Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Generalization, Stimulus”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,675 records · Page 93Linked to original sources

The minimum contrast requirements for stereopsis.

A number of researchers have compared the contrast requirements for stereopsis with those for detection of the stereoscopic stimulus, but they have generally failed to allow for the fact that stereopsis requires a detectable stimulus in both eyes at the same time. It is argued that the most appropriate detection threshold for this comparison is that for simultaneous monocular detection (SMD) of the stereoscopic half images. Experiments in which this comparison threshold has been used are summarised and the hypothesis generated that, on using stimuli that are localised in both space and spatial frequency (e.g. Gabor patches or differences of Gaussians), a range of disparities can always be found over which contrast thresholds for depth identification are less than or equal to this SMD threshold (the SMD hypothesis). It is argued that the success of this hypothesis in describing data obtained with these stimuli is consistent with the notions of labelled lines for disparity sign and the size--disparity correlation. Last, experiments are reported in which contrast thresholds for stereoscopic depth identification (front/back) were measured with interocular differences in contrast. The data obtained are consistent with the presence of both inhibitory and excitatory interactions between the eyes when unequal monocular contrasts are presented. The implications of these results and the SMD hypothesis for theories of stereopsis and binocular function are discussed.

Contrast Sensitivity↗

Postural reactions induced by vertical motion of visual scenes and the effects of weightlessness.

Postural reactions induced by vertical optokinetic stimulation were recorded for 5 subjects in a ground-based study, and for one astronaut before, during, and after a 25-day spaceflight. On the ground, the amplitude of visually-induced postural reactions generally increased with stimulus velocity and saturated around 60 degrees/s, with an angle of body tilt which never exceeded 2-3 degrees. For velocities higher than 20 degrees/s, backward body tilt during upgoing optokinetic stimulation was larger than forward body tilt during downgoing stimulation. In weightlessness, the angle of body tilt was reduced compared to ground values, but after the flight the postural reactions were larger than before the flight. If the limited angle of body tilt on Earth is due to an inhibition from the graviceptive inputs which do not confirm the visual inputs, the larger angle of tilt might reflect that this inhibition was less effective after spaceflight. This ineffectiveness might reflect a confusion between body tilt and translation as the result of adaptation to weightlessness.

Adult↗

Respiratory and electrocortical responses to acoustic stimulation.

Although sleep-related obstructive apnea is most often associated with transient arousal, the impact of this arousal on respiratory control remains unclear. We employed binaural tone bursts (.5 second duration) to elicit repetitive transient arousals from sleep during polygraphic recordings in 5 adult volunteers. By this method, we elicited repetitive transient arousals with a mean duration of approximately 10 seconds from all stages of sleep. With respect to the 3 pre-stimulus breaths, acoustic stimulation was associated with increased tidal volume and decreased inspiratory duration for at least 4 breaths. These respiratory responses to acoustic stimulation were not significantly influenced by either presence of transient arousal from sleep or the sleep state from which arousal occurred. We conclude that transient electro-cortical state changes may be repeatedly evoked from all sleep stages by transient acoustic stimulation in normal sleepers. This sensory stimulation represents a significant respiratory stimulus even when generalized arousal from sleep does not occur.

Acoustic Stimulation↗

Odour concentration affects odour identity in honeybees.

The fact that most types of sensory stimuli occur naturally over a large range of intensities is a challenge to early sensory processing. Sensory mechanisms appear to be optimized to extract perceptually significant stimulus fluctuations that can be analysed in a manner largely independent of the absolute stimulus intensity. This general principle may not, however, extend to olfaction; many studies have suggested that olfactory stimuli are not perceptually invariant with respect to odour intensity. For many animals, absolute odour intensity may be a feature in itself, such that it forms a part of odour identity and thus plays an important role in discrimination alongside other odour properties such as the molecular identity of the odorant. The experiments with honeybees reported here show a departure from odour-concentration invariance and are consistent with a lower-concentration regime in which odour concentration contributes to overall odour identity and a higher-concentration regime in which it may not. We argue that this could be a natural consequence of odour coding and suggest how an 'intensity feature' might be useful to the honeybee in natural odour detection and discrimination.

Acyclic Monoterpenes↗

The effect of inducing ventricular fibrillation with 50-Hz pacing versus T wave stimulation on the ability to defibrillate.

