Shortening of subjective visual intervals followed by repetitive stimulation

Our previous research demonstrated that repetitive tone stimulation shortened the perceived duration of the preceding auditory time interval. In this study, we examined whether repetitive visual stimulation influences the perception of preceding visual time intervals. Results showed that a time interval followed by a high-frequency visual flicker was perceived as shorter than that followed by a low-frequency visual flicker. The perceived duration decreased as the frequency of the visual flicker increased. The visual flicker presented in one hemifield shortened the apparent time interval in the other hemifield. A final experiment showed that repetitive tone stimulation also shortened the perceived duration of preceding visual time intervals. We concluded that visual flicker shortened the perceived duration of preceding visual time intervals in the same way as repetitive auditory stimulation shortened the subjective duration of preceding tones.     

CRITICAL FREQUENCY OF FLICKER AS A FUNCTION OF INTENSITY OF ILLUMINATION FOR THE EYE OF THE BEE

The bee''s characteristic response to a movement of its visual field is used for the study of the relation between critical frequency of flicker and illumination. The critical flicker frequency varies with illumination in such a way that with increasing flicker frequency the intensity of illumination must be increased to produce a threshold response in the bee. The illuminations required to give a response in a bee at different flicker frequencies closely correspond to the intensities for threshold response in visual acuity tests. This is due to the different thresholds of excitability of the elements of the ommatidial mosaic. An analysis of the variation of the values for threshold intensities at the several flicker frequencies shows that the variation depends upon flicker frequency and upon the number of elements functioning at different intensities.     

The visual cortex produces gamma band echo in response to broadband visual flicker

The aim of this study is to uncover the network dynamics of the human visual cortex by driving it with a broadband random visual flicker. We here applied a broadband flicker (1–720 Hz) while measuring the MEG and then estimated the temporal response function (TRF) between the visual input and the MEG response. This TRF revealed an early response in the 40–60 Hz gamma range as well as in the 8–12 Hz alpha band. While the gamma band response is novel, the latter has been termed the alpha band perceptual echo. The gamma echo preceded the alpha perceptual echo. The dominant frequency of the gamma echo was subject-specific thereby reflecting the individual dynamical properties of the early visual cortex. To understand the neuronal mechanisms generating the gamma echo, we implemented a pyramidal-interneuron gamma (PING) model that produces gamma oscillations in the presence of constant input currents. Applying a broadband input current mimicking the visual stimulation allowed us to estimate TRF between the input current and the population response (akin to the local field potentials). The TRF revealed a gamma echo that was similar to the one we observed in the MEG data. Our results suggest that the visual gamma echo can be explained by the dynamics of the PING model even in the absence of sustained gamma oscillations.     

Effects of taurine supplementation on VDT work induced visual stress

Summary. In order to evaluate the effects of dietary taurine supplementation on visual fatigue induced by visual display terminals (VDT) work, 25 male college students aged from 20 to 24 years who were not engaged in VDT work were selected to participate in the study. Volunteers were randomly assigned to either the taurine supplementation (n=13) or the placebo supplementation control group (n=12). Before and after 12 days of taurine (3g/day) or placebo supplementation, two identical 2.5-hr VDT work tests were performed while recording the P100, N75 and N145 latencies and P100 amplitude of pattern visual evoked potential (PVEP) and the frequency of critical flicker fusion (CFF). Following 2.5-hr of VDT work, the P100 and N75 latencies of PVEP increased (P<0.01) while the P100 amplitude decreased significantly (P<0.01). The frequency of CFF also reduced significantly (P<0.01). After 12 days of taurine supplementation, the reduction in P100 amplitude after VDT work alleviated significantly (P<0.05). The results suggest that taurine supplementation alleviates visual fatigue induced by VDT work.     

稳态视觉诱发电位神经网络间的相互作用

稳态视觉诱发电位(steady-state visual evoked potential,SSVEP)不同于瞬态视觉诱发电位,有其独特的产生机理。当用两种不同频率的闪光同时刺激时,每种频率闪光诱发的SSVEP之间是否会相互影响?它们与对应单一频率闪光刺激时产生的SSVEP的关系怎样?作者用!波段频率8.3Hz与"波段频率20Hz的闪光分别及同时刺激10个被试的双眼,发现在同时刺激时,每种频率闪光的SSVEP比对应单频刺激时的SSVEP略小,但位置分布无明显变化。这说明不同频率SSVEP的产生网络是彼此独立的,在被同时激活时,每个网络产生的信号并不相互影响。     

