternative forced-choice procedure was disrupted by this manipulation, supporting the former class of models. A particular computational scheme, edge orientation from motion (EOFM) instantiating a motion-precedes-form model is described and tested in Experiment 2. The EOFM model should be disrupted when initiating element changes occur in a certain type of sequential order, relative to randomly arranged changes. Sequential changes markedly disrupted performance, supporting this EOFM approach. The results favor motion-precedes-form models of SBF and are consistent with the particular computational scheme proposed.

Form Perception↗
PubMed1997

Motion interference: perturbing perceived direction.

The minimum stimulus necessary to define motion is a change in position from one location to another in time, but past studies have provided evidence that the human motion system integrates motion over more than two positions. In this study we demonstrate strong sequential interactions affecting perceived direction in apparent-motion sequences; a perturbing dot can bias the perceived direction of motion between two test dots to which it is relatively close in space (up to 100 min arc) and time (up to 300 msec). These sequential interactions suggest a motion mechanism sensitive to the spatial characteristics of motion trajectories; the interactions are greatest for evenly spaced targets positioned along a single axis. The implications for motion-detection models and models based on attention as a mechanism to create apparent motion are discussed.

Humans↗
PubMed1998

Local and global factors affecting the coherent motion of gratings presented in multiple apertures.

Using stimuli composed of two independent gratings viewed through multiple apertures, we investigate a number of parameters affecting the integration of locally ambiguous motions into globally coherent motion. In four experiments, we varied local factors (grating spatial frequency, speed, contrast, duty cycle, orientation) and global factors (degree of similarity and common fate between the gratings, and symmetry in the configuration of the grating pattern) and examined their effects on global motion coherence. Our results, confirming accounts offered by previous investigators, indicate that local competition between motion signals generated by contours (ambiguous) and their line terminations (unambiguous) is important in determining global motion coherence in multiple-aperture stimuli. Our results also indicate that global factors can affect perceived coherence independently of local motion signals, suggesting the involvement of higher-level motion areas and a role for non-motion processes such as those involved in pattern and form perception. Comparing motion coherence with other two-dimensional (2-D) stimuli (plaids) shows that 2-D multiple-aperture stimuli are not analogous and that coherence models derived from plaid stimuli do not account for the data.

Humans↗
PubMed1999

Second-order processing of four-stroke apparent motion.

In four-stroke apparent motion displays, pattern elements oscillate between two adjacent positions and synchronously reverse in contrast, but appear to move unidirectionally. For example, if rightward shifts preserve contrast but leftward shifts reverse contrast, consistent rightward motion is seen. In conventional first-order displays, elements reverse in luminance contrast (e.g. light elements become dark, and vice-versa). The resulting perception can be explained by responses in elementary motion detectors turned to spatio-temporal orientation. Second-order motion displays contain texture-defined elements, and there is some evidence that they excite second-order motion detectors that extract spatio-temporal orientation following the application of a non-linear 'texture-grabbing' transform by the visual system. We generated a variety of second-order four-stroke displays, containing texture-contrast reversals instead of luminance contrast reversals, and used their effectiveness as a diagnostic test for the presence of various forms of non-linear transform in the second-order motion system. Displays containing only forward or only reversed phi motion sequences were also tested. Displays defined by variation in luminance, contrast, orientation, and size were effective. Displays defined by variation in motion, dynamism, and stereo were partially or wholly ineffective. Results obtained with contrast-reversing and four-stroke displays indicate that only relatively simple non-linear transforms (involving spatial filtering and rectification) are available during second-order energy-based motion analysis.

Contrast Sensitivity↗
PubMed1999

Infants code the direction of chromatic quadrature motion.

The present experiment uses a quadrature motion paradigm to investigate the motion correspondence cues used by young infants for coding the direction of motion of red/green isoluminant gratings. Three-month-old infants and adults were tested with 0.25 c/d luminance-modulated or red/green isoluminant gratings, either moving continuously or shifted in spatial quadrature. Both direction-of-motion and detection thresholds were measured, and motion:detection (M:D) threshold ratios were examined. Infants, like adults, could code the direction of motion of red/green quadrature-shifted gratings. In adults, M:D ratios were similar for continuous and quadrature motion. In infants, M:D ratios were higher for quadrature than for continuous motion, but elevations of similar magnitude were seen for both luminance-modulated and red/green gratings. The results suggest that frequency-doubled signals, such as those often seen in the magnocellular (M-cell) pathway, are not necessary for coding the direction of motion of isoluminant gratings in infant subjects. Two other theoretical options--mediation by the scatter of isoluminance points in the M-cell population, and parvocellular (P-cell) mediation--are discussed.

Adult↗
PubMed1999

Stereoscopic (cyclopean) motion sensing.