When testing an ICD, there are at least two techniques for inducing ventricular fibrillation: (1) high frequency (approximately equal to 50 Hz) pacing; and (2) a single T wave stimulus. It is generally assumed that these two methods yield similar results. This study directly tested this assumption. In six dogs, one defibrillation electrode was placed in the right ventricular (RV) apex and the second was placed cutaneously on the left thorax. All defibrillation and T wave stimuli were biphasic between these two electrodes. Pacing was monophasic from the tip of the RV catheter to the cutaneous patch. The voltage which defibrillates 50% of the time (DF50) was measured using a 10-step Bayesian up-down method. Observations for two DF50 measurements were randomly interleaved. For one DF50 measurement, fibrillation was induced with 99 pacing stimuli at a 20-ms pacing interval (50-Hz pacing). For the second DF50 measurement, fibrillation was induced with a single defibrillation shock of approximately 1/2 J delivered at a time corresponding to the peak of the T wave in the lead II electrogram (T wave stimuli). The average DF50 when measured after fibrillation induced with 50-Hz pacing was 379 +/- 54.6 V, as compared to 382 +/- 50.3 V when fibrillation was induced with T wave stimuli. The difference of 3 V was not statistically significant. If these results are confirmed in humans, it is reasonable to assume that the efficacy of a defibrillation shock is the same whether T wave stimuli or 50-Hz pacing are used to induce fibrillation.

Animals↗

The afferent connexions and laminar distribution of cells in area 18 of the cat.

1. The receptive field properties, laminar distribution and afferent connectivity of cells in area 18 of the cat are described. 2. Testing with both moving and stationary stimuli revealed three main receptive field types which have been termed S, C and B, respectively (cf. Henry, 1977; Henry, Lund & Harvey, 1978). All three classes may show end-zone inhibition and units exhibiting this property have been designated SH, CH and BH. 3. S cells can be divided into spatially separate lights and/or dark edge response regions when tested with moving edges and usually have separate ON and/or OFF areas when tested with stationary flashing stimuli. They are the most commonly encountered cell type in area 18 and occur most frequently in laminae IIIb, IVa and VI. 4. Both C and B cells have spatially coincident light and dark edge response regions and give mixed ON and OFF discharges when tested with stationary flashing stimuli. Compared to B cells however, C cells have large receptive fields, they are broadly tuned for stimulus orientation and generally have a relatively high rate of spontaneous activity. C cells are more common than B cells and are encountered most often in laminae IVb and V. 5. Electrical stimulation of the optic chiasm (OX) and optic radiation (OR) was used to examine the afferent connectivity of parastriate neurons. Cells driven from both OX and OR have been divided into two main groups and it is argued that group 1 cells are directly, and group 2 cells are indirectly, excited by rapidly conducting afferent fibres. Group 1 cells are found most often in laminae IIIb, IVa, IVb and VI, and their distribution closely follows the anatomically defined laminar disposition of geniculocortical afferent terminals. Group 2 neurones predominate in laminae II-IIIa, IIIA and V. 6. The majority of S and SH cells are directly driven, whereas most C and CH cells have OX and OR latencies suggestive of indirect activation by thalamic afferents. 7. The intrinsic organization and possible functional role of area 18 is discussed in the light of these results.

Afferent Pathways↗

Recruitment of motor units in response to transcranial magnetic stimulation in man.

1. Short-latency responses of single motor units (SMUs) and surface electromyographic activity (EMG) to transcranial magnetic stimulation (TMS) were examined in five different hand and forearm muscles of human subjects. 2. The response probability, P (number of extra spikes in the response peak above background per stimulus), was, in general, higher at the lower voluntary discharge rate of the motor unit than at the higher rate. 3. Increasing the strength of TMS increased the response probability of a tonically firing motor unit and at the same time recruited new units which discharged phasically during the response peak. This demonstrates rate coding and recruitment of motor units by excitatory inputs resulting from TMS when the motoneurone pool is tonically facilitated by a constant voluntary drive. 4. Next, TMS was delivered without any voluntary facilitation of motoneurones. The order of recruitment for up to four different motor units discharged by TMS was compared to that observed with voluntary input. The threshold of recruitment for each of the two inputs was estimated from the surface EMG value at which the unit was recruited. For these motoneurone pools (eleven sets of observations), the order of recruitment was the same with TMS and voluntary inputs. 5. From these data it is concluded that, despite the complex and phasic nature of the descending corticospinal volleys generated by TMS, it produces orderly recruitment and rate coding of motoneurones similar to that found for voluntary activation.