INTENSITY AND CRITICAL FREQUENCY FOR VISUAL FLICKER

Using the rotating striped cylinder device previously employed for determination of the flicker response function with lower animals, corresponding measurements have been made with human observers. The curves based upon the relation between critical flash frequency and critical intensity for the signalling of the recognition of flicker have the properties of human flicker fusion data as obtained by other methods. They also have the quantitative properties of the flicker curves provided by the motor responses of insects and fishes to the seen movement of flashes. This applies to the variation found in repeated measurements as well as to the nature of the analytical function describing the connection between flash frequency and intensity. The data for human visual flicker and those for the responses of lower animals are therefore essentially homologous.     

Approach behaviour and embryonic visual experience in chicks: studies on the effect of rate of visual flicker

It has been demonstrated that visual stimulation during the latter part of embryonic development will have its effect on subsequent approach behaviour in the chick. Stimulation here had been of a non-specific type, i.e. mere presence or absence of illumination. This study was conducted to see how much specific stimulation like visual flicker applied during the latter part of embryonic development would affect approach to the same or similar stimuli. In experiment 1 extremely slow flicker (6·6 and 20 c/min) was applied to the eggs under incubation. Treatment groups were tested for approach on flickering and non-flickering stimuli after hatching. Results show that exposing the eggs to flicker has an effect on approach behaviour. Groups that received flicker at a rate of 20 c/min approach faster than those which received flicker at the rate of 6·6 c/min. A significant improvement over trials was only found in the group which received flicker of 20 c/min during the embryonic period. In experiment 2 which employed a range of very much faster flicker no significant treatment effects became apparent. These results suggest that visual flicker as embryonic stimulation is effective in priming the embryo to yield better approach performance after hatching. Results of experiment 2 indicate that the effect of flicker as embryonic stimulation may operate over a certain range in affecting subsequent approach performance.     

The Frequency-Response Electroretinogram Distinguishes Cone and Abnormal Rod Function in rd12 Mice

Early studies on Rpe65 knockout mice reported that remaining visual function was attributable to cone function. However, this finding has been challenged more and more as time has passed. Electroretinograms (ERGs) showed that rd12 mice, a spontaneous animal model of RPE65 Leber’s congenital amaurosis, had sizeable photopic responses. Unfortunately, the recorded ERG waveform was difficult to interpret because of a remarkably delayed peak-time, which resembles a rod response more than a cone response. Here, we compare flicker ERGs in animals with normal rod and cone function (C57BL/6J mice), pure rod function (cpfl5 mice), and pure cone function (Rho^-/- mice) under different adaptation levels and stimulus intensities. These responses were then compared with those obtained from rd12 mice. Our results showed that normal rods respond to low frequency flicker (5 and 15 Hz) and that normal cones respond to both low and high frequency flicker (5–35 Hz). As was seen in cpfl5 mice, rd12 mice had recordable responses to low frequency flicker (5 and 15Hz), but not to high frequency flicker (25 and 35 Hz). We hypothesize that abnormal rods may be the source of residual vision in rd12 mice, which is proved correct here with double mutant rd12mice. In this study, we show, for the first time, that frequency-response ERGs can effectively distinguish cone- and rod-driven responses in the rd12 mouse. It is another simple and valid method for evaluating the respective contributions of retinal rods and cones.     

Opponent and nonopponent contributions to the zebrafish electroretinogram using heterochromatic flicker photometry

While some lower vertebrates, such as zebrafish, do not appear to possess anatomically separate pathways of processing visual information (such as M-pathways and P-pathways), it is believed that separate processing of the visual stimulus (such as luminance and chromatic processing) is a basic requirement of vertebrate vision. In this study, spectral sensitivity functions were obtained from electroretinogram responses to heterochromatic flicker photometry stimuli at several flicker rates, including a low flicker rate (2 Hz), in an attempt to predominantly stimulate chromatic processes and a high flicker rate (16 Hz), in an attempt to predominantly stimulate luminance processes. In addition, chromatic adaptation was used to isolate and examine the temporal properties of the different cone-type contributions to the electroretinogram response. Spectral sensitivity functions based on responses to heterochromatic stimuli of a low flicker rate appeared to receive both opponent and nonopponent contributions; however, when the stimulus flicker rate was high, spectral sensitivity appeared to be a function of only nonopponent mechanisms. Also, the differences in cone contributions to the spectral sensitivity functions across the different flicker rates appear to be related to the temporal properties of the cone contributions to the electroretinogram response.     

A model for the origin and properties of flicker-induced geometric phosphenes

We present a model for flicker phosphenes, the spontaneous appearance of geometric patterns in the visual field when a subject is exposed to diffuse flickering light. We suggest that the phenomenon results from interaction of cortical lateral inhibition with resonant periodic stimuli. We find that the best temporal frequency for eliciting phosphenes is a multiple of intrinsic (damped) oscillatory rhythms in the cortex. We show how both the quantitative and qualitative aspects of the patterns change with frequency of stimulation and provide an explanation for these differences. We use Floquet theory combined with the theory of pattern formation to derive the parameter regimes where the phosphenes occur. We use symmetric bifurcation theory to show why low frequency flicker should produce hexagonal patterns while high frequency produces pinwheels, targets, and spirals.     

Effect of the Fatigue Induced by a 110-km Ultramarathon on Tibial Impact Acceleration and Lower Leg Kinematics

Ultramarathon runners are exposed to a high number of impact shocks and to severe neuromuscular fatigue. Runners may manage mechanical stress and muscle fatigue by changing their running kinematics. Our purposes were to study (i) the effects of a 110-km mountain ultramarathon (MUM) on tibial shock acceleration and lower limb kinematics, and (ii) whether kinematic changes are modulated according to the severity of neuromuscular fatigue. Twenty-three runners participated in the study. Pre- and post-MUM, neuromuscular tests were performed to assess knee extensor (KE) and plantar flexor (PF) central and peripheral fatigue, and a treadmill running bouts was completed during which step frequency, peak acceleration, median frequency and impact frequency content were measured from tibial acceleration, as well as foot-to-treadmill, tibia-to-treadmill, and ankle flexion angles at initial contact, and ankle range of motion using video analysis. Large neuromuscular fatigue, including peripheral changes and deficits in voluntary activation, was observed in KE and PF. MVC decrements of ~35% for KE and of ~28% for PF were noted. Among biomechanical variables, step frequency increased by ~2.7% and the ankle range of motion decreased by ~4.1% post-MUM. Runners adopting a non rearfoot strike pre-MUM adopted a less plantarflexed foot strike pattern post-MUM while those adopting a rearfoot strike pre-MUM tended to adopt a less dorsiflexed foot strike pattern post-MUM. Positive correlations were observed between percent changes in peripheral PF fatigue and the ankle range of motion. Peripheral PF fatigue was also significantly correlated to both percent changes in step frequency and the ankle angle at contact. This study suggests that in a fatigued state, ultratrail runners use compensatory/protective adjustments leading to a flatter foot landing and this is done in a fatigue dose-dependent manner. This strategy may aim at minimizing the overall load applied to the musculoskeletal system, including impact shock and muscle stretch.     

Conscious awareness of flicker in humans involves frontal and parietal cortex

Even when confined to the same spatial location, flickering and steady light evoke very different conscious experiences because of their distinct temporal patterns. The neural basis of such differences in subjective experience remains uncertain . Here, we used functional MRI in humans to examine the neural structures involved in awareness of flicker. Participants viewed a single point source of light that flickered at the critical flicker fusion (CFF) threshold, where the same stimulus is sometimes perceived as flickering and sometimes as steady (fused) . We were thus able to compare brain activity for conscious percepts that differed qualitatively (flickering or fused) but were evoked by identical physical stimuli. Greater brain activation was observed on flicker (versus fused) trials in regions of frontal and parietal cortex previously associated with visual awareness in tasks that did not require detection of temporal patterns . In contrast, greater activation was observed on fused (versus flicker) trials in occipital extrastriate cortex. Our findings indicate that activity of higher-level cortical areas is important for awareness of temporally distinct visual events in the context of a nonspatial task, and they thus suggest that frontal and parietal regions may play a general role in visual awareness.     

THRESHOLD INTENSITY OF ILLUMINATION AND FLICKER FREQUENCY FOR THE EYE OF THE SUN-FISH

The sun-fish Lepomis responds to a moving system of stripes by a motion of its body. By changing the velocity of motion of the stripe system different flicker frequencies can be produced and thus the relation of flicker frequency to critical intensity of illumination can be studied. Threshold illumination varies with flicker frequency in such a way that with increasing flicker frequency the intensity of illumination must be increased to produce a threshold response in the fish. The curve of critical illumination as a function of frequency is made up of two distinct parts. For an intensity range below 0.04 millilambert and flicker frequencies below 10 per second, the rods are in function. For higher intensities and flicker frequencies above 10, the cones come into play. The maximum frequency of flicker which can be perceived by the fish''s eye is slightly above 50 per second. The flicker curve for the eye of Lepomis can easily be compared with that for the human eye. The extent of the curve for the fish is greater at low illuminations, the fish being capable of distinguishing flicker at illuminations lower than can the human eye. The transition of rod vision to cone vision occurs for the fish and for the human eye at the same intensity and flicker frequency. The maximum frequency of flicker which can be perceived is for both about the same.     

Spatially localized distortions of event time

A fundamental question about the perception of time is whether the neural mechanisms underlying temporal judgements are universal and centralized in the brain or modality specific and distributed. Time perception has traditionally been thought to be entirely dissociated from spatial vision. Here we show that the apparent duration of a dynamic stimulus can be manipulated in a local region of visual space by adapting to oscillatory motion or flicker. This implicates spatially localized temporal mechanisms in duration perception. We do not see concomitant changes in the time of onset or offset of the test patterns, demonstrating a direct local effect on duration perception rather than an indirect effect on the time course of neural processing. The effects of adaptation on duration perception can also be dissociated from motion or flicker perception per se. Although 20 Hz adaptation reduces both the apparent temporal frequency and duration of a 10 Hz test stimulus, 5 Hz adaptation increases apparent temporal frequency but has little effect on duration perception. We conclude that there is a peripheral, spatially localized, essentially visual component involved in sensing the duration of visual events.     

ON CRITICAL FREQUENCY AND CRITICAL ILLUMINATION FOR RESPONSE TO FLICKERED LIGHT

The curve of mean critical flicker frequency as a function of illumination has been determined for the reaction of the sunfish Lepomis to flicker. It exhibits expected quantitative disagreements with the curve of mean critical illumination as a function of flicker frequency in the same organism. The form of the dependence of the variation of critical frequency of flicker upon illumination can be predicted from a knowledge of the way in which variation of critical illumination depends upon flicker frequency. It is pointed out that these findings have an important bearing upon the interpretation of the data of intensity discrimination.     

Temporal properties of the lens eyes of the box jellyfish Tripedalia cystophora

Box jellyfish (Cubomedusae) are visually orientating animals which posses a total of 24 eyes of 4 morphological types; 2 pigment cup eyes (pit eye and slit eye) and 2 lens eyes [upper lens-eye (ule) and lower lens-eye (lle)]. In this study, we use electroretinograms (ERGs) to explore temporal properties of the two lens eyes. We find that the ERG of both lens eyes are complex and using sinusoidal flicker stimuli we find that both lens eyes have slow temporal resolution. The average flicker fusion frequency (FFF) was found to be approximately 10 Hz for the ule and 8 Hz for the lle. Differences in the FFF and response patterns between the two lens eyes suggest that the ule and lle filter information differently in the temporal domain and thus are tuned to perform different visual tasks. The data collected in this study support the idea that the visual system of box jellyfish is a collection of special purpose eyes.     

How Long Depends on How Fast—Perceived Flicker Dilates Subjective Duration

How do humans perceive the passage of time and the duration of events without a dedicated sensory system for timing? Previous studies have demonstrated that when a stimulus changes over time, its duration is subjectively dilated, indicating that duration judgments are based on the number of changes within an interval. In this study, we tested predictions derived from three different accounts describing the relation between a changing stimulus and its subjective duration as either based on (1) the objective rate of changes of the stimulus, (2) the perceived saliency of the changes, or (3) the neural energy expended in processing the stimulus. We used visual stimuli flickering at different frequencies (4–166 Hz) to study how the number of changes affects subjective duration. To this end, we assessed the subjective duration of these stimuli and measured participants'' behavioral flicker fusion threshold (the highest frequency perceived as flicker), as well as their threshold for a frequency-specific neural response to the flicker using EEG. We found that only consciously perceived flicker dilated perceived duration, such that a 2 s long stimulus flickering at 4 Hz was perceived as lasting as long as a 2.7 s steady stimulus. This effect was most pronounced at the slowest flicker frequencies, at which participants reported the most consistent flicker perception. Flicker frequencies higher than the flicker fusion threshold did not affect perceived duration at all, even if they evoked a significant frequency-specific neural response. In sum, our findings indicate that time perception in the peri-second range is driven by the subjective saliency of the stimulus'' temporal features rather than the objective rate of stimulus changes or the neural response to the changes.     

Temporal modulation of luminance adapts time constant of fly movement detectors

The time constant of movement detectors in the fly visual system has been proposed to adapt in response to moving stimuli (de Ruyter van Steveninck et al. 1986). The objective of the present study is to analyse, whether this adaptation can be induced as well, if the luminance of a stationary uniform field is modulated in time. The experiments were done on motion-sensitive wide-field neurones of the lobula plate, the posterior part of the third visual ganglion of the blowfly, calliphora erythrocephala. These cells are assumed to receive input from large retinotopic arrays of movement detectors. In order to demonstrate that our results concern the properties of the movement detectors rather than those of a particular wide-field cell we recorded from two different types of them, the H1- and the HSE-cell. Both cell types respond to a brief movement stimulus in their preferred direction with a transient excitation. This response decays about exponentially. The time constant of this decay reflects, in a first approximation, the time constant of the presynaptic movement detectors. It was determined after prestimulation of the cell by the following stimuli: (a) periodic stationary grating; (b) uniform field, the intensity of which was modulated sinusoidally in time (flicker stimulation); (c) periodic grating moving front-to-back; (d) periodic grating moving back-to-front. The decay of the response is significantly faster not only after movement but also after flicker stimulation as compared with pre-stimulation with a stationary stimulus. This is interpreted as an adaptation of the movement detector's time constant. The finding that flicker stimulation also leads to an adaptation shows that movement is not necessary for this process. Instead the adaptation of the time constant appears to be governed mainly by the temporal modulation (i.e., contrast frequency) of the signal in each visual channel.     

Critical flicker detection frequency and double pulse recognition threshold do not depend on the spectral properties of stimuli

We have measured the critical flicker detection frequency (CFDF) and double pulse recognition threshold (DPT) using three LEDs with power peaks at 460, 525 and 625 nm for target illumination. Brightness equalization was performed by customized heterochromatic flicker photometry (cHFP). Reference luminance levels were 170 cd/m² (blue LED, 60 subjects), 4 cd/m² (green LED, 20 subjects), and 1 cd/m² (green LED, 20 subjects). The measurement at 1 cd/m² was preceded by 15 min of dark adaptation. The angle of view for the target was 3°, and the duration of stimuli was 1 ms. An experimental pulse generator with three channels and a projector was used. No differences in CFDF at different spectral properties of stimulus were observed at all three levels of luminance. Thus, it is concluded that temporal vision resolution does not depend on the spectral properties of visual stimuli.     

Compressive fatigue properties of a commercially available acrylic bone cement for vertebroplasty

Acrylic bone cements are widely used for fixation of joint prostheses as well as for vertebral body augmentation procedures of vertebroplasty and balloon kyphoplasty, with the cement zone(s) being subjected to repeated mechanical loading in each of these applications. Although, in vertebroplasty and balloon kyphoplasty, the cement zone is exposed to mainly cyclical compressive load, the compressive fatigue properties of acrylic bone cements used in these procedures are yet to be determined. The purposes of the present study were to determine the compressive fatigue properties of a commercially available cement brand used in vertebroplasty, including the effect of frequency on these properties; to identify the cement failure modes under compressive cyclical load; and to introduce a screening method that may be used to shorten the lengthy character of the standardized fatigue tests. Osteopal \({^\circledR } \mathrm{V}\) was used as the model cement in this study. The combinations of maximum stress and frequency used were 50.0, 55.0, 60.0, 62.5 and 75.5 MPa at 2 Hz; and of 40.0, 55.0, 60.0, 62.5 or 75.5 MPa at 10 Hz. Through analysis of nominal strain-number of loading cycles results, three cement failure modes were identified. The estimated mean fatigue limit at 2 Hz (55.4 MPa) was significantly higher than that at 10 Hz (41.1 MPa). The estimated fatigue limit at 2 Hz is much higher than stresses commonly found in the spine and also higher than that for other acrylic bone cements tested in a full tension–compression fatigue test, which indicates that tension–compression fatigue testing may substantially underestimate the performance of cements intended for vertebroplasty. A screening method was introduced which may be used to shorten the time spent in performing compressive fatigue tests on specimens of acrylic bone cement for use in vertebral body augmentation procedures.