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At least 19 recordsLinked to original sources
PubMed1976

The role of pattern goodness in the reproduction of backward masked patterns.

Four experiments investigated the role of pattern goodness in backward masking using five- and four-dot patterns constructed by placing dots in the cells of a 3 x 3 matrix. In Experiment 1, subjects rated the goodness of these patterns and the results replicated previous work showing that good patterns had few alternatives. In Experiment 2, the dot patterns were the target stimuli in a backward masking task using a variety of masking stimuli. For all masking, good patterns were reproduced more accurately than poor patterns. In Experiment 3, the goodness of the masking stimulus was varied. The results indicated that good patterns were reproduced more accurately (replicating Experiment 2) and that good patterns were less effective as stimulus than were poor patterns. In Experiment 4, a long interstimulus interval which precluded masking was used to determine whether goodness affected encoding or memory. At these intervals, there were no differences among patterns, suggesting that the effect of pattern goodness was on rate of encoding. These results demonstrate the importance of configural properties in pattern perception.

Discrimination, Psychological↗
PubMed1992

Analysis of pulmonary venous flow velocity patterns in hypertensive hearts: its complementary value in the interpretation of mitral flow velocity patterns.

Although the Doppler mitral flow velocity pattern changes in accordance with the degree of left ventricular diastolic dysfunction, it is "normalized" in the presence of heart failure. In this study the pulmonary venous flow velocity pattern was characterized in 43 hypertensive patients with and without heart failure to clarify whether analysis of the pulmonary venous flow velocity pattern provides complementary information in the interpretation of the mitral flow velocity pattern. The mitral flow velocity pattern in 32 hypertensive patients without heart failure was characterized by decreases in the peak early diastolic filling velocity (E) and the ratio of E to peak filling velocity at atrial contraction. The mitral flow velocity pattern was "normalized" in 11 patients with heart failure, with no differences in any mitral flow velocity pattern indexes as compared with 24 normal subjects. The pulmonary venous flow velocity pattern in hypertensive patients without heart failure was characterized by a decreased peak diastolic forward flow velocity (D) and an increased ratio of peak systolic forward flow velocity (S) to D (S/D ratio). In patients with heart failure, D was higher and the S/D ratio was lower compared with hypertensive patients without heart failure (p less than 0.01, p less than 0.01) and normal subjects (p less than 0.01, p less than 0.01). Thus the pulmonary venous flow velocity pattern appeared to be more reliable than the mitral flow velocity pattern in differentiating subgroups of patients with hypertension. Analysis of the pulmonary venous flow velocity pattern in conjunction with the mitral flow velocity pattern provides important and complementary information in the interpretation of the mitral flow velocity pattern in hypertensive patients with and without heart failure.

Blood Flow Velocity↗
PubMed1976

Spatial distribution of potentials evoked by half-field pattern-reversal and pattern-onset stimuli.

Spatial distributions of visual potentials (VEPs) evoked by half-field checkerboard pattern-reversal and pattern-onset stimuli were studied in 13 subjects, using an 11 lead unipolar array. The main aim was to confirm findings, obtained by previous workers with bipolar recordings, that half-field pattern-reversal VEP's are confined to the contralateral hemisphere and that half-field pattern-onset VEPs are asymmetrical, with greater right hemisphere involvement. Pattern-reversal VEP's contained four consistent peaks, designated here by polarity and peak latency as: (a) P95, positivity contra-lateral and negativity ipsilateral to the field stimulated; (b) P125, predominantly ipsilateral positivity; (c) N165, predominantly ipsilateral negativity; (d) P225; predominantly midline positivity. Pattern-onset VEPs contained three consistent peaks: (a) P125, mainly contraleteral positivity; (B) N175, mainly contralateral negativity; (c) P225, midline positivity. Distributions of pattern-reversal and pattern-onset peaks resembled one another only for P225, suggesting different cortical representation for the other events of the two kinds of VEP. Bipolar pattern-reversal VEPs were largely contralateral, but unipolar recordings showed that this was due to steeper contralateral potential gradients, as ipislateral activity was widespread. Pattern-onset peaks did not differ in amplitude with respect to the half-field stimulated. Previously reported asymmetries were not confirmed. The P125 and N175 pattern-onset peaks were almost entirely restricted to the contralateral hemisphere, but the distributions by half-field were mirror-images of one another. Half-field pattern-onset stimuli could be used to investigate the responsiveness of each hemisphere, although differential hemispheric involvement was not shown. Several differences in amplitude and distribution resulted from varying the width of the vertical central dark strip.