This paper reviews literature on the motion processing of dynamic change in binocular disparity, called stereoscopic (cyclopean) motion. Studies investigating the visual processing of stereoscopic motion in the Z-axis, stereoscopic motion in the X/Y plane, and cyclopean motion are discussed. It is concluded that stereoscopic motion is processed by a motion-sensing system composed of special-purpose mechanisms that function like low-level motion sensors. For animals with binocular vision, low-level motion processing may involve, at least in part, stereoscopic processing.

Animals↗
PubMed1999

Position-based motion perception for color and texture stimuli: effects of contrast and speed.

Motion can be perceived either through low-level, motion-energy detection or through tracking the change in position of features. Previously we have shown that, while luminance-based motion likely is detected with velocity-sensitive motion-energy units, patterns defined by texture or binocular disparity ('second-order' stimuli) were tracked by a position-sensitive mechanism (Seiffert & Cavanagh (1998) Vision Research, 38, 3569-3582). Here, we use the same technique, measuring motion amplitude thresholds of oscillating gratings over a range of temporal frequencies and find that the motion of low-contrast equiluminant red/green gratings is also detected with position tracking. In addition, we find that as contrast or speed increases these results change: high-contrast or high-speed equiluminant color or texture-based motion is detected by velocity-sensitive mechanisms. These results help resolve the dispute over the processes which detect the motion of non-luminance based stimuli. Both systems are available, but their relative efficiency changes as a function of contrast and speed. A position-tracking process is more sensitive at low contrasts and low speeds whereas a motion-energy system is more sensitive at high contrasts and high speeds.

Color Perception↗
PubMed2000

The role of relative motion computation in 'direction repulsion'.

When two sets of intermixed dots move in different directions the perceived direction of each is considerably shifted [Marshak & Sekuler (1979). Science, 205, 1399-1401; Mather & Moulden, (1980). Quarterly Journal of Experimental Psychology, 32, 325-333)]. This phenomenon has been attributed to 'repulsive' interactions between channels tuned to different directions of motion. However, we report that it is not only the relative direction, but also the density and speed of the sets, which determines the magnitude of the apparent shift. These results are difficult to reconcile with the notion of 'repulsive' interactions, and we describe an alternative, functionally motivated explanation. In the natural environment, observed motion results from objects moving over background surfaces that may themselves be mobile. Disentanglement of motion signals therefore necessitates a computation of relative motion. We propose that the phenomenon of 'direction repulsion' results from a deliberate adjustment of observed motion to compensate for an inferred source of 'background' motion. A simple scheme to do this subtracts the weighted vector-sum of all motion signals from observed motion. This relative motion computation quantitatively predicts the observed effects of the density of dot sets on perceived direction. The effects of speed cannot be reconciled with the scheme as it stands, but this could be due to the model's failure to consider the effect of temporal frequency on the effective contrast of the sets.

Female↗
PubMed2001

Opioid receptor involvement in the adaptation to motion sickness in Suncus murinus.

The aim of the present study was to investigate an opioid receptor involvement in the adaptation response to motion sickness in Suncus murinus. Different groups of animals were treated intraperitoneally with either saline, morphine (0.1 and 1.0 mg/kg), naloxone (1.0, 10.0 and 5.0 mg/kg) or a combination of naloxone plus morphine in the absence or 30 min prior to a horizontal motion stimulus of 1 Hz and 40 mm amplitude. For the study of adaptation, different groups received saline on the first trial, and in subsequent trials (every 2 days) they received either saline, naloxone (1.0 and 10.0 mg/kg, i.p.) or morphine (0.1 mg/kg, i.p.) 30 min prior to the motion stimulus. Pretreatment with morphine caused a dose-related reduction in emesis induced by a single challenge to a motion stimulus. Pretreatment with naloxone alone did not induce emesis in its own right nor did it modify emesis induced by a single challenge to a motion stimulus. However, pretreatment with naloxone (5.0 mg/kg, i.p.) revealed an emetic response to morphine (P<.001) (1.0 mg/kg, i.p.) and antagonised the reduction of motion sickness induced by morphine. In animals that received saline or naloxone (1.0 mg/kg), a motion stimulus inducing emesis decreased the responsiveness of animals to a second and subsequent motion stimulus challenge when applied every 2 days for 11 trials. However, the animals receiving naloxone 10.0 mg/kg prior to the second and subsequent challenges showed no significant reduction in the intensity of emesis compared to the first trial. The data are revealing of an emetic potential of morphine when administered in the presence of a naloxone pretreatment. The administration of naloxone is also revealing of an additional inhibitory opioid system whose activation by endogenous opioid(s) may play a role in the adaptation to motion sickness on repeated challenge in S. murinus.

Adaptation, Psychological↗