Action Potentials↗

Intensity difference limens at high frequencies.

Thresholds for amplitude modulation detection were obtained from four subjects at frequencies of 2, 4, 6, 8, and 10 kHz for sensation levels of 15, 30, 45, and 60 dB and modulation rates of 2, 4, and 8 Hz. High-frequency difference limens calculated from amplitude modulation thresholds were found to change nonmonotonically as a function of sensation level, independent of modulation rate. This nonmonotonic relation stemmed mainly from a gradual reduction of the difference limen at the lowest sensation level with increasing frequency. Difference limens for pulsed tone discrimination were also measured in two of the subjects at 2, 6, and 10 kHz and sensation levels of 15, 30, 45, and 60 dB. The relation between intensity discrimination and sensation level was similar to that found for amplitude modulation detection. These findings are interpreted as indicating that the nonmonotonic relation between sensation level and intensity resolution is a general characteristic of stimulus processing at higher frequencies.

Adult↗

Role of primate visual area V4 in the processing of 3-D shape characteristics defined by disparity.

We studied the responses of V4 neurons in awake, fixating monkeys to a diverse set of stereoscopic stimuli, including zero-order disparity (frontoparallel) stimuli, surfaces oriented in depth, and convex and concave shapes presented at various mean disparities. The responses of many V4 cells were significantly modulated across each of these stimulus subsets. In general, V4 cells were broadly tuned for zero-order disparity, and at any given disparity value, about four-fifths of the cells responded significantly above background. The response modulation by flat surfaces oriented in depth was significant for about one-quarter of cells, and the responses of about one-third of the cells were significantly modulated by convex or concave surfaces at various mean disparities. However, we encountered no cells that unambiguously distinguished a given three-dimensional (3-D) shape independent of mean disparity. Thus 3-D shapes defined by disparity are unlikely to be represented explicitly at the level of individual V4 cells. Nonetheless, V4 cells likely play an important role in the processing of 3-D shape characteristics defined by disparity as a part of a distributed network.

Analysis of Variance↗

Nonlinear encoding of tactile patterns in the barrel cortex.

Cells in the rodent barrel cortex respond to vibrissa deflection with a brief excitatory component and a longer suppressive component. The response to a given deflection is thus scaled because of suppression induced by a preceding deflection, causing the neuronal response to be linked to the temporal properties of the peripheral stimulus. A paired-deflection stimulus was used to characterize the postexcitatory suppression and a 3-deflection stimulus was used to investigate the nonlinear response to patterns of whisker deflections in barbiturate-anesthetized Sprague-Dawley rats. The postexcitatory suppression was not dependent on a sensory-evoked action potential to the first deflection, implying that it is likely a subthreshold property of the network. The suppression induced by a deflection served to suppress both the excitatory and suppressive components of a subsequent neuronal response, thus effectively disinhibiting it. Two different response properties were observed in the recorded cells. Approximately 65% responded to a vibrissa deflection with an excitatory component followed by a suppressive component and 35% responded with excitation, suppression, and a subsequent rebound in excitation. Based on these observations of postexcitatory dynamics, a prediction method was used to estimate neuronal responses to more complex stimulus trains. Using the 2nd-order representation obtained from the paired-deflection stimulus, responses to general periodic deflection patterns were well predicted. A higher cutoff frequency was predicted for rebound cells compared with cells not exhibiting rebound excitation, consistent with experimental observations. The method also predicted the response of neurons to a random aperiodic deflection pattern. Therefore the temporal structure of cortical dynamics after a single deflection dictates the response to complex temporal patterns, which are more representative of stimuli encountered under natural conditions.

Algorithms↗

Increase of neuronal response variability at higher processing levels as revealed by simultaneous recordings.

A key problem for neuronal information processing is the variability of spike trains, something that is likely to constrain the encoding of sensory signals. We measured interspike-interval variability (coefficient of variation) as well as spike-count variability (Fano factor) in the metathoracic auditory system of locusts. We performed simultaneous intracellular recordings at the first three processing levels to establish identical physiological conditions. This allows us to assess whether variability is generated anew or is reduced during synaptic transmission and processing. Both the interspike-interval variability as well as the spike-count variability revealed similar trends and showed an increase from the periphery to higher processing levels. This result was confirmed by single-cell recordings. A comparison of ascending interneurons coding for sound direction and those encoding sound patterns showed that the latter respond more reliably to repeated stimulus presentations. In general, the variability of spiking responses was much lower than expected from a Poisson process. Furthermore, we observed a strong dependence of variability on the spike rate, which differed at the three levels investigated. The differences in spike rates account for most of the differences in variability observed between processing levels. For auditory receptors, we found a good agreement between the Fano factor and the squared coefficient of variation, suggesting similarities to a renewal process of spike generation at the periphery. At the level of interneurons, the Fano factor was lower than the squared coefficient of variation; this indicates a higher reliability than expected from the interspike-interval distribution.

Acoustic Stimulation↗

Control of size and excitability of mechanosensory receptive fields in dorsal column nuclei by homolateral dorsal horn neurons.

Both accidental and experimental lesions of the spinal cord suggest that neuronal processes occurring in the spinal cord modify the relay of information through the dorsal column-lemniscal pathway. How such interactions might occur has not been adequately explained. To address this issue, the receptive fields of mechanosensory neurons of the dorsal column nuclei were studied before and after manipulation of the spinal dorsal horn. After either a cervical or lumbar laminectomy and exposure of the dorsal column nuclei in anesthetized cats, the representation of the hindlimb or of the forelimb was defined by multiunit recordings in both the dorsal column nuclei and in the ipsilateral spinal cord. Next, a single cell was isolated in the dorsal column nuclei, and its receptive field carefully defined. Each cell could be activated by light mechanical stimuli from a well-defined cutaneous receptive field. Generally the adequate stimulus was movement of a few hairs or rapid skin indentation. Subsequently a pipette containing either lidocaine or cobalt chloride was lowered into the ipsilateral dorsal horn at the site in the somatosensory representation in the spinal cord corresponding to the receptive field of the neuron isolated in the dorsal column nuclei. Injection of several hundred nanoliters of either lidocaine or cobalt chloride into the dorsal horn produced an enlargement of the receptive field of the neuron being studied in the dorsal column nuclei. The experiment was repeated 16 times, and receptive field enlargements of 147-563% were observed in 15 cases. These data suggest that the dorsal horn exerts a tonic inhibitory control on the mechanosensory signals relayed through the dorsal column-lemniscal pathway. Because published data from other laboratories have shown that receptive field size is controlled by signals arising from the skin, we infer that the control of neuronal excitability, receptive field size and location for lemniscal neurons is determined by tonic afferent activity that is relayed through a synapse in the dorsal horn. This influence of dorsal horn neurons on the relay of mechanosensory information through the lemniscal pathways must modify our traditional views concerning the relative independence of these two systems.

Animals↗

Light-dark asymmetries in the Craik-Cornsweet-O'Brien illusion and a new model of brightness coding.

With the aid of a matching technique, the magnitude of induced brightness in bars bordered with Craik-Cornsweet-O'Brien (CCOB) edges was investigated as a function of the width and amplitude of those edges. Data were collected for stimuli with the sloping part of the edge on both the inside and outside of the bar, and also for stimuli with both positive-going and negative-going edges. The results confirmed previous reports that induced brightness was greater for CCOB stimuli with negative-going, as opposed to positive-going, edges and greater for CCOB stimuli whose edges contained outer, as opposed to inner gradients. A model of brightness coding is offered to provide an explanation for the specific anisotropies observed, as well as the general effects of stimulus amplitude and width on induced brightness. The model assumes that a symbolic description of brightness is generated separately from each of a number of different-sized 2DG (second difference of a Gaussian) filters, and the resulting brightness profile obtained by averaging across the separate descriptions. The ability of other brightness models to account for the data is also discussed.

Contrast Sensitivity↗

In search of the emotional self: an fMRI study using positive and negative emotional words.

OBJECTIVE: The authors used functional magnetic resonance imaging (fMRI) to define the neural regions mediating self-referential processing of emotional stimuli and to explore how these regions are influenced by the emotional valence of the stimulus. METHOD: Ten healthy subjects were presented with words describing positive and negative personality traits during fMRI scanning in three different conditions. In the self-referential processing condition, subjects judged whether they thought each trait described them. In the other-referential processing condition, subjects judged whether the stimulus described a generally desirable trait. In the letter-recognition control condition, subjects indicated whether the word contained a specific target letter. RESULTS: The self-referential condition induced bilateral activation in the dorsomedial prefrontal cortex, whereas the other-referential condition induced activation in lateral prefrontal areas. Activation in the right dorsomedial prefrontal cortex was unique to the self-referential condition regardless of the valence of the words, although positive words produced a more robust activation than did negative words. In the self-referential condition, differences between the processing of positive and negative words were seen in regions outside the medial frontal cortex, with reductions in the insula, temporal and occipital regions, and inferior parietal regions associated with negative words. CONCLUSIONS: A widely distributed network of brain areas contributes to emotional processing. Among these regions, the right dorsomedial prefrontal cortex is one main area mediating self-reference. By providing a personal perspective in the evaluation of emotional stimuli, the right dorsomedial prefrontal cortex may mediate cognitive processes, such as those involved in psychotherapy, that guide self-regulation of emotional experience.

Adult↗

Neural mechanisms of the ultrafast activities.

A brief review of previous studies is presented on ultra-fast activities > 300 Hz (high frequency oscillations, HFOs) overlying the cortical response in the somatosensory evoked potential (SEP) or magnetic field (SEF). The characteristics of somatosensory HFOs are described in terms of reproducibility and origin (area 3b and 1) of the HFOs, changes during a wake-sleep cycle, effects of higher stimulus rate or tactile interference, etc. Also, several hypotheses on the neural mechanisms of the HFOs are introduced; the early HFO burst is probably generated from action potentials of thalamocortical fibers at the time when they arrive at the area 3b (and 1), since this component is resistant to higher stimulus rate > 10Hz or general anesthesia: by contrast, the late HFO burst is sensitive to higher stimulus rate, reflecting activities of a postsynaptic neural network in the somatosensory cortices, area 3b and 1. As to possible mechanisms of the late HFO burst genesis, an interneuron hypothesis, a fast inhibitory postsynaptic potential (IPSP) hypothesis of the pyramidal cell and a chattering cell hypothesis will be discussed on the basis of physiological and pathological features of the somatosensory HFOs.

Action Potentials↗

Non-infantile neuronopathic Gaucher's disease: a clinicopathologic study.

Two siblings with Gaucher's disease developed a chronic, slowly progressive neurologic disorder in early adult life. Stimulus-sensitive myoclonus, generalized seizures, supranuclear gaze palsies, and cerebellar ataxia were the main clinical features. Autopsy disclosed perivascular Gaucher cells in the brain, and nerve cell loss and neuronophagia in the brainstem, cerebellum, and spinal cord. From these observations and the literature, there seem to be three clinically distinct neurologic syndromes in Gaucher's disease, depending on the age at which symptoms begin, but the neuropathologic changes are essentially the same in all of them. A modified classification of Gaucher's disease, based on these observations, is proposed.

Adult↗

The effects of differential and lag reinforcement schedules on varied verbal responding by individuals with autism.

Variability has been shown to be a reinforceable dimension of behavior. One procedure that has been demonstrated to increase variability in basic research is the lag reinforcement schedule. On this type of schedule, a response is reinforced if it differs from a specified number of previous responses. Lag schedules are rarely used, however, for increasing response variability in applied settings. The purpose of the present study was to investigate the effects of a lag schedule of differential reinforcement on varied and appropriate verbal responding to social questions by 3 males with autism. A reversal design with a multiple baseline across subjects was used to evaluate the effects of the lag schedule. During baseline, differential reinforcement of appropriate responding (DRA) resulted in little or no varied responding. During the intervention, a Lag 1 requirement was added to the DRA (Lag 1/DRA) resulting in an increase in the percentage of trials with varied and appropriate verbal responding for 2 of the 3 participants. In addition, an increase in the cumulative number of novel verbal responses was also observed for the same 2 participants. These results are discussed in terms of reinforcement schedules that support variability, generalization, and potential stimulus control over varied responding.

Adult↗

REACTION TIME AS A FUNCTION OF STIMULUS INTENSITY FOR THE MONKEY.

Monkeys were trained to release a telegraph key in response to a visual or auditory stimulus. The latency of the key release response was measured for different stimulus intensities. In general, the relation between latency and intensity is inverse and exponential with greater variability of latency at the lower intensities. Some preliminary data involving differential reinforcement of short latencies are presented.

Animals↗