Adolescent↗
PubMed1990

Limits of auditory patterns discrimination for patterns with various durations and numbers of components.

In three experiments, listeners' abilities to detect changes in randomly generated tonal sequences were determined for sequences or "patterns" ranging in total duration from 62.5 ms to 2 s. Experiment 1 utilized an adaptive-tracking procedure, with n, the number of pattern components, as the dependent variable, and included a variety of spectral and temporal discrimination tasks with isochronous patterns. When the to-be-detected change was the only variation on a given dimension (e.g., the presence or location of a brief pause), patterns were discriminable when the absolute duration of the changed element, or pause, exceeded a critical value. However, when each pattern component varied on the dimension of the to-be-detected change (e.g., frequency), discriminability was strongly related to the number of tones in the pattern, and only weakly to the durations of either the target components or the total pattern. This dependence of discrimination performance on n was also demonstrated with anisochronous patterns in experiment 2. Experiment 3 revealed the same dependence of performance on the number of components per pattern as did experiments 1 and 2, but with delta f/f as the dependent variable, rather than n. The number of pattern components and the proportional duration of the target components, relative to total pattern duration, were confounded in these experiments. Additional research is therefore required to determine whether number or proportional target-tone duration is the primary determinant of pattern discriminability.

Adult↗
PubMed1991

The pattern electroretinogram in retinal and optic nerve disease. A quantitative comparison of the pattern of visual dysfunction.

A retrospective analysis was performed on the transient and steady-state pattern electroretinograms recorded from 42 patients with glaucoma, 13 patients with senile dementia of the Alzheimer's type, 58 patients with diabetes mellitus, and 92 control subjects to evaluate the pattern of electroretinographic changes associated with retinal and optic nerve disease. The amplitudes of both the initial positive component (N1 to P1) and the subsequent negative component (P1 to N2) of the transient (4 rps) responses were measured. From these measurements the (P1 to N2)/(N1 to P1) was derived. The N1 to P1 amplitude of the steady-state pattern electroretinogram also was measured. In the glaucoma patients all three amplitude measures, as well as the amplitude ratio of the components of the transient response, were reduced significantly compared with age-matched controls (p less than 0.05). A similar pattern was detected in the patients with Alzheimer's disease, but in this case the only statistically significant amplitude reduction was in the steady-state pattern electroretinogram. A different pattern was observed among the diabetic patients (both with and without retinopathy). Only minor reductions in the amplitude of the transient pattern electroretinogram, which were not statistically significant, were noted. In addition, the ratio of the amplitudes of the components of the transient response did not differ from age-matched controls. The amplitude of the steady-state pattern electroretinogram was reduced in diabetics, but this was significant only for those patients with retinopathy (p less than 0.01). These findings support the suggestion that an analysis of both the positive and negative components of the pattern electroretinogram may be useful for differentiating the contributions of retinal and optic nerve dysfunction to visual impairment. The results also indicate that in both retinal and optic nerve disease the steady-state pattern electroretinogram can be an earlier sign of dysfunction than the transient pattern electroretinogram.

Adult↗
PubMed1990

Neural mechanisms generating respiratory pattern in mammalian brain stem-spinal cord in vitro. I. Spatiotemporal patterns of motor and medullary neuron activity.

1. An analysis of the spatial and temporal patterns of activity of neurons of the respiratory motor-pattern generation system in an in vitro neonatal rat brain stem-spinal cord preparation is presented. Impulse discharge patterns of spinal and cranial moto-neurons as well as respiratory neurons in the medulla were analyzed. Patterns of motoneuronal discharge were characterized at the population level from recordings of motor-nerve discharge and at the single-cell level from intracellular recordings. These patterns were compared to patterns generated in the neonatal rat and adult mammal in vivo to establish the correspondence between in vitro and in vivo states. 2. The in vitro system generated a complex spatiotemporal pattern of spinal and cranial motoneuron activity during inspiratory (I) and expiratory (E) phases of the respiratory cycle. The respiratory cycle consisted of three distinct phases of neuronal activity (I, early E, and late E phase) similar to the temporal organization of the cycle in the intact mammal. The spike discharge pattern of motoneurons during the I phase consisted of a rapidly peaking-slowly decrementing discharge envelope with a high degree of synchronization on a time scale of 25-50 ms (approximately 20-40 Hz). A similar pattern was generated in the neonate in vivo under conditions comparable with the in vitro state (i.e., nervous system isolated from mechanosensory afferent inputs). However, the I-phase-motoneuron discharge pattern and cycle-phase durations differed from those characteristic of the intact neonatal or adult systems in vivo. This difference could be accounted for primarily by removal of vagal mechanosensory afferent inputs. 3. The synaptic drive potentials of spinal motoneurons during the I phase in vitro consisted of a rapidly peaking-slowly decrementing potential envelope similar in shape to the spike-frequency histogram of single motoneurons and the envelope of the motoneuron-population discharge. The drive potentials had prominent high-frequency amplitude fluctuations superimposed on the slower drive-potential envelope that were temporally correlated with the generation of motoneuron action potentials. The dominant frequency components of these fast-membrane-potential oscillations (20-35 Hz) were similar to the frequency components of the amplitude fluctuations in the motoneuron-population discharge. One class of medullary neurons with I-phase discharge also exhibited a rapidly peaking-slowly decrementing pattern of impulse discharge and synaptic drive potential with similar high-frequency components.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1985

Internal representations and operations in the visual comparison of transformed patterns: effects of pattern point-inversion, position symmetry, and separation.

A scheme for visual pattern recognition is described. It is supposed, amongst other things, that patterns are internally represented by the visual system in terms of local features, spatial-order relations between local features, and global spatial relations specifying approximate pattern position with respect to the point of fixation. It is further supposed that there are two distinct types of internal operation that may be applied to the components of internal representations in the process of pattern comparison: typically a discrete spatial-order-reversal operation and a continuous position-shift operation. Some general predictions of the scheme are tested against data obtained in an experiment using random-dot patterns that were subjected to rigid transformations and presented at various locations along the horizontal meridian. Patterns were presented sequentially, in pairs, to subjects in a "same-different" comparison task. Pattern pairs were to be responded to as "same" if they were identical or related by point-inversion (planar rotation through 180 degrees) or responded to as "different". Extending earlier findings, the present results showed that "same"-detection performance for identical and point-inverted patterns depended differentially on the distance between the patterns and the symmetry of the pattern positions about the point of fixation in a manner consistent with the predictions of the scheme.

Adult↗
PubMed1979

Transformation and relational-structure schemes for visual pattern recognition. Two models tested experimentally with rotated random-dot patterns.

Two models for visual pattern recognition are described; the one based on application of internal compensatory transformations to pattern representations, the other based on encoding of patterns in terms of local features and spatial relations between these local features. These transformations and relational-structure models are each endowed with the same experimentally observed invariance properties, which include independence to pattern translation and pattern jitter, and, depending on the particular versions of the models, independence to pattern reflection and inversion (180 degrees rotation). Each model is tested by comparing the predicted recognition performance with experimentally determined recognition performance using as stimuli random-dot patterns that were variously rotated in the plane. The level of visual recognition of such patterns is known to depend strongly on rotation angle. It is shown that the relational-structure model equipped with an invariance to pattern inversion gives responses which are in close agreement with the experimental data over all pattern rotation angles. In contrast, the transformation model equipped with the same invariances gives poor agreement to the experimental data. Some implications of these results are considered.

Field Dependence-Independence↗
PubMedDate not supplied

The influence of pattern size on amplitude, latency and wave form of retinal and cortical potentials elicited by checkerboard pattern reversal and stimulus onset-offset.

Transient pattern electroretinograms (PERGs) and visual evoked potentials (VEPs) were recorded with checkerboard pattern reversal and equiluminance stimulus onset-offset, elicited by a high quality moving mirror stimulator. Different sized checkerboard patterns (0.35-4.2 c/deg) were used as stimulus patterns. The wave forms of the equiluminance stimulus onset responses were similar to ERGs evoked with luminance decrease and the stimulus offset PERGs were like ERGs elicited by luminance increase. The PERG c wave and the VEP showed spatial frequency tuning with pattern reversal and stimulus offset. Spatial frequency tuning was not detectable with PERG a and b waves. Pattern reversal and stimulus onset evoked PERGs had no major spectral components above 40 Hz; stimulus offset evoked PERGs contained components up to 55.3 Hz. Retino-cortical time--measured as a latency difference of the PERG b wave to VEP P100--was identical with pattern reversal and stimulus onset and about 12 msec longer with stimulus offset. Our results suggest that the 3 stimulation modes, reversal, onset and offset induce different types of processing at the retinal and cortical levels. PERG a and b waves to our high luminance/contrast stimuli contain no pattern specific information and the c waves are the sum of luminance and pattern specific responses.

Cerebral Cortex↗
PubMed1989

Pattern-contingent color aftereffects on noninduced patterns.

In a series of experiments, we found that in addition to expected reports of color aftereffects on patterns viewed during induction, reliable and predictable reports of color were given by subjects to patterns they did not view during induction. These reports to noninduced patterns were generally to patterns that were orthogonal to the patterns seen during induction. Induction with, for example, a red vertical grating led to appropriate aftereffects (i.e., green) on that vertical pattern and to the complementary aftereffect (i.e., pink) on a horizontal grating. We suggest that such color aftereffects on noninduced patterns are based on a shift in the activity of orientation coding mechanisms as a result of viewing the inducing patterns. We further propose that the results are consistent with the Lie transformation group theory of neuropsychology and that they add to a growing body of research demonstrating the applicability of this theory to the understanding of pattern-contingent color aftereffects.

Attention↗
PubMed1990

Modeling the Drosophila pair-rule pattern by reaction-diffusion: gap input and pattern control in a 4-morphogen system.

Various reaction-diffusion models will produce striped patterns, but the most effective models so far devised to do this require two matched pairs of interacting morphogens, i.e. four substances in all. This paper examines the behavior of one such model, of a fairly generalized type, and its application to the process of pair-rule pattern formation during Drosophila embryogenesis. It is assumed that the two self-activating morphogens required by the model, expressed in complementary out-of-phase stripes, are products of early-acting pair-rule genes. Possible candidates include the primary pair-rule genes, hairy and runt. The conditions under which regular stripes are generated by the model are then examined, with emphasis on the way pre-existing patterns act to control stripe formation via their effect on rates of reaction within the pair-rule system, specifically rates of pair-rule gene transcription, to show how gap gene products may act during pattern formation. A fully symmetrical set of reactions, in which rates of formation, self- and cross-activation are exactly matched, gives unaligned stripes. Pronounced asymmetries in this regard, e.g. differential rates of formation or self-activation, destabilize stripes or produce local interruptions in the pattern like those seen in gap mutants. A limited degree of asymmetry, coupled with a gradient in the value of one or more parameters will give a correctly aligned, well-controlled pattern of stripes. The experimental evidence indicates that gap genes could be responsible for both of these effects: they activate the pair-rule system asymmetrically and, when first expressed, generate a sufficiently complex landscape of concentration peaks and gradations to provide the local cues needed to correctly position and align the pair-rule stripes. In this respect, the pair-rule system can be viewed as having an intrinsic pattern-forming capability, but it depends on the input of gap genes for pattern control. Gradients are involved, but from this analysis, it is the graded distribution of gap products that is important, not the overall antero-posterior gradient. The uniform spacing of stripes, despite underlying peaks and troughs of gap gene expression, shows that pattern wavelength is relatively insensitive to parameter change, also a property of the model.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1986

Patterns of breathing in response to alternating patterns of alveolar carbon dioxide pressures in man.

The time profile of alveolar PCO2 within the respiratory cycle has been forced to follow contrasting patterns in alternate breaths, in two different ways. Within-breath changes (w.b.c., with a CO2-rich inspirate supplied early or late in alternate inspirations) involved minimal alternation of end-tidal PCO2. Between-breath changes (b.b.c., with whole inspirates of CO2-free or CO2-rich gas) involved large swings of end-tidal PCO2. As previously reported (Metias, Cunningham, Howson, Petersen & Wolff, 1981), both patterns of forcing were associated with alternation of ventilation, but only when hypoxia was present. The patterns of the alternating reflex responses in 118 runs on four human subjects in steady hypoxia are described in terms of alternation of inspiratory and expiratory tidal volume, time and mean flow. These patterns often disappeared, or changed unpredictably in mid-run. The inspiratory pattern of reflex alternation depended in part on the type of forcing, but alternation of inspiratory tidal volume was usually observed with both types. No single pattern of expiratory alternation emerged as predominant. The pattern of reflex expiratory alternation was surprisingly independent of the pattern of inspiratory alternation: indeed, in w.b.c., but not in b.b.c., alternation of mean expiratory flow and of mean inspiratory flow were mutually exclusive. It is concluded that in man, as in cats and dogs, the arterial chemoreceptor pathway has access to various parts of the respiratory pattern generator, the exact response depending to some extent on the timing within the respiratory cycle. In particular, expiratory variables may be influenced directly through the arterial chemoreceptor pathway, i.e. without any supposedly mediating inspiratory alternation being demonstrable. The results are discussed briefly in relation to some current views on the organization of respiratory control.

Carbon Dioxide↗
PubMed1989

Differences between pattern onset and pattern reversal retinal responses.

The pattern-evoked electroretinogram was recorded to pattern onset-offset and pattern reversal stimuli in two color-normal subjects with either luminance contrast of black-red (600 nm) and black-green (526 nm) square-wave stripe patterns or color contrast red-green patterns. The size of the onset response shows a spatial tuning with luminance contrast patterns and only a simple low-pass filter function with color contrast patterns. The peak latency of the response to luminance contrast increases with increasing spatial frequency but stays constant with color contrast patterns. The size of the reversal responses, however, shows only a low-pass filter function under both contrast conditions. The peak latency to luminance contrast shows a slight increase and to color contrast it remains constant with increasing spatial frequency. The differences noted under the various stimulus conditions must take into account the possible effects of different luminance modulation depths of onset and reversal stimuli, the modulation transfer function of the eye, and the activity of luminance-antagonistic and color-antagonistic receptive fields.

Color Perception↗
PubMed1985

Incidence of finger pattern types and pattern intensity in a Spanish population (Tierra de Campos).

The incidence of finger pattern types and the pattern intensity distribution in a Spanish sample (417 males and 416 females) drawn from the geographical area of Tierra de Campos have been studied. Sexual and bilateral differences for both dermatoglyphic traits were explored by means of chi 2-test and Mann-Whitney U-test, showing significant differences in all cases, excepting the sexual difference between left hands for pattern intensity. Kolmogorov test for distribution normality showed that pattern intensity was not normally distributed, being the distributions right skewed because of the low frequency of classes with fewer triradii. The results obtained in Tierra de Campos were compared with those observed in other Spanish and Portuguese populations, showing more heterogeneity in the pattern types than in pattern intensity. This could imply that arches account for the main source of variation between populations. Moreover, pattern type frequencies and pattern intensity in Tierra de Campos are, as expected, within the variation ranges of Southeuropean-Mediterranean populations and Caucasians as a whole, although the incidence of radial loops is located in the lower extremes of the corresponding variation ranges.

Dermatoglyphics↗
PubMed1988

Solid perception mechanism by a shading pattern: spatial frequency components in a corrugated wave pattern.

Illumination allows solid object perception to be obtained and depicted by a shading pattern produced by lighting. The shading cue, as one of solid perception cues (Gibson 1979), was investigated in regard to a white corrugated wave shape, using computer graphic device: Tospix-2. The reason the corrugated wave was chosen, is that an alternately bright and dark pattern, produced by shading, can be conveniently analyzed into contained spatial frequencies. This paper reports spatial frequency properties contained in the shading pattern. The shading patterns, input into the computer graphic device, are analyzed by Fourier Transformation by the same device. After the filtration by various spatial frequency low and high pass filters, Inverse Fourier Transformation is carried out for the residual components. The result of the analysis indicates that the third through higher harmonics components are important in regard to presenting a solid reality feeling in solid perception. Sakata (1983) also reported that an edged pattern, superimposed onto a lower sinusoidal pattern, was important in solid perception. The third through higher harmonics components express the changing position of luminance on the pattern, and a slanted plane relating to the light direction. Detection of a solid shape, constructed with flat planes, is assumed to be on the bottom of the perfect curved solid perception mechanism. Apparent evidence for this assumption, in difficult visual conditions, is that a flat paneled solid is seen before the curved solid. This mechanism is explained by two spatial frequency neural network systems, assumed as having correspondence with higher spatial frequency detection and lower spatial frequency detection.

Computer Graphics↗
PubMed1992

Effects of pattern element density upon displacement limits for motion detection in random binary luminance patterns.

The upper motion displacement threshold (Dmax) was determined with two-frame motion sequences of random binary luminance patterns, over a range of pattern element sizes and densities. Dmax was little affected by density at small element sizes (less than 5 arcmin), in agreement with previous reports. However, at larger element sizes (greater than 9 arcmin) Dmax increased as element density was reduced in the range 50-5%. We explain our findings by a model which takes into account spatial-frequency filtering prior to motion detection, and the effects of pattern density upon the statistics of random binary patterns. We also implicate the dependence of Dmax upon the contrast energy of the elements in broadband patterns, and provide a direct demonstration that Dmax is contrast limited over a wide range of pattern contrasts (72-2.5%). Previous reports that Dmax is independent of density should be modified to take into account the complex effects of density upon the statistics of random patterns, and the existence of physiological filtering prior to motion detection.

Humans↗
PubMed1979

Cell number in relation to primary pattern formation in the embryo of Xenopus laevis. I. The cell cycle during new pattern formation in response to implanted organizers.

Results are presented which offer strong evidence that extensive alteration of the fates of embryonic Xenopus cells occurs independently of the schedule of cell division, after operations which lead to a doubling of the axial pattern of mesodermal differentiation in the gastrula. The experimental strategy was to make estimates of total mesodermal cell numbers and mitotic index in closely matched sets, each of three synchronous sibling embryos, fixed during the ten hours following the close of gastrulation. Within each set two embryos, an unoperated control and a sham-operated embryo whose own dorsal-lip (organizer) cells had been replaced with an equivalent graft, were developing normally. The third, experimental embryo had received an organizer implant to replace an equivalent number of cells from its ventral marginal zone, and was thus developing two axial mesodermal patterns of differentiation in relation to two dorsal midlines, the extra pattern embracing much host tissue. Mitotic index was also determined, in specific regions and throughout the mesoderm, in similar sets of embryos but at mid-gastrula stages. The conclusions are justified by the results of a control investigation which show that there is normally no difference in cell cycle time along the presumptive dorso-ventral mesodermal, dimension, during the interval between time of operations and the determination of pattern. The lack of any enhancement of mesodermal cell number in late embryos with dual axia patterns, or intervening enhancement of mitotic index in younger operated embryos, thus suggests that new patterns may be determined in the Xenopus gastrula without generation of extra cells. The results are discussed in relation to recent ideas about pattern formation, and the concepts of morphallaxis and epimorphosis.

Animals